SRX6631984 GSM3995471 SRP217050 SRS5194652 GSM3995471 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using Dynabeads mRNA Direct Kit (Thermo Fisher Scientific). NGS libraries were prepared using a modified version of Transeq, as described (Jaitin et al., 2014) We used a derivation of the MARS-seq as described (Jaitin et al. Science 2014), developed for single cell MARS-seq to produce 3' exprssion libraries with a minimum of 3 replicates per sample. 3' RNA-seq for digital gene expression quantitation (single end protocol R2 used for 7N barcode + 8N UMI in fastq header) NextSeq 500 gds 303995471 GSM3995471 SRX6631985 GSM3995472 SRP217050 SRS5194653 GSM3995472 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using Dynabeads mRNA Direct Kit (Thermo Fisher Scientific). NGS libraries were prepared using a modified version of Transeq, as described (Jaitin et al., 2014) We used a derivation of the MARS-seq as described (Jaitin et al. Science 2014), developed for single cell MARS-seq to produce 3' exprssion libraries with a minimum of 3 replicates per sample. 3' RNA-seq for digital gene expression quantitation (single end protocol R2 used for 7N barcode + 8N UMI in fastq header) NextSeq 500 gds 303995472 GSM3995472 SRX6631986 GSM3995473 SRP217050 SRS5194654 GSM3995473 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using Dynabeads mRNA Direct Kit (Thermo Fisher Scientific). NGS libraries were prepared using a modified version of Transeq, as described (Jaitin et al., 2014) We used a derivation of the MARS-seq as described (Jaitin et al. Science 2014), developed for single cell MARS-seq to produce 3' exprssion libraries with a minimum of 3 replicates per sample. 3' RNA-seq for digital gene expression quantitation (single end protocol R2 used for 7N barcode + 8N UMI in fastq header) NextSeq 500 gds 303995473 GSM3995473 SRX6631987 GSM3995474 SRP217050 SRS5194655 GSM3995474 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using Dynabeads mRNA Direct Kit (Thermo Fisher Scientific). NGS libraries were prepared using a modified version of Transeq, as described (Jaitin et al., 2014) We used a derivation of the MARS-seq as described (Jaitin et al. Science 2014), developed for single cell MARS-seq to produce 3' exprssion libraries with a minimum of 3 replicates per sample. 3' RNA-seq for digital gene expression quantitation (single end protocol R2 used for 7N barcode + 8N UMI in fastq header) NextSeq 500 gds 303995474 GSM3995474 SRX6631988 GSM3995475 SRP217050 SRS5194656 GSM3995475 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using Dynabeads mRNA Direct Kit (Thermo Fisher Scientific). NGS libraries were prepared using a modified version of Transeq, as described (Jaitin et al., 2014) We used a derivation of the MARS-seq as described (Jaitin et al. Science 2014), developed for single cell MARS-seq to produce 3' exprssion libraries with a minimum of 3 replicates per sample. 3' RNA-seq for digital gene expression quantitation (single end protocol R2 used for 7N barcode + 8N UMI in fastq header) NextSeq 500 gds 303995475 GSM3995475 SRX6631989 GSM3995476 SRP217050 SRS5194657 GSM3995476 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using Dynabeads mRNA Direct Kit (Thermo Fisher Scientific). NGS libraries were prepared using a modified version of Transeq, as described (Jaitin et al., 2014) We used a derivation of the MARS-seq as described (Jaitin et al. Science 2014), developed for single cell MARS-seq to produce 3' exprssion libraries with a minimum of 3 replicates per sample. 3' RNA-seq for digital gene expression quantitation (single end protocol R2 used for 7N barcode + 8N UMI in fastq header) NextSeq 500 gds 303995476 GSM3995476