SRX6478752 D6_iPSC_S6_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129030 D6_iPSC_S6_L006_R1_001 D6_iPSC_S6_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478753 D6_iPSC_S6_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129032 D6_iPSC_S6_L005_R1_001 D6_iPSC_S6_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478754 D6_iPSC_S6_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129036 D6_iPSC_S6_L008_R1_001 D6_iPSC_S6_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478755 D6_iPSC_S6_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129031 D6_iPSC_S6_L007_R1_001 D6_iPSC_S6_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478756 D6_iPSC_S6_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129033 D6_iPSC_S6_L002_R1_001 D6_iPSC_S6_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478757 D6_iPSC_S6_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129034 D6_iPSC_S6_L001_R1_001 D6_iPSC_S6_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478758 D6_iPSC_S6_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129035 D6_iPSC_S6_L004_R1_001 D6_iPSC_S6_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478759 D6_iPSC_S6_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129037 D6_iPSC_S6_L003_R1_001 D6_iPSC_S6_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478760 D6_iPSC_S7_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129038 D6_iPSC_S7_L002_R1_001 D6_iPSC_S7_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478761 D6_iPSC_S7_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129039 D6_iPSC_S7_L001_R1_001 D6_iPSC_S7_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478762 D8_iPSC_S38_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129040 D8_iPSC_S38_L004_R1_001 D8_iPSC_S38_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478763 D8_iPSC_S38_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129041 D8_iPSC_S38_L003_R1_001 D8_iPSC_S38_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478764 D8_iPSC_S38_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129042 D8_iPSC_S38_L006_R1_001 D8_iPSC_S38_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478765 D8_iPSC_S38_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129043 D8_iPSC_S38_L005_R1_001 D8_iPSC_S38_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478766 D8_iPSC_S38_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129044 D8_iPSC_S38_L008_R1_001 D8_iPSC_S38_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478767 D8_iPSC_S38_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129045 D8_iPSC_S38_L007_R1_001 D8_iPSC_S38_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478768 D8_iPSC_S39_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129046 D8_iPSC_S39_L002_R1_001 D8_iPSC_S39_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478769 D8_iPSC_S39_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129047 D8_iPSC_S39_L001_R1_001 D8_iPSC_S39_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478770 D8_iPSC_S39_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129048 D8_iPSC_S39_L004_R1_001 D8_iPSC_S39_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478771 D8_iPSC_S39_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129049 D8_iPSC_S39_L003_R1_001 D8_iPSC_S39_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478772 D2_S19_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129050 D2_S19_L007_R1_001 D2_S19_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478773 D2_S19_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129051 D2_S19_L008_R1_001 D2_S19_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478774 D5_S26_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129052 D5_S26_L007_R1_001 D5_S26_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478775 D5_S26_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129053 D5_S26_L008_R1_001 D5_S26_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478776 D5_S26_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129054 D5_S26_L005_R1_001 D5_S26_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478777 D5_S26_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129055 D5_S26_L006_R1_001 D5_S26_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478778 D5_S27_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129056 D5_S27_L003_R1_001 D5_S27_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478779 D5_S27_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129057 D5_S27_L004_R1_001 D5_S27_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478780 D5_S27_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129058 D5_S27_L001_R1_001 D5_S27_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478781 D5_S27_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129059 D5_S27_L002_R1_001 D5_S27_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478782 D5_S27_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129060 D5_S27_L005_R1_001 D5_S27_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478783 D5_S27_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129062 D5_S27_L006_R1_001 D5_S27_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478784 D2_S20_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129061 D2_S20_L001_R1_001 D2_S20_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478785 D2_S20_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129063 D2_S20_L002_R1_001 D2_S20_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478786 D10_iPSC_S15_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129064 D10_iPSC_S15_L004_R1_001 D10_iPSC_S15_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478787 D10_iPSC_S15_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129065 D10_iPSC_S15_L003_R1_001 D10_iPSC_S15_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478788 D10_iPSC_S15_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129066 D10_iPSC_S15_L006_R1_001 D10_iPSC_S15_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478789 D10_iPSC_S15_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129067 D10_iPSC_S15_L005_R1_001 D10_iPSC_S15_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478790 D10_iPSC_S15_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129068 D10_iPSC_S15_L008_R1_001 D10_iPSC_S15_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478791 D10_iPSC_S15_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129069 D10_iPSC_S15_L007_R1_001 D10_iPSC_S15_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478792 D10_iPSC_S16_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129070 D10_iPSC_S16_L002_R1_001 D10_iPSC_S16_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478793 D10_iPSC_S16_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129071 D10_iPSC_S16_L001_R1_001 D10_iPSC_S16_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478794 D10_iPSC_S16_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129072 D10_iPSC_S16_L004_R1_001 D10_iPSC_S16_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478795 D10_iPSC_S16_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129073 D10_iPSC_S16_L003_R1_001 D10_iPSC_S16_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478796 iPSC_S56_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129074 iPSC_S56_L007_R1_001 iPSC_S56_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478797 iPSC_S56_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129075 iPSC_S56_L008_R1_001 iPSC_S56_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478798 MEF_S29_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129076 MEF_S29_L001_R1_001 MEF_S29_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478799 MEF_S29_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129077 MEF_S29_L002_R1_001 MEF_S29_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478800 iPSC_S56_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129078 iPSC_S56_L003_R1_001 iPSC_S56_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478801 iPSC_S56_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129079 iPSC_S56_L004_R1_001 iPSC_S56_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478802 iPSC_S56_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129080 iPSC_S56_L005_R1_001 iPSC_S56_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478803 iPSC_S56_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129081 iPSC_S56_L006_R1_001 iPSC_S56_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478804 MEF_S29_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129082 MEF_S29_L003_R1_001 MEF_S29_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478805 MEF_S29_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129083 MEF_S29_L004_R1_001 MEF_S29_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478806 D7_iNSC_S44_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129084 D7_iNSC_S44_L002_R1_001 D7_iNSC_S44_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478807 D7_iNSC_S44_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129085 D7_iNSC_S44_L001_R1_001 D7_iNSC_S44_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478808 D7_iNSC_S43_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129086 D7_iNSC_S43_L002_R1_001 D7_iNSC_S43_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478809 D7_iNSC_S43_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129087 D7_iNSC_S43_L001_R1_001 D7_iNSC_S43_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478810 D7_iNSC_S43_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129088 D7_iNSC_S43_L004_R1_001 D7_iNSC_S43_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478811 D7_iNSC_S43_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129089 D7_iNSC_S43_L003_R1_001 D7_iNSC_S43_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478812 D7_iNSC_S43_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129090 D7_iNSC_S43_L006_R1_001 D7_iNSC_S43_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478813 D7_iNSC_S43_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129091 D7_iNSC_S43_L005_R1_001 D7_iNSC_S43_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478814 D7_iNSC_S43_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129092 D7_iNSC_S43_L008_R1_001 D7_iNSC_S43_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478815 D7_iNSC_S43_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129093 D7_iNSC_S43_L007_R1_001 D7_iNSC_S43_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478816 D6_iNSC_S4_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129094 D6_iNSC_S4_L003_R1_001 D6_iNSC_S4_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478817 D6_iNSC_S4_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129095 D6_iNSC_S4_L004_R1_001 D6_iNSC_S4_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478818 D6_iNSC_S4_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129098 D6_iNSC_S4_L001_R1_001 D6_iNSC_S4_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478819 D6_iNSC_S4_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129096 D6_iNSC_S4_L002_R1_001 D6_iNSC_S4_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478820 D6_iNSC_S3_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129097 D6_iNSC_S3_L007_R1_001 D6_iNSC_S3_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478821 D6_iNSC_S3_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129099 D6_iNSC_S3_L008_R1_001 D6_iNSC_S3_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478822 D6_iNSC_S3_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129101 D6_iNSC_S3_L005_R1_001 D6_iNSC_S3_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478823 D6_iNSC_S3_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129100 D6_iNSC_S3_L006_R1_001 D6_iNSC_S3_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478824 D6_iNSC_S4_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129102 D6_iNSC_S4_L005_R1_001 D6_iNSC_S4_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478825 D6_iNSC_S4_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129103 D6_iNSC_S4_L006_R1_001 D6_iNSC_S4_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478826 D8_iPSC_S40_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129104 D8_iPSC_S40_L005_R1_001 D8_iPSC_S40_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478827 D8_iPSC_S40_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129105 D8_iPSC_S40_L006_R1_001 D8_iPSC_S40_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478828 D8_iPSC_S39_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129106 D8_iPSC_S39_L005_R1_001 D8_iPSC_S39_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478829 D8_iPSC_S39_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129107 D8_iPSC_S39_L006_R1_001 D8_iPSC_S39_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478830 D8_iPSC_S39_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129108 D8_iPSC_S39_L007_R1_001 D8_iPSC_S39_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478831 D8_iPSC_S39_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129109 D8_iPSC_S39_L008_R1_001 D8_iPSC_S39_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478832 D8_iPSC_S40_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129110 D8_iPSC_S40_L001_R1_001 D8_iPSC_S40_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478833 D8_iPSC_S40_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129111 D8_iPSC_S40_L002_R1_001 D8_iPSC_S40_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478834 D8_iPSC_S40_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129112 D8_iPSC_S40_L003_R1_001 D8_iPSC_S40_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478835 D8_iPSC_S40_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129113 D8_iPSC_S40_L004_R1_001 D8_iPSC_S40_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478836 D2_S20_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129115 D2_S20_L008_R1_001 D2_S20_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478837 D2_S20_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129118 D2_S20_L007_R1_001 D2_S20_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478838 D4_S21_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129114 D4_S21_L002_R1_001 D4_S21_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478839 D4_S21_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129116 D4_S21_L001_R1_001 D4_S21_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478840 D4_S23_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129117 D4_S23_L008_R1_001 D4_S23_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478841 D4_S23_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129119 D4_S23_L007_R1_001 D4_S23_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478842 D2_S20_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129120 D2_S20_L006_R1_001 D2_S20_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478843 D2_S20_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129121 D2_S20_L005_R1_001 D2_S20_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478844 D4_S23_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129122 D4_S23_L004_R1_001 D4_S23_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478845 D4_S23_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129123 D4_S23_L003_R1_001 D4_S23_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478846 D4_S23_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129124 D4_S23_L006_R1_001 D4_S23_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478847 D4_S23_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129125 D4_S23_L005_R1_001 D4_S23_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478848 D4_S22_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129126 D4_S22_L008_R1_001 D4_S22_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478849 D4_S22_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129127 D4_S22_L007_R1_001 D4_S22_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478850 D4_S23_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129128 D4_S23_L002_R1_001 D4_S23_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478851 D4_S23_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129129 D4_S23_L001_R1_001 D4_S23_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478852 D7_iNSC_S41_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129133 D7_iNSC_S41_L007_R1_001 D7_iNSC_S41_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478853 D7_iNSC_S41_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129130 D7_iNSC_S41_L008_R1_001 D7_iNSC_S41_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478854 D7_iNSC_S42_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129131 D7_iNSC_S42_L001_R1_001 D7_iNSC_S42_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478855 D7_iNSC_S42_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129132 D7_iNSC_S42_L002_R1_001 D7_iNSC_S42_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478856 D7_iNSC_S42_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129134 D7_iNSC_S42_L003_R1_001 D7_iNSC_S42_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478857 D7_iNSC_S42_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129135 D7_iNSC_S42_L004_R1_001 D7_iNSC_S42_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478858 D7_iNSC_S42_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129136 D7_iNSC_S42_L005_R1_001 D7_iNSC_S42_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478859 D7_iNSC_S42_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129137 D7_iNSC_S42_L006_R1_001 D7_iNSC_S42_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478860 D7_iNSC_S42_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129139 D7_iNSC_S42_L007_R1_001 D7_iNSC_S42_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478861 D7_iNSC_S42_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129138 D7_iNSC_S42_L008_R1_001 D7_iNSC_S42_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478862 MEF_S32_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129140 MEF_S32_L008_R1_001 MEF_S32_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478863 MEF_S32_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129141 MEF_S32_L007_R1_001 MEF_S32_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478864 MEF_S32_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129142 MEF_S32_L006_R1_001 MEF_S32_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478865 MEF_S32_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129143 MEF_S32_L005_R1_001 MEF_S32_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478866 MEF_S32_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129144 MEF_S32_L004_R1_001 MEF_S32_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478867 MEF_S32_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129145 MEF_S32_L003_R1_001 MEF_S32_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478868 MEF_S32_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129146 MEF_S32_L002_R1_001 MEF_S32_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478869 MEF_S32_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129147 MEF_S32_L001_R1_001 MEF_S32_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478870 D8_iNSC_S35_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129148 D8_iNSC_S35_L005_R1_001 D8_iNSC_S35_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478871 D8_iNSC_S35_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129149 D8_iNSC_S35_L006_R1_001 D8_iNSC_S35_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478872 D8_iNSC_S35_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129150 D8_iNSC_S35_L001_R1_001 D8_iNSC_S35_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478873 D8_iNSC_S35_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129151 D8_iNSC_S35_L002_R1_001 D8_iNSC_S35_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478874 D8_iNSC_S35_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129152 D8_iNSC_S35_L003_R1_001 D8_iNSC_S35_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478875 D8_iNSC_S35_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129153 D8_iNSC_S35_L004_R1_001 D8_iNSC_S35_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478876 D8_iNSC_S34_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129154 D8_iNSC_S34_L005_R1_001 D8_iNSC_S34_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478877 D8_iNSC_S34_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129155 D8_iNSC_S34_L006_R1_001 D8_iNSC_S34_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478878 D8_iNSC_S34_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129156 D8_iNSC_S34_L007_R1_001 D8_iNSC_S34_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478879 D8_iNSC_S34_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129157 D8_iNSC_S34_L008_R1_001 D8_iNSC_S34_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478880 D5_S27_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129158 D5_S27_L008_R1_001 D5_S27_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478881 D5_S27_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129159 D5_S27_L007_R1_001 D5_S27_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478882 D5_S28_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129160 D5_S28_L002_R1_001 D5_S28_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478883 D5_S28_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129161 D5_S28_L001_R1_001 D5_S28_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478884 D5_S28_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129162 D5_S28_L004_R1_001 D5_S28_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478885 D5_S28_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129163 D5_S28_L003_R1_001 D5_S28_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478886 D5_S28_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129164 D5_S28_L006_R1_001 D5_S28_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478887 D5_S28_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129165 D5_S28_L005_R1_001 D5_S28_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478888 D5_S28_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129166 D5_S28_L008_R1_001 D5_S28_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478889 D5_S28_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129167 D5_S28_L007_R1_001 D5_S28_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478890 D2_S20_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129168 D2_S20_L004_R1_001 D2_S20_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478891 D2_S20_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129169 D2_S20_L003_R1_001 D2_S20_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478892 D10_iPSC_S14_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129170 D10_iPSC_S14_L003_R1_001 D10_iPSC_S14_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478893 D10_iPSC_S14_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129171 D10_iPSC_S14_L004_R1_001 D10_iPSC_S14_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478894 D10_iPSC_S14_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129172 D10_iPSC_S14_L001_R1_001 D10_iPSC_S14_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478895 D10_iPSC_S14_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129173 D10_iPSC_S14_L002_R1_001 D10_iPSC_S14_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478896 D10_iPSC_S14_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129174 D10_iPSC_S14_L007_R1_001 D10_iPSC_S14_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478897 D10_iPSC_S14_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129175 D10_iPSC_S14_L008_R1_001 D10_iPSC_S14_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478898 D10_iPSC_S14_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129176 D10_iPSC_S14_L005_R1_001 D10_iPSC_S14_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478899 D10_iPSC_S14_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129177 D10_iPSC_S14_L006_R1_001 D10_iPSC_S14_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478900 D4_S21_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129178 D4_S21_L004_R1_001 D4_S21_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478901 D10_iPSC_S15_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129179 D10_iPSC_S15_L001_R1_001 D10_iPSC_S15_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478902 D10_iPSC_S15_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129180 D10_iPSC_S15_L002_R1_001 D10_iPSC_S15_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478903 D7_iPSC_S45_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129181 D7_iPSC_S45_L003_R1_001 D7_iPSC_S45_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478904 D4_S21_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129182 D4_S21_L003_R1_001 D4_S21_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478905 D7_iPSC_S45_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129183 D7_iPSC_S45_L004_R1_001 D7_iPSC_S45_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478906 iPSC_S54_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129184 iPSC_S54_L008_R1_001 iPSC_S54_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478907 iPSC_S54_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129185 iPSC_S54_L007_R1_001 iPSC_S54_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478908 iPSC_S55_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129186 iPSC_S55_L004_R1_001 iPSC_S55_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478909 iPSC_S55_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129187 iPSC_S55_L003_R1_001 iPSC_S55_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478910 iPSC_S55_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129188 iPSC_S55_L002_R1_001 iPSC_S55_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478911 iPSC_S55_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129189 iPSC_S55_L001_R1_001 iPSC_S55_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478912 iPSC_S55_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129190 iPSC_S55_L008_R1_001 iPSC_S55_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478913 iPSC_S55_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129191 iPSC_S55_L007_R1_001 iPSC_S55_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478914 iPSC_S55_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129192 iPSC_S55_L006_R1_001 iPSC_S55_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478915 iPSC_S55_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129193 iPSC_S55_L005_R1_001 iPSC_S55_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478916 iPSC_S56_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129194 iPSC_S56_L002_R1_001 iPSC_S56_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478917 iPSC_S56_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129195 iPSC_S56_L001_R1_001 iPSC_S56_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478918 D7_iPSC_S47_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129196 D7_iPSC_S47_L003_R1_001 D7_iPSC_S47_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478919 D7_iPSC_S47_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129197 D7_iPSC_S47_L004_R1_001 D7_iPSC_S47_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478920 D7_iPSC_S47_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129198 D7_iPSC_S47_L005_R1_001 D7_iPSC_S47_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478921 D7_iPSC_S47_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129199 D7_iPSC_S47_L006_R1_001 D7_iPSC_S47_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478922 D7_iPSC_S46_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129200 D7_iPSC_S46_L007_R1_001 D7_iPSC_S46_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478923 D7_iPSC_S46_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129201 D7_iPSC_S46_L008_R1_001 D7_iPSC_S46_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478924 D7_iPSC_S47_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129202 D7_iPSC_S47_L001_R1_001 D7_iPSC_S47_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478925 D7_iPSC_S47_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129203 D7_iPSC_S47_L002_R1_001 D7_iPSC_S47_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478926 D7_iPSC_S47_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129204 D7_iPSC_S47_L007_R1_001 D7_iPSC_S47_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478927 D7_iPSC_S47_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129205 D7_iPSC_S47_L008_R1_001 D7_iPSC_S47_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478928 D6_iPSC_S5_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129206 D6_iPSC_S5_L004_R1_001 D6_iPSC_S5_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478929 D6_iPSC_S5_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129207 D6_iPSC_S5_L003_R1_001 D6_iPSC_S5_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478930 D6_iPSC_S5_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129208 D6_iPSC_S5_L006_R1_001 D6_iPSC_S5_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478931 D6_iPSC_S5_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129209 D6_iPSC_S5_L005_R1_001 D6_iPSC_S5_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478932 D6_iNSC_S4_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129210 D6_iNSC_S4_L008_R1_001 D6_iNSC_S4_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478933 D6_iNSC_S4_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129211 D6_iNSC_S4_L007_R1_001 D6_iNSC_S4_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478934 D6_iPSC_S5_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129212 D6_iPSC_S5_L002_R1_001 D6_iPSC_S5_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478935 D6_iPSC_S5_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129213 D6_iPSC_S5_L001_R1_001 D6_iPSC_S5_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478936 D6_iPSC_S5_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129214 D6_iPSC_S5_L008_R1_001 D6_iPSC_S5_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478937 D6_iPSC_S5_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129215 D6_iPSC_S5_L007_R1_001 D6_iPSC_S5_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478938 iNSC_S49_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129216 iNSC_S49_L006_R1_001 iNSC_S49_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478939 iNSC_S49_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129217 iNSC_S49_L005_R1_001 iNSC_S49_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478940 iNSC_S49_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129218 iNSC_S49_L004_R1_001 iNSC_S49_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478941 iNSC_S49_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129219 iNSC_S49_L003_R1_001 iNSC_S49_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478942 iNSC_S49_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129220 iNSC_S49_L002_R1_001 iNSC_S49_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478943 iNSC_S49_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129221 iNSC_S49_L001_R1_001 iNSC_S49_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478944 D8_iPSC_S40_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129222 D8_iPSC_S40_L008_R1_001 D8_iPSC_S40_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478945 D8_iPSC_S40_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129223 D8_iPSC_S40_L007_R1_001 D8_iPSC_S40_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478946 D8_iNSC_S34_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129224 D8_iNSC_S34_L001_R1_001 D8_iNSC_S34_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478947 D8_iNSC_S34_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129225 D8_iNSC_S34_L002_R1_001 D8_iNSC_S34_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478948 D8_iNSC_S33_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129226 D8_iNSC_S33_L007_R1_001 D8_iNSC_S33_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478949 D8_iNSC_S33_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129227 D8_iNSC_S33_L008_R1_001 D8_iNSC_S33_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478950 D8_iNSC_S33_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129228 D8_iNSC_S33_L005_R1_001 D8_iNSC_S33_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478951 D8_iNSC_S33_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129229 D8_iNSC_S33_L006_R1_001 D8_iNSC_S33_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478952 D8_iNSC_S33_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129230 D8_iNSC_S33_L003_R1_001 D8_iNSC_S33_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478953 D8_iNSC_S33_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129231 D8_iNSC_S33_L004_R1_001 D8_iNSC_S33_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478954 D10_iNSC_S11_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129232 D10_iNSC_S11_L002_R1_001 D10_iNSC_S11_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478955 D10_iNSC_S11_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129233 D10_iNSC_S11_L001_R1_001 D10_iNSC_S11_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478956 D10_iNSC_S10_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129234 D10_iNSC_S10_L006_R1_001 D10_iNSC_S10_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478957 D10_iNSC_S10_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129235 D10_iNSC_S10_L005_R1_001 D10_iNSC_S10_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478958 D10_iNSC_S10_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129236 D10_iNSC_S10_L008_R1_001 D10_iNSC_S10_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478959 D10_iNSC_S10_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129237 D10_iNSC_S10_L007_R1_001 D10_iNSC_S10_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478960 D10_iNSC_S10_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129238 D10_iNSC_S10_L002_R1_001 D10_iNSC_S10_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478961 D10_iNSC_S10_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129239 D10_iNSC_S10_L001_R1_001 D10_iNSC_S10_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478962 D10_iNSC_S10_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129240 D10_iNSC_S10_L004_R1_001 D10_iNSC_S10_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478963 D10_iNSC_S10_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129241 D10_iNSC_S10_L003_R1_001 D10_iNSC_S10_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478964 D5_S25_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129242 D5_S25_L001_R1_001 D5_S25_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478965 D5_S25_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129243 D5_S25_L002_R1_001 D5_S25_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478966 D2_S19_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129244 D2_S19_L005_R1_001 D2_S19_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478967 D2_S19_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129245 D2_S19_L006_R1_001 D2_S19_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478968 D2_S19_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129246 D2_S19_L003_R1_001 D2_S19_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478969 D2_S19_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129247 D2_S19_L004_R1_001 D2_S19_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478970 D2_S19_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129248 D2_S19_L001_R1_001 D2_S19_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478971 D2_S19_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129249 D2_S19_L002_R1_001 D2_S19_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478972 D4_S24_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129250 D4_S24_L001_R1_001 D4_S24_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478973 D4_S24_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129251 D4_S24_L002_R1_001 D4_S24_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478974 D4_S24_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129252 D4_S24_L003_R1_001 D4_S24_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478975 D4_S24_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129253 D4_S24_L004_R1_001 D4_S24_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478976 D4_S24_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129254 D4_S24_L005_R1_001 D4_S24_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478977 D4_S24_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129255 D4_S24_L006_R1_001 D4_S24_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478978 D4_S24_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129256 D4_S24_L007_R1_001 D4_S24_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478979 D4_S24_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129257 D4_S24_L008_R1_001 D4_S24_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478980 D10_iPSC_S13_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129258 D10_iPSC_S13_L008_R1_001 D10_iPSC_S13_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478981 D10_iPSC_S13_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129259 D10_iPSC_S13_L007_R1_001 D10_iPSC_S13_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478982 D10_iPSC_S13_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129260 D10_iPSC_S13_L002_R1_001 D10_iPSC_S13_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478983 D10_iPSC_S13_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129261 D10_iPSC_S13_L001_R1_001 D10_iPSC_S13_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478984 D10_iNSC_S9_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129262 D10_iNSC_S9_L008_R1_001 D10_iNSC_S9_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478985 D10_iNSC_S9_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129263 D10_iNSC_S9_L007_R1_001 D10_iNSC_S9_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478986 D10_iPSC_S13_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129264 D10_iPSC_S13_L006_R1_001 D10_iPSC_S13_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478987 D10_iPSC_S13_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129265 D10_iPSC_S13_L005_R1_001 D10_iPSC_S13_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478988 D10_iPSC_S13_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129266 D10_iPSC_S13_L004_R1_001 D10_iPSC_S13_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478989 D10_iPSC_S13_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129267 D10_iPSC_S13_L003_R1_001 D10_iPSC_S13_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478990 D8_iPSC_S37_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129268 D8_iPSC_S37_L007_R1_001 D8_iPSC_S37_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478991 D8_iPSC_S37_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129269 D8_iPSC_S37_L008_R1_001 D8_iPSC_S37_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478992 D7_iPSC_S48_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129270 D7_iPSC_S48_L008_R1_001 D7_iPSC_S48_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478993 D7_iPSC_S48_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129271 D7_iPSC_S48_L007_R1_001 D7_iPSC_S48_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478994 MEF_S31_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129272 MEF_S31_L007_R1_001 MEF_S31_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478995 MEF_S31_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129273 MEF_S31_L008_R1_001 MEF_S31_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478996 MEF_S31_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129274 MEF_S31_L001_R1_001 MEF_S31_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478997 MEF_S31_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129275 MEF_S31_L002_R1_001 MEF_S31_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478998 MEF_S30_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129276 MEF_S30_L007_R1_001 MEF_S30_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6478999 MEF_S30_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129278 MEF_S30_L008_R1_001 MEF_S30_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479000 MEF_S31_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129277 MEF_S31_L005_R1_001 MEF_S31_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479001 MEF_S31_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129279 MEF_S31_L006_R1_001 MEF_S31_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479002 MEF_S31_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129280 MEF_S31_L003_R1_001 MEF_S31_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479003 MEF_S31_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129281 MEF_S31_L004_R1_001 MEF_S31_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479004 D8_iNSC_S36_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129282 D8_iNSC_S36_L008_R1_001 D8_iNSC_S36_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479005 D8_iNSC_S36_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129283 D8_iNSC_S36_L007_R1_001 D8_iNSC_S36_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479006 D8_iNSC_S36_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129284 D8_iNSC_S36_L002_R1_001 D8_iNSC_S36_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479007 D8_iNSC_S36_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129285 D8_iNSC_S36_L001_R1_001 D8_iNSC_S36_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479008 D8_iNSC_S35_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129286 D8_iNSC_S35_L008_R1_001 D8_iNSC_S35_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479009 D8_iNSC_S35_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129287 D8_iNSC_S35_L007_R1_001 D8_iNSC_S35_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479010 D8_iNSC_S36_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129288 D8_iNSC_S36_L006_R1_001 D8_iNSC_S36_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479011 D8_iNSC_S36_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129289 D8_iNSC_S36_L005_R1_001 D8_iNSC_S36_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479012 D8_iNSC_S36_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129290 D8_iNSC_S36_L004_R1_001 D8_iNSC_S36_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479013 D8_iNSC_S36_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129291 D8_iNSC_S36_L003_R1_001 D8_iNSC_S36_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479014 iPSC_S53_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129292 iPSC_S53_L001_R1_001 iPSC_S53_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479015 iPSC_S53_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129293 iPSC_S53_L002_R1_001 iPSC_S53_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479016 iPSC_S53_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129294 iPSC_S53_L003_R1_001 iPSC_S53_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479017 iPSC_S53_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129295 iPSC_S53_L004_R1_001 iPSC_S53_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479018 iNSC_S52_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129296 iNSC_S52_L005_R1_001 iNSC_S52_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479019 iNSC_S52_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129297 iNSC_S52_L006_R1_001 iNSC_S52_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479020 D7_iNSC_S41_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129298 D7_iNSC_S41_L006_R1_001 D7_iNSC_S41_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479021 D7_iNSC_S41_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129299 D7_iNSC_S41_L005_R1_001 D7_iNSC_S41_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479022 D7_iNSC_S41_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129300 D7_iNSC_S41_L004_R1_001 D7_iNSC_S41_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479023 D7_iNSC_S41_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129301 D7_iNSC_S41_L003_R1_001 D7_iNSC_S41_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479024 D7_iNSC_S41_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129302 D7_iNSC_S41_L002_R1_001 D7_iNSC_S41_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479025 D7_iNSC_S41_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129303 D7_iNSC_S41_L001_R1_001 D7_iNSC_S41_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479026 D6_iPSC_S8_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129304 D6_iPSC_S8_L008_R1_001 D6_iPSC_S8_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479027 iPSC_S53_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129305 iPSC_S53_L006_R1_001 iPSC_S53_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479028 D6_iPSC_S8_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129306 D6_iPSC_S8_L006_R1_001 D6_iPSC_S8_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479029 D6_iPSC_S8_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129307 D6_iPSC_S8_L005_R1_001 D6_iPSC_S8_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479030 iNSC_S52_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129308 iNSC_S52_L007_R1_001 iNSC_S52_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479031 D6_iNSC_S2_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129309 D6_iNSC_S2_L001_R1_001 D6_iNSC_S2_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479032 D6_iNSC_S2_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129311 D6_iNSC_S2_L002_R1_001 D6_iNSC_S2_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479033 D6_iNSC_S1_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129310 D6_iNSC_S1_L005_R1_001 D6_iNSC_S1_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479034 D6_iNSC_S1_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129312 D6_iNSC_S1_L006_R1_001 D6_iNSC_S1_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479035 D6_iNSC_S1_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129313 D6_iNSC_S1_L007_R1_001 D6_iNSC_S1_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479036 D6_iNSC_S1_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129314 D6_iNSC_S1_L008_R1_001 D6_iNSC_S1_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479037 D6_iNSC_S1_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129315 D6_iNSC_S1_L001_R1_001 D6_iNSC_S1_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479038 D6_iNSC_S1_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129316 D6_iNSC_S1_L002_R1_001 D6_iNSC_S1_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479039 D6_iNSC_S1_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129317 D6_iNSC_S1_L003_R1_001 D6_iNSC_S1_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479040 D6_iNSC_S1_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129319 D6_iNSC_S1_L004_R1_001 D6_iNSC_S1_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479041 iNSC_S51_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129318 iNSC_S51_L001_R1_001 iNSC_S51_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479042 iNSC_S51_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129320 iNSC_S51_L002_R1_001 iNSC_S51_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479043 iNSC_S50_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129321 iNSC_S50_L007_R1_001 iNSC_S50_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479044 iNSC_S50_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129322 iNSC_S50_L008_R1_001 iNSC_S50_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479045 iNSC_S50_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129323 iNSC_S50_L005_R1_001 iNSC_S50_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479046 iNSC_S50_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129324 iNSC_S50_L006_R1_001 iNSC_S50_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479047 iNSC_S50_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129325 iNSC_S50_L003_R1_001 iNSC_S50_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479048 iNSC_S50_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129326 iNSC_S50_L004_R1_001 iNSC_S50_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479049 iNSC_S50_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129327 iNSC_S50_L001_R1_001 iNSC_S50_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479050 iNSC_S50_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129328 iNSC_S50_L002_R1_001 iNSC_S50_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479051 D2_S18_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129329 D2_S18_L008_R1_001 D2_S18_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479052 D2_S18_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129330 D2_S18_L007_R1_001 D2_S18_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479053 D2_S18_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129331 D2_S18_L006_R1_001 D2_S18_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479054 D2_S18_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129332 D2_S18_L005_R1_001 D2_S18_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479055 D2_S18_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129333 D2_S18_L004_R1_001 D2_S18_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479056 D2_S18_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129334 D2_S18_L003_R1_001 D2_S18_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479057 D2_S18_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129335 D2_S18_L002_R1_001 D2_S18_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479058 D2_S18_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129336 D2_S18_L001_R1_001 D2_S18_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479059 D2_S17_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129337 D2_S17_L008_R1_001 D2_S17_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479060 D2_S17_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129338 D2_S17_L007_R1_001 D2_S17_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479061 iNSC_S49_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129339 iNSC_S49_L008_R1_001 iNSC_S49_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479062 iNSC_S49_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129340 iNSC_S49_L007_R1_001 iNSC_S49_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479063 D10_iPSC_S16_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129341 D10_iPSC_S16_L005_R1_001 D10_iPSC_S16_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479064 D10_iPSC_S16_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129342 D10_iPSC_S16_L006_R1_001 D10_iPSC_S16_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479065 D10_iPSC_S16_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129343 D10_iPSC_S16_L007_R1_001 D10_iPSC_S16_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479066 D10_iPSC_S16_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129344 D10_iPSC_S16_L008_R1_001 D10_iPSC_S16_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479067 D2_S17_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129345 D2_S17_L001_R1_001 D2_S17_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479068 D2_S17_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129346 D2_S17_L002_R1_001 D2_S17_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479069 D2_S17_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129347 D2_S17_L003_R1_001 D2_S17_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479070 D2_S17_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129350 D2_S17_L004_R1_001 D2_S17_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479071 D6_iPSC_S8_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129348 D6_iPSC_S8_L001_R1_001 D6_iPSC_S8_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479072 D6_iPSC_S8_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129349 D6_iPSC_S8_L002_R1_001 D6_iPSC_S8_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479073 D6_iPSC_S7_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129351 D6_iPSC_S7_L007_R1_001 D6_iPSC_S7_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479074 D6_iPSC_S7_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129352 D6_iPSC_S7_L008_R1_001 D6_iPSC_S7_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479075 D6_iPSC_S7_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129353 D6_iPSC_S7_L005_R1_001 D6_iPSC_S7_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479076 D6_iPSC_S7_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129354 D6_iPSC_S7_L006_R1_001 D6_iPSC_S7_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479077 D6_iPSC_S7_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129355 D6_iPSC_S7_L003_R1_001 D6_iPSC_S7_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479078 D6_iPSC_S7_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129356 D6_iPSC_S7_L004_R1_001 D6_iPSC_S7_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479079 iNSC_S52_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129357 iNSC_S52_L008_R1_001 iNSC_S52_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479080 D6_iPSC_S8_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129358 D6_iPSC_S8_L003_R1_001 D6_iPSC_S8_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479081 D6_iPSC_S8_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129359 D6_iPSC_S8_L004_R1_001 D6_iPSC_S8_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479082 iPSC_S53_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129360 iPSC_S53_L005_R1_001 iPSC_S53_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479083 D6_iPSC_S8_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129361 D6_iPSC_S8_L007_R1_001 D6_iPSC_S8_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479084 D7_iPSC_S45_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129362 D7_iPSC_S45_L008_R1_001 D7_iPSC_S45_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479085 D7_iPSC_S45_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129363 D7_iPSC_S45_L007_R1_001 D7_iPSC_S45_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479086 D7_iPSC_S45_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129364 D7_iPSC_S45_L006_R1_001 D7_iPSC_S45_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479087 D7_iPSC_S45_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129365 D7_iPSC_S45_L005_R1_001 D7_iPSC_S45_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479088 D7_iPSC_S46_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129366 D7_iPSC_S46_L004_R1_001 D7_iPSC_S46_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479089 D7_iPSC_S46_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129367 D7_iPSC_S46_L003_R1_001 D7_iPSC_S46_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479090 D7_iPSC_S46_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129368 D7_iPSC_S46_L002_R1_001 D7_iPSC_S46_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479091 D7_iPSC_S46_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129369 D7_iPSC_S46_L001_R1_001 D7_iPSC_S46_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479092 D7_iPSC_S46_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129370 D7_iPSC_S46_L006_R1_001 D7_iPSC_S46_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479093 D7_iPSC_S46_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129371 D7_iPSC_S46_L005_R1_001 D7_iPSC_S46_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479094 D8_iPSC_S37_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129372 D8_iPSC_S37_L003_R1_001 D8_iPSC_S37_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479095 D8_iPSC_S37_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129373 D8_iPSC_S37_L004_R1_001 D8_iPSC_S37_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479096 D8_iPSC_S37_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129374 D8_iPSC_S37_L001_R1_001 D8_iPSC_S37_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479097 D8_iPSC_S37_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129375 D8_iPSC_S37_L002_R1_001 D8_iPSC_S37_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479098 D8_iNSC_S33_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129376 D8_iNSC_S33_L002_R1_001 D8_iNSC_S33_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479099 D8_iNSC_S33_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129377 D8_iNSC_S33_L001_R1_001 D8_iNSC_S33_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479100 D8_iPSC_S37_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129378 D8_iPSC_S37_L005_R1_001 D8_iPSC_S37_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479101 D8_iPSC_S37_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129379 D8_iPSC_S37_L006_R1_001 D8_iPSC_S37_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479102 D7_iPSC_S48_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129380 D7_iPSC_S48_L006_R1_001 D7_iPSC_S48_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479103 D7_iPSC_S48_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129381 D7_iPSC_S48_L005_R1_001 D7_iPSC_S48_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479104 D8_iPSC_S38_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129382 D8_iPSC_S38_L001_R1_001 D8_iPSC_S38_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479105 D8_iPSC_S38_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129383 D8_iPSC_S38_L002_R1_001 D8_iPSC_S38_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479106 D7_iPSC_S48_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129384 D7_iPSC_S48_L002_R1_001 D7_iPSC_S48_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479107 D7_iPSC_S48_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129385 D7_iPSC_S48_L001_R1_001 D7_iPSC_S48_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479108 D7_iPSC_S48_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129386 D7_iPSC_S48_L004_R1_001 D7_iPSC_S48_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479109 D7_iPSC_S48_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129387 D7_iPSC_S48_L003_R1_001 D7_iPSC_S48_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479110 D5_S26_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129388 D5_S26_L002_R1_001 D5_S26_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479111 D5_S26_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129389 D5_S26_L001_R1_001 D5_S26_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479112 D5_S25_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129390 D5_S25_L008_R1_001 D5_S25_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479113 D5_S25_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129391 D5_S25_L007_R1_001 D5_S25_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479114 D5_S25_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129392 D5_S25_L006_R1_001 D5_S25_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479115 D5_S25_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129393 D5_S25_L005_R1_001 D5_S25_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479116 D5_S25_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129394 D5_S25_L004_R1_001 D5_S25_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479117 D5_S25_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129395 D5_S25_L003_R1_001 D5_S25_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479118 D5_S26_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129396 D5_S26_L004_R1_001 D5_S26_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479119 D5_S26_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129397 D5_S26_L003_R1_001 D5_S26_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479120 D10_iNSC_S9_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129398 D10_iNSC_S9_L001_R1_001 D10_iNSC_S9_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479121 D10_iNSC_S9_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129399 D10_iNSC_S9_L002_R1_001 D10_iNSC_S9_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479122 D10_iNSC_S9_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129400 D10_iNSC_S9_L003_R1_001 D10_iNSC_S9_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479123 D10_iNSC_S9_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129401 D10_iNSC_S9_L004_R1_001 D10_iNSC_S9_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479124 D10_iNSC_S12_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129402 D10_iNSC_S12_L005_R1_001 D10_iNSC_S12_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479125 D10_iNSC_S12_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129403 D10_iNSC_S12_L006_R1_001 D10_iNSC_S12_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479126 D10_iNSC_S12_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129404 D10_iNSC_S12_L007_R1_001 D10_iNSC_S12_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479127 D10_iNSC_S12_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129405 D10_iNSC_S12_L008_R1_001 D10_iNSC_S12_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479128 D10_iNSC_S9_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129406 D10_iNSC_S9_L005_R1_001 D10_iNSC_S9_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479129 D10_iNSC_S9_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129407 D10_iNSC_S9_L006_R1_001 D10_iNSC_S9_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479130 MEF_S30_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129408 MEF_S30_L006_R1_001 MEF_S30_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479131 MEF_S30_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129409 MEF_S30_L005_R1_001 MEF_S30_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479132 MEF_S29_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129410 MEF_S29_L006_R1_001 MEF_S29_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479133 MEF_S29_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129411 MEF_S29_L005_R1_001 MEF_S29_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479134 MEF_S29_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129413 MEF_S29_L008_R1_001 MEF_S29_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479135 MEF_S29_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129412 MEF_S29_L007_R1_001 MEF_S29_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479136 MEF_S30_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129414 MEF_S30_L002_R1_001 MEF_S30_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479137 MEF_S30_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129415 MEF_S30_L001_R1_001 MEF_S30_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479138 MEF_S30_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129416 MEF_S30_L004_R1_001 MEF_S30_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479139 MEF_S30_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129417 MEF_S30_L003_R1_001 MEF_S30_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479140 D8_iNSC_S34_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129418 D8_iNSC_S34_L003_R1_001 D8_iNSC_S34_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479141 D8_iNSC_S34_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129419 D8_iNSC_S34_L004_R1_001 D8_iNSC_S34_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479142 iPSC_S54_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129420 iPSC_S54_L002_R1_001 iPSC_S54_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479143 iPSC_S54_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129421 iPSC_S54_L001_R1_001 iPSC_S54_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479144 iPSC_S53_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129422 iPSC_S53_L008_R1_001 iPSC_S53_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479145 iPSC_S53_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129423 iPSC_S53_L007_R1_001 iPSC_S53_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479146 iPSC_S54_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129424 iPSC_S54_L006_R1_001 iPSC_S54_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479147 iPSC_S54_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129425 iPSC_S54_L005_R1_001 iPSC_S54_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479148 iPSC_S54_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129426 iPSC_S54_L004_R1_001 iPSC_S54_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479149 iPSC_S54_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129427 iPSC_S54_L003_R1_001 iPSC_S54_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479150 D7_iNSC_S44_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129428 D7_iNSC_S44_L005_R1_001 D7_iNSC_S44_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479151 D7_iNSC_S44_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129429 D7_iNSC_S44_L006_R1_001 D7_iNSC_S44_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479152 D7_iNSC_S44_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129430 D7_iNSC_S44_L003_R1_001 D7_iNSC_S44_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479153 D7_iNSC_S44_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129431 D7_iNSC_S44_L004_R1_001 D7_iNSC_S44_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479154 D7_iPSC_S45_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129432 D7_iPSC_S45_L001_R1_001 D7_iPSC_S45_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479155 D7_iPSC_S45_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129433 D7_iPSC_S45_L002_R1_001 D7_iPSC_S45_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479156 D7_iNSC_S44_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129436 D7_iNSC_S44_L007_R1_001 D7_iNSC_S44_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479157 D7_iNSC_S44_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129434 D7_iNSC_S44_L008_R1_001 D7_iNSC_S44_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479158 D6_iNSC_S3_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129435 D6_iNSC_S3_L004_R1_001 D6_iNSC_S3_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479159 D6_iNSC_S3_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129437 D6_iNSC_S3_L003_R1_001 D6_iNSC_S3_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479160 D6_iNSC_S2_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129438 D6_iNSC_S2_L006_R1_001 D6_iNSC_S2_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479161 D6_iNSC_S2_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129439 D6_iNSC_S2_L005_R1_001 D6_iNSC_S2_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479162 D6_iNSC_S2_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129440 D6_iNSC_S2_L004_R1_001 D6_iNSC_S2_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479163 D6_iNSC_S2_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129441 D6_iNSC_S2_L003_R1_001 D6_iNSC_S2_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479164 D6_iNSC_S3_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129442 D6_iNSC_S3_L002_R1_001 D6_iNSC_S3_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479165 D6_iNSC_S3_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129443 D6_iNSC_S3_L001_R1_001 D6_iNSC_S3_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479166 D6_iNSC_S2_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129444 D6_iNSC_S2_L008_R1_001 D6_iNSC_S2_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479167 D6_iNSC_S2_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129445 D6_iNSC_S2_L007_R1_001 D6_iNSC_S2_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479168 iNSC_S52_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129446 iNSC_S52_L004_R1_001 iNSC_S52_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479169 iNSC_S52_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129447 iNSC_S52_L003_R1_001 iNSC_S52_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479170 iNSC_S51_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129448 iNSC_S51_L008_R1_001 iNSC_S51_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479171 iNSC_S51_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129449 iNSC_S51_L007_R1_001 iNSC_S51_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479172 iNSC_S52_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129450 iNSC_S52_L002_R1_001 iNSC_S52_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479173 iNSC_S52_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129451 iNSC_S52_L001_R1_001 iNSC_S52_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479174 iNSC_S51_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129452 iNSC_S51_L004_R1_001 iNSC_S51_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479175 iNSC_S51_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129453 iNSC_S51_L003_R1_001 iNSC_S51_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479176 iNSC_S51_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129454 iNSC_S51_L006_R1_001 iNSC_S51_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479177 iNSC_S51_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129455 iNSC_S51_L005_R1_001 iNSC_S51_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479178 D2_S17_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129456 D2_S17_L005_R1_001 D2_S17_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479179 D2_S17_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129457 D2_S17_L006_R1_001 D2_S17_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479180 D4_S22_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129458 D4_S22_L005_R1_001 D4_S22_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479181 D4_S22_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129459 D4_S22_L006_R1_001 D4_S22_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479182 D4_S22_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129460 D4_S22_L003_R1_001 D4_S22_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479183 D4_S22_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129461 D4_S22_L004_R1_001 D4_S22_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479184 D4_S22_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129462 D4_S22_L001_R1_001 D4_S22_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479185 D4_S22_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129463 D4_S22_L002_R1_001 D4_S22_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479186 D4_S21_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129464 D4_S21_L007_R1_001 D4_S21_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479187 D4_S21_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129465 D4_S21_L008_R1_001 D4_S21_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479188 D4_S21_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129466 D4_S21_L005_R1_001 D4_S21_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479189 D4_S21_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129467 D4_S21_L006_R1_001 D4_S21_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479190 D10_iNSC_S12_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129468 D10_iNSC_S12_L004_R1_001 D10_iNSC_S12_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479191 D10_iNSC_S12_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129469 D10_iNSC_S12_L003_R1_001 D10_iNSC_S12_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479192 D10_iNSC_S11_L008_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129470 D10_iNSC_S11_L008_R1_001 D10_iNSC_S11_L008_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479193 D10_iNSC_S11_L007_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129471 D10_iNSC_S11_L007_R1_001 D10_iNSC_S11_L007_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479194 D10_iNSC_S12_L002_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129472 D10_iNSC_S12_L002_R1_001 D10_iNSC_S12_L002_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479195 D10_iNSC_S12_L001_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129473 D10_iNSC_S12_L001_R1_001 D10_iNSC_S12_L001_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479196 D10_iNSC_S11_L004_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129474 D10_iNSC_S11_L004_R1_001 D10_iNSC_S11_L004_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479197 D10_iNSC_S11_L003_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129475 D10_iNSC_S11_L003_R1_001 D10_iNSC_S11_L003_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479198 D10_iNSC_S11_L006_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129476 D10_iNSC_S11_L006_R1_001 D10_iNSC_S11_L006_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000 SRX6479199 D10_iNSC_S11_L005_R1_001 SRP215688 bp0 scRNA-seq libraries were generated using the Chromium Single Cell 3 Reagent Kit v2 (PN-120267, 10X Genomics), Chromium Single Cell A Chip Kit (PN-120236, 10X Genomics) and Chromium Single Cell i7 Multiplex Kit (PN-120262, 10X Genomics). The cell viability was estimated to be over 90% by trypan blue staining under the microscope. Cells were diluted to 2105 ~ 2106 cells/mL with 0.04% BSA in DPBS and loaded on the Chromium microfluidic platform, aiming to capture 3,000 cells per each channel. Subsequent library preparation was performed according to the manufacturers instructions provided. Libraries were sequenced on an Illumina HiSeq 4000 platform (2100bp). SRS5129477 D10_iNSC_S11_L005_R1_001 D10_iNSC_S11_L005_R1_001 RNA-Seq TRANSCRIPTOMIC cDNA Illumina HiSeq 4000