| GSE64016 | GSM1562389 | Illumina HiSeq 2500 | Homo sapiens | H1_Exp1.003 | single H1 hESC | cell type: human embryonic stem cells; passages: 30-35; treatment: not sorted |
| GSE64016 | GSM1562654 | Illumina HiSeq 2500 | Homo sapiens | G1_Exp1.046 | single H1-Fucci cell sorted from G1 phase of the cell cycle only | cell type: human embryonic stem cells; passages: 35-40; treatment: FACS sorted |
| GSE69405 | GSM1702774 | Illumina HiSeq 2500 | Homo sapiens | LC-MBT-15_SC79 | PDX, LC-MBT-15 | cell type: PDX |
| GSE71315 | GSM1832427 | Illumina HiSeq 2500 | Homo sapiens | A2_N701_S503 | Cerebral Cortex GW20.5 | tissue: Cerebral Cortex; developmental stage: GW20.5 |
| GSE75140 | GSM1957078 | Illumina HiSeq 2500 | Homo sapiens | whOrg1_H2_hOrg33d_c1 | iPSC 409B2[33 days] | Stage: 33 days; tissue: Dissociated whole cerebral organoid |
| GSE75140 | GSM1957334 | Illumina HiSeq 2500 | Homo sapiens | whOrg5_D10_hOrg65d | iPSC 409B2[65 days] | Stage: 65 days; tissue: Dissociated whole cerebral organoid |
| GSE75140 | GSM1957623 | Illumina HiSeq 2500 | Homo sapiens | fetal1_D2_fetal_12wpc_c1 | fetal human cortex 1[12 weeks post-conception] | Stage: 12 weeks post-conception; tissue: Fetal neocortex |
| GSE69292 | GSM1697190 | Illumina HiSeq 2500 | Homo sapiens | q14_0 | hiF-T cell | well number: 56; reprogramming time point (day): 10 |
| GSE63818 | GSM1677690 | Illumina HiSeq 2500 | Homo sapiens | F_PGC_17W_embryo1_sc16 | Primordial Germ Cells[female 17 week gestation] | developmental stage: 17 week gestation; gender: female |
| GSE68596 | GSM1676569.25 | Illumina HiSeq 2500 | Homo sapiens | Single cell mRNA sequencing data from KMB7 cells | Cell line KBM7, derived from a patient with chronic myeloid leukemia | cell line: KBM7; cell type: myeloid leukemia; ploidy: 1N |
