SRX3453306 GSM2879525 SRP126323 SRS2742012 GSM2879525 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879525 GSM2879525 GEO Accession GSM2879525 SRX3453307 GSM2879526 SRP126323 SRS2742009 GSM2879526 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879526 GSM2879526 GEO Accession GSM2879526 SRX3453308 GSM2879527 SRP126323 SRS2742011 GSM2879527 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879527 GSM2879527 GEO Accession GSM2879527 SRX3453309 GSM2879528 SRP126323 SRS2742010 GSM2879528 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879528 GSM2879528 GEO Accession GSM2879528 SRX3453310 GSM2879529 SRP126323 SRS2742013 GSM2879529 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879529 GSM2879529 GEO Accession GSM2879529 SRX3453311 GSM2879530 SRP126323 SRS2742014 GSM2879530 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879530 GSM2879530 GEO Accession GSM2879530 SRX3453312 GSM2879531 SRP126323 SRS2742015 GSM2879531 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879531 GSM2879531 GEO Accession GSM2879531 SRX3453313 GSM2879532 SRP126323 SRS2742016 GSM2879532 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879532 GSM2879532 GEO Accession GSM2879532 SRX3453314 GSM2879533 SRP126323 SRS2742017 GSM2879533 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879533 GSM2879533 GEO Accession GSM2879533 SRX3453315 GSM2879534 SRP126323 SRS2742018 GSM2879534 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was reversed transcribed by SuperScript II reverse transcriptase (Invitrogen). The double-stranded cDNA was amplified using KAPA HiFi HotStart ReadyMix (KAPA Biosystems) and purified using 1: 0.75 ratio of AMPure XP beads (Bechman Coulter). Amplified cDNA (~5 ng) was then used to construct Illumina sequencing libraries using Illumina's Nextera DNA sample preparation kit following the manufacturer's instructions. Illumina HiSeq 2500 gds 302879534 GSM2879534 GEO Accession GSM2879534