SRX10502026 GSM5224069 SRP313155 SRS8626564 GSM5224069 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224069 GSM5224069 GEO Accession GSM5224069 SRX10502027 GSM5224070 SRP313155 SRS8626565 GSM5224070 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224070 GSM5224070 GEO Accession GSM5224070 SRX10502028 GSM5224071 SRP313155 SRS8626566 GSM5224071 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224071 GSM5224071 GEO Accession GSM5224071 SRX10502029 GSM5224072 SRP313155 SRS8626567 GSM5224072 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224072 GSM5224072 GEO Accession GSM5224072 SRX10502030 GSM5224073 SRP313155 SRS8626568 GSM5224073 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224073 GSM5224073 GEO Accession GSM5224073 SRX10502031 GSM5224074 SRP313155 SRS8626569 GSM5224074 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224074 GSM5224074 GEO Accession GSM5224074 SRX10502032 GSM5224075 SRP313155 SRS8626570 GSM5224075 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224075 GSM5224075 GEO Accession GSM5224075 SRX10502033 GSM5224076 SRP313155 SRS8626571 GSM5224076 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224076 GSM5224076 GEO Accession GSM5224076 SRX10502034 GSM5224077 SRP313155 SRS8626572 GSM5224077 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224077 GSM5224077 GEO Accession GSM5224077 SRX10502035 GSM5224078 SRP313155 SRS8626574 GSM5224078 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224078 GSM5224078 GEO Accession GSM5224078 SRX10502036 GSM5224079 SRP313155 SRS8626573 GSM5224079 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224079 GSM5224079 GEO Accession GSM5224079 SRX10502037 GSM5224080 SRP313155 SRS8626575 GSM5224080 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224080 GSM5224080 GEO Accession GSM5224080 SRX10502038 GSM5224081 SRP313155 SRS8626576 GSM5224081 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224081 GSM5224081 GEO Accession GSM5224081 SRX10502039 GSM5224082 SRP313155 SRS8626577 GSM5224082 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224082 GSM5224082 GEO Accession GSM5224082 SRX10502040 GSM5224083 SRP313155 SRS8626578 GSM5224083 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224083 GSM5224083 GEO Accession GSM5224083 SRX10502041 GSM5224084 SRP313155 SRS8626579 GSM5224084 RNA-Seq TRANSCRIPTOMIC cDNA Cellular RNA was harvested using the RNeasy Plus Mini Kit with QIAshredder homogenization columns (Qiagen). RNA-seq libraries were prepared using the Kapa mRNA HyperPrep RNA-seq library construction kit (Kapa/Roche), with 6 min fragmentation at 94 °C and 9 PCR cycles of final amplification and duplex barcoding. Libraries were quantified using the Fragment Analyzer and qPCR before being sequenced on an Illumina HiSeq 2000 using 40-bp single-end reads in High Output mode. Illumina HiSeq 2000 gds 305224084 GSM5224084 GEO Accession GSM5224084