SRX18285812 GSM6734705 SRP408256 SRS15777590 GSM6734705 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734705 GSM6734705 SRX18285813 GSM6734706 SRP408256 SRS15777591 GSM6734706 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734706 GSM6734706 SRX18285814 GSM6734707 SRP408256 SRS15777592 GSM6734707 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734707 GSM6734707 SRX18285815 GSM6734708 SRP408256 SRS15777593 GSM6734708 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734708 GSM6734708 SRX18285816 GSM6734709 SRP408256 SRS15777594 GSM6734709 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734709 GSM6734709 SRX18285817 GSM6734710 SRP408256 SRS15777595 GSM6734710 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734710 GSM6734710 SRX18285818 GSM6734711 SRP408256 SRS15777596 GSM6734711 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734711 GSM6734711 SRX18285819 GSM6734712 SRP408256 SRS15777597 GSM6734712 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734712 GSM6734712 SRX18285820 GSM6734713 SRP408256 SRS15777598 GSM6734713 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA The purity of RNA was determined by NanoPhotometer (IMPLEN, CA, USA). RNA integrity and concentration was assessed using the RNA Nano6000 Assay Kit of the Bioanalyzer 2100 system (Agilent Technologies, CA, USA). Qualified RNA was subjected to construct double stranded PCR library using MGI Easy RNA library preparation kit. Sequencing was performed on DNBSEQ-T7 and 150bp double ended sequencing reads was obtained. The volume of single-cell suspension that was required to generate single-cell GEMs (gel beads in the emulsion) per sample was loaded onto the Chromium Controller (DNBSEQ-T7). Libraries were prepared using the DNBelab C series single-cell RNA library preparation kit according to the manufacturer's specifications. Final library quantification and quality control were performed using a Qubit 3.0 and LabChip GX Touch, followed by sequencing on DNBSEQ-T7. DNBSEQ-T7 gds 306734713 GSM6734713