SRX15048417 GSM6077379_r1 SRP372852 PRJNA833401 SRS12794418 GSM6077379 GSM6077379 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048418 GSM6077380_r1 SRP372852 PRJNA833401 SRS12794554 GSM6077380 GSM6077380 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048419 GSM6077381_r1 SRP372852 PRJNA833401 SRS12794417 GSM6077381 GSM6077381 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048420 GSM6077382_r1 SRP372852 PRJNA833401 SRS12794419 GSM6077382 GSM6077382 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048421 GSM6077383_r1 SRP372852 PRJNA833401 SRS12794420 GSM6077383 GSM6077383 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048422 GSM6077384_r1 SRP372852 PRJNA833401 SRS12794422 GSM6077384 GSM6077384 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048423 GSM6077385_r1 SRP372852 PRJNA833401 SRS12794423 GSM6077385 GSM6077385 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048424 GSM6077386_r1 SRP372852 PRJNA833401 SRS12794421 GSM6077386 GSM6077386 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048425 GSM6077387_r1 SRP372852 PRJNA833401 SRS12794424 GSM6077387 GSM6077387 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048426 GSM6077388_r1 SRP372852 PRJNA833401 SRS12794425 GSM6077388 GSM6077388 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048427 GSM6077389_r1 SRP372852 PRJNA833401 SRS12794426 GSM6077389 GSM6077389 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 SRX15048428 GSM6077390_r1 SRP372852 PRJNA833401 SRS12794427 GSM6077390 GSM6077390 RNA-Seq TRANSCRIPTOMIC cDNA Cells from multiple wells were washed with PBS and pooled to generate a pellet of 0.8x10^6 cells per treatment condition.Total RNA extracted according to the manufacturer's instructions . QC was performed for RNA integrity by Agilent Tapestation and concentration by Qubit assay. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000