SRX6492111 GSM3964244 SRP216269 SRS5140707 GSM3964244 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964244 GSM3964244 SRX6492112 GSM3964245 SRP216269 SRS5140708 GSM3964245 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964245 GSM3964245 SRX6492113 GSM3964246 SRP216269 SRS5140709 GSM3964246 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964246 GSM3964246 SRX6492114 GSM3964247 SRP216269 SRS5140710 GSM3964247 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964247 GSM3964247 SRX6492115 GSM3964248 SRP216269 SRS5140711 GSM3964248 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964248 GSM3964248 SRX6492116 GSM3964249 SRP216269 SRS5140712 GSM3964249 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964249 GSM3964249 SRX6492117 GSM3964250 SRP216269 SRS5140713 GSM3964250 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964250 GSM3964250 SRX6492118 GSM3964251 SRP216269 SRS5140714 GSM3964251 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964251 GSM3964251 SRX6492119 GSM3964252 SRP216269 SRS5140715 GSM3964252 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964252 GSM3964252 SRX6492120 GSM3964253 SRP216269 SRS5140716 GSM3964253 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964253 GSM3964253 SRX6492121 GSM3964254 SRP216269 SRS5140717 GSM3964254 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964254 GSM3964254 SRX6492122 GSM3964255 SRP216269 SRS5140718 GSM3964255 RNA-Seq TRANSCRIPTOMIC cDNA RNA from lysed cells was barcoded through reverse transcription in individual GEMs. Barcoded cDNAs were pooled and cleanup by using DynaBeads® MyOne Silane Beads (Invitrogen, 37002D). Single-cell RNA-seq libraries were prepared using Single Cell 3′ Library Gel Bead Kit V2 (10x Genomics, 120237). Sequencing was performed with using multiple NextSeq 500/550 High Output Kit v2 on an Illumina NextSeq with pair end 150bp (PE150). On average, sequencing generated 100-200K reads per cell on average over the libraries. NextSeq 500 gds 303964255 GSM3964255