SRX2766637 GSM2590076 SRP105328 SRS2150775 GSM2590076 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590076 GSM2590076 GEO Accession GSM2590076 SRX2766638 GSM2590077 SRP105328 SRS2150774 GSM2590077 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590077 GSM2590077 GEO Accession GSM2590077 SRX2766639 GSM2590078 SRP105328 SRS2150773 GSM2590078 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590078 GSM2590078 GEO Accession GSM2590078 SRX2766640 GSM2590079 SRP105328 SRS2150776 GSM2590079 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590079 GSM2590079 GEO Accession GSM2590079 SRX2766641 GSM2590080 SRP105328 SRS2150777 GSM2590080 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590080 GSM2590080 GEO Accession GSM2590080 SRX2766642 GSM2590081 SRP105328 SRS2150778 GSM2590081 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590081 GSM2590081 GEO Accession GSM2590081 SRX2766643 GSM2590082 SRP105328 SRS2150779 GSM2590082 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590082 GSM2590082 GEO Accession GSM2590082 SRX2766644 GSM2590083 SRP105328 SRS2150780 GSM2590083 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590083 GSM2590083 GEO Accession GSM2590083 SRX2766645 GSM2590084 SRP105328 SRS2150781 GSM2590084 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590084 GSM2590084 GEO Accession GSM2590084 SRX2766646 GSM2590085 SRP105328 SRS2150782 GSM2590085 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590085 GSM2590085 GEO Accession GSM2590085 SRX2766647 GSM2590086 SRP105328 SRS2150783 GSM2590086 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590086 GSM2590086 GEO Accession GSM2590086 SRX2766648 GSM2590087 SRP105328 SRS2150784 GSM2590087 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590087 GSM2590087 GEO Accession GSM2590087 SRX2766649 GSM2590088 SRP105328 SRS2150785 GSM2590088 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590088 GSM2590088 GEO Accession GSM2590088 SRX2766650 GSM2590089 SRP105328 SRS2150787 GSM2590089 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590089 GSM2590089 GEO Accession GSM2590089 SRX2766651 GSM2590090 SRP105328 SRS2150786 GSM2590090 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590090 GSM2590090 GEO Accession GSM2590090 SRX2766652 GSM2590091 SRP105328 SRS2150788 GSM2590091 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590091 GSM2590091 GEO Accession GSM2590091 SRX2766653 GSM2590092 SRP105328 SRS2150789 GSM2590092 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590092 GSM2590092 GEO Accession GSM2590092 SRX2766654 GSM2590093 SRP105328 SRS2150790 GSM2590093 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590093 GSM2590093 GEO Accession GSM2590093 SRX2766655 GSM2590094 SRP105328 SRS2150791 GSM2590094 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590094 GSM2590094 GEO Accession GSM2590094 SRX2766656 GSM2590095 SRP105328 SRS2150792 GSM2590095 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590095 GSM2590095 GEO Accession GSM2590095 SRX2766657 GSM2590096 SRP105328 SRS2150793 GSM2590096 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590096 GSM2590096 GEO Accession GSM2590096 SRX2766658 GSM2590097 SRP105328 SRS2150794 GSM2590097 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590097 GSM2590097 GEO Accession GSM2590097 SRX2766659 GSM2590098 SRP105328 SRS2150795 GSM2590098 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590098 GSM2590098 GEO Accession GSM2590098 SRX2766660 GSM2590099 SRP105328 SRS2150796 GSM2590099 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590099 GSM2590099 GEO Accession GSM2590099 SRX2766661 GSM2590100 SRP105328 SRS2150798 GSM2590100 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590100 GSM2590100 GEO Accession GSM2590100 SRX2766662 GSM2590101 SRP105328 SRS2150797 GSM2590101 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590101 GSM2590101 GEO Accession GSM2590101 SRX2766663 GSM2590102 SRP105328 SRS2150799 GSM2590102 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590102 GSM2590102 GEO Accession GSM2590102 SRX2766664 GSM2590103 SRP105328 SRS2150801 GSM2590103 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590103 GSM2590103 GEO Accession GSM2590103 SRX2766665 GSM2590104 SRP105328 SRS2150800 GSM2590104 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590104 GSM2590104 GEO Accession GSM2590104 SRX2766666 GSM2590105 SRP105328 SRS2150802 GSM2590105 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590105 GSM2590105 GEO Accession GSM2590105 SRX2766667 GSM2590106 SRP105328 SRS2150803 GSM2590106 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590106 GSM2590106 GEO Accession GSM2590106 SRX2766668 GSM2590107 SRP105328 SRS2150804 GSM2590107 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590107 GSM2590107 GEO Accession GSM2590107 SRX2766669 GSM2590108 SRP105328 SRS2150805 GSM2590108 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590108 GSM2590108 GEO Accession GSM2590108 SRX2766670 GSM2590109 SRP105328 SRS2150806 GSM2590109 RNA-Seq TRANSCRIPTOMIC cDNA For RNA extraction, we used Trizol kit by following manufacturer's instructions Trizol-isolated RNA was enriched for Poly(A+) RNA with biotinylated oligo(dT), converted to cDNA with Superscript III (Invitrogen). Next, a terminal transferase (NEB, cat.no.M0315S) was used to add a ddNTP to the 3’-end of the cDNA. After the second-strand cDNA synthesis, 23 cycles of PCR were performed to amplify the cDNA. The length of 200-400nt PCR product was subjected to deep sequencing. Illumina HiSeq 2500 gds 302590109 GSM2590109 GEO Accession GSM2590109