SRX3770849 GSM3032497 SRP134089 SRS3025493 GSM3032497 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from cells by using TRIzol reagent (Thermo Fisher Scientific) and treated with DNase I (Takara). Conventional RNA-seq library protocol after 3′ adapter ligation and size fractionation (100-500 nt) without fragmentation step NextSeq 500 gds 303032497 GSM3032497 GEO Accession GSM3032497 SRX3770850 GSM3032498 SRP134089 SRS3025494 GSM3032498 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from cells by using TRIzol reagent (Thermo Fisher Scientific) and treated with DNase I (Takara). Conventional RNA-seq library protocol after 3′ adapter ligation and size fractionation (100-500 nt) without fragmentation step NextSeq 500 gds 303032498 GSM3032498 GEO Accession GSM3032498 SRX3770851 GSM3032499 SRP134089 SRS3025496 GSM3032499 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from cells by using TRIzol reagent (Thermo Fisher Scientific) and treated with DNase I (Takara). Conventional RNA-seq library protocol after 3′ adapter ligation and size fractionation (100-500 nt) without fragmentation step NextSeq 500 gds 303032499 GSM3032499 GEO Accession GSM3032499 SRX3770852 GSM3032500 SRP134089 SRS3025495 GSM3032500 RNA-Seq TRANSCRIPTOMIC cDNA Total RNAs were extracted from cells by using TRIzol reagent (Thermo Fisher Scientific) and treated with DNase I (Takara). Conventional RNA-seq library protocol after 3′ adapter ligation and size fractionation (100-500 nt) without fragmentation step NextSeq 500 gds 303032500 GSM3032500 GEO Accession GSM3032500