SRX1515204 GSM2027030 SRP068025 SRS1233913 GSM2027030 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA was performed according to the manufacturer's instructions. Poly-A containing mRNA molecules was purified from total RNA (0.6 µg; RIN >7) using poly-T oligo-attached magnetic beads from TruSeq RNA Sample Prep Kit v2 (Illumina; RS-122-2001). Subsequent library construction of the RNA-seq library according to the manufacturer's instructions. Libraries were prepared with 13 cycles of PCR. Sequencing was performed using the single-read 50bp approach on HiSeq 2000 high output mode. Illumina HiSeq 2000 gds 302027030 GEO Accession GSM2027030 SRX1515205 GSM2027031 SRP068025 SRS1233914 GSM2027031 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA was performed according to the manufacturer's instructions. Poly-A containing mRNA molecules was purified from total RNA (0.6 µg; RIN >7) using poly-T oligo-attached magnetic beads from TruSeq RNA Sample Prep Kit v2 (Illumina; RS-122-2001). Subsequent library construction of the RNA-seq library according to the manufacturer's instructions. Libraries were prepared with 13 cycles of PCR. Sequencing was performed using the single-read 50bp approach on HiSeq 2000 high output mode. Illumina HiSeq 2000 gds 302027031 GEO Accession GSM2027031 SRX1515206 GSM2027032 SRP068025 SRS1233912 GSM2027032 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA was performed according to the manufacturer's instructions. Poly-A containing mRNA molecules was purified from total RNA (0.6 µg; RIN >7) using poly-T oligo-attached magnetic beads from TruSeq RNA Sample Prep Kit v2 (Illumina; RS-122-2001). Subsequent library construction of the RNA-seq library according to the manufacturer's instructions. Libraries were prepared with 13 cycles of PCR. Sequencing was performed using the single-read 50bp approach on HiSeq 2000 high output mode. Illumina HiSeq 2000 gds 302027032 GEO Accession GSM2027032 SRX1515207 GSM2027033 SRP068025 SRS1233911 GSM2027033 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA was performed according to the manufacturer's instructions. Poly-A containing mRNA molecules was purified from total RNA (0.6 µg; RIN >7) using poly-T oligo-attached magnetic beads from TruSeq RNA Sample Prep Kit v2 (Illumina; RS-122-2001). Subsequent library construction of the RNA-seq library according to the manufacturer's instructions. Libraries were prepared with 13 cycles of PCR. Sequencing was performed using the single-read 50bp approach on HiSeq 2000 high output mode. Illumina HiSeq 2000 gds 302027033 GEO Accession GSM2027033