SRX3509840 GSM2901750 SRP127506 SRS2792905 GSM2901750 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901750 GSM2901750 GEO Accession GSM2901750 SRX3509841 GSM2901751 SRP127506 SRS2792906 GSM2901751 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901751 GSM2901751 GEO Accession GSM2901751 SRX3509842 GSM2901752 SRP127506 SRS2792904 GSM2901752 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901752 GSM2901752 GEO Accession GSM2901752 SRX3509843 GSM2901753 SRP127506 SRS2792910 GSM2901753 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901753 GSM2901753 GEO Accession GSM2901753 SRX3509844 GSM2901754 SRP127506 SRS2792903 GSM2901754 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901754 GSM2901754 GEO Accession GSM2901754 SRX3509845 GSM2901755 SRP127506 SRS2792907 GSM2901755 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901755 GSM2901755 GEO Accession GSM2901755 SRX3509846 GSM2901756 SRP127506 SRS2792913 GSM2901756 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901756 GSM2901756 GEO Accession GSM2901756 SRX3509847 GSM2901757 SRP127506 SRS2792914 GSM2901757 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901757 GSM2901757 GEO Accession GSM2901757 SRX3509848 GSM2901758 SRP127506 SRS2792908 GSM2901758 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901758 GSM2901758 GEO Accession GSM2901758 SRX3509849 GSM2901759 SRP127506 SRS2792912 GSM2901759 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901759 GSM2901759 GEO Accession GSM2901759 SRX3509850 GSM2901760 SRP127506 SRS2792909 GSM2901760 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901760 GSM2901760 GEO Accession GSM2901760 SRX3509851 GSM2901761 SRP127506 SRS2792911 GSM2901761 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using RNeasy Mini Kit from QIAGEN. Integrity and quantity of RNA was evaluated by Agilent 2100, following the manufacturer's instructions. The mRNA and non-coding RNAs are enriched by removing rRNA using RNaseH. Mixed with the fragmentation buffer, target RNA were fragmented into short fragments and cDNA was synthesized using the RNA fragments as templates by N6 random primer, followed by end reparation and ligated with adapters. The quantity and quality of the cDNA libraries were assessed using an Agilent 2100 BioAnalyzer (Agilent Technologies). BGISEQ-500 gds 302901761 GSM2901761 GEO Accession GSM2901761