SRX3375298 GSM2845429 SRP124633 SRS2671723 GSM2845429 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845429 GSM2845429 GEO Accession GSM2845429 SRX3375299 GSM2845430 SRP124633 SRS2671722 GSM2845430 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845430 GSM2845430 GEO Accession GSM2845430 SRX3375300 GSM2845431 SRP124633 SRS2671726 GSM2845431 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845431 GSM2845431 GEO Accession GSM2845431 SRX3375301 GSM2845432 SRP124633 SRS2671724 GSM2845432 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845432 GSM2845432 GEO Accession GSM2845432 SRX3375302 GSM2845433 SRP124633 SRS2671725 GSM2845433 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845433 GSM2845433 GEO Accession GSM2845433 SRX3375303 GSM2845434 SRP124633 SRS2671729 GSM2845434 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845434 GSM2845434 GEO Accession GSM2845434 SRX3375305 GSM2845435 SRP124633 SRS2671728 GSM2845435 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845435 GSM2845435 GEO Accession GSM2845435 SRX3375306 GSM2845436 SRP124633 SRS2671732 GSM2845436 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845436 GSM2845436 GEO Accession GSM2845436 SRX3375307 GSM2845437 SRP124633 SRS2671730 GSM2845437 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845437 GSM2845437 GEO Accession GSM2845437 SRX3375308 GSM2845438 SRP124633 SRS2671731 GSM2845438 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845438 GSM2845438 GEO Accession GSM2845438 SRX3375309 GSM2845439 SRP124633 SRS2671738 GSM2845439 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was treated with RQ1 DNase (Promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260 nm/280 nm (A260/A280) using Smartspec Plus (BioRad). RNA integrity was further verified by 1.5% agrose gel electrophoresis. For each sample, 5 μg of total RNA was used for RNA-seq library preparation. Polyadenylated mRNAs were purified and concentrated with oligo(dT)-conjugated magnetic beads (Invitrogen). Purified mRNAs were fragmented at 95℃ followed by end repair and 5' adaptor ligation. Then mRNA reverse transcription was performed with RT primer harboring 3' adaptor sequence and randomized hexamer. The cDNAs were purified and amplified with RNA-Seq Library Preparation Kit (Gnomegen). And PCR products corresponding to 200-500 bps were purified, quantified and stored at -80 ℃ until before sequencing. Illumina HiSeq 2000 gds 302845439 GSM2845439 GEO Accession GSM2845439