SHOGoiN Cell Marker : From Gene Expression Data

No.Sample IdSHOGoiN Cell IdSource OrganismSource Cell TypeSource TissueProject IdData IDAssay Instrumentation IDAssay InstrumentationAssay Description
1GSM12689609000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032910GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
2GSM1268961 9000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032911GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
3GSM12689629000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032912GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
4GSM12689649000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032914GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
5GSM12689659000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032915GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
6GSM12689669000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032916GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
7GSM12689679000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032917GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
8GSM12689689000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032918GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
9GSM12689699000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032919GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
10GSM12689709000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032920GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
11GSM12689719000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032921GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
12GSM12689729000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032922GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
13GSM12689739000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032923GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
14GSM12689749000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032924GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
15GSM12689769000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032926GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
16GSM12689779000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032927GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
17GSM12689789000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032928GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
18GSM12689799000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032929GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
19GSM12689809000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032930GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
20GSM12689819000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032931GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
21GSM12689839000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032933GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
22GSM12689859000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032935GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
23GSM12689869000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032936GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
24GSM12689879000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032937GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
25GSM12689889000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032938GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
26GSM12689899000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032939GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
27GSM12689909000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032940GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
28GSM12689919000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032941GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
29GSM12689929000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032942GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
30GSM12689939000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032943GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
31GSM12689949000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032944GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
32GSM12689959000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032945GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
33GSM12689969000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032946GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
34GSM12689979000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032947GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
35GSM12689989000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032948GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
36GSM12689999000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032949GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
37GSM12690009000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032950GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
38GSM12690019000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032951GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
39GSM12690029000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032952GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
40GSM12690039000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032953GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
41GSM12690049000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032954GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
42GSM12690069000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032956GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
43GSM12690079000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032957GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
44GSM12690089000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032958GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
45GSM12690109000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032960GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
46GSM12690119000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032961GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
47GSM12690129000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032962GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
48GSM12690139000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032963GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
49GSM12690149000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032964GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
50GSM12690159000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032965GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
51GSM12690169000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032966GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
52GSM12690179000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032967GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
53GSM12690189000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032968GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
54GSM12690199000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032969GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
55GSM12690209000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032970GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
56GSM12690219000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032971GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
57GSM12690229000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032972GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
58GSM12690239000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032973GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
59GSM12690249000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032974GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
60GSM12690259000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032975GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
61GSM12690269000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032976GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
62GSM12690279000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032977GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
63GSM12690289000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032978GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
64GSM12690309000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032980GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
65GSM12690319000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032981GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
66GSM12690329000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032982GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
67GSM12690339000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032983GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
68GSM12690349000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032984GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
69GSM12690359000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032985GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
70GSM12690389000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032988GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
71GSM12690399000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032989GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
72GSM12690409000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032990GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
73GSM12690419000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032991GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
74GSM12690429000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032992GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
75GSM12690449000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032994GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
76GSM12690459000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032995GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
77GSM12690469000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032996GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
78GSM12690479000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032997GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
79GSM12690489000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032998GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
80GSM12690499000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1032999GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
81GSM12690519000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1033001GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
82GSM12690529000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1033002GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
83GSM12690539000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1033003GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
84GSM12690559000201-738HumanMyoblast T0Skeletal Muscle TissueSRP033135SRR1033005GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
85GSM12690569000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033006GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
86GSM12690589000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033008GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
87GSM12690599000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033009GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
88GSM12690609000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033010GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
89GSM12690629000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033012GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
90GSM12690639000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033013GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
91GSM12690649000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033014GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
92GSM12690659000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033015GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
93GSM12690689000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033018GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
94GSM12690699000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033019GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
95GSM12690709000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033020GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
96GSM12690729000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033022GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
97GSM12690739000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033023GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
98GSM12690749000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033024GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
99GSM12690759000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033025GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
100GSM12690769000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033026GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
101GSM12690789000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033028GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
102GSM12690809000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033030GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
103GSM12690819000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033031GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
104GSM12690829000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033032GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
105GSM12690849000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033034GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
106GSM12690869000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033036GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
107GSM12690879000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033037GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
108GSM12690889000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033038GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
109GSM12690899000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033039GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
110GSM12690909000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033040GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
111GSM12690919000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033041GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
112GSM12690929000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033042GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
113GSM12690939000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033043GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
114GSM12690949000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033044GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
115GSM12690959000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033045GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
116GSM12690969000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033046GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
117GSM12690979000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033047GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
118GSM12690989000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033048GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
119GSM12690999000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033049GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
120GSM12691009000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033050GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
121GSM12691019000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033051GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
122GSM12691029000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033052GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
123GSM12691049000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033054GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
124GSM12691059000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033055GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
125GSM12691079000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033057GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
126GSM12691089000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033058GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
127GSM12691109000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033060GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
128GSM12691129000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033062GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
129GSM12691139000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033063GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
130GSM12691149000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033064GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
131GSM12691159000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033065GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
132GSM12691169000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033066GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
133GSM12691179000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033067GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
134GSM12691189000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033068GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
135GSM12691199000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033069GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
136GSM12691209000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033070GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
137GSM12691219000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033071GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
138GSM12691229000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033072GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
139GSM12691239000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033073GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
140GSM12691249000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033074GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
141GSM12691259000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033075GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
142GSM12691269000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033076GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
143GSM12691279000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033077GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
144GSM12691289000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033078GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
145GSM12691299000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033079GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
146GSM12691309000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033080GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
147GSM12691319000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033081GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
148GSM12691329000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033082GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
149GSM12691339000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033083GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
150GSM12691359000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033085GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
151GSM12691379000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033087GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
152GSM12691389000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033088GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
153GSM12691399000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033089GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
154GSM12691409000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033090GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
155GSM12691419000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033091GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
156GSM12691429000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033092GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
157GSM12691449000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033094GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
158GSM12691469000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033096GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
159GSM12691489000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033098GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
160GSM12691519000201-738HumanMyoblast T24Skeletal Muscle TissueSRP033135SRR1033101GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
161GSM12691529000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033102GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
162GSM12691539000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033103GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
163GSM12691549000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033104GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
164GSM12691559000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033105GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
165GSM12691569000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033106GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
166GSM12691579000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033107GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
167GSM12691589000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033108GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
168GSM12691599000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033109GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
169GSM12691609000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033110GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
170GSM12691619000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033111GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
171GSM12691629000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033112GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
172GSM12691639000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033113GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
173GSM12691649000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033114GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
174GSM12691659000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033115GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
175GSM12691669000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033116GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
176GSM12691679000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033117GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
177GSM12691689000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033118GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
178GSM12691699000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033119GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
179GSM12691709000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033120GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
180GSM12691719000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033121GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
181GSM12691739000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033123GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
182GSM12691749000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033124GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
183GSM12691759000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033125GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
184GSM12691769000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033126GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
185GSM12691779000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033127GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
186GSM12691789000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033128GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
187GSM12691799000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033129GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
188GSM12691809000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033130GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
189GSM12691819000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033131GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
190GSM12691829000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033132GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
191GSM12691839000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033133GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
192GSM12691849000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033134GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
193GSM12691859000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033135GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
194GSM12691869000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033136GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
195GSM12691889000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033138GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
196GSM12691899000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033139GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
197GSM12691909000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033140GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
198GSM12691919000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033141GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
199GSM12691929000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033142GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
200GSM12691939000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033143GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
201GSM12691949000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033144GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
202GSM12691959000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033145GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
203GSM12691969000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033146GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
204GSM12691979000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033147GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
205GSM12691989000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033148GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
206GSM12691999000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033149GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
207GSM12692009000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033150GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
208GSM12692019000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033151GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
209GSM12692029000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033152GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
210GSM12692039000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033153GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
211GSM12692049000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033154GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
212GSM12692059000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033155GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
213GSM12692069000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033156GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
214GSM12692079000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033157GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
215GSM12692089000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033158GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
216GSM12692099000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033159GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
217GSM12692109000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033160GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
218GSM12692119000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033161GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
219GSM12692129000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033162GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
220GSM12692139000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033163GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
221GSM12692149000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033164GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
222GSM12692169000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033166GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
223GSM12692189000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033168GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
224GSM12692209000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033170GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
225GSM12692219000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033171GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
226GSM12692229000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033172GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
227GSM12692239000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033173GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
228GSM12692249000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033174GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
229GSM12692259000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033175GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
230GSM12692269000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033176GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
231GSM12692309000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033180GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
232GSM12692319000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033181GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
233GSM12692329000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033182GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
234GSM12692339000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033183GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
235GSM12692349000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033184GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
236GSM12692359000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033185GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
237GSM12692369000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033186GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
238GSM12692379000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033187GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
239GSM12692399000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033189GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
240GSM12692409000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033190GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
241GSM12692419000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033191GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
242GSM12692429000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033192GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
243GSM12692439000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033193GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
244GSM12692449000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033194GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
245GSM12692469000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033196GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
246GSM12692479000201-738HumanMyoblast T48Skeletal Muscle TissueSRP033135SRR1033197GPL16791HiSeq 2500
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
247GSM12692489000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033198GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
248GSM12692499000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033199GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
249GSM12692509000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033200GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
250GSM12692519000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033201GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
251GSM12692529000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033202GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
252GSM12692539000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033203GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
253GSM12692549000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033204GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
254GSM12692559000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033205GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
255GSM12692569000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033206GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
256GSM12692579000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033207GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
257GSM12692589000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033208GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
258GSM12692599000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033209GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
259GSM12692609000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033210GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
260GSM12692619000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033211GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
261GSM12692629000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033212GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
262GSM12692649000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033214GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
263GSM12692659000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033215GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
264GSM12692669000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033216GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
265GSM12692679000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033217GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
266GSM12692689000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033218GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
267GSM12692699000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033219GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
268GSM12692709000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033220GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
269GSM12692719000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033221GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
270GSM12692729000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033222GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
271GSM12692739000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033223GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
272GSM12692749000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033224GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
273GSM12692759000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033225GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
274GSM12692769000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033226GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
275GSM12692779000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033227GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
276GSM12692789000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033228GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
277GSM12692809000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033230GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
278GSM12692819000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033231GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
279GSM12692829000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033232GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
280GSM12692839000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033233GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
281GSM12692849000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033234GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
282GSM12692869000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033236GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
283GSM12692879000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033237GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
284GSM12692899000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033239GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
285GSM12692909000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033240GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
286GSM12692919000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033241GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
287GSM12692929000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033242GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
288GSM12692939000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033243GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
289GSM12692949000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033244GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
290GSM12692959000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033245GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
291GSM12692969000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033246GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
292GSM12692979000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033247GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
293GSM12692989000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033248GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
294GSM12693019000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033251GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
295GSM12693039000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033253GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
296GSM12693049000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033254GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
297GSM12693059000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033255GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
298GSM12693079000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033257GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
299GSM12693089000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033258GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
300GSM12693099000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033259GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
301GSM12693119000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033261GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
302GSM12693129000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033262GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
303GSM12693149000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033264GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
304GSM12693159000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033265GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
305GSM12693169000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033266GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
306GSM12693189000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033268GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
307GSM12693199000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033269GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
308GSM12693209000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033270GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
309GSM12693219000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033271GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
310GSM12693229000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033272GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
311GSM12693239000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033273GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
312GSM12693249000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033274GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
313GSM12693259000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033275GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
314GSM12693279000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033277GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
315GSM12693289000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033278GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
316GSM12693299000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033279GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
317GSM12693309000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033280GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
318GSM12693319000201-738HumanMyoblast T72Skeletal Muscle TissueSRP033135SRR1033281GPL11154HiSeq 2000
[TruSeq] - HSMM in either growth or differentiation medium were dissociated, washed and resuspended in complete media containing 0.1U/ul of RNaseOUT (Lifetech). Each time point was collected in three independent biological replicates for regular mRNA sequencing while for single cell mRNA sequencing the independent replicates were pooled in equal amounts. For bulk RNA-Seq libraries, total RNA was extracted with Trizol and mRNA libraries were produced starting from 100ng of total RNA using the TruSeq mRNA-Seq library kit (Illumina) according to manufacturer's instructions.
319GSM9675060000000-004HumanLeucocyteBloodSRP014428SRR522079GPL15520MiSeq
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
320GSM9675070000000-004HumanLeucocyteBloodSRP014428SRR522080GPL15520MiSeq
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
321GSM9675089020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522081GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
322GSM9675099020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522082GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
323GSM9675109020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522083GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
324GSM9675119020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522084GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
325GSM9675129020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522085GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
326GSM9675139020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522086GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
327GSM9675149020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522087GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
328GSM9675159020000-715HumanEmbryonic Stem CellEmbryoSRP014428SRR522088GPL10999Genome Analyzer IIx
cDNA was generated as described in the manual for SMARTer Ultra Low RNA Kit for Illumina sequencing marketed by Clontech. Then, a sequencing library was generated using the Epicentre Nextera sample preparation kit, with 5 min tagmentation at 55C with 0.25 ul transposase and 4 ul 5x HMW Nextera reaction buffer, then 35 ul of PB, then 88 ul SPRI XP beads.
329GSM1080212NAHumanBlood CellBloodSRP018525SRR689250GPL11154HiSeq 2000
Targeted enrichment was performed with Agilent 50M kit. Libraries were prepared using an Illumina paired-end DNA sample prep kit (Illumina) following the manufacturer's protocols
330GSM11601126020700-755HumanSecondary OocyteOvarian FollicleSRP018525SRR893046GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
331GSM11601136020700-755HumanSecondary OocyteOvarian FollicleSRP018525SRR893047GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
332GSM11601146020700-755HumanSecondary OocyteOvarian FollicleSRP018525SRR893048GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
333GSM1160115NAHumanTwo-pronuclear ZygoteZygoteSRP018525SRR893049GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
334GSM1160116NAHumanTwo-pronuclear ZygoteZygoteSRP018525SRR893050GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
335GSM1160117NAHumanTwo-pronuclear ZygoteZygoteSRP018525SRR893051GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
336GSM1160118NAHumanZygoteZygoteSRP018525SRR893052GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
337GSM1160119NAHumanZygoteZygoteSRP018525SRR893053GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
338GSM1160120NAHuman2-cell Embryo Cell2-cell EmbryoSRP018525SRR893054GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
339GSM1160121NAHuman2-cell Embryo Cell2-cell EmbryoSRP018525SRR893055GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
340GSM1160122NAHuman2-cell Embryo Cell2-cell EmbryoSRP018525SRR893056GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
341GSM1160123NAHuman4-cell Embryo Cell4-cell EmbryoSRP018525SRR893057GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
342GSM1160124NAHuman4-cell Embryo Cell4-cell EmbryoSRP018525SRR893058GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
343GSM1160125NAHuman4-cell Embryo Cell4-cell EmbryoSRP018525SRR893059GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
344GSM1160126NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893060GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
345GSM1160127NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893061GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
346GSM1160128NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893062GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
347GSM1160129NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893063GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
348GSM1160130NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893064GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
349GSM1160131NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893065GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
350GSM1160132NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893066GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
351GSM1160133NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893067GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
352GSM1160134NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893068GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
353GSM1160135NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893069GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
354GSM1160136NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893070GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
355GSM1160137NAHuman8-cell Embryo Cell8-cell EmbryoSRP018525SRR893071GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
356GSM1160138NAHumanMorula CellMorulaSRP018525SRR893072GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
357GSM1160139NAHumanMorula CellMorulaSRP018525SRR893073GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
358GSM1160140NAHumanMorula CellMorulaSRP018525SRR893074GPL11154HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
359GSM1657871NAHumanNACortex (temporal Lobe)SRP057196SRR1974543GPL18573NextSeq 500
NA
360GSM1657872NAHumanNACortex (temporal Lobe)SRP057196SRR1974544GPL18573NextSeq 500
NA
361GSM1657873NAHumanNACortex (temporal Lobe)SRP057196SRR1974545GPL18573NextSeq 500
NA
362GSM1657874NAHumanNACortex (temporal Lobe)SRP057196SRR1974546GPL18573NextSeq 500
NA
363GSM1657875NAHumanNACortex (temporal Lobe)SRP057196SRR1974547GPL18573NextSeq 500
NA
364GSM1657876NAHumanNACortex (temporal Lobe)SRP057196SRR1974548GPL18573NextSeq 500
NA
365GSM1657877NAHumanNACortex (temporal Lobe)SRP057196SRR1974549GPL18573NextSeq 500
NA
366GSM1657878NAHumanNACortex (temporal Lobe)SRP057196SRR1974550GPL18573NextSeq 500
NA
367GSM1657879NAHumanNACortex (temporal Lobe)SRP057196SRR1974551GPL18573NextSeq 500
NA
368GSM1657880NAHumanNACortex (temporal Lobe)SRP057196SRR1974552GPL18573NextSeq 500
NA
369GSM1657881NAHumanNACortex (temporal Lobe)SRP057196SRR1974553GPL18573NextSeq 500
NA
370GSM1657882NAHumanNACortex (temporal Lobe)SRP057196SRR1974554GPL18573NextSeq 500
NA
371GSM1657883NAHumanNACortex (temporal Lobe)SRP057196SRR1974555GPL18573NextSeq 500
NA
372GSM1657884NAHumanNACortex (temporal Lobe)SRP057196SRR1974556GPL18573NextSeq 500
NA
373GSM1657885NAHumanNACortex (temporal Lobe)SRP057196SRR1974557GPL18573NextSeq 500
NA
374GSM1657886NAHumanNACortex (temporal Lobe)SRP057196SRR1974558GPL18573NextSeq 500
NA
375GSM1657887NAHumanNACortex (temporal Lobe)SRP057196SRR1974559GPL18573NextSeq 500
NA
376GSM1657888NAHumanNACortex (temporal Lobe)SRP057196SRR1974560GPL18573NextSeq 500
NA
377GSM1657889NAHumanNACortex (temporal Lobe)SRP057196SRR1974561GPL18573NextSeq 500
NA
378GSM1657890NAHumanNACortex (temporal Lobe)SRP057196SRR1974562GPL18573NextSeq 500
NA
379GSM1657891NAHumanNACortex (temporal Lobe)SRP057196SRR1974563GPL18573NextSeq 500
NA
380GSM1657892NAHumanNACortex (temporal Lobe)SRP057196SRR1974564GPL18573NextSeq 500
NA
381GSM1657893NAHumanNACortex (temporal Lobe)SRP057196SRR1974565GPL18573NextSeq 500
NA
382GSM1657894NAHumanNACortex (temporal Lobe)SRP057196SRR1974566GPL18573NextSeq 500
NA
383GSM1657895NAHumanNACortex (temporal Lobe)SRP057196SRR1974567GPL18573NextSeq 500
NA
384GSM1657896NAHumanNACortex (temporal Lobe)SRP057196SRR1974568GPL18573NextSeq 500
NA
385GSM1657897NAHumanNACortex (temporal Lobe)SRP057196SRR1974569GPL18573NextSeq 500
NA
386GSM1657898NAHumanNACortex (temporal Lobe)SRP057196SRR1974570GPL18573NextSeq 500
NA
387GSM1657899NAHumanNACortex (temporal Lobe)SRP057196SRR1974571GPL18573NextSeq 500
NA
388GSM1657900NAHumanNACortex (temporal Lobe)SRP057196SRR1974572GPL18573NextSeq 500
NA
389GSM1657901NAHumanNACortex (temporal Lobe)SRP057196SRR1974573GPL18573NextSeq 500
NA
390GSM1657902NAHumanNACortex (temporal Lobe)SRP057196SRR1974574GPL18573NextSeq 500
NA
391GSM1657903NAHumanNACortex (temporal Lobe)SRP057196SRR1974575GPL18573NextSeq 500
NA
392GSM1657904NAHumanNACortex (temporal Lobe)SRP057196SRR1974576GPL18573NextSeq 500
NA
393GSM1657905NAHumanNACortex (temporal Lobe)SRP057196SRR1974577GPL18573NextSeq 500
NA
394GSM1657906NAHumanNACortex (temporal Lobe)SRP057196SRR1974578GPL18573NextSeq 500
NA
395GSM1657907NAHumanNACortex (temporal Lobe)SRP057196SRR1974579GPL18573NextSeq 500
NA
396GSM1657908NAHumanNACortex (temporal Lobe)SRP057196SRR1974580GPL18573NextSeq 500
NA
397GSM1657909NAHumanNACortex (temporal Lobe)SRP057196SRR1974581GPL18573NextSeq 500
NA
398GSM1657910NAHumanNACortex (temporal Lobe)SRP057196SRR1974582GPL18573NextSeq 500
NA
399GSM1657911NAHumanNACortex (temporal Lobe)SRP057196SRR1974583GPL18573NextSeq 500
NA
400GSM1657912NAHumanNACortex (temporal Lobe)SRP057196SRR1974584GPL18573NextSeq 500
NA
401GSM1657913NAHumanNACortex (temporal Lobe)SRP057196SRR1974585GPL18573NextSeq 500
NA
402GSM1657914NAHumanNACortex (temporal Lobe)SRP057196SRR1974586GPL18573NextSeq 500
NA
403GSM1657915NAHumanNACortex (temporal Lobe)SRP057196SRR1974587GPL18573NextSeq 500
NA
404GSM1657916NAHumanNACortex (temporal Lobe)SRP057196SRR1974588GPL18573NextSeq 500
NA
405GSM1657917NAHumanNACortex (temporal Lobe)SRP057196SRR1974589GPL18573NextSeq 500
NA
406GSM1657918NAHumanNACortex (temporal Lobe)SRP057196SRR1974590GPL18573NextSeq 500
NA
407GSM1657919NAHumanNACortex (temporal Lobe)SRP057196SRR1974591GPL18573NextSeq 500
NA
408GSM1657920NAHumanNACortex (temporal Lobe)SRP057196SRR1974592GPL18573NextSeq 500
NA
409GSM1657921NAHumanNACortex (temporal Lobe)SRP057196SRR1974593GPL18573NextSeq 500
NA
410GSM1657922NAHumanNACortex (temporal Lobe)SRP057196SRR1974594GPL18573NextSeq 500
NA
411GSM1657923NAHumanNACortex (temporal Lobe)SRP057196SRR1974595GPL18573NextSeq 500
NA
412GSM1657924NAHumanNACortex (temporal Lobe)SRP057196SRR1974596GPL18573NextSeq 500
NA
413GSM1657925NAHumanNACortex (temporal Lobe)SRP057196SRR1974597GPL18573NextSeq 500
NA
414GSM1657926NAHumanNACortex (temporal Lobe)SRP057196SRR1974598GPL18573NextSeq 500
NA
415GSM1657927NAHumanNACortex (temporal Lobe)SRP057196SRR1974599GPL18573NextSeq 500
NA
416GSM1657928NAHumanNACortex (temporal Lobe)SRP057196SRR1974600GPL18573NextSeq 500
NA
417GSM1657929NAHumanNACortex (temporal Lobe)SRP057196SRR1974601GPL18573NextSeq 500
NA
418GSM1657930NAHumanNACortex (temporal Lobe)SRP057196SRR1974602GPL18573NextSeq 500
NA
419GSM1657931NAHumanNACortex (temporal Lobe)SRP057196SRR1974603GPL18573NextSeq 500
NA
420GSM1657932NAHumanNACortex (temporal Lobe)SRP057196SRR1974604GPL18573NextSeq 500
NA
421GSM1657933NAHumanNACortex (temporal Lobe)SRP057196SRR1974605GPL18573NextSeq 500
NA
422GSM1657934NAHumanNACortex (temporal Lobe)SRP057196SRR1974606GPL18573NextSeq 500
NA
423GSM1657935NAHumanNACortex (temporal Lobe)SRP057196SRR1974607GPL18573NextSeq 500
NA
424GSM1657936NAHumanNACortex (temporal Lobe)SRP057196SRR1974608GPL18573NextSeq 500
NA
425GSM1657937NAHumanNACortex (temporal Lobe)SRP057196SRR1974609GPL18573NextSeq 500
NA
426GSM1657938NAHumanNACortex (temporal Lobe)SRP057196SRR1974610GPL18573NextSeq 500
NA
427GSM1657939NAHumanNACortex (temporal Lobe)SRP057196SRR1974611GPL18573NextSeq 500
NA
428GSM1657940NAHumanNACortex (temporal Lobe)SRP057196SRR1974612GPL18573NextSeq 500
NA
429GSM1657941NAHumanNACortex (temporal Lobe)SRP057196SRR1974613GPL18573NextSeq 500
NA
430GSM1657942NAHumanNACortex (temporal Lobe)SRP057196SRR1974614GPL18573NextSeq 500
NA
431GSM1657943NAHumanNACortex (temporal Lobe)SRP057196SRR1974615GPL18573NextSeq 500
NA
432GSM1657944NAHumanNACortex (temporal Lobe)SRP057196SRR1974616GPL18573NextSeq 500
NA
433GSM1657945NAHumanNACortex (temporal Lobe)SRP057196SRR1974617GPL18573NextSeq 500
NA
434GSM1657946NAHumanNACortex (temporal Lobe)SRP057196SRR1974618GPL18573NextSeq 500
NA
435GSM1657947NAHumanNACortex (temporal Lobe)SRP057196SRR1974619GPL18573NextSeq 500
NA
436GSM1657948NAHumanNACortex (temporal Lobe)SRP057196SRR1974620GPL18573NextSeq 500
NA
437GSM1657949NAHumanNACortex (temporal Lobe)SRP057196SRR1974621GPL18573NextSeq 500
NA
438GSM1657950NAHumanNACortex (temporal Lobe)SRP057196SRR1974622GPL18573NextSeq 500
NA
439GSM1657951NAHumanNACortex (temporal Lobe)SRP057196SRR1974623GPL18573NextSeq 500
NA
440GSM1657952NAHumanNACortex (temporal Lobe)SRP057196SRR1974624GPL18573NextSeq 500
NA
441GSM1657953NAHumanNACortex (temporal Lobe)SRP057196SRR1974625GPL18573NextSeq 500
NA
442GSM1657954NAHumanNACortex (temporal Lobe)SRP057196SRR1974626GPL18573NextSeq 500
NA
443GSM1657955NAHumanNACortex (temporal Lobe)SRP057196SRR1974627GPL18573NextSeq 500
NA
444GSM1657956NAHumanNACortex (temporal Lobe)SRP057196SRR1974628GPL18573NextSeq 500
NA
445GSM1657957NAHumanNACortex (temporal Lobe)SRP057196SRR1974629GPL18573NextSeq 500
NA
446GSM1657958NAHumanNACortex (temporal Lobe)SRP057196SRR1974630GPL18573NextSeq 500
NA
447GSM1657959NAHumanNACortex (temporal Lobe)SRP057196SRR1974631GPL18573NextSeq 500
NA
448GSM1657960NAHumanNACortex (temporal Lobe)SRP057196SRR1974632GPL18573NextSeq 500
NA
449GSM1657961NAHumanNACortex (temporal Lobe)SRP057196SRR1974633GPL18573NextSeq 500
NA
450GSM1657962NAHumanNACortex (temporal Lobe)SRP057196SRR1974634GPL18573NextSeq 500
NA
451GSM1657963NAHumanNACortex (temporal Lobe)SRP057196SRR1974635GPL18573NextSeq 500
NA
452GSM1657964NAHumanNACortex (temporal Lobe)SRP057196SRR1974636GPL18573NextSeq 500
NA
453GSM1657965NAHumanNACortex (temporal Lobe)SRP057196SRR1974637GPL18573NextSeq 500
NA
454GSM1657966NAHumanNACortex (temporal Lobe)SRP057196SRR1974638GPL18573NextSeq 500
NA
455GSM1657967NAHumanNACortex (temporal Lobe)SRP057196SRR1974639GPL18573NextSeq 500
NA
456GSM1657968NAHumanNACortex (temporal Lobe)SRP057196SRR1974640GPL18573NextSeq 500
NA
457GSM1657969NAHumanNACortex (temporal Lobe)SRP057196SRR1974641GPL18573NextSeq 500
NA
458GSM1657970NAHumanNACortex (temporal Lobe)SRP057196SRR1974642GPL18573NextSeq 500
NA
459GSM1657971NAHumanNACortex (temporal Lobe)SRP057196SRR1974643GPL18573NextSeq 500
NA
460GSM1657972NAHumanNACortex (temporal Lobe)SRP057196SRR1974644GPL18573NextSeq 500
NA
461GSM1657973NAHumanNACortex (temporal Lobe)SRP057196SRR1974645GPL18573NextSeq 500
NA
462GSM1657974NAHumanNACortex (temporal Lobe)SRP057196SRR1974646GPL18573NextSeq 500
NA
463GSM1657975NAHumanNACortex (temporal Lobe)SRP057196SRR1974647GPL18573NextSeq 500
NA
464GSM1657976NAHumanNACortex (temporal Lobe)SRP057196SRR1974648GPL18573NextSeq 500
NA
465GSM1657977NAHumanNACortex (temporal Lobe)SRP057196SRR1974649GPL18573NextSeq 500
NA
466GSM1657978NAHumanNACortex (temporal Lobe)SRP057196SRR1974650GPL18573NextSeq 500
NA
467GSM1657979NAHumanNACortex (temporal Lobe)SRP057196SRR1974651GPL18573NextSeq 500
NA
468GSM1657980NAHumanNACortex (temporal Lobe)SRP057196SRR1974652GPL18573NextSeq 500
NA
469GSM1657981NAHumanNACortex (temporal Lobe)SRP057196SRR1974653GPL18573NextSeq 500
NA
470GSM1657982NAHumanNACortex (temporal Lobe)SRP057196SRR1974654GPL18573NextSeq 500
NA
471GSM1657983NAHumanNACortex (temporal Lobe)SRP057196SRR1974655GPL18573NextSeq 500
NA
472GSM1657984NAHumanNACortex (temporal Lobe)SRP057196SRR1974656GPL18573NextSeq 500
NA
473GSM1657985NAHumanNACortex (temporal Lobe)SRP057196SRR1974657GPL18573NextSeq 500
NA
474GSM1657986NAHumanNACortex (temporal Lobe)SRP057196SRR1974658GPL18573NextSeq 500
NA
475GSM1657987NAHumanNACortex (temporal Lobe)SRP057196SRR1974659GPL18573NextSeq 500
NA
476GSM1657988NAHumanNACortex (temporal Lobe)SRP057196SRR1974660GPL18573NextSeq 500
NA
477GSM1657989NAHumanNACortex (temporal Lobe)SRP057196SRR1974661GPL18573NextSeq 500
NA
478GSM1657990NAHumanNACortex (temporal Lobe)SRP057196SRR1974662GPL18573NextSeq 500
NA
479GSM1657991NAHumanNACortex (temporal Lobe)SRP057196SRR1974663GPL18573NextSeq 500
NA
480GSM1657992NAHumanNACortex (temporal Lobe)SRP057196SRR1974664GPL15520MiSeq
NA
481GSM1657993NAHumanNACortex (temporal Lobe)SRP057196SRR1974665GPL15520MiSeq
NA
482GSM1657994NAHumanNACortex (temporal Lobe)SRP057196SRR1974666GPL15520MiSeq
NA
483GSM1657995NAHumanNACortex (temporal Lobe)SRP057196SRR1974667GPL15520MiSeq
NA
484GSM1657996NAHumanNACortex (temporal Lobe)SRP057196SRR1974668GPL15520MiSeq
NA
485GSM1657997NAHumanNACortex (temporal Lobe)SRP057196SRR1974669GPL15520MiSeq
NA
486GSM1657998NAHumanNACortex (temporal Lobe)SRP057196SRR1974670GPL15520MiSeq
NA
487GSM1657999NAHumanNACortex (temporal Lobe)SRP057196SRR1974671GPL15520MiSeq
NA
488GSM1658000NAHumanNACortex (temporal Lobe)SRP057196SRR1974672GPL15520MiSeq
NA
489GSM1658001NAHumanNACortex (temporal Lobe)SRP057196SRR1974673GPL15520MiSeq
NA
490GSM1658002NAHumanNACortex (temporal Lobe)SRP057196SRR1974674GPL15520MiSeq
NA
491GSM1658003NAHumanNACortex (temporal Lobe)SRP057196SRR1974675GPL15520MiSeq
NA
492GSM1658004NAHumanNACortex (temporal Lobe)SRP057196SRR1974676GPL15520MiSeq
NA
493GSM1658005NAHumanNACortex (temporal Lobe)SRP057196SRR1974677GPL15520MiSeq
NA
494GSM1658006NAHumanNACortex (temporal Lobe)SRP057196SRR1974678GPL18573NextSeq 500
NA
495GSM1658007NAHumanNACortex (temporal Lobe)SRP057196SRR1974679GPL18573NextSeq 500
NA
496GSM1658008NAHumanNACortex (temporal Lobe)SRP057196SRR1974680GPL18573NextSeq 500
NA
497GSM1658009NAHumanNACortex (temporal Lobe)SRP057196SRR1974681GPL18573NextSeq 500
NA
498GSM1658010NAHumanNACortex (temporal Lobe)SRP057196SRR1974682GPL18573NextSeq 500
NA
499GSM1658011NAHumanNACortex (temporal Lobe)SRP057196SRR1974683GPL18573NextSeq 500
NA
500GSM1658012NAHumanNACortex (temporal Lobe)SRP057196SRR1974684GPL18573NextSeq 500
NA
501GSM1658013NAHumanNACortex (temporal Lobe)SRP057196SRR1974685GPL18573NextSeq 500
NA
502GSM1658014NAHumanNACortex (temporal Lobe)SRP057196SRR1974686GPL18573NextSeq 500
NA
503GSM1658015NAHumanNACortex (temporal Lobe)SRP057196SRR1974687GPL18573NextSeq 500
NA
504GSM1658016NAHumanNACortex (temporal Lobe)SRP057196SRR1974688GPL18573NextSeq 500
NA
505GSM1658017NAHumanNACortex (temporal Lobe)SRP057196SRR1974689GPL18573NextSeq 500
NA
506GSM1658018NAHumanNACortex (temporal Lobe)SRP057196SRR1974690GPL18573NextSeq 500
NA
507GSM1658019NAHumanNACortex (temporal Lobe)SRP057196SRR1974691GPL18573NextSeq 500
NA
508GSM1658020NAHumanNACortex (temporal Lobe)SRP057196SRR1974692GPL18573NextSeq 500
NA
509GSM1658021NAHumanNACortex (temporal Lobe)SRP057196SRR1974693GPL18573NextSeq 500
NA
510GSM1658022NAHumanNACortex (temporal Lobe)SRP057196SRR1974694GPL18573NextSeq 500
NA
511GSM1658023NAHumanNACortex (temporal Lobe)SRP057196SRR1974695GPL18573NextSeq 500
NA
512GSM1658024NAHumanNACortex (temporal Lobe)SRP057196SRR1974696GPL18573NextSeq 500
NA
513GSM1658025NAHumanNACortex (temporal Lobe)SRP057196SRR1974697GPL18573NextSeq 500
NA
514GSM1658026NAHumanNACortex (temporal Lobe)SRP057196SRR1974698GPL18573NextSeq 500
NA
515GSM1658027NAHumanNACortex (temporal Lobe)SRP057196SRR1974699GPL18573NextSeq 500
NA
516GSM1658028NAHumanNACortex (temporal Lobe)SRP057196SRR1974700GPL18573NextSeq 500
NA
517GSM1658029NAHumanNACortex (temporal Lobe)SRP057196SRR1974701GPL18573NextSeq 500
NA
518GSM1658030NAHumanNACortex (temporal Lobe)SRP057196SRR1974702GPL18573NextSeq 500
NA
519GSM1658031NAHumanNACortex (temporal Lobe)SRP057196SRR1974703GPL18573NextSeq 500
NA
520GSM1658032NAHumanNACortex (temporal Lobe)SRP057196SRR1974704GPL18573NextSeq 500
NA
521GSM1658033NAHumanNACortex (temporal Lobe)SRP057196SRR1974705GPL18573NextSeq 500
NA
522GSM1658034NAHumanNACortex (temporal Lobe)SRP057196SRR1974706GPL18573NextSeq 500
NA
523GSM1658035NAHumanNACortex (temporal Lobe)SRP057196SRR1974707GPL18573NextSeq 500
NA
524GSM1658036NAHumanNACortex (temporal Lobe)SRP057196SRR1974708GPL18573NextSeq 500
NA
525GSM1658037NAHumanNACortex (temporal Lobe)SRP057196SRR1974709GPL18573NextSeq 500
NA
526GSM1658038NAHumanNACortex (temporal Lobe)SRP057196SRR1974710GPL18573NextSeq 500
NA
527GSM1658039NAHumanNACortex (temporal Lobe)SRP057196SRR1974711GPL18573NextSeq 500
NA
528GSM1658040NAHumanNACortex (temporal Lobe)SRP057196SRR1974712GPL18573NextSeq 500
NA
529GSM1658041NAHumanNACortex (temporal Lobe)SRP057196SRR1974713GPL18573NextSeq 500
NA
530GSM1658042NAHumanNACortex (temporal Lobe)SRP057196SRR1974714GPL18573NextSeq 500
NA
531GSM1658043NAHumanNACortex (temporal Lobe)SRP057196SRR1974715GPL18573NextSeq 500
NA
532GSM1658044NAHumanNACortex (temporal Lobe)SRP057196SRR1974716GPL18573NextSeq 500
NA
533GSM1658045NAHumanNACortex (temporal Lobe)SRP057196SRR1974717GPL18573NextSeq 500
NA
534GSM1658046NAHumanNACortex (temporal Lobe)SRP057196SRR1974718GPL18573NextSeq 500
NA
535GSM1658047NAHumanNACortex (temporal Lobe)SRP057196SRR1974719GPL18573NextSeq 500
NA
536GSM1658048NAHumanNACortex (temporal Lobe)SRP057196SRR1974720GPL18573NextSeq 500
NA
537GSM1658049NAHumanNACortex (temporal Lobe)SRP057196SRR1974721GPL18573NextSeq 500
NA
538GSM1658050NAHumanNACortex (temporal Lobe)SRP057196SRR1974722GPL18573NextSeq 500
NA
539GSM1658051NAHumanNACortex (temporal Lobe)SRP057196SRR1974723GPL18573NextSeq 500
NA
540GSM1658052NAHumanNACortex (temporal Lobe)SRP057196SRR1974724GPL18573NextSeq 500
NA
541GSM1658053NAHumanNACortex (temporal Lobe)SRP057196SRR1974725GPL18573NextSeq 500
NA
542GSM1658054NAHumanNACortex (temporal Lobe)SRP057196SRR1974726GPL18573NextSeq 500
NA
543GSM1658055NAHumanNACortex (temporal Lobe)SRP057196SRR1974727GPL18573NextSeq 500
NA
544GSM1658056NAHumanNACortex (temporal Lobe)SRP057196SRR1974728GPL18573NextSeq 500
NA
545GSM1658057NAHumanNACortex (temporal Lobe)SRP057196SRR1974729GPL18573NextSeq 500
NA
546GSM1658058NAHumanNACortex (temporal Lobe)SRP057196SRR1974730GPL18573NextSeq 500
NA
547GSM1658059NAHumanNACortex (temporal Lobe)SRP057196SRR1974731GPL18573NextSeq 500
NA
548GSM1658060NAHumanNACortex (temporal Lobe)SRP057196SRR1974732GPL18573NextSeq 500
NA
549GSM1658061NAHumanNACortex (temporal Lobe)SRP057196SRR1974733GPL18573NextSeq 500
NA
550GSM1658062NAHumanNACortex (temporal Lobe)SRP057196SRR1974734GPL18573NextSeq 500
NA
551GSM1658063NAHumanNACortex (temporal Lobe)SRP057196SRR1974735GPL18573NextSeq 500
NA
552GSM1658064NAHumanNACortex (temporal Lobe)SRP057196SRR1974736GPL18573NextSeq 500
NA
553GSM1658065NAHumanNACortex (temporal Lobe)SRP057196SRR1974737GPL18573NextSeq 500
NA
554GSM1658066NAHumanNACortex (temporal Lobe)SRP057196SRR1974738GPL18573NextSeq 500
NA
555GSM1658067NAHumanNACortex (temporal Lobe)SRP057196SRR1974739GPL18573NextSeq 500
NA
556GSM1658068NAHumanNACortex (temporal Lobe)SRP057196SRR1974740GPL18573NextSeq 500
NA
557GSM1658069NAHumanNACortex (temporal Lobe)SRP057196SRR1974741GPL18573NextSeq 500
NA
558GSM1658070NAHumanNACortex (temporal Lobe)SRP057196SRR1974742GPL18573NextSeq 500
NA
559GSM1658071NAHumanNACortex (temporal Lobe)SRP057196SRR1974743GPL18573NextSeq 500
NA
560GSM1658072NAHumanNACortex (temporal Lobe)SRP057196SRR1974744GPL18573NextSeq 500
NA
561GSM1658073NAHumanNACortex (temporal Lobe)SRP057196SRR1974745GPL18573NextSeq 500
NA
562GSM1658074NAHumanNACortex (temporal Lobe)SRP057196SRR1974746GPL18573NextSeq 500
NA
563GSM1658075NAHumanNACortex (temporal Lobe)SRP057196SRR1974747GPL18573NextSeq 500
NA
564GSM1658076NAHumanNACortex (temporal Lobe)SRP057196SRR1974748GPL18573NextSeq 500
NA
565GSM1658077NAHumanNACortex (temporal Lobe)SRP057196SRR1974749GPL18573NextSeq 500
NA
566GSM1658078NAHumanNACortex (temporal Lobe)SRP057196SRR1974750GPL18573NextSeq 500
NA
567GSM1658079NAHumanNACortex (temporal Lobe)SRP057196SRR1974751GPL18573NextSeq 500
NA
568GSM1658080NAHumanNACortex (temporal Lobe)SRP057196SRR1974752GPL18573NextSeq 500
NA
569GSM1658081NAHumanNACortex (temporal Lobe)SRP057196SRR1974753GPL18573NextSeq 500
NA
570GSM1658082NAHumanNACortex (temporal Lobe)SRP057196SRR1974754GPL18573NextSeq 500
NA
571GSM1658083NAHumanNACortex (temporal Lobe)SRP057196SRR1974755GPL18573NextSeq 500
NA
572GSM1658084NAHumanNACortex (temporal Lobe)SRP057196SRR1974756GPL18573NextSeq 500
NA
573GSM1658085NAHumanNACortex (temporal Lobe)SRP057196SRR1974757GPL18573NextSeq 500
NA
574GSM1658086NAHumanNACortex (temporal Lobe)SRP057196SRR1974758GPL18573NextSeq 500
NA
575GSM1658087NAHumanNACortex (temporal Lobe)SRP057196SRR1974759GPL18573NextSeq 500
NA
576GSM1658088NAHumanNACortex (temporal Lobe)SRP057196SRR1974760GPL18573NextSeq 500
NA
577GSM1658089NAHumanNACortex (temporal Lobe)SRP057196SRR1974761GPL18573NextSeq 500
NA
578GSM1658090NAHumanNACortex (temporal Lobe)SRP057196SRR1974762GPL18573NextSeq 500
NA
579GSM1658091NAHumanNACortex (temporal Lobe)SRP057196SRR1974763GPL18573NextSeq 500
NA
580GSM1658092NAHumanNACortex (temporal Lobe)SRP057196SRR1974764GPL18573NextSeq 500
NA
581GSM1658093NAHumanNACortex (temporal Lobe)SRP057196SRR1974765GPL18573NextSeq 500
NA
582GSM1658094NAHumanNACortex (temporal Lobe)SRP057196SRR1974766GPL18573NextSeq 500
NA
583GSM1658095NAHumanNACortex (temporal Lobe)SRP057196SRR1974767GPL18573NextSeq 500
NA
584GSM1658096NAHumanNACortex (temporal Lobe)SRP057196SRR1974768GPL18573NextSeq 500
NA
585GSM1658097NAHumanNACortex (temporal Lobe)SRP057196SRR1974769GPL18573NextSeq 500
NA
586GSM1658098NAHumanNACortex (temporal Lobe)SRP057196SRR1974770GPL18573NextSeq 500
NA
587GSM1658099NAHumanNACortex (temporal Lobe)SRP057196SRR1974771GPL18573NextSeq 500
NA
588GSM1658100NAHumanNACortex (temporal Lobe)SRP057196SRR1974772GPL18573NextSeq 500
NA
589GSM1658101NAHumanNACortex (temporal Lobe)SRP057196SRR1974773GPL18573NextSeq 500
NA
590GSM1658102NAHumanNACortex (temporal Lobe)SRP057196SRR1974774GPL18573NextSeq 500
NA
591GSM1658103NAHumanNACortex (temporal Lobe)SRP057196SRR1974775GPL18573NextSeq 500
NA
592GSM1658104NAHumanNACortex (temporal Lobe)SRP057196SRR1974776GPL18573NextSeq 500
NA
593GSM1658105NAHumanNACortex (temporal Lobe)SRP057196SRR1974777GPL18573NextSeq 500
NA
594GSM1658106NAHumanNACortex (temporal Lobe)SRP057196SRR1974778GPL18573NextSeq 500
NA
595GSM1658107NAHumanNACortex (temporal Lobe)SRP057196SRR1974779GPL18573NextSeq 500
NA
596GSM1658108NAHumanNACortex (temporal Lobe)SRP057196SRR1974780GPL18573NextSeq 500
NA
597GSM1658109NAHumanNACortex (temporal Lobe)SRP057196SRR1974781GPL18573NextSeq 500
NA
598GSM1658110NAHumanNACortex (temporal Lobe)SRP057196SRR1974782GPL18573NextSeq 500
NA
599GSM1658111NAHumanNACortex (temporal Lobe)SRP057196SRR1974783GPL18573NextSeq 500
NA
600GSM1658112NAHumanNACortex (temporal Lobe)SRP057196SRR1974784GPL18573NextSeq 500
NA
601GSM1658113NAHumanNACortex (temporal Lobe)SRP057196SRR1974785GPL18573NextSeq 500
NA
602GSM1658114NAHumanNACortex (temporal Lobe)SRP057196SRR1974786GPL18573NextSeq 500
NA
603GSM1658115NAHumanNACortex (temporal Lobe)SRP057196SRR1974787GPL18573NextSeq 500
NA
604GSM1658116NAHumanNACortex (temporal Lobe)SRP057196SRR1974788GPL18573NextSeq 500
NA
605GSM1658117NAHumanNACortex (temporal Lobe)SRP057196SRR1974789GPL18573NextSeq 500
NA
606GSM1658118NAHumanNACortex (temporal Lobe)SRP057196SRR1974790GPL18573NextSeq 500
NA
607GSM1658119NAHumanNACortex (temporal Lobe)SRP057196SRR1974791GPL18573NextSeq 500
NA
608GSM1658120NAHumanNACortex (temporal Lobe)SRP057196SRR1974792GPL18573NextSeq 500
NA
609GSM1658121NAHumanNACortex (temporal Lobe)SRP057196SRR1974793GPL18573NextSeq 500
NA
610GSM1658122NAHumanNACortex (temporal Lobe)SRP057196SRR1974794GPL18573NextSeq 500
NA
611GSM1658123NAHumanNACortex (temporal Lobe)SRP057196SRR1974795GPL18573NextSeq 500
NA
612GSM1658124NAHumanNACortex (temporal Lobe)SRP057196SRR1974796GPL18573NextSeq 500
NA
613GSM1658125NAHumanNACortex (temporal Lobe)SRP057196SRR1974797GPL18573NextSeq 500
NA
614GSM1658126NAHumanNACortex (temporal Lobe)SRP057196SRR1974798GPL18573NextSeq 500
NA
615GSM1658127NAHumanNACortex (temporal Lobe)SRP057196SRR1974799GPL18573NextSeq 500
NA
616GSM1658128NAHumanNACortex (temporal Lobe)SRP057196SRR1974800GPL18573NextSeq 500
NA
617GSM1658129NAHumanNACortex (temporal Lobe)SRP057196SRR1974801GPL18573NextSeq 500
NA
618GSM1658130NAHumanNACortex (temporal Lobe)SRP057196SRR1974802GPL18573NextSeq 500
NA
619GSM1658131NAHumanNACortex (temporal Lobe)SRP057196SRR1974803GPL18573NextSeq 500
NA
620GSM1658132NAHumanNACortex (temporal Lobe)SRP057196SRR1974804GPL18573NextSeq 500
NA
621GSM1658133NAHumanNACortex (temporal Lobe)SRP057196SRR1974805GPL18573NextSeq 500
NA
622GSM1658134NAHumanNACortex (temporal Lobe)SRP057196SRR1974806GPL18573NextSeq 500
NA
623GSM1658135NAHumanNACortex (temporal Lobe)SRP057196SRR1974807GPL18573NextSeq 500
NA
624GSM1658136NAHumanNACortex (temporal Lobe)SRP057196SRR1974808GPL18573NextSeq 500
NA
625GSM1658137NAHumanNACortex (temporal Lobe)SRP057196SRR1974809GPL18573NextSeq 500
NA
626GSM1658138NAHumanNACortex (temporal Lobe)SRP057196SRR1974810GPL18573NextSeq 500
NA
627GSM1658139NAHumanNACortex (temporal Lobe)SRP057196SRR1974811GPL18573NextSeq 500
NA
628GSM1658140NAHumanNACortex (temporal Lobe)SRP057196SRR1974812GPL18573NextSeq 500
NA
629GSM1658141NAHumanNACortex (temporal Lobe)SRP057196SRR1974813GPL18573NextSeq 500
NA
630GSM1658142NAHumanNACortex (temporal Lobe)SRP057196SRR1974814GPL18573NextSeq 500
NA
631GSM1658143NAHumanNACortex (temporal Lobe)SRP057196SRR1974815GPL18573NextSeq 500
NA
632GSM1658144NAHumanNACortex (temporal Lobe)SRP057196SRR1974816GPL18573NextSeq 500
NA
633GSM1658145NAHumanNACortex (temporal Lobe)SRP057196SRR1974817GPL18573NextSeq 500
NA
634GSM1658146NAHumanNACortex (temporal Lobe)SRP057196SRR1974818GPL18573NextSeq 500
NA
635GSM1658147NAHumanNACortex (temporal Lobe)SRP057196SRR1974819GPL18573NextSeq 500
NA
636GSM1658148NAHumanNACortex (temporal Lobe)SRP057196SRR1974820GPL18573NextSeq 500
NA
637GSM1658149NAHumanNACortex (temporal Lobe)SRP057196SRR1974821GPL18573NextSeq 500
NA
638GSM1658150NAHumanNACortex (temporal Lobe)SRP057196SRR1974822GPL18573NextSeq 500
NA
639GSM1658151NAHumanNACortex (temporal Lobe)SRP057196SRR1974823GPL18573NextSeq 500
NA
640GSM1658152NAHumanNACortex (temporal Lobe)SRP057196SRR1974824GPL18573NextSeq 500
NA
641GSM1658153NAHumanNACortex (temporal Lobe)SRP057196SRR1974825GPL18573NextSeq 500
NA
642GSM1658154NAHumanNACortex (temporal Lobe)SRP057196SRR1974826GPL18573NextSeq 500
NA
643GSM1658155NAHumanNACortex (temporal Lobe)SRP057196SRR1974827GPL18573NextSeq 500
NA
644GSM1658156NAHumanNACortex (temporal Lobe)SRP057196SRR1974828GPL18573NextSeq 500
NA
645GSM1658157NAHumanNACortex (temporal Lobe)SRP057196SRR1974829GPL18573NextSeq 500
NA
646GSM1658158NAHumanNACortex (temporal Lobe)SRP057196SRR1974830GPL18573NextSeq 500
NA
647GSM1658159NAHumanNACortex (temporal Lobe)SRP057196SRR1974831GPL18573NextSeq 500
NA
648GSM1658160NAHumanNACortex (temporal Lobe)SRP057196SRR1974832GPL18573NextSeq 500
NA
649GSM1658161NAHumanNACortex (temporal Lobe)SRP057196SRR1974833GPL18573NextSeq 500
NA
650GSM1658162NAHumanNACortex (temporal Lobe)SRP057196SRR1974834GPL18573NextSeq 500
NA
651GSM1658163NAHumanNACortex (temporal Lobe)SRP057196SRR1974835GPL18573NextSeq 500
NA
652GSM1658164NAHumanNACortex (temporal Lobe)SRP057196SRR1974836GPL18573NextSeq 500
NA
653GSM1658165NAHumanNACortex (temporal Lobe)SRP057196SRR1974837GPL18573NextSeq 500
NA
654GSM1658166NAHumanNACortex (temporal Lobe)SRP057196SRR1974838GPL18573NextSeq 500
NA
655GSM1658167NAHumanNACortex (temporal Lobe)SRP057196SRR1974839GPL18573NextSeq 500
NA
656GSM1658168NAHumanNACortex (temporal Lobe)SRP057196SRR1974840GPL18573NextSeq 500
NA
657GSM1658169NAHumanNACortex (temporal Lobe)SRP057196SRR1974841GPL18573NextSeq 500
NA
658GSM1658170NAHumanNACortex (temporal Lobe)SRP057196SRR1974842GPL18573NextSeq 500
NA
659GSM1658171NAHumanNACortex (temporal Lobe)SRP057196SRR1974843GPL18573NextSeq 500
NA
660GSM1658172NAHumanNACortex (temporal Lobe)SRP057196SRR1974844GPL18573NextSeq 500
NA
661GSM1658173NAHumanNACortex (temporal Lobe)SRP057196SRR1974845GPL18573NextSeq 500
NA
662GSM1658174NAHumanNACortex (temporal Lobe)SRP057196SRR1974846GPL18573NextSeq 500
NA
663GSM1658175NAHumanNACortex (temporal Lobe)SRP057196SRR1974847GPL18573NextSeq 500
NA
664GSM1658176NAHumanNACortex (temporal Lobe)SRP057196SRR1974848GPL18573NextSeq 500
NA
665GSM1658177NAHumanNACortex (temporal Lobe)SRP057196SRR1974849GPL18573NextSeq 500
NA
666GSM1658178NAHumanNACortex (temporal Lobe)SRP057196SRR1974850GPL18573NextSeq 500
NA
667GSM1658179NAHumanNACortex (temporal Lobe)SRP057196SRR1974851GPL18573NextSeq 500
NA
668GSM1658180NAHumanNACortex (temporal Lobe)SRP057196SRR1974852GPL18573NextSeq 500
NA
669GSM1658181NAHumanNACortex (temporal Lobe)SRP057196SRR1974853GPL18573NextSeq 500
NA
670GSM1658182NAHumanNACortex (temporal Lobe)SRP057196SRR1974854GPL18573NextSeq 500
NA
671GSM1658183NAHumanNACortex (temporal Lobe)SRP057196SRR1974855GPL18573NextSeq 500
NA
672GSM1658184NAHumanNACortex (temporal Lobe)SRP057196SRR1974856GPL15520MiSeq
NA
673GSM1658185NAHumanNACortex (temporal Lobe)SRP057196SRR1974857GPL15520MiSeq
NA
674GSM1658186NAHumanNACortex (temporal Lobe)SRP057196SRR1974858GPL15520MiSeq
NA
675GSM1658187NAHumanNACortex (temporal Lobe)SRP057196SRR1974859GPL15520MiSeq
NA
676GSM1658188NAHumanNACortex (temporal Lobe)SRP057196SRR1974860GPL15520MiSeq
NA
677GSM1658189NAHumanNACortex (temporal Lobe)SRP057196SRR1974861GPL15520MiSeq
NA
678GSM1658190NAHumanNACortex (temporal Lobe)SRP057196SRR1974862GPL15520MiSeq
NA
679GSM1658191NAHumanNACortex (temporal Lobe)SRP057196SRR1974863GPL15520MiSeq
NA
680GSM1658192NAHumanNACortex (temporal Lobe)SRP057196SRR1974864GPL15520MiSeq
NA
681GSM1658193NAHumanNACortex (temporal Lobe)SRP057196SRR1974865GPL15520MiSeq
NA
682GSM1658194NAHumanNACortex (temporal Lobe)SRP057196SRR1974866GPL15520MiSeq
NA
683GSM1658195NAHumanNACortex (temporal Lobe)SRP057196SRR1974867GPL15520MiSeq
NA
684GSM1658196NAHumanNACortex (temporal Lobe)SRP057196SRR1974868GPL15520MiSeq
NA
685GSM1658197NAHumanNACortex (temporal Lobe)SRP057196SRR1974869GPL15520MiSeq
NA
686GSM1658198NAHumanNACortex (temporal Lobe)SRP057196SRR1974870GPL15520MiSeq
NA
687GSM1658199NAHumanNACortex (temporal Lobe)SRP057196SRR1974871GPL15520MiSeq
NA
688GSM1658200NAHumanNACortex (temporal Lobe)SRP057196SRR1974872GPL15520MiSeq
NA
689GSM1658201NAHumanNACortex (temporal Lobe)SRP057196SRR1974873GPL15520MiSeq
NA
690GSM1658202NAHumanNACortex (temporal Lobe)SRP057196SRR1974874GPL15520MiSeq
NA
691GSM1658203NAHumanNACortexSRP057196SRR1974875GPL15520MiSeq
NA
692GSM1658204NAHumanNACortexSRP057196SRR1974876GPL15520MiSeq
NA
693GSM1658205NAHumanNACortexSRP057196SRR1974877GPL15520MiSeq
NA
694GSM1658206NAHumanNACortexSRP057196SRR1974878GPL15520MiSeq
NA
695GSM1658207NAHumanNACortexSRP057196SRR1974879GPL15520MiSeq
NA
696GSM1658208NAHumanNACortexSRP057196SRR1974880GPL15520MiSeq
NA
697GSM1658209NAHumanNACortexSRP057196SRR1974881GPL15520MiSeq
NA
698GSM1658210NAHumanNACortexSRP057196SRR1974882GPL15520MiSeq
NA
699GSM1658211NAHumanNACortexSRP057196SRR1974883GPL15520MiSeq
NA
700GSM1658212NAHumanNACortexSRP057196SRR1974884GPL15520MiSeq
NA
701GSM1658213NAHumanNACortexSRP057196SRR1974885GPL15520MiSeq
NA
702GSM1658214NAHumanNACortexSRP057196SRR1974886GPL15520MiSeq
NA
703GSM1658215NAHumanNACortexSRP057196SRR1974887GPL15520MiSeq
NA
704GSM1658216NAHumanNACortexSRP057196SRR1974888GPL15520MiSeq
NA
705GSM1658217NAHumanNACortexSRP057196SRR1974889GPL15520MiSeq
NA
706GSM1658218NAHumanNACortexSRP057196SRR1974890GPL15520MiSeq
NA
707GSM1658219NAHumanNACortexSRP057196SRR1974891GPL15520MiSeq
NA
708GSM1658220NAHumanNACortexSRP057196SRR1974892GPL15520MiSeq
NA
709GSM1658221NAHumanNACortexSRP057196SRR1974893GPL15520MiSeq
NA
710GSM1658222NAHumanNACortexSRP057196SRR1974894GPL15520MiSeq
NA
711GSM1658223NAHumanNACortexSRP057196SRR1974895GPL15520MiSeq
NA
712GSM1658224NAHumanNACortexSRP057196SRR1974896GPL15520MiSeq
NA
713GSM1658225NAHumanNACortexSRP057196SRR1974897GPL15520MiSeq
NA
714GSM1658226NAHumanNACortexSRP057196SRR1974898GPL15520MiSeq
NA
715GSM1658227NAHumanNACortexSRP057196SRR1974899GPL15520MiSeq
NA
716GSM1658228NAHumanNACortexSRP057196SRR1974900GPL15520MiSeq
NA
717GSM1658229NAHumanNACortexSRP057196SRR1974901GPL15520MiSeq
NA
718GSM1658230NAHumanNACortexSRP057196SRR1974902GPL15520MiSeq
NA
719GSM1658231NAHumanNACortexSRP057196SRR1974903GPL15520MiSeq
NA
720GSM1658232NAHumanNACortexSRP057196SRR1974904GPL15520MiSeq
NA
721GSM1658233NAHumanNACortexSRP057196SRR1974905GPL15520MiSeq
NA
722GSM1658234NAHumanNACortexSRP057196SRR1974906GPL15520MiSeq
NA
723GSM1658235NAHumanNACortexSRP057196SRR1974907GPL15520MiSeq
NA
724GSM1658236NAHumanNACortexSRP057196SRR1974908GPL15520MiSeq
NA
725GSM1658237NAHumanNACortexSRP057196SRR1974909GPL15520MiSeq
NA
726GSM1658238NAHumanNACortexSRP057196SRR1974910GPL15520MiSeq
NA
727GSM1658239NAHumanNACortexSRP057196SRR1974911GPL15520MiSeq
NA
728GSM1658240NAHumanNACortexSRP057196SRR1974912GPL15520MiSeq
NA
729GSM1658241NAHumanNACortexSRP057196SRR1974913GPL15520MiSeq
NA
730GSM1658242NAHumanNACortexSRP057196SRR1974914GPL15520MiSeq
NA
731GSM1658243NAHumanNACortexSRP057196SRR1974915GPL15520MiSeq
NA
732GSM1658244NAHumanNACortexSRP057196SRR1974916GPL15520MiSeq
NA
733GSM1658245NAHumanNACortexSRP057196SRR1974917GPL15520MiSeq
NA
734GSM1658246NAHumanNACortexSRP057196SRR1974918GPL15520MiSeq
NA
735GSM1658247NAHumanNACortexSRP057196SRR1974919GPL15520MiSeq
NA
736GSM1658248NAHumanNACortexSRP057196SRR1974920GPL15520MiSeq
NA
737GSM1658249NAHumanNACortexSRP057196SRR1974921GPL15520MiSeq
NA
738GSM1658251NAHumanNACortexSRP057196SRR1974922GPL15520MiSeq
NA
739GSM1658253NAHumanNACortexSRP057196SRR1974923GPL15520MiSeq
NA
740GSM1658255NAHumanNACortexSRP057196SRR1974924GPL15520MiSeq
NA
741GSM1658257NAHumanNACortexSRP057196SRR1974925GPL15520MiSeq
NA
742GSM1658259NAHumanNACortexSRP057196SRR1974926GPL15520MiSeq
NA
743GSM1658262NAHumanNACortexSRP057196SRR1974927GPL15520MiSeq
NA
744GSM1658264NAHumanNACortexSRP057196SRR1974928GPL15520MiSeq
NA
745GSM1658266NAHumanNACortexSRP057196SRR1974929GPL15520MiSeq
NA
746GSM1658268NAHumanNACortexSRP057196SRR1974930GPL15520MiSeq
NA
747GSM1658270NAHumanNACortexSRP057196SRR1974931GPL15520MiSeq
NA
748GSM1658272NAHumanNACortexSRP057196SRR1974932GPL15520MiSeq
NA
749GSM1658275NAHumanNACortexSRP057196SRR1974933GPL15520MiSeq
NA
750GSM1658277NAHumanNACortexSRP057196SRR1974934GPL15520MiSeq
NA
751GSM1658279NAHumanNACortexSRP057196SRR1974935GPL15520MiSeq
NA
752GSM1658281NAHumanNACortexSRP057196SRR1974936GPL15520MiSeq
NA
753GSM1658284NAHumanNACortexSRP057196SRR1974937GPL15520MiSeq
NA
754GSM1658286NAHumanNACortexSRP057196SRR1974938GPL15520MiSeq
NA
755GSM1658288NAHumanNACortexSRP057196SRR1974939GPL15520MiSeq
NA
756GSM1658290NAHumanNACortexSRP057196SRR1974940GPL15520MiSeq
NA
757GSM1658292NAHumanNACortexSRP057196SRR1974941GPL15520MiSeq
NA
758GSM1658294NAHumanNACortexSRP057196SRR1974942GPL15520MiSeq
NA
759GSM1658297NAHumanNACortexSRP057196SRR1974943GPL15520MiSeq
NA
760GSM1658299NAHumanNACortexSRP057196SRR1974944GPL15520MiSeq
NA
761GSM1658301NAHumanNACortexSRP057196SRR1974945GPL15520MiSeq
NA
762GSM1658304NAHumanNACortexSRP057196SRR1974946GPL15520MiSeq
NA
763GSM1658305NAHumanNACortex (temporal Lobe)SRP057196SRR1974947GPL15520MiSeq
NA
764GSM1658306NAHumanNACortex (temporal Lobe)SRP057196SRR1974948GPL15520MiSeq
NA
765GSM1658307NAHumanNACortex (temporal Lobe)SRP057196SRR1974949GPL15520MiSeq
NA
766GSM1658308NAHumanNACortex (temporal Lobe)SRP057196SRR1974950GPL15520MiSeq
NA
767GSM1658309NAHumanNACortex (temporal Lobe)SRP057196SRR1974951GPL15520MiSeq
NA
768GSM1658310NAHumanNACortex (temporal Lobe)SRP057196SRR1974952GPL15520MiSeq
NA
769GSM1658311NAHumanNACortex (temporal Lobe)SRP057196SRR1974953GPL15520MiSeq
NA
770GSM1658312NAHumanNACortex (temporal Lobe)SRP057196SRR1974954GPL15520MiSeq
NA
771GSM1658313NAHumanNACortex (temporal Lobe)SRP057196SRR1974955GPL15520MiSeq
NA
772GSM1658314NAHumanNACortex (temporal Lobe)SRP057196SRR1974956GPL15520MiSeq
NA
773GSM1658315NAHumanNACortex (temporal Lobe)SRP057196SRR1974957GPL15520MiSeq
NA
774GSM1658316NAHumanNACortex (temporal Lobe)SRP057196SRR1974958GPL15520MiSeq
NA
775GSM1658317NAHumanNACortex (temporal Lobe)SRP057196SRR1974959GPL15520MiSeq
NA
776GSM1658318NAHumanNACortex (temporal Lobe)SRP057196SRR1974960GPL15520MiSeq
NA
777GSM1658319NAHumanNACortex (temporal Lobe)SRP057196SRR1974961GPL15520MiSeq
NA
778GSM1658320NAHumanNACortex (temporal Lobe)SRP057196SRR1974962GPL15520MiSeq
NA
779GSM1658321NAHumanNACortex (temporal Lobe)SRP057196SRR1974963GPL15520MiSeq
NA
780GSM1658322NAHumanNACortex (temporal Lobe)SRP057196SRR1974964GPL15520MiSeq
NA
781GSM1658323NAHumanNACortex (temporal Lobe)SRP057196SRR1974965GPL15520MiSeq
NA
782GSM1658324NAHumanNACortex (temporal Lobe)SRP057196SRR1974966GPL15520MiSeq
NA
783GSM1658325NAHumanNACortex (temporal Lobe)SRP057196SRR1974967GPL15520MiSeq
NA
784GSM1658326NAHumanNACortex (temporal Lobe)SRP057196SRR1974968GPL15520MiSeq
NA
785GSM1658327NAHumanNACortex (temporal Lobe)SRP057196SRR1974969GPL15520MiSeq
NA
786GSM1658328NAHumanNACortex (temporal Lobe)SRP057196SRR1974970GPL15520MiSeq
NA
787GSM1658329NAHumanNACortex (temporal Lobe)SRP057196SRR1974971GPL15520MiSeq
NA
788GSM1658330NAHumanNACortex (temporal Lobe)SRP057196SRR1974972GPL15520MiSeq
NA
789GSM1658331NAHumanNACortex (temporal Lobe)SRP057196SRR1974973GPL15520MiSeq
NA
790GSM1658332NAHumanNACortex (temporal Lobe)SRP057196SRR1974974GPL15520MiSeq
NA
791GSM1658333NAHumanNACortex (temporal Lobe)SRP057196SRR1974975GPL15520MiSeq
NA
792GSM1658334NAHumanNACortex (temporal Lobe)SRP057196SRR1974976GPL15520MiSeq
NA
793GSM1658335NAHumanNACortex (temporal Lobe)SRP057196SRR1974977GPL15520MiSeq
NA
794GSM1658336NAHumanNACortex (temporal Lobe)SRP057196SRR1974978GPL15520MiSeq
NA
795GSM1658337NAHumanNACortex (temporal Lobe)SRP057196SRR1974979GPL15520MiSeq
NA
796GSM1658338NAHumanNACortex (temporal Lobe)SRP057196SRR1974980GPL18573NextSeq 500
NA
797GSM1658339NAHumanNACortex (temporal Lobe)SRP057196SRR1974981GPL18573NextSeq 500
NA
798GSM1658340NAHumanNACortex (temporal Lobe)SRP057196SRR1974982GPL18573NextSeq 500
NA
799GSM1658341NAHumanNACortex (temporal Lobe)SRP057196SRR1974983GPL18573NextSeq 500
NA
800GSM1658342NAHumanNACortex (temporal Lobe)SRP057196SRR1974984GPL18573NextSeq 500
NA
801GSM1658343NAHumanNACortex (temporal Lobe)SRP057196SRR1974985GPL18573NextSeq 500
NA
802GSM1658344NAHumanNACortex (temporal Lobe)SRP057196SRR1974986GPL18573NextSeq 500
NA
803GSM1658345NAHumanNACortex (temporal Lobe)SRP057196SRR1974987GPL18573NextSeq 500
NA
804GSM1658346NAHumanNACortex (temporal Lobe)SRP057196SRR1974988GPL18573NextSeq 500
NA
805GSM1658347NAHumanNACortex (temporal Lobe)SRP057196SRR1974989GPL18573NextSeq 500
NA
806GSM1658348NAHumanNACortex (temporal Lobe)SRP057196SRR1974990GPL18573NextSeq 500
NA
807GSM1658349NAHumanNACortex (temporal Lobe)SRP057196SRR1974991GPL18573NextSeq 500
NA
808GSM1658350NAHumanNACortex (temporal Lobe)SRP057196SRR1974992GPL18573NextSeq 500
NA
809GSM1658351NAHumanNACortex (temporal Lobe)SRP057196SRR1974993GPL18573NextSeq 500
NA
810GSM1658352NAHumanNACortex (temporal Lobe)SRP057196SRR1974994GPL18573NextSeq 500
NA
811GSM1658353NAHumanNACortex (temporal Lobe)SRP057196SRR1974995GPL18573NextSeq 500
NA
812GSM1658354NAHumanNACortex (temporal Lobe)SRP057196SRR1974996GPL18573NextSeq 500
NA
813GSM1658355NAHumanNACortex (temporal Lobe)SRP057196SRR1974997GPL18573NextSeq 500
NA
814GSM1658356NAHumanNACortex (temporal Lobe)SRP057196SRR1974998GPL18573NextSeq 500
NA
815GSM1658357NAHumanNACortex (temporal Lobe)SRP057196SRR1974999GPL18573NextSeq 500
NA
816GSM1658358NAHumanNACortex (temporal Lobe)SRP057196SRR1975000GPL18573NextSeq 500
NA
817GSM1658359NAHumanNACortex (temporal Lobe)SRP057196SRR1975001GPL18573NextSeq 500
NA
818GSM1658360NAHumanNACortex (temporal Lobe)SRP057196SRR1975002GPL18573NextSeq 500
NA
819GSM1658361NAHumanNACortex (temporal Lobe)SRP057196SRR1975003GPL18573NextSeq 500
NA
820GSM1658362NAHumanNACortex (temporal Lobe)SRP057196SRR1975004GPL18573NextSeq 500
NA
821GSM1658363NAHumanNACortex (temporal Lobe)SRP057196SRR1975005GPL18573NextSeq 500
NA
822GSM1658364NAHumanNACortex (temporal Lobe)SRP057196SRR1975006GPL18573NextSeq 500
NA
823GSM1658365NAHumanNACortex (temporal Lobe)SRP057196SRR1975007GPL18573NextSeq 500
NA
824GSM1658366NAHumanNACortex (temporal Lobe)SRP057196SRR1975008GPL18573NextSeq 500
NA
825GSM1617398NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813952GPL11154HiSeq 2000
NA
826GSM1617399NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813953GPL11154HiSeq 2000
NA
827GSM1617400NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813954GPL11154HiSeq 2000
NA
828GSM1617401NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813955GPL11154HiSeq 2000
NA
829GSM1617402NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813956GPL11154HiSeq 2000
NA
830GSM1617403NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813957GPL11154HiSeq 2000
NA
831GSM1617404NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813958GPL11154HiSeq 2000
NA
832GSM1617405NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813959GPL11154HiSeq 2000
NA
833GSM1617406NAHumanRadial Glial CellCerebral CortexSRP055440SRR1813960GPL11154HiSeq 2000
NA
834GSM1677473NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013442GPL16791HiSeq 2500
NA
835GSM1677474NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013443GPL16791HiSeq 2500
NA
836GSM1677475NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013444GPL16791HiSeq 2500
NA
837GSM1677476NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013445GPL16791HiSeq 2500
NA
838GSM1677477NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013446GPL16791HiSeq 2500
NA
839GSM1677478NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013447GPL16791HiSeq 2500
NA
840GSM1677479NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013448GPL16791HiSeq 2500
NA
841GSM1677480NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013449GPL16791HiSeq 2500
NA
842GSM1677481NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013450GPL16791HiSeq 2500
NA
843GSM1677482NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013451GPL16791HiSeq 2500
NA
844GSM1677483NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013452GPL16791HiSeq 2500
NA
845GSM1677484NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013453GPL16791HiSeq 2500
NA
846GSM1677485NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013454GPL16791HiSeq 2500
NA
847GSM1677486NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013455GPL16791HiSeq 2500
NA
848GSM1677487NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013456GPL16791HiSeq 2500
NA
849GSM1677488NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013457GPL16791HiSeq 2500
NA
850GSM1677489NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013458GPL16791HiSeq 2500
NA
851GSM1677490NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013459GPL16791HiSeq 2500
NA
852GSM1677491NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013460GPL16791HiSeq 2500
NA
853GSM1677492NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013461GPL16791HiSeq 2500
NA
854GSM1677493NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013462GPL16791HiSeq 2500
NA
855GSM1677494NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013463GPL16791HiSeq 2500
NA
856GSM1677495NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013464GPL16791HiSeq 2500
NA
857GSM1677496NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013465GPL16791HiSeq 2500
NA
858GSM1677497NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013466GPL16791HiSeq 2500
NA
859GSM1677498NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013467GPL16791HiSeq 2500
NA
860GSM1677499NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013468GPL16791HiSeq 2500
NA
861GSM1677500NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013469GPL16791HiSeq 2500
NA
862GSM1677501NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013470GPL16791HiSeq 2500
NA
863GSM1677502NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013471GPL16791HiSeq 2500
NA
864GSM1677503NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013472GPL16791HiSeq 2500
NA
865GSM1677504NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013473GPL16791HiSeq 2500
NA
866GSM1677505NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013474GPL16791HiSeq 2500
NA
867GSM1677506NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013475GPL16791HiSeq 2500
NA
868GSM1677507NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013476GPL16791HiSeq 2500
NA
869GSM1677508NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013477GPL16791HiSeq 2500
NA
870GSM1677509NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013478GPL16791HiSeq 2500
NA
871GSM1677510NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013479GPL16791HiSeq 2500
NA
872GSM1677511NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013480GPL16791HiSeq 2500
NA
873GSM1677512NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013481GPL16791HiSeq 2500
NA
874GSM1677513NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013482GPL16791HiSeq 2500
NA
875GSM1677514NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013483GPL16791HiSeq 2500
NA
876GSM1677515NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013484GPL16791HiSeq 2500
NA
877GSM1677516NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013485GPL16791HiSeq 2500
NA
878GSM1677517NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013486GPL16791HiSeq 2500
NA
879GSM1677518NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013487GPL16791HiSeq 2500
NA
880GSM1677519NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013488GPL16791HiSeq 2500
NA
881GSM1677520NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013489GPL16791HiSeq 2500
NA
882GSM1677521NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013490GPL16791HiSeq 2500
NA
883GSM1677522NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013491GPL16791HiSeq 2500
NA
884GSM1677523NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013492GPL16791HiSeq 2500
NA
885GSM1677524NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013493GPL16791HiSeq 2500
NA
886GSM1677525NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013494GPL16791HiSeq 2500
NA
887GSM1677526NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013495GPL16791HiSeq 2500
NA
888GSM1677527NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013496GPL16791HiSeq 2500
NA
889GSM1677528NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013497GPL16791HiSeq 2500
NA
890GSM1677529NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013498GPL16791HiSeq 2500
NA
891GSM1677530NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013499GPL16791HiSeq 2500
NA
892GSM1677531NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013500GPL16791HiSeq 2500
NA
893GSM1677532NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013501GPL16791HiSeq 2500
NA
894GSM1677533NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013502GPL16791HiSeq 2500
NA
895GSM1677534NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013503GPL16791HiSeq 2500
NA
896GSM1677535NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013504GPL16791HiSeq 2500
NA
897GSM1677536NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013505GPL16791HiSeq 2500
NA
898GSM1677537NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013506GPL16791HiSeq 2500
NA
899GSM1677538NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013507GPL16791HiSeq 2500
NA
900GSM1677539NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013508GPL16791HiSeq 2500
NA
901GSM1677540NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013509GPL16791HiSeq 2500
NA
902GSM1677541NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013510GPL16791HiSeq 2500
NA
903GSM1677542NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013511GPL16791HiSeq 2500
NA
904GSM1677543NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013512GPL16791HiSeq 2500
NA
905GSM1677544NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013513GPL16791HiSeq 2500
NA
906GSM1677545NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013514GPL16791HiSeq 2500
NA
907GSM1677546NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013515GPL16791HiSeq 2500
NA
908GSM1677547NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013516GPL16791HiSeq 2500
NA
909GSM1677548NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013517GPL16791HiSeq 2500
NA
910GSM1677549NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013518GPL16791HiSeq 2500
NA
911GSM1677550NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013519GPL16791HiSeq 2500
NA
912GSM1677551NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013520GPL16791HiSeq 2500
NA
913GSM1677552NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013521GPL16791HiSeq 2500
NA
914GSM1677553NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013522GPL16791HiSeq 2500
NA
915GSM1677554NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013523GPL16791HiSeq 2500
NA
916GSM1677555NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013524GPL16791HiSeq 2500
NA
917GSM1677556NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013525GPL16791HiSeq 2500
NA
918GSM1677557NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013526GPL16791HiSeq 2500
NA
919GSM1677558NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013527GPL16791HiSeq 2500
NA
920GSM1677559NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013528GPL16791HiSeq 2500
NA
921GSM1677560NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013529GPL16791HiSeq 2500
NA
922GSM1677561NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013530GPL16791HiSeq 2500
NA
923GSM1677562NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013531GPL16791HiSeq 2500
NA
924GSM1677563NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013532GPL16791HiSeq 2500
NA
925GSM1677564NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013533GPL16791HiSeq 2500
NA
926GSM1677565NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013534GPL16791HiSeq 2500
NA
927GSM1677566NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013535GPL16791HiSeq 2500
NA
928GSM1677567NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013536GPL16791HiSeq 2500
NA
929GSM1677568NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013537GPL16791HiSeq 2500
NA
930GSM1677569NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013538GPL16791HiSeq 2500
NA
931GSM1677570NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013539GPL16791HiSeq 2500
NA
932GSM1677571NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013540GPL16791HiSeq 2500
NA
933GSM1677572NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013541GPL16791HiSeq 2500
NA
934GSM1677573NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013542GPL16791HiSeq 2500
NA
935GSM1677574NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013543GPL16791HiSeq 2500
NA
936GSM1677575NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013544GPL16791HiSeq 2500
NA
937GSM1677576NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013545GPL16791HiSeq 2500
NA
938GSM1677577NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013546GPL16791HiSeq 2500
NA
939GSM1677578NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013547GPL16791HiSeq 2500
NA
940GSM1677579NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013548GPL16791HiSeq 2500
NA
941GSM1677580NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013549GPL16791HiSeq 2500
NA
942GSM1677581NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013550GPL16791HiSeq 2500
NA
943GSM1677582NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013551GPL16791HiSeq 2500
NA
944GSM1677583NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013552GPL16791HiSeq 2500
NA
945GSM1677584NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013553GPL16791HiSeq 2500
NA
946GSM1677585NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013554GPL16791HiSeq 2500
NA
947GSM1677586NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013555GPL16791HiSeq 2500
NA
948GSM1677587NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013556GPL16791HiSeq 2500
NA
949GSM1677588NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013557GPL16791HiSeq 2500
NA
950GSM1677589NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013558GPL16791HiSeq 2500
NA
951GSM1677590NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013559GPL16791HiSeq 2500
NA
952GSM1677591NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013560GPL16791HiSeq 2500
NA
953GSM1677592NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013561GPL16791HiSeq 2500
NA
954GSM1677593NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013562GPL16791HiSeq 2500
NA
955GSM1677594NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013563GPL16791HiSeq 2500
NA
956GSM1677595NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013564GPL16791HiSeq 2500
NA
957GSM1677596NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013565GPL16791HiSeq 2500
NA
958GSM1677597NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013566GPL16791HiSeq 2500
NA
959GSM1677598NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013567GPL16791HiSeq 2500
NA
960GSM1677599NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013568GPL16791HiSeq 2500
NA
961GSM1677600NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013569GPL16791HiSeq 2500
NA
962GSM1677601NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013570GPL16791HiSeq 2500
NA
963GSM1677602NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013571GPL16791HiSeq 2500
NA
964GSM1677603NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013572GPL16791HiSeq 2500
NA
965GSM1677604NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013573GPL16791HiSeq 2500
NA
966GSM1677605NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013574GPL16791HiSeq 2500
NA
967GSM1677606NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013575GPL16791HiSeq 2500
NA
968GSM1677607NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013576GPL16791HiSeq 2500
NA
969GSM1677608NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013577GPL16791HiSeq 2500
NA
970GSM1677609NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013578GPL16791HiSeq 2500
NA
971GSM1677610NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013579GPL16791HiSeq 2500
NA
972GSM1677611NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013580GPL16791HiSeq 2500
NA
973GSM1677612NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013581GPL16791HiSeq 2500
NA
974GSM1677613NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013582GPL16791HiSeq 2500
NA
975GSM1677614NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013583GPL16791HiSeq 2500
NA
976GSM1677615NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013584GPL16791HiSeq 2500
NA
977GSM1677616NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013585GPL16791HiSeq 2500
NA
978GSM1677617NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013586GPL16791HiSeq 2500
NA
979GSM1677618NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013587GPL16791HiSeq 2500
NA
980GSM1677619NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013588GPL16791HiSeq 2500
NA
981GSM1677620NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013589GPL16791HiSeq 2500
NA
982GSM1677621NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013590GPL16791HiSeq 2500
NA
983GSM1677622NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013591GPL16791HiSeq 2500
NA
984GSM1677623NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013592GPL16791HiSeq 2500
NA
985GSM1677624NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013593GPL16791HiSeq 2500
NA
986GSM1677625NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013594GPL16791HiSeq 2500
NA
987GSM1677626NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013595GPL16791HiSeq 2500
NA
988GSM1677627NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013596GPL16791HiSeq 2500
NA
989GSM1677628NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013597GPL16791HiSeq 2500
NA
990GSM1677629NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013598GPL16791HiSeq 2500
NA
991GSM1677630NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013599GPL16791HiSeq 2500
NA
992GSM1677631NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013600GPL16791HiSeq 2500
NA
993GSM1677632NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013601GPL16791HiSeq 2500
NA
994GSM1677633NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013602GPL16791HiSeq 2500
NA
995GSM1677634NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013603GPL16791HiSeq 2500
NA
996GSM1677635NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013604GPL16791HiSeq 2500
NA
997GSM1677636NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013605GPL16791HiSeq 2500
NA
998GSM1677637NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013606GPL16791HiSeq 2500
NA
999GSM1677638NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013607GPL16791HiSeq 2500
NA
1000GSM1677639NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013608GPL16791HiSeq 2500
NA
1001GSM1677640NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013609GPL16791HiSeq 2500
NA
1002GSM1677641NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013610GPL16791HiSeq 2500
NA
1003GSM1677642NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013611GPL16791HiSeq 2500
NA
1004GSM1677643NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013612GPL16791HiSeq 2500
NA
1005GSM1677644NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013613GPL16791HiSeq 2500
NA
1006GSM1677645NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013614GPL16791HiSeq 2500
NA
1007GSM1677646NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013615GPL16791HiSeq 2500
NA
1008GSM1677647NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013616GPL16791HiSeq 2500
NA
1009GSM1677648NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013617GPL16791HiSeq 2500
NA
1010GSM1677649NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013618GPL16791HiSeq 2500
NA
1011GSM1677650NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013619GPL16791HiSeq 2500
NA
1012GSM1677651NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013620GPL16791HiSeq 2500
NA
1013GSM1677652NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013621GPL16791HiSeq 2500
NA
1014GSM1677653NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013622GPL16791HiSeq 2500
NA
1015GSM1677654NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013623GPL16791HiSeq 2500
NA
1016GSM1677655NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013624GPL16791HiSeq 2500
NA
1017GSM1677656NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013625GPL16791HiSeq 2500
NA
1018GSM1677657NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013626GPL16791HiSeq 2500
NA
1019GSM1677658NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013627GPL16791HiSeq 2500
NA
1020GSM1677659NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013628GPL16791HiSeq 2500
NA
1021GSM1677660NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013629GPL16791HiSeq 2500
NA
1022GSM1677661NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013630GPL16791HiSeq 2500
NA
1023GSM1677662NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013631GPL16791HiSeq 2500
NA
1024GSM1677663NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013632GPL16791HiSeq 2500
NA
1025GSM1677664NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013633GPL16791HiSeq 2500
NA
1026GSM1677665NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013634GPL16791HiSeq 2500
NA
1027GSM1677666NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013635GPL16791HiSeq 2500
NA
1028GSM1677667NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013636GPL16791HiSeq 2500
NA
1029GSM1677668NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013637GPL16791HiSeq 2500
NA
1030GSM1677669NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013638GPL16791HiSeq 2500
NA
1031GSM1677670NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013639GPL16791HiSeq 2500
NA
1032GSM1677671NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013640GPL16791HiSeq 2500
NA
1033GSM1677672NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013641GPL16791HiSeq 2500
NA
1034GSM1677673NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013642GPL16791HiSeq 2500
NA
1035GSM1677674NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013643GPL16791HiSeq 2500
NA
1036GSM1677675NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013644GPL16791HiSeq 2500
NA
1037GSM1677676NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013645GPL16791HiSeq 2500
NA
1038GSM1677677NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013646GPL16791HiSeq 2500
NA
1039GSM1677678NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013647GPL16791HiSeq 2500
NA
1040GSM1677679NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013648GPL16791HiSeq 2500
NA
1041GSM1677680NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013649GPL16791HiSeq 2500
NA
1042GSM1677681NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013650GPL16791HiSeq 2500
NA
1043GSM1677682NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013651GPL16791HiSeq 2500
NA
1044GSM1677683NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013652GPL16791HiSeq 2500
NA
1045GSM1677684NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013653GPL16791HiSeq 2500
NA
1046GSM1677685NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013654GPL16791HiSeq 2500
NA
1047GSM1677686NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013655GPL16791HiSeq 2500
NA
1048GSM1677687NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013656GPL16791HiSeq 2500
NA
1049GSM1677688NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013657GPL16791HiSeq 2500
NA
1050GSM1677689NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013658GPL16791HiSeq 2500
NA
1051GSM1677690NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013659GPL16791HiSeq 2500
NA
1052GSM1677691NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013660GPL16791HiSeq 2500
NA
1053GSM1677692NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013661GPL16791HiSeq 2500
NA
1054GSM1677693NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013662GPL16791HiSeq 2500
NA
1055GSM1677694NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013663GPL16791HiSeq 2500
NA
1056GSM1677695NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013664GPL16791HiSeq 2500
NA
1057GSM1677696NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013665GPL16791HiSeq 2500
NA
1058GSM1677697NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013666GPL16791HiSeq 2500
NA
1059GSM1677698NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013667GPL16791HiSeq 2500
NA
1060GSM1677699NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013668GPL16791HiSeq 2500
NA
1061GSM1677700NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013669GPL16791HiSeq 2500
NA
1062GSM1677701NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013670GPL16791HiSeq 2500
NA
1063GSM1677702NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013671GPL16791HiSeq 2500
NA
1064GSM1677703NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013672GPL16791HiSeq 2500
NA
1065GSM1677704NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013673GPL16791HiSeq 2500
NA
1066GSM1677705NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013674GPL16791HiSeq 2500
NA
1067GSM1677706NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013675GPL16791HiSeq 2500
NA
1068GSM1677707NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013676GPL16791HiSeq 2500
NA
1069GSM1677708NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013677GPL16791HiSeq 2500
NA
1070GSM1677709NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013678GPL16791HiSeq 2500
NA
1071GSM1677710NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013679GPL16791HiSeq 2500
NA
1072GSM1677711NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013680GPL16791HiSeq 2500
NA
1073GSM1677712NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013681GPL16791HiSeq 2500
NA
1074GSM1677713NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013682GPL16791HiSeq 2500
NA
1075GSM1677714NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013683GPL16791HiSeq 2500
NA
1076GSM1677715NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013684GPL16791HiSeq 2500
NA
1077GSM1677716NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013685GPL16791HiSeq 2500
NA
1078GSM1677717NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013686GPL16791HiSeq 2500
NA
1079GSM1677718NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013687GPL16791HiSeq 2500
NA
1080GSM1677719NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013688GPL16791HiSeq 2500
NA
1081GSM1677720NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013689GPL16791HiSeq 2500
NA
1082GSM1677721NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013690GPL16791HiSeq 2500
NA
1083GSM1677722NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013691GPL16791HiSeq 2500
NA
1084GSM1677723NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013692GPL16791HiSeq 2500
NA
1085GSM1677724NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013693GPL16791HiSeq 2500
NA
1086GSM1677725NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013694GPL16791HiSeq 2500
NA
1087GSM1677726NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013695GPL16791HiSeq 2500
NA
1088GSM1677727NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013696GPL16791HiSeq 2500
NA
1089GSM1677728NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013697GPL16791HiSeq 2500
NA
1090GSM1677729NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013698GPL16791HiSeq 2500
NA
1091GSM1677730NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013699GPL16791HiSeq 2500
NA
1092GSM1677731NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013700GPL16791HiSeq 2500
NA
1093GSM1677732NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013701GPL16791HiSeq 2500
NA
1094GSM1677733NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013702GPL16791HiSeq 2500
NA
1095GSM1677734NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013703GPL16791HiSeq 2500
NA
1096GSM1677735NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013704GPL16791HiSeq 2500
NA
1097GSM1677736NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013705GPL16791HiSeq 2500
NA
1098GSM1677737NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013706GPL16791HiSeq 2500
NA
1099GSM1677738NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013707GPL16791HiSeq 2500
NA
1100GSM1677739NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013708GPL16791HiSeq 2500
NA
1101GSM1677740NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013709GPL16791HiSeq 2500
NA
1102GSM1677741NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013710GPL16791HiSeq 2500
NA
1103GSM1677742NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013711GPL16791HiSeq 2500
NA
1104GSM1677743NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013712GPL16791HiSeq 2500
NA
1105GSM1677744NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013713GPL16791HiSeq 2500
NA
1106GSM1677745NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013714GPL16791HiSeq 2500
NA
1107GSM1677746NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013715GPL16791HiSeq 2500
NA
1108GSM1677747NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013716GPL16791HiSeq 2500
NA
1109GSM1677748NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013717GPL16791HiSeq 2500
NA
1110GSM1677749NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013718GPL16791HiSeq 2500
NA
1111GSM1677750NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013719GPL16791HiSeq 2500
NA
1112GSM1677751NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013720GPL16791HiSeq 2500
NA
1113GSM1677752NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013721GPL16791HiSeq 2500
NA
1114GSM1677753NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013722GPL16791HiSeq 2500
NA
1115GSM1677754NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013723GPL16791HiSeq 2500
NA
1116GSM1677755NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013724GPL16791HiSeq 2500
NA
1117GSM1677756NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013725GPL16791HiSeq 2500
NA
1118GSM1677757NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013726GPL16791HiSeq 2500
NA
1119GSM1677758NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013727GPL16791HiSeq 2500
NA
1120GSM1677759NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013728GPL16791HiSeq 2500
NA
1121GSM1677760NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013729GPL16791HiSeq 2500
NA
1122GSM1677761NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013730GPL16791HiSeq 2500
NA
1123GSM1677762NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013731GPL16791HiSeq 2500
NA
1124GSM1677763NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013732GPL16791HiSeq 2500
NA
1125GSM1677764NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013733GPL16791HiSeq 2500
NA
1126GSM1677765NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013734GPL16791HiSeq 2500
NA
1127GSM1677766NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013735GPL16791HiSeq 2500
NA
1128GSM1677767NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013736GPL16791HiSeq 2500
NA
1129GSM1677768NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013737GPL16791HiSeq 2500
NA
1130GSM1677769NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013738GPL16791HiSeq 2500
NA
1131GSM1677770NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013739GPL16791HiSeq 2500
NA
1132GSM1677771NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013740GPL16791HiSeq 2500
NA
1133GSM1677772NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013741GPL16791HiSeq 2500
NA
1134GSM1677773NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013742GPL16791HiSeq 2500
NA
1135GSM1677774NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013743GPL16791HiSeq 2500
NA
1136GSM1677775NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013744GPL16791HiSeq 2500
NA
1137GSM1677776NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013745GPL16791HiSeq 2500
NA
1138GSM1677777NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013746GPL16791HiSeq 2500
NA
1139GSM1677778NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013747GPL16791HiSeq 2500
NA
1140GSM1677779NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013748GPL16791HiSeq 2500
NA
1141GSM1677780NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013749GPL16791HiSeq 2500
NA
1142GSM1677781NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013750GPL16791HiSeq 2500
NA
1143GSM1677782NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013751GPL16791HiSeq 2500
NA
1144GSM1677783NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013752GPL16791HiSeq 2500
NA
1145GSM1677784NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013753GPL16791HiSeq 2500
NA
1146GSM1677785NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013754GPL16791HiSeq 2500
NA
1147GSM1677786NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013755GPL16791HiSeq 2500
NA
1148GSM1677787NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013756GPL16791HiSeq 2500
NA
1149GSM1677788NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013757GPL16791HiSeq 2500
NA
1150GSM1677789NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013758GPL16791HiSeq 2500
NA
1151GSM1677790NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013759GPL16791HiSeq 2500
NA
1152GSM1677791NAHumanGonadal Somatic CellEmbryoSRP050499SRR2013760GPL16791HiSeq 2500
NA
1153GSM1677792NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013761GPL16791HiSeq 2500
NA
1154GSM1677793NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013762GPL16791HiSeq 2500
NA
1155GSM1677794NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013763GPL16791HiSeq 2500
NA
1156GSM1677795NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013764GPL16791HiSeq 2500
NA
1157GSM1677796NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013765GPL16791HiSeq 2500
NA
1158GSM1677797NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013766GPL16791HiSeq 2500
NA
1159GSM1677798NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013767GPL16791HiSeq 2500
NA
1160GSM1677799NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013768GPL16791HiSeq 2500
NA
1161GSM1677800NAHumanPrimordial Germ CellEmbryoSRP050499SRR2013769GPL16791HiSeq 2500
NA
1162GSM1538995NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643167GPL11154HiSeq 2000
NA
1163GSM1538995NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643168GPL11154HiSeq 2000
NA
1164GSM1538995NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643169GPL11154HiSeq 2000
NA
1165GSM1538995NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643170GPL11154HiSeq 2000
NA
1166GSM1538996NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643171GPL11154HiSeq 2000
NA
1167GSM1538996NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643172GPL11154HiSeq 2000
NA
1168GSM1538996NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643173GPL11154HiSeq 2000
NA
1169GSM1538996NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643174GPL11154HiSeq 2000
NA
1170GSM1538997NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643175GPL11154HiSeq 2000
NA
1171GSM1538997NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643176GPL11154HiSeq 2000
NA
1172GSM1538997NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643177GPL11154HiSeq 2000
NA
1173GSM1538997NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643178GPL11154HiSeq 2000
NA
1174GSM1538998NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643179GPL11154HiSeq 2000
NA
1175GSM1538998NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643180GPL11154HiSeq 2000
NA
1176GSM1538998NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643181GPL11154HiSeq 2000
NA
1177GSM1538998NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643182GPL11154HiSeq 2000
NA
1178GSM1538999NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643183GPL11154HiSeq 2000
NA
1179GSM1538999NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643184GPL11154HiSeq 2000
NA
1180GSM1538999NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643185GPL11154HiSeq 2000
NA
1181GSM1538999NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643186GPL11154HiSeq 2000
NA
1182GSM1539000NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643187GPL11154HiSeq 2000
NA
1183GSM1539000NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643188GPL11154HiSeq 2000
NA
1184GSM1539000NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643189GPL11154HiSeq 2000
NA
1185GSM1539000NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643190GPL11154HiSeq 2000
NA
1186GSM1539001NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643191GPL11154HiSeq 2000
NA
1187GSM1539001NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643192GPL11154HiSeq 2000
NA
1188GSM1539002NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643193GPL11154HiSeq 2000
NA
1189GSM1539002NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643194GPL11154HiSeq 2000
NA
1190GSM1539003NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643195GPL11154HiSeq 2000
NA
1191GSM1539003NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643196GPL11154HiSeq 2000
NA
1192GSM1539004NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643197GPL11154HiSeq 2000
NA
1193GSM1539004NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643198GPL11154HiSeq 2000
NA
1194GSM1539005NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643199GPL11154HiSeq 2000
NA
1195GSM1539005NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643200GPL11154HiSeq 2000
NA
1196GSM1539006NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643201GPL11154HiSeq 2000
NA
1197GSM1539006NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643202GPL11154HiSeq 2000
NA
1198GSM1539007NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643203GPL11154HiSeq 2000
NA
1199GSM1539007NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643204GPL11154HiSeq 2000
NA
1200GSM1539008NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643205GPL11154HiSeq 2000
NA
1201GSM1539008NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643206GPL11154HiSeq 2000
NA
1202GSM1539008NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643207GPL11154HiSeq 2000
NA
1203GSM1539008NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643208GPL11154HiSeq 2000
NA
1204GSM1539009NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643209GPL11154HiSeq 2000
NA
1205GSM1539009NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643210GPL11154HiSeq 2000
NA
1206GSM1539010NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643211GPL11154HiSeq 2000
NA
1207GSM1539010NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643212GPL11154HiSeq 2000
NA
1208GSM1539010NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643213GPL11154HiSeq 2000
NA
1209GSM1539010NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643214GPL11154HiSeq 2000
NA
1210GSM1539011NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643215GPL11154HiSeq 2000
NA
1211GSM1539011NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643216GPL11154HiSeq 2000
NA
1212GSM1539011NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643217GPL11154HiSeq 2000
NA
1213GSM1539011NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643218GPL11154HiSeq 2000
NA
1214GSM1539012NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643219GPL11154HiSeq 2000
NA
1215GSM1539012NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643220GPL11154HiSeq 2000
NA
1216GSM1539013NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643221GPL11154HiSeq 2000
NA
1217GSM1539013NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643222GPL11154HiSeq 2000
NA
1218GSM1539014NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643223GPL11154HiSeq 2000
NA
1219GSM1539014NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643224GPL11154HiSeq 2000
NA
1220GSM1539014NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643225GPL11154HiSeq 2000
NA
1221GSM1539014NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643226GPL11154HiSeq 2000
NA
1222GSM1539015NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643227GPL11154HiSeq 2000
NA
1223GSM1539015NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643228GPL11154HiSeq 2000
NA
1224GSM1539016NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643229GPL11154HiSeq 2000
NA
1225GSM1539017NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643230GPL11154HiSeq 2000
NA
1226GSM1539018NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643231GPL11154HiSeq 2000
NA
1227GSM1539019NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643232GPL11154HiSeq 2000
NA
1228GSM1539020NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643233GPL11154HiSeq 2000
NA
1229GSM1539020NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643234GPL11154HiSeq 2000
NA
1230GSM1539021NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643235GPL11154HiSeq 2000
NA
1231GSM1539022NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643236GPL11154HiSeq 2000
NA
1232GSM1539022NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643237GPL11154HiSeq 2000
NA
1233GSM1539023NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643238GPL11154HiSeq 2000
NA
1234GSM1539023NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643239GPL11154HiSeq 2000
NA
1235GSM1539023NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643240GPL11154HiSeq 2000
NA
1236GSM1539023NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643241GPL11154HiSeq 2000
NA
1237GSM1539024NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643242GPL11154HiSeq 2000
NA
1238GSM1539025NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643243GPL11154HiSeq 2000
NA
1239GSM1539026NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643244GPL11154HiSeq 2000
NA
1240GSM1539026NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643245GPL11154HiSeq 2000
NA
1241GSM1539026NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643246GPL11154HiSeq 2000
NA
1242GSM1539026NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643247GPL11154HiSeq 2000
NA
1243GSM1539027NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643248GPL11154HiSeq 2000
NA
1244GSM1539028NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643249GPL11154HiSeq 2000
NA
1245GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643250GPL11154HiSeq 2000
NA
1246GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643251GPL11154HiSeq 2000
NA
1247GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643252GPL11154HiSeq 2000
NA
1248GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643253GPL11154HiSeq 2000
NA
1249GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643254GPL11154HiSeq 2000
NA
1250GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643255GPL11154HiSeq 2000
NA
1251GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643256GPL11154HiSeq 2000
NA
1252GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643257GPL11154HiSeq 2000
NA
1253GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643258GPL11154HiSeq 2000
NA
1254GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643259GPL11154HiSeq 2000
NA
1255GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643260GPL11154HiSeq 2000
NA
1256GSM1539029NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643261GPL11154HiSeq 2000
NA
1257GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643262GPL11154HiSeq 2000
NA
1258GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643263GPL11154HiSeq 2000
NA
1259GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643264GPL11154HiSeq 2000
NA
1260GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643265GPL11154HiSeq 2000
NA
1261GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643266GPL11154HiSeq 2000
NA
1262GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643267GPL11154HiSeq 2000
NA
1263GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643268GPL11154HiSeq 2000
NA
1264GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643269GPL11154HiSeq 2000
NA
1265GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643270GPL11154HiSeq 2000
NA
1266GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643271GPL11154HiSeq 2000
NA
1267GSM1539030NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643272GPL11154HiSeq 2000
NA
1268GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643273GPL11154HiSeq 2000
NA
1269GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643274GPL11154HiSeq 2000
NA
1270GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643275GPL11154HiSeq 2000
NA
1271GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643276GPL11154HiSeq 2000
NA
1272GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643277GPL11154HiSeq 2000
NA
1273GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643278GPL11154HiSeq 2000
NA
1274GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643279GPL11154HiSeq 2000
NA
1275GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643280GPL11154HiSeq 2000
NA
1276GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643281GPL11154HiSeq 2000
NA
1277GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643282GPL11154HiSeq 2000
NA
1278GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643283GPL11154HiSeq 2000
NA
1279GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643284GPL11154HiSeq 2000
NA
1280GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643285GPL11154HiSeq 2000
NA
1281GSM1539031NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643286GPL11154HiSeq 2000
NA
1282GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643287GPL11154HiSeq 2000
NA
1283GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643288GPL11154HiSeq 2000
NA
1284GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643289GPL11154HiSeq 2000
NA
1285GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643290GPL11154HiSeq 2000
NA
1286GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643291GPL11154HiSeq 2000
NA
1287GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643292GPL11154HiSeq 2000
NA
1288GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643293GPL11154HiSeq 2000
NA
1289GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643294GPL11154HiSeq 2000
NA
1290GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643295GPL11154HiSeq 2000
NA
1291GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643296GPL11154HiSeq 2000
NA
1292GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643297GPL11154HiSeq 2000
NA
1293GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643298GPL11154HiSeq 2000
NA
1294GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643299GPL11154HiSeq 2000
NA
1295GSM1539032NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643300GPL11154HiSeq 2000
NA
1296GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643301GPL11154HiSeq 2000
NA
1297GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643302GPL11154HiSeq 2000
NA
1298GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643303GPL11154HiSeq 2000
NA
1299GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643304GPL11154HiSeq 2000
NA
1300GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643305GPL11154HiSeq 2000
NA
1301GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643306GPL11154HiSeq 2000
NA
1302GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643307GPL11154HiSeq 2000
NA
1303GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643308GPL11154HiSeq 2000
NA
1304GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643309GPL11154HiSeq 2000
NA
1305GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643310GPL11154HiSeq 2000
NA
1306GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643311GPL11154HiSeq 2000
NA
1307GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643312GPL11154HiSeq 2000
NA
1308GSM1539033NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643313GPL11154HiSeq 2000
NA
1309GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643314GPL11154HiSeq 2000
NA
1310GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643315GPL11154HiSeq 2000
NA
1311GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643316GPL11154HiSeq 2000
NA
1312GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643317GPL11154HiSeq 2000
NA
1313GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643318GPL11154HiSeq 2000
NA
1314GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643319GPL11154HiSeq 2000
NA
1315GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643320GPL11154HiSeq 2000
NA
1316GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643321GPL11154HiSeq 2000
NA
1317GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643322GPL11154HiSeq 2000
NA
1318GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643323GPL11154HiSeq 2000
NA
1319GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643324GPL11154HiSeq 2000
NA
1320GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643325GPL11154HiSeq 2000
NA
1321GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643326GPL11154HiSeq 2000
NA
1322GSM1539034NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643327GPL11154HiSeq 2000
NA
1323GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643328GPL11154HiSeq 2000
NA
1324GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643329GPL11154HiSeq 2000
NA
1325GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643330GPL11154HiSeq 2000
NA
1326GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643331GPL11154HiSeq 2000
NA
1327GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643332GPL11154HiSeq 2000
NA
1328GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643333GPL11154HiSeq 2000
NA
1329GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643334GPL11154HiSeq 2000
NA
1330GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643335GPL11154HiSeq 2000
NA
1331GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643336GPL11154HiSeq 2000
NA
1332GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643337GPL11154HiSeq 2000
NA
1333GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643338GPL11154HiSeq 2000
NA
1334GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643339GPL11154HiSeq 2000
NA
1335GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643340GPL11154HiSeq 2000
NA
1336GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643341GPL11154HiSeq 2000
NA
1337GSM1539035NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643342GPL11154HiSeq 2000
NA
1338GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643343GPL11154HiSeq 2000
NA
1339GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643344GPL11154HiSeq 2000
NA
1340GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643345GPL11154HiSeq 2000
NA
1341GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643346GPL11154HiSeq 2000
NA
1342GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643347GPL11154HiSeq 2000
NA
1343GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643348GPL11154HiSeq 2000
NA
1344GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643349GPL11154HiSeq 2000
NA
1345GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643350GPL11154HiSeq 2000
NA
1346GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643351GPL11154HiSeq 2000
NA
1347GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643352GPL11154HiSeq 2000
NA
1348GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643353GPL11154HiSeq 2000
NA
1349GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643354GPL11154HiSeq 2000
NA
1350GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643355GPL11154HiSeq 2000
NA
1351GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643356GPL11154HiSeq 2000
NA
1352GSM1539036NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643357GPL11154HiSeq 2000
NA
1353GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643358GPL11154HiSeq 2000
NA
1354GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643359GPL11154HiSeq 2000
NA
1355GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643360GPL11154HiSeq 2000
NA
1356GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643361GPL11154HiSeq 2000
NA
1357GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643362GPL11154HiSeq 2000
NA
1358GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643363GPL11154HiSeq 2000
NA
1359GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643364GPL11154HiSeq 2000
NA
1360GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643365GPL11154HiSeq 2000
NA
1361GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643366GPL11154HiSeq 2000
NA
1362GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643367GPL11154HiSeq 2000
NA
1363GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643368GPL11154HiSeq 2000
NA
1364GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643369GPL11154HiSeq 2000
NA
1365GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643370GPL11154HiSeq 2000
NA
1366GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643371GPL11154HiSeq 2000
NA
1367GSM1539037NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643372GPL11154HiSeq 2000
NA
1368GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643373GPL11154HiSeq 2000
NA
1369GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643374GPL11154HiSeq 2000
NA
1370GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643375GPL11154HiSeq 2000
NA
1371GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643376GPL11154HiSeq 2000
NA
1372GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643377GPL11154HiSeq 2000
NA
1373GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643378GPL11154HiSeq 2000
NA
1374GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643379GPL11154HiSeq 2000
NA
1375GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643380GPL11154HiSeq 2000
NA
1376GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643381GPL11154HiSeq 2000
NA
1377GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643382GPL11154HiSeq 2000
NA
1378GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643383GPL11154HiSeq 2000
NA
1379GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643384GPL11154HiSeq 2000
NA
1380GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643385GPL11154HiSeq 2000
NA
1381GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643386GPL11154HiSeq 2000
NA
1382GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643387GPL11154HiSeq 2000
NA
1383GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643388GPL11154HiSeq 2000
NA
1384GSM1539038NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643389GPL11154HiSeq 2000
NA
1385GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643390GPL11154HiSeq 2000
NA
1386GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643391GPL11154HiSeq 2000
NA
1387GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643392GPL11154HiSeq 2000
NA
1388GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643393GPL11154HiSeq 2000
NA
1389GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643394GPL11154HiSeq 2000
NA
1390GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643395GPL11154HiSeq 2000
NA
1391GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643396GPL11154HiSeq 2000
NA
1392GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643397GPL11154HiSeq 2000
NA
1393GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643398GPL11154HiSeq 2000
NA
1394GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643399GPL11154HiSeq 2000
NA
1395GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643400GPL11154HiSeq 2000
NA
1396GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643401GPL11154HiSeq 2000
NA
1397GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643402GPL11154HiSeq 2000
NA
1398GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643403GPL11154HiSeq 2000
NA
1399GSM1539039NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643404GPL11154HiSeq 2000
NA
1400GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643405GPL11154HiSeq 2000
NA
1401GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643406GPL11154HiSeq 2000
NA
1402GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643407GPL11154HiSeq 2000
NA
1403GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643408GPL11154HiSeq 2000
NA
1404GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643409GPL11154HiSeq 2000
NA
1405GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643410GPL11154HiSeq 2000
NA
1406GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643411GPL11154HiSeq 2000
NA
1407GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643412GPL11154HiSeq 2000
NA
1408GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643413GPL11154HiSeq 2000
NA
1409GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643414GPL11154HiSeq 2000
NA
1410GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643415GPL11154HiSeq 2000
NA
1411GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643416GPL11154HiSeq 2000
NA
1412GSM1539040NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643417GPL11154HiSeq 2000
NA
1413GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643418GPL11154HiSeq 2000
NA
1414GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643419GPL11154HiSeq 2000
NA
1415GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643420GPL11154HiSeq 2000
NA
1416GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643421GPL11154HiSeq 2000
NA
1417GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643422GPL11154HiSeq 2000
NA
1418GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643423GPL11154HiSeq 2000
NA
1419GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643424GPL11154HiSeq 2000
NA
1420GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643425GPL11154HiSeq 2000
NA
1421GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643426GPL11154HiSeq 2000
NA
1422GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643427GPL11154HiSeq 2000
NA
1423GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643428GPL11154HiSeq 2000
NA
1424GSM1539041NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643429GPL11154HiSeq 2000
NA
1425GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643430GPL11154HiSeq 2000
NA
1426GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643431GPL11154HiSeq 2000
NA
1427GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643432GPL11154HiSeq 2000
NA
1428GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643433GPL11154HiSeq 2000
NA
1429GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643434GPL11154HiSeq 2000
NA
1430GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643435GPL11154HiSeq 2000
NA
1431GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643436GPL11154HiSeq 2000
NA
1432GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643437GPL11154HiSeq 2000
NA
1433GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643438GPL11154HiSeq 2000
NA
1434GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643439GPL11154HiSeq 2000
NA
1435GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643440GPL11154HiSeq 2000
NA
1436GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643441GPL11154HiSeq 2000
NA
1437GSM1539042NAHumanSkin Fibroblast-derived IPSCSkinSRP049593SRR1643442GPL11154HiSeq 2000
NA
1438GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643443GPL11154HiSeq 2000
NA
1439GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643444GPL11154HiSeq 2000
NA
1440GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643445GPL11154HiSeq 2000
NA
1441GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643446GPL11154HiSeq 2000
NA
1442GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643447GPL11154HiSeq 2000
NA
1443GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643448GPL11154HiSeq 2000
NA
1444GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643449GPL11154HiSeq 2000
NA
1445GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643450GPL11154HiSeq 2000
NA
1446GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643451GPL11154HiSeq 2000
NA
1447GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643452GPL11154HiSeq 2000
NA
1448GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643453GPL11154HiSeq 2000
NA
1449GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643454GPL11154HiSeq 2000
NA
1450GSM1539043NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643455GPL11154HiSeq 2000
NA
1451GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643456GPL11154HiSeq 2000
NA
1452GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643457GPL11154HiSeq 2000
NA
1453GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643458GPL11154HiSeq 2000
NA
1454GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643459GPL11154HiSeq 2000
NA
1455GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643460GPL11154HiSeq 2000
NA
1456GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643461GPL11154HiSeq 2000
NA
1457GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643462GPL11154HiSeq 2000
NA
1458GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643463GPL11154HiSeq 2000
NA
1459GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643464GPL11154HiSeq 2000
NA
1460GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643465GPL11154HiSeq 2000
NA
1461GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643466GPL11154HiSeq 2000
NA
1462GSM1539044NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643467GPL11154HiSeq 2000
NA
1463GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643468GPL11154HiSeq 2000
NA
1464GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643469GPL11154HiSeq 2000
NA
1465GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643470GPL11154HiSeq 2000
NA
1466GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643471GPL11154HiSeq 2000
NA
1467GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643472GPL11154HiSeq 2000
NA
1468GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643473GPL11154HiSeq 2000
NA
1469GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643474GPL11154HiSeq 2000
NA
1470GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643475GPL11154HiSeq 2000
NA
1471GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643476GPL11154HiSeq 2000
NA
1472GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643477GPL11154HiSeq 2000
NA
1473GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643478GPL11154HiSeq 2000
NA
1474GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643479GPL11154HiSeq 2000
NA
1475GSM1539045NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643480GPL11154HiSeq 2000
NA
1476GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643481GPL11154HiSeq 2000
NA
1477GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643482GPL11154HiSeq 2000
NA
1478GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643483GPL11154HiSeq 2000
NA
1479GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643484GPL11154HiSeq 2000
NA
1480GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643485GPL11154HiSeq 2000
NA
1481GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643486GPL11154HiSeq 2000
NA
1482GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643487GPL11154HiSeq 2000
NA
1483GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643488GPL11154HiSeq 2000
NA
1484GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643489GPL11154HiSeq 2000
NA
1485GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643490GPL11154HiSeq 2000
NA
1486GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643491GPL11154HiSeq 2000
NA
1487GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643492GPL11154HiSeq 2000
NA
1488GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643493GPL11154HiSeq 2000
NA
1489GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643494GPL11154HiSeq 2000
NA
1490GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643495GPL11154HiSeq 2000
NA
1491GSM1539046NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643496GPL11154HiSeq 2000
NA
1492GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643497GPL11154HiSeq 2000
NA
1493GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643498GPL11154HiSeq 2000
NA
1494GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643499GPL11154HiSeq 2000
NA
1495GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643500GPL11154HiSeq 2000
NA
1496GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643501GPL11154HiSeq 2000
NA
1497GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643502GPL11154HiSeq 2000
NA
1498GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643503GPL11154HiSeq 2000
NA
1499GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643504GPL11154HiSeq 2000
NA
1500GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643505GPL11154HiSeq 2000
NA
1501GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643506GPL11154HiSeq 2000
NA
1502GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643507GPL11154HiSeq 2000
NA
1503GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643508GPL11154HiSeq 2000
NA
1504GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643509GPL11154HiSeq 2000
NA
1505GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643510GPL11154HiSeq 2000
NA
1506GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643511GPL11154HiSeq 2000
NA
1507GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643512GPL11154HiSeq 2000
NA
1508GSM1539047NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643513GPL11154HiSeq 2000
NA
1509GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643514GPL11154HiSeq 2000
NA
1510GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643515GPL11154HiSeq 2000
NA
1511GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643516GPL11154HiSeq 2000
NA
1512GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643517GPL11154HiSeq 2000
NA
1513GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643518GPL11154HiSeq 2000
NA
1514GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643519GPL11154HiSeq 2000
NA
1515GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643520GPL11154HiSeq 2000
NA
1516GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643521GPL11154HiSeq 2000
NA
1517GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643522GPL11154HiSeq 2000
NA
1518GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643523GPL11154HiSeq 2000
NA
1519GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643524GPL11154HiSeq 2000
NA
1520GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643525GPL11154HiSeq 2000
NA
1521GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643526GPL11154HiSeq 2000
NA
1522GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643527GPL11154HiSeq 2000
NA
1523GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643528GPL11154HiSeq 2000
NA
1524GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643529GPL11154HiSeq 2000
NA
1525GSM1539048NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643530GPL11154HiSeq 2000
NA
1526GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643531GPL11154HiSeq 2000
NA
1527GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643532GPL11154HiSeq 2000
NA
1528GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643533GPL11154HiSeq 2000
NA
1529GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643534GPL11154HiSeq 2000
NA
1530GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643535GPL11154HiSeq 2000
NA
1531GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643536GPL11154HiSeq 2000
NA
1532GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643537GPL11154HiSeq 2000
NA
1533GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643538GPL11154HiSeq 2000
NA
1534GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643539GPL11154HiSeq 2000
NA
1535GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643540GPL11154HiSeq 2000
NA
1536GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643541GPL11154HiSeq 2000
NA
1537GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643542GPL11154HiSeq 2000
NA
1538GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643543GPL11154HiSeq 2000
NA
1539GSM1539049NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643544GPL11154HiSeq 2000
NA
1540GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643545GPL11154HiSeq 2000
NA
1541GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643546GPL11154HiSeq 2000
NA
1542GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643547GPL11154HiSeq 2000
NA
1543GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643548GPL11154HiSeq 2000
NA
1544GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643549GPL11154HiSeq 2000
NA
1545GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643550GPL11154HiSeq 2000
NA
1546GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643551GPL11154HiSeq 2000
NA
1547GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643552GPL11154HiSeq 2000
NA
1548GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643553GPL11154HiSeq 2000
NA
1549GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643554GPL11154HiSeq 2000
NA
1550GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643555GPL11154HiSeq 2000
NA
1551GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643556GPL11154HiSeq 2000
NA
1552GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643557GPL11154HiSeq 2000
NA
1553GSM1539050NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643558GPL11154HiSeq 2000
NA
1554GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643559GPL11154HiSeq 2000
NA
1555GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643560GPL11154HiSeq 2000
NA
1556GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643561GPL11154HiSeq 2000
NA
1557GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643562GPL11154HiSeq 2000
NA
1558GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643563GPL11154HiSeq 2000
NA
1559GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643564GPL11154HiSeq 2000
NA
1560GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643565GPL11154HiSeq 2000
NA
1561GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643566GPL11154HiSeq 2000
NA
1562GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643567GPL11154HiSeq 2000
NA
1563GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643568GPL11154HiSeq 2000
NA
1564GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643569GPL11154HiSeq 2000
NA
1565GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643570GPL11154HiSeq 2000
NA
1566GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643571GPL11154HiSeq 2000
NA
1567GSM1539051NAHumanMesenchymal Stem Cells (MSC), IPSC-derivedNASRP049593SRR1643572GPL11154HiSeq 2000
NA
1568SAMN02870137NAHumanB CellBloodSRP043513SRR1449123GPL11154HiSeq 2000
NA
1569SAMN02870136 NAHumanB CellBloodSRP043513SRR1449124GPL11154HiSeq 2000
NA
1570GSM1297624NAHumanAdipose Derived Stem CellNASRP034712SRR1058003GPL11154HiSeq 2000
NA
1571GSM1297625NAHumanAdipose Derived Stem CellNASRP034712SRR1058004GPL11154HiSeq 2000
NA
1572GSM1297626NAHumanAdipose Derived Stem CellNASRP034712SRR1058005GPL11154HiSeq 2000
NA
1573GSM1297627NAHumanAdipose Derived Stem CellNASRP034712SRR1058006GPL11154HiSeq 2000
NA
1574GSM1297628NAHumanAdipose Derived Stem CellNASRP034712SRR1058007GPL11154HiSeq 2000
NA
1575GSM1297629NAHumanAdipose Derived Stem CellNASRP034712SRR1058008GPL11154HiSeq 2000
NA
1576GSM1297630NAHumanAdipose Derived Stem CellNASRP034712SRR1058009GPL11154HiSeq 2000
NA
1577GSM1297631NAHumanAdipose Derived Stem CellNASRP034712SRR1058010GPL11154HiSeq 2000
NA
1578GSM1297632NAHumanAdipose Derived Stem CellNASRP034712SRR1058011GPL11154HiSeq 2000
NA
1579GSM1297633NAHumanAdipose Derived Stem CellNASRP034712SRR1058012GPL11154HiSeq 2000
NA
1580GSM1297634NAHumanAdipose Derived Stem CellNASRP034712SRR1058013GPL11154HiSeq 2000
NA
1581GSM1297635NAHumanAdipose Derived Stem CellNASRP034712SRR1058014GPL11154HiSeq 2000
NA
1582GSM1297636NAHumanAdipose Derived Stem CellNASRP034712SRR1058015GPL11154HiSeq 2000
NA
1583GSM1297637NAHumanAdipose Derived Stem CellNASRP034712SRR1058016GPL11154HiSeq 2000
NA
1584GSM1297638NAHumanAdipose Derived Stem CellNASRP034712SRR1058017GPL11154HiSeq 2000
NA
1585GSM1297639NAHumanAdipose Derived Stem CellNASRP034712SRR1058018GPL11154HiSeq 2000
NA
1586GSM1297640NAHumanAdipose Derived Stem CellNASRP034712SRR1058019GPL11154HiSeq 2000
NA
1587GSM1297641NAHumanAdipose Derived Stem CellNASRP034712SRR1058020GPL11154HiSeq 2000
NA
1588GSM1297642NAHumanAdipose Derived Stem CellNASRP034712SRR1058021GPL11154HiSeq 2000
NA
1589GSM1297643NAHumanAdipose Derived Stem CellNASRP034712SRR1058022GPL11154HiSeq 2000
NA
1590GSM1297644NAHumanAdipose Derived Stem CellNASRP034712SRR1058023GPL11154HiSeq 2000
NA
1591GSM1297645NAHumanAdipose Derived Stem CellNASRP034712SRR1058024GPL11154HiSeq 2000
NA
1592GSM1297646NAHumanAdipose Derived Stem CellNASRP034712SRR1058025GPL11154HiSeq 2000
NA
1593GSM1297647NAHumanAdipose Derived Stem CellNASRP034712SRR1058026GPL16791HiSeq 2500
NA
1594GSM1297648NAHumanAdipose Derived Stem CellNASRP034712SRR1058027GPL16791HiSeq 2500
NA
1595GSM1297649NAHumanAdipose Derived Stem CellNASRP034712SRR1058028GPL16791HiSeq 2500
NA
1596GSM1297650NAHumanAdipose Derived Stem CellNASRP034712SRR1058029GPL16791HiSeq 2500
NA
1597GSM1297651NAHumanAdipose Derived Stem CellNASRP034712SRR1058030GPL16791HiSeq 2500
NA
1598GSM1297652NAHumanAdipose Derived Stem CellNASRP034712SRR1058031GPL16791HiSeq 2500
NA
1599GSM1297653NAHumanAdipose Derived Stem CellNASRP034712SRR1058032GPL16791HiSeq 2500
NA
1600GSM1297654NAHumanAdipose Derived Stem CellNASRP034712SRR1058033GPL16791HiSeq 2500
NA
1601GSM1297655NAHumanAdipose Derived Stem CellNASRP034712SRR1058034GPL16791HiSeq 2500
NA
1602GSM1297656NAHumanAdipose Derived Stem CellNASRP034712SRR1058035GPL16791HiSeq 2500
NA
1603GSM1297657NAHumanAdipose Derived Stem CellNASRP034712SRR1058036GPL16791HiSeq 2500
NA
1604GSM1297658NAHumanAdipose Derived Stem CellNASRP034712SRR1058037GPL16791HiSeq 2500
NA
1605GSM1297659NAHumanAdipose Derived Stem CellNASRP034712SRR1058038GPL16791HiSeq 2500
NA
1606GSM1297660NAHumanAdipose Derived Stem CellNASRP034712SRR1058039GPL16791HiSeq 2500
NA
1607GSM1297661NAHumanAdipose Derived Stem CellNASRP034712SRR1058040GPL16791HiSeq 2500
NA
1608GSM1297662NAHumanAdipose Derived Stem CellNASRP034712SRR1058041GPL16791HiSeq 2500
NA
1609GSM1297663NAHumanAdipose Derived Stem CellNASRP034712SRR1058042GPL16791HiSeq 2500
NA
1610GSM1297664NAHumanAdipose Derived Stem CellNASRP034712SRR1058043GPL16791HiSeq 2500
NA
1611GSM1297665NAHumanAdipose Derived Stem CellNASRP034712SRR1058044GPL16791HiSeq 2500
NA
1612GSM1297666NAHumanAdipose Derived Stem CellNASRP034712SRR1058045GPL16791HiSeq 2500
NA
1613GSM1297667NAHumanAdipose Derived Stem CellNASRP034712SRR1058046GPL16791HiSeq 2500
NA
1614GSM12689071020000-189MouseNeuronCerebral CortexSRP033139SRR1033318GPL13112HiSeq 2000
Individual cells were collected by Pipette. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Samples. Included as a column of the SAMPLES section above, labelled "protocol: extract protocol"Samples were prepared for multiplexed paired-end Illumina sequencing using TruSeq according to manufacturer instructions.
1615GSM12689081020000-189MouseNeuronCerebral CortexSRP033139SRR1033319GPL13112HiSeq 2000
Individual cells were collected by Pipette. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Samples. Included as a column of the SAMPLES section above, labelled "protocol: extract protocol"Samples were prepared for multiplexed paired-end Illumina sequencing using TruSeq according to manufacturer instructions.
1616GSM12689101020000-189MouseNeuronCerebral CortexSRP033139SRR1033321GPL13112HiSeq 2000
Individual cells were collected by Pipette. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Samples. Included as a column of the SAMPLES section above, labelled "protocol: extract protocol"Samples were prepared for multiplexed paired-end Illumina sequencing using TruSeq according to manufacturer instructions.
1617GSM12689111020000-189MouseNeuronCerebral CortexSRP033139SRR1033322GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1618GSM12689121020000-189MouseNeuronCerebral CortexSRP033139SRR1033323GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1619GSM12689131020000-189MouseNeuronCerebral CortexSRP033139SRR1033324GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1620GSM12689141020000-189MouseNeuronCerebral CortexSRP033139SRR1033325GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1621GSM12689151020900-134MouseNeuronHippocampusSRP033139SRR1033326GPL13112HiSeq 2000
Individual cells were collected by Pipette. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Samples. Included as a column of the SAMPLES section above, labelled "protocol: extract protocol"Samples were prepared for multiplexed paired-end Illumina sequencing using TruSeq according to manufacturer instructions.
1622GSM12689161020900-134MouseNeuronHippocampusSRP033139SRR1033327GPL13112HiSeq 2000
Individual cells were collected by Pipette. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Samples. Included as a column of the SAMPLES section above, labelled "protocol: extract protocol"Samples were prepared for multiplexed paired-end Illumina sequencing using TruSeq according to manufacturer instructions.
1623GSM12689171020900-134MouseNeuronHippocampusSRP033139SRR1033328GPL13112HiSeq 2000
Individual cells were collected by Pipette. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Samples. Included as a column of the SAMPLES section above, labelled "protocol: extract protocol"Samples were prepared for multiplexed paired-end Illumina sequencing using TruSeq according to manufacturer instructions.
1624GSM12689181020900-134MouseNeuronHippocampusSRP033139SRR1033329GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1625GSM12689191020900-134MouseNeuronHippocampusSRP033139SRR1033330GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1626GSM12689201020900-134MouseNeuronHippocampusSRP033139SRR1033331GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1627GSM12689211020900-134MouseNeuronHippocampusSRP033139SRR1033332GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. Photolysis was performed using the 405 nm laser at 30% power and 50 µs per pixel. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based method.Protocols applicable only to a subset of Sampl
1628GSM12689251020900-134MouseNeuronHippocampusSRP033139SRR1033336GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1629GSM12689261020900-134MouseNeuronHippocampusSRP033139SRR1033337GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1630GSM12689271020900-134MouseNeuronHippocampusSRP033139SRR1033338GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1631GSM12689281020900-134MouseNeuronHippocampusSRP033139SRR1033339GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1632GSM12689291020900-134MouseNeuronHippocampusSRP033139SRR1033340GPL13112HiSeq 2000
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1633GSM12689301020000-189MouseNeuronCerebral CortexSRP033139SRR1033341GPL17021HiSeq 2500
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1634GSM12689311020000-189MouseNeuronCerebral CortexSRP033139SRR1033342GPL17021HiSeq 2500
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1635GSM12689321020900-134MouseNeuronHippocampusSRP033139SRR1033343GPL17021HiSeq 2500
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1636GSM12689331020900-134MouseNeuronHippocampusSRP033139SRR1033344GPL17021HiSeq 2500
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1637GSM12689341020900-134MouseNeuronHippocampusSRP033139SRR1033345GPL17021HiSeq 2500
Individual cells were collected by TIVA. Imaging and photolysis were performed in the CA1 area of the hippocampus immediately on cells using a confocal microscope (Zeiss 710 Meta, 40x water objective, N.A. 1.0). Photolysis was performed using the 405 nm laser for uncaging at 80% power and 100.85 µs per pixel. Loading was confirmed by detecting Cy5 signal in the emission range excited by 561 nm, and uncaging was performed using the 405 nm laser while recording FRET excited by 514 nm and simultaneous capturing in Cy3 (538-599nm) and Cy5 (637-704nm) emission ranges. In some experiments, a line-scan analysis was performed using a 4-pixel-width line and averaging pixel values. After uncaging a single cell in the tissue, the imaged field and surrounding area, including the photolysed cell, was isolated by aspiration using a wide bore glass pipette, and further processed for mRNA analysis. Collected samples were individually amplified using 3 rounds of a linear in vitro-transcription-based m
1638GSM9674876020700-755MouseSecondary OocyteOvarian FollicleSRP014428SRR522060GPL13112HiSeq 2000
cDNA was generated as described in the manual for "SMARTer Ultra Low RNA Kit for Illumina sequencing" marketed by Clontech. Then, a sequencing library was generated as described in Illumina's "Ultra Low Input mRNA-Seq Guide".
1639GSM9674886020700-755MouseSecondary OocyteOvarian FollicleSRP014428SRR522061GPL13112HiSeq 2000
cDNA was generated as described in the manual for "SMARTer Ultra Low RNA Kit for Illumina sequencing" marketed by Clontech. Then, a sequencing library was generated as described in Illumina's "Ultra Low Input mRNA-Seq Guide".
1640GSM9674896020700-755MouseSecondary OocyteOvarian FollicleSRP014428SRR522062GPL13112HiSeq 2000
cDNA was generated as described in the manual for "SMARTer Ultra Low RNA Kit for Illumina sequencing" marketed by Clontech. Then, a sequencing library was generated as described in Illumina's "Ultra Low Input mRNA-Seq Guide".
1641GSM10801956020700-755MouseSecondary OocyteOvarian FollicleSRP018525SRR689233GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1642GSM10801966020700-755MouseSecondary OocyteOvarian FollicleSRP018525SRR689234GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1643GSM1080200NAMouse2-cell Embryo Cell2-cell EmbryoSRP018525SRR689238GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1644GSM1080201NAMouse2-cell Embryo Cell2-cell EmbryoSRP018525SRR689239GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1645GSM1080202NAMouse2-cell Embryo Cell2-cell EmbryoSRP018525SRR689240GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1646GSM1080203NAMouse4-cell Embryo Cell4-cell EmbryoSRP018525SRR689241GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1647GSM1080204NAMouse4-cell Embryo Cell4-cell EmbryoSRP018525SRR689242GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1648GSM1080205NAMouse4-cell Embryo Cell4-cell EmbryoSRP018525SRR689243GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1649GSM1080206NAMouse8-cell Embryo Cell8-cell EmbryoSRP018525SRR689244GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1650GSM1080207NAMouse8-cell Embryo Cell8-cell EmbryoSRP018525SRR689245GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1651GSM1080208NAMouse8-cell Embryo Cell8-cell EmbryoSRP018525SRR689246GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1652GSM1080209NAMouseMorula CellMorulaSRP018525SRR689247GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1653GSM1080210NAMouseMorula CellMorulaSRP018525SRR689248GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1654GSM1080211NAMouseMorula CellMorulaSRP018525SRR689249GPL13112HiSeq 2000
RNA was isolated from single cells or single morula embryos and amplified as previously described (Tang et al., 2010, Nat Protoc). Library construction was performed following Illumina manufacturer suggestions.
1655GSM13057773150000-009MouseMacrophageSpleenSRP035326SRR1106612GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1656GSM13057783150000-009MouseMacrophageSpleenSRP035326SRR1106613GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1657GSM13057793150000-009MouseMacrophageSpleenSRP035326SRR1106614GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1658GSM13057803150000-009MouseMacrophageSpleenSRP035326SRR1106615GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1659GSM13057813150000-009MouseMacrophageSpleenSRP035326SRR1106616GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1660GSM13057823150000-009MouseMacrophageSpleenSRP035326SRR1106617GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1661GSM13057833150000-009MouseMacrophageSpleenSRP035326SRR1106618GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1662GSM13057843150000-009MouseMacrophageSpleenSRP035326SRR1106619GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1663GSM13057853150000-009MouseMacrophageSpleenSRP035326SRR1106620GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1664GSM13057863150000-009MouseMacrophageSpleenSRP035326SRR1106621GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1665GSM13057873150000-009MouseMacrophageSpleenSRP035326SRR1106622GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1666GSM13057883150000-009MouseMacrophageSpleenSRP035326SRR1106623GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1667GSM13057893150000-009MouseMacrophageSpleenSRP035326SRR1106624GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1668GSM13057903150000-009MouseMacrophageSpleenSRP035326SRR1106625GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1669GSM13057913150000-009MouseMacrophageSpleenSRP035326SRR1106626GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system. single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1670GSM13057923150000-009MouseMacrophageSpleenSRP035326SRR1106627GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1671GSM13057933150000-009MouseMacrophageSpleenSRP035326SRR1106628GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1672GSM13057943150000-009MouseMacrophageSpleenSRP035326SRR1106629GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1673GSM13057953150000-009MouseMacrophageSpleenSRP035326SRR1106630GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1674GSM13057963150000-009MouseMacrophageSpleenSRP035326SRR1106631GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1675GSM13057973150000-009MouseMacrophageSpleenSRP035326SRR1106632GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1676GSM13057983150000-009MouseMacrophageSpleenSRP035326SRR1106633GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1677GSM13057993150000-009MouseMacrophageSpleenSRP035326SRR1106634GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1678GSM13058003150000-009MouseMacrophageSpleenSRP035326SRR1106635GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1679GSM13058013150000-009MouseMacrophageSpleenSRP035326SRR1106636GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1680GSM13058023150000-009MouseMacrophageSpleenSRP035326SRR1106637GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1681GSM13058033150000-009MouseMacrophageSpleenSRP035326SRR1106638GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1682GSM13058043150000-009MouseMacrophageSpleenSRP035326SRR1106639GPL13112HiSeq 2000
Each mouse was euthanized and spleen removed, homogenized to single cell suspension, red cells removed by selective lysis, and for all samples except for samples 11 and 12, the cell suspensions were enriched for CD11c-positive cells with anti-mouse CD11c antibodies coupled to magentic beads and the MACS system.single cell RNA-seq for gene expression quantitation: 3' end mRNA libraries were prepared for sequencing using a method developed at Dr. Ido Amit's lab, Weizmann Institute of Science
1683GSM12718623100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033853GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1684GSM12718633100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033854GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1685GSM12718643100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033855GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1686GSM12718653100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033856GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1687GSM12718663100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033857GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1688GSM12718673100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033858GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1689GSM12718683100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033859GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1690GSM12718693100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033860GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1691GSM12718703100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033861GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1692GSM12718713100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033862GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1693GSM12718723100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033863GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1694GSM12718733100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033864GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1695GSM12718743100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033865GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1696GSM12718753100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033866GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1697GSM12718763100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033867GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1698GSM12718773100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033868GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1699GSM12718783100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033869GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1700GSM12718793100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033870GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1701GSM12718803100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033871GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1702GSM12718813100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033872GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1703GSM12718843100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033875GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1704GSM12718853100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033876GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1705GSM12718863100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033877GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1706GSM12718873100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033878GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1707GSM12718883100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033879GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1708GSM12718893100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033880GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1709GSM12718903100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033881GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1710GSM12718913100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033882GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1711GSM12718923100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033883GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1712GSM12718933100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033884GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1713GSM12718943100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033885GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1714GSM12718953100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033886GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1715GSM12718963100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033887GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1716GSM12718973100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033888GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1717GSM12718983100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033889GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1718GSM12718993100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033890GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1719GSM12719003100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033891GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1720GSM12719013100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033892GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1721GSM12719023100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033893GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1722GSM12719033100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033894GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1723GSM12719043100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033895GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1724GSM12719053100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033896GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1725GSM12719063100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033897GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1726GSM12719073100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033898GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1727GSM12719083100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033899GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1728GSM12719093100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033900GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1729GSM12719103100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033901GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1730GSM12719113100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033902GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1731GSM12719123100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033903GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1732GSM12719133100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033904GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1733GSM12719143100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033905GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1734GSM12719153100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033906GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1735GSM12719163100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033907GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1736GSM12719173100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033908GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1737GSM12719183100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033909GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1738GSM12719193100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033910GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1739GSM12719203100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033911GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1740GSM12719213100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033912GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1741GSM12719223100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033913GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1742GSM12719233100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033914GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1743GSM12719243100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033915GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1744GSM12719253100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033916GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1745GSM12719263100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033917GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1746GSM12719273100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033918GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1747GSM12719283100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033919GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1748GSM12719293100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033920GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1749GSM12719303100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033921GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1750GSM12719313100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033922GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1751GSM12719323100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033923GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1752GSM12719333100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033924GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1753GSM12719343100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033925GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1754GSM12719353100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033926GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1755GSM12719363100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033927GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1756GSM12719373100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033928GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1757GSM12719383100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033929GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1758GSM12719393100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033930GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1759GSM12719403100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033931GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1760GSM12719413100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033932GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1761GSM12719423100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033933GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1762GSM12719433100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033934GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1763GSM12719453100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033936GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1764GSM12719463100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033937GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1765GSM12719473100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033938GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1766GSM12719483100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033939GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1767GSM12719493100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033940GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1768GSM12719503100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033941GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1769GSM12719513100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033942GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1770GSM12719523100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033943GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1771GSM12719533100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033944GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1772GSM12719543100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033945GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1773GSM12719553100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033946GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1774GSM12719563100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033947GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1775GSM12719573100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033948GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1776GSM12719583100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033949GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1777GSM12719593100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033950GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1778GSM12719603100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033951GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1779GSM12719613100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033952GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1780GSM12719623100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033953GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1781GSM12719633100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033954GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1782GSM12719643100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033955GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1783GSM12719653100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033956GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1784GSM12719663100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033957GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1785GSM12719673100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033958GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1786GSM12719683100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033959GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1787GSM12719693100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033960GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1788GSM12719703100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033961GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1789GSM12719713100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033962GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1790GSM12719723100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033963GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1791GSM12719733100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033964GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1792GSM12719743100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033965GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1793GSM12719753100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033966GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1794GSM12719763100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033967GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1795GSM12719773100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033968GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1796GSM12719783100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033969GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1797GSM12719793100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033970GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1798GSM12719803100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033971GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1799GSM12719813100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033972GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1800GSM12719823100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033973GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1801GSM12719833100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033974GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1802GSM12719843100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033975GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1803GSM12719853100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033976GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1804GSM12719863100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033977GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1805GSM12719873100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033978GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1806GSM12719883100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033979GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1807GSM12719893100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033980GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1808GSM12719903100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033981GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1809GSM12719913100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033982GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1810GSM12719923100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033983GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1811GSM12719933100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033984GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1812GSM12719943100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033985GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1813GSM12719953100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033986GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1814GSM12719963100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033987GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1815GSM12719973100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033988GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1816GSM12719983100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033989GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1817GSM12719993100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033990GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1818GSM12720003100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033991GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1819GSM12720013100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033992GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1820GSM12720023100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033993GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1821GSM12720033100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033994GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1822GSM12720043100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033995GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1823GSM12720053100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033996GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1824GSM12720063100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033997GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1825GSM12720073100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033998GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1826GSM12720083100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1033999GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1827GSM12720093100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034000GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1828GSM12720103100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034001GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1829GSM12720113100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034002GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1830GSM12720123100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034003GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1831GSM12720133100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034004GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1832GSM12720143100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034005GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1833GSM12720153100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034006GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1834GSM12720163100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034007GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1835GSM12720173100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034008GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1836GSM12720183100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034009GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1837GSM12720193100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034010GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1838GSM12720203100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034011GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1839GSM12720213100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034012GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1840GSM12720223100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034013GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1841GSM12720233100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034014GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1842GSM12720243100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034015GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1843GSM12720253100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034016GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1844GSM12720263100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034017GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1845GSM12720273100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034018GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1846GSM12720283100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034019GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1847GSM12720293100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034020GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1848GSM12720303100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034021GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1849GSM12720313100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034022GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1850GSM12720323100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034023GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1851GSM12720333100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034024GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1852GSM12720343100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034025GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1853GSM12720353100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034026GPL13112HiSeq 2000
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1854GSM12720363100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034027GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1855GSM12720373100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034028GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1856GSM12720383100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034029GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1857GSM12720393100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034030GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1858GSM12720403100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034031GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1859GSM12720413100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034032GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1860GSM12720423100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034033GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1861GSM12720433100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034034GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1862GSM12720443100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034035GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1863GSM12720453100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034036GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1864GSM12720463100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034037GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1865GSM12720473100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034038GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1866GSM12720483100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034039GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1867GSM12720493100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034040GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1868GSM12720503100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034041GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1869GSM12720513100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034042GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1870GSM12720523100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034043GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1871GSM12720533100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034044GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1872GSM12720543100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034045GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1873GSM12720553100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034046GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1874GSM12720563100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034047GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1875GSM12720573100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034048GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1876GSM12720583100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034049GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1877GSM12720593100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034050GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1878GSM12720603100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034051GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1879GSM12720613100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034052GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1880GSM12720623100200-254MouseType II PneumocyteDistal Lung EpitheliumSRP033209SRR1034053GPL16417MiSeq
Cells were loaded into the Fluidigm C1 microfluidic platform, where single cells were captured. Lysis of single cells, reverse-transcription of mRNA into cDNA as well as preamplification of cDNA occured within the microfluidic device using reagents provided by Fluidigm as well as the SMARTer Ultra Low RNA kit for Illumina (Clontech). External RNA spike-in transcripts (ERCC spike-in Mix, Ambion) were added to all single cell lysis reactions. As a bulk control, cDNA was prepared from approximately 200 cells in a PCR tube using the same protocol and reagents as used for the single cells. In addition, one "no cell control" was prepared using reagents without any cell input in a PCR tube.Libraries were prepared using Illumina Nextera XT kit per illumina's protocols.
1881GSM12800639020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043197, SRR1043198GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1882GSM12800649020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043199, SRR1043200GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1883GSM12800659020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043201, SRR1043202GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1884GSM12800669020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043203, SRR1043204GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1885GSM12800679020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043205, SRR1043206GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1886GSM12800689020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043207, SRR1043208GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1887GSM12800699020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043209, SRR1043210GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1888GSM12800709020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043211, SRR1043212GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1889GSM12800719020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043213, SRR1043214GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1890GSM12800729020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043215, SRR1043216GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1891GSM12800739020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043217, SRR1043218GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1892GSM12800749020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043219, SRR1043220GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1893GSM12800759020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043221, SRR1043222GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1894GSM12800769020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043223, SRR1043224GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1895GSM12800779020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043225, SRR1043226GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1896GSM12800789020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043227, SRR1043228GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1897GSM12800799020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043229, SRR1043230GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1898GSM12800809020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043231, SRR1043232GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1899GSM12800819020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043233, SRR1043234GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1900GSM12800829020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043235, SRR1043236GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1901GSM12800839020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043237, SRR1043238GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1902GSM12800849020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043239, SRR1043240GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1903GSM12800859020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043241, SRR1043242GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1904GSM12800869020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043243, SRR1043244GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1905GSM12800879020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043245, SRR1043246GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1906GSM12800889020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043247, SRR1043248GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1907GSM12800899020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043249, SRR1043250GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1908GSM12800909020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043251, SRR1043252GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1909GSM12800919020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043253, SRR1043254GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1910GSM12800929020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043255, SRR1043256GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1911GSM12800939020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043257, SRR1043258GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1912GSM12800949020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043259, SRR1043260GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1913GSM12800959020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043261, SRR1043262GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1914GSM12800969020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043263, SRR1043264GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1915GSM12800979020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043265, SRR1043266GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1916GSM12800989020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043267, SRR1043268GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1917GSM12800999020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043269, SRR1043270GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1918GSM12801009020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043271, SRR1043272GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1919GSM12801019020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043273, SRR1043274GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1920GSM12801029020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043275, SRR1043276GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1921GSM12801039020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043277, SRR1043278GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1922GSM12801049020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043279, SRR1043280GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1923GSM12801059020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043281, SRR1043282GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1924GSM12801069020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043283, SRR1043284GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1925GSM12801079020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043285, SRR1043286GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1926GSM12801089020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043287, SRR1043288GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1927GSM12801099020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043289, SRR1043290GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1928GSM12801109020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043291, SRR1043292GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1929GSM12801119020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043293, SRR1043294GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1930GSM12801129020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043295, SRR1043296GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1931GSM12801139020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043297, SRR1043298GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1932GSM12801149020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043299, SRR1043300GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1933GSM12801159020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043301, SRR1043302GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1934GSM12801169020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043303, SRR1043304GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1935GSM12801179020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043305, SRR1043306GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1936GSM12801189020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043307, SRR1043308GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1937GSM12801199020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043309, SRR1043310GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1938GSM12801209020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043311, SRR1043312GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1939GSM12801219020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043313, SRR1043314GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1940GSM12801229020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043315, SRR1043316GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1941GSM12801239020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043317, SRR1043318GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1942GSM12801249020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043319, SRR1043320GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1943GSM12801259020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043321, SRR1043322GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1944GSM12801269020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043323, SRR1043324GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1945GSM12801279020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043325, SRR1043326GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1946GSM12801289020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043327, SRR1043328GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1947GSM12801299020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043329, SRR1043330GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1948GSM12801309020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043331, SRR1043332GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1949GSM12801319020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043333, SRR1043334GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1950GSM12801329020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043335, SRR1043336GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1951GSM12801339020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043337, SRR1043338GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1952GSM12801349020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043339, SRR1043340GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1953GSM12801359020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043341, SRR1043342GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1954GSM12801369020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043343, SRR1043344GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1955GSM12801379020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043345, SRR1043346GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1956GSM12801389020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043347, SRR1043348GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1957GSM12801399020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043349, SRR1043350GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1958GSM12801409020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043351, SRR1043352GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1959GSM12801419020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043353, SRR1043354GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1960GSM12801429020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043355, SRR1043356GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1961GSM12801439020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043357, SRR1043358GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1962GSM12801449020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043359, SRR1043360GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1963GSM12801459020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043361, SRR1043362GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1964GSM12801469020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043363, SRR1043364GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1965GSM12801479020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043365, SRR1043366GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1966GSM12801489020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043367, SRR1043368GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1967GSM12801499020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043369, SRR1043370GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1968GSM12801509020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043371, SRR1043372GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1969GSM12801519020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043373, SRR1043374GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1970GSM12801529020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043375, SRR1043376GPL13112HiSeq 2000
A 30 _L aliquot of ~12000 cells was thawed and 20 _L C1 Suspension Reagent was added (all "C1" reagents were from Fluidigm, Inc.). 5 _L of this mix was loaded according to the manufacturer's protocol on a C1 Single-Cell AutoPrep IFC microfludic chip designed for 10-17 _m cells, and the chip was then processed on a Fluidigm C1 instrument using the "mRNA Seq: Cell Load (1772x/1773x)" script. This captured one cell in each of up to 96 capture chambers, and took approximately 30 minutes. The plate was then transferred to an automated microscope (Nikon TE2000E) and an image was acquired from each site using _Manager (http://micro-manager.org), which took less than 15 minutes.20 _L lysis buffer (0.15% Triton X-100, 1 U/_L TaKaRa RNase inhibitor, 4 _M reverse transcription primer C1-P1-T31, 5% C1 Loading Reagent and 1:50,000 Life Technologies ERCC Spike-In Mix 1), reverse transcription mix (1x SuperScript II First-Strand Buffer supplemented with 3 mM MgCl2, 1.5 mM dNTP, 4 mM DTT, 3.3% C1 Load
1971GSM12801539020000-715MouseEmbryonic Stem CellEmbryoSRP022764SRR1043377, SRR1043378GPL13112HiSeq 2000
A 30 _L aliquot of ~12000