SRX5391932 GSM3612189 SRP186290 SRS4379762 GSM3612189 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612189 GSM3612189 GEO Accession GSM3612189 SRX5391933 GSM3612190 SRP186290 SRS4379763 GSM3612190 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612190 GSM3612190 GEO Accession GSM3612190 SRX5391934 GSM3612191 SRP186290 SRS4379764 GSM3612191 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612191 GSM3612191 GEO Accession GSM3612191 SRX5391935 GSM3612192 SRP186290 SRS4379765 GSM3612192 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612192 GSM3612192 GEO Accession GSM3612192 SRX5391936 GSM3612193 SRP186290 SRS4379766 GSM3612193 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612193 GSM3612193 GEO Accession GSM3612193 SRX5391937 GSM3612194 SRP186290 SRS4379767 GSM3612194 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612194 GSM3612194 GEO Accession GSM3612194 SRX5391938 GSM3612195 SRP186290 SRS4379768 GSM3612195 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612195 GSM3612195 GEO Accession GSM3612195 SRX5391939 GSM3612196 SRP186290 SRS4379769 GSM3612196 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612196 GSM3612196 GEO Accession GSM3612196 SRX5391940 GSM3612197 SRP186290 SRS4379770 GSM3612197 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612197 GSM3612197 GEO Accession GSM3612197 SRX5391941 GSM3612198 SRP186290 SRS4379771 GSM3612198 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612198 GSM3612198 GEO Accession GSM3612198 SRX5391942 GSM3612199 SRP186290 SRS4379772 GSM3612199 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612199 GSM3612199 GEO Accession GSM3612199 SRX5391943 GSM3612200 SRP186290 SRS4379773 GSM3612200 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612200 GSM3612200 GEO Accession GSM3612200 SRX5391944 GSM3612201 SRP186290 SRS4379774 GSM3612201 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612201 GSM3612201 GEO Accession GSM3612201 SRX5391945 GSM3612202 SRP186290 SRS4379775 GSM3612202 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612202 GSM3612202 GEO Accession GSM3612202 SRX5391946 GSM3612203 SRP186290 SRS4379776 GSM3612203 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612203 GSM3612203 GEO Accession GSM3612203 SRX5391947 GSM3612204 SRP186290 SRS4379777 GSM3612204 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612204 GSM3612204 GEO Accession GSM3612204 SRX5391948 GSM3612205 SRP186290 SRS4379778 GSM3612205 RNA-Seq TRANSCRIPTOMIC cDNA RNA were extracted using Trizol standard protocol After ribogreen quantification and quality control on bioAnalyser, 500ng of total RNA underwent library preparation using the Truseq Stranded Total RNA library preparation chemistry (Illumina), with 6 cycles of PCR. Samples were barcoded and run on a Hiseq 2500 1T in a 50bp/50bp Paired end run, using the TruSeq SBS Kit v3 (Illumina). An average of 51 million paired reads were generated per sample and the percent of mRNA bases was 58% on average. Illumina HiSeq 2500 gds 303612205 GSM3612205 GEO Accession GSM3612205