SRX3893061 GSM3082906 SRP137723 SRS3130871 GSM3082906 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082906 GSM3082906 GEO Accession GSM3082906 SRX3893062 GSM3082907 SRP137723 SRS3130872 GSM3082907 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082907 GSM3082907 GEO Accession GSM3082907 SRX3893063 GSM3082908 SRP137723 SRS3130873 GSM3082908 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082908 GSM3082908 GEO Accession GSM3082908 SRX3893064 GSM3082909 SRP137723 SRS3130874 GSM3082909 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082909 GSM3082909 GEO Accession GSM3082909 SRX3893065 GSM3082910 SRP137723 SRS3130875 GSM3082910 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082910 GSM3082910 GEO Accession GSM3082910 SRX3893066 GSM3082911 SRP137723 SRS3130876 GSM3082911 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082911 GSM3082911 GEO Accession GSM3082911 SRX3893067 GSM3082912 SRP137723 SRS3130877 GSM3082912 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082912 GSM3082912 GEO Accession GSM3082912 SRX3893068 GSM3082913 SRP137723 SRS3130878 GSM3082913 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082913 GSM3082913 GEO Accession GSM3082913 SRX3893069 GSM3082914 SRP137723 SRS3130879 GSM3082914 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082914 GSM3082914 GEO Accession GSM3082914 SRX3893070 GSM3082915 SRP137723 SRS3130880 GSM3082915 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082915 GSM3082915 GEO Accession GSM3082915 SRX3893071 GSM3082916 SRP137723 SRS3130881 GSM3082916 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082916 GSM3082916 GEO Accession GSM3082916 SRX3893072 GSM3082917 SRP137723 SRS3130882 GSM3082917 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082917 GSM3082917 GEO Accession GSM3082917 SRX3893073 GSM3082918 SRP137723 SRS3130883 GSM3082918 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082918 GSM3082918 GEO Accession GSM3082918 SRX3893074 GSM3082919 SRP137723 SRS3130884 GSM3082919 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082919 GSM3082919 GEO Accession GSM3082919 SRX3893075 GSM3082920 SRP137723 SRS3130885 GSM3082920 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Zymo Direct-Zol RNA MiniPrep Plus (cat# R2070, Irvine, CA) as per the manufacturer's instructions. Total RNA was quantified and 260/280 ratios determined using Nanodrop (all samples with a 260/280>1.97). 1μg of total RNA was used as starting material for each sample. RNA sequencing and library preparation was performed by the UCLA Technology Center for Genomics and Bioinformatics using the KAPA Stranded mRNA-seq kit (Roche Sequencing, cat#KK8421, Pleasanton, CA, USA), according to the manufacturer's instructions. The work flow consisted of mRNA enrichment, cDNA generation, end repair to generate blunt ends, A-tailing, adaptor ligation and PCR amplification. Different adaptors were used for multiplexing samples in one lane. Sequencing was performed on the HiSeq3000 System for a single-read 50 run (Illumina). Illumina HiSeq 3000 gds 303082920 GSM3082920 GEO Accession GSM3082920