SRX892624 GSM1620040 SRP055558 PRJNA276574 SRS858840 SAMN03378766 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620040 GSM1620040 GEO Accession GSM1620040 SRX892625 GSM1620041 SRP055558 PRJNA276574 SRS858839 SAMN03378771 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620041 GSM1620041 GEO Accession GSM1620041 SRX892626 GSM1620042 SRP055558 PRJNA276574 SRS858838 SAMN03378764 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620042 GSM1620042 GEO Accession GSM1620042 SRX892627 GSM1620043 SRP055558 PRJNA276574 SRS858836 SAMN03378769 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620043 GSM1620043 GEO Accession GSM1620043 SRX892628 GSM1620044 SRP055558 PRJNA276574 SRS858837 SAMN03378773 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620044 GSM1620044 GEO Accession GSM1620044 SRX892629 GSM1620045 SRP055558 PRJNA276574 SRS858841 SAMN03378767 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620045 GSM1620045 GEO Accession GSM1620045 SRX892630 GSM1620046 SRP055558 PRJNA276574 SRS858835 SAMN03378772 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620046 GSM1620046 GEO Accession GSM1620046 SRX892631 GSM1620047 SRP055558 PRJNA276574 SRS858834 SAMN03378774 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620047 GSM1620047 GEO Accession GSM1620047 SRX892632 GSM1620048 SRP055558 PRJNA276574 SRS858833 SAMN03378762 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). Illumina HiSeq 2500 gds 301620048 GSM1620048 GEO Accession GSM1620048 SRX892633 GSM1620049 SRP055558 PRJNA276574 SRS858832 SAMN03378768 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620049 GSM1620049 GEO Accession GSM1620049 SRX892634 GSM1620050 SRP055558 PRJNA276574 SRS858831 SAMN03378763 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620050 GSM1620050 GEO Accession GSM1620050 SRX892635 GSM1620051 SRP055558 PRJNA276574 SRS858830 SAMN03378765 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620051 GSM1620051 GEO Accession GSM1620051 SRX892636 GSM1620052 SRP055558 PRJNA276574 SRS858829 SAMN03378770 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620052 GSM1620052 GEO Accession GSM1620052 SRX892637 GSM1620053 SRP055558 PRJNA276574 SRS858828 SAMN03378776 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620053 GSM1620053 GEO Accession GSM1620053 SRX892638 GSM1620054 SRP055558 PRJNA276574 SRS858826 SAMN03378778 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620054 GSM1620054 GEO Accession GSM1620054 SRX892639 GSM1620055 SRP055558 PRJNA276574 SRS858825 SAMN03378777 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620055 GSM1620055 GEO Accession GSM1620055 SRX892640 GSM1620056 SRP055558 PRJNA276574 SRS858827 SAMN03378775 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated using Arcturus PicoPure RNA isolation kit (Life Technologies). Double stranded cDNA was generated from total RNA using a DNA-RNA chimeric primer mix and reverse transcriptase, and cDNA was amplified by the SPIA amplification process developed by NuGEN (Ovation RNA-Seq System V2 kit (Neugen)). The amplified double stranded cDNA was fragmented to an average size of 200 bases using Covaris S-S series sonication system. The fragmented cDNA was end-repaired, and adaptors and barcodes were ligated before PCR-based library preparation using Ovation Ultralow DRMultiplex Systems (Nugen). NextSeq 500 gds 301620056 GSM1620056 GEO Accession GSM1620056