SRX3372302 GSM2844171 SRP124497 SRS2669639 GSM2844171 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Trizol reagent and a QC was conducted using the Agilent Bioanalyzer. Total RNA was treated with Dnase I and mRNA was enriched using the oligo (dT) magnetic beads. mRNA was fragmented into short fragments and cDNA was synthesized using random hexamer primer. The double strand cDNA was purified with magentic beads. End reparation and 3'-end single nucleotide adenine addition was performed. Finally, sequencing adaptors were ligated to the fragments. The fragments were enriched by PCR amplification. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 302844171 GSM2844171 GEO Accession GSM2844171 SRX3372303 GSM2844172 SRP124497 SRS2669640 GSM2844172 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Trizol reagent and a QC was conducted using the Agilent Bioanalyzer. Total RNA was treated with Dnase I and mRNA was enriched using the oligo (dT) magnetic beads. mRNA was fragmented into short fragments and cDNA was synthesized using random hexamer primer. The double strand cDNA was purified with magentic beads. End reparation and 3'-end single nucleotide adenine addition was performed. Finally, sequencing adaptors were ligated to the fragments. The fragments were enriched by PCR amplification. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 302844172 GSM2844172 GEO Accession GSM2844172 SRX3372304 GSM2844173 SRP124497 SRS2669637 GSM2844173 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Trizol reagent and a QC was conducted using the Agilent Bioanalyzer. Total RNA was treated with Dnase I and mRNA was enriched using the oligo (dT) magnetic beads. mRNA was fragmented into short fragments and cDNA was synthesized using random hexamer primer. The double strand cDNA was purified with magentic beads. End reparation and 3'-end single nucleotide adenine addition was performed. Finally, sequencing adaptors were ligated to the fragments. The fragments were enriched by PCR amplification. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 302844173 GSM2844173 GEO Accession GSM2844173 SRX3372305 GSM2844174 SRP124497 SRS2669638 GSM2844174 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using the Trizol reagent and a QC was conducted using the Agilent Bioanalyzer. Total RNA was treated with Dnase I and mRNA was enriched using the oligo (dT) magnetic beads. mRNA was fragmented into short fragments and cDNA was synthesized using random hexamer primer. The double strand cDNA was purified with magentic beads. End reparation and 3'-end single nucleotide adenine addition was performed. Finally, sequencing adaptors were ligated to the fragments. The fragments were enriched by PCR amplification. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 302844174 GSM2844174 GEO Accession GSM2844174