SRX1310939 GSM1904045 SRP064574 SRS1103606 GSM1904045 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904045 GEO Accession GSM1904045 SRX1310940 GSM1904046 SRP064574 SRS1103609 GSM1904046 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904046 GEO Accession GSM1904046 SRX1310941 GSM1904047 SRP064574 SRS1103607 GSM1904047 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904047 GEO Accession GSM1904047 SRX1310942 GSM1904048 SRP064574 SRS1103605 GSM1904048 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904048 GEO Accession GSM1904048 SRX1310943 GSM1904049 SRP064574 SRS1103603 GSM1904049 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904049 GEO Accession GSM1904049 SRX1310944 GSM1904050 SRP064574 SRS1103602 GSM1904050 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904050 GEO Accession GSM1904050 SRX1310945 GSM1904051 SRP064574 SRS1103601 GSM1904051 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904051 GEO Accession GSM1904051 SRX1310946 GSM1904052 SRP064574 SRS1103604 GSM1904052 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904052 GEO Accession GSM1904052 SRX1310947 GSM1904053 SRP064574 SRS1103600 GSM1904053 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904053 GEO Accession GSM1904053 SRX1310948 GSM1904054 SRP064574 SRS1103599 GSM1904054 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904054 GEO Accession GSM1904054 SRX1310949 GSM1904055 SRP064574 SRS1103597 GSM1904055 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904055 GEO Accession GSM1904055 SRX1310950 GSM1904056 SRP064574 SRS1103596 GSM1904056 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904056 GEO Accession GSM1904056 SRX1310951 GSM1904057 SRP064574 SRS1103598 GSM1904057 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904057 GEO Accession GSM1904057 SRX1310952 GSM1904058 SRP064574 SRS1103595 GSM1904058 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904058 GEO Accession GSM1904058 SRX1310953 GSM1904059 SRP064574 SRS1103594 GSM1904059 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904059 GEO Accession GSM1904059 SRX1310954 GSM1904060 SRP064574 SRS1103592 GSM1904060 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904060 GEO Accession GSM1904060 SRX1310955 GSM1904061 SRP064574 SRS1103591 GSM1904061 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904061 GEO Accession GSM1904061 SRX1310956 GSM1904062 SRP064574 SRS1103593 GSM1904062 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904062 GEO Accession GSM1904062 SRX1310957 GSM1904063 SRP064574 SRS1103590 GSM1904063 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904063 GEO Accession GSM1904063 SRX1310958 GSM1904064 SRP064574 SRS1103589 GSM1904064 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904064 GEO Accession GSM1904064 SRX1310959 GSM1904065 SRP064574 SRS1103570 GSM1904065 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904065 GEO Accession GSM1904065 SRX1310960 GSM1904066 SRP064574 SRS1103588 GSM1904066 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904066 GEO Accession GSM1904066 SRX1310961 GSM1904067 SRP064574 SRS1103586 GSM1904067 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904067 GEO Accession GSM1904067 SRX1310962 GSM1904068 SRP064574 SRS1103585 GSM1904068 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904068 GEO Accession GSM1904068 SRX1310963 GSM1904069 SRP064574 SRS1103587 GSM1904069 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904069 GEO Accession GSM1904069 SRX1310964 GSM1904070 SRP064574 SRS1103584 GSM1904070 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904070 GEO Accession GSM1904070 SRX1310965 GSM1904071 SRP064574 SRS1103583 GSM1904071 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904071 GEO Accession GSM1904071 SRX1310966 GSM1904072 SRP064574 SRS1103582 GSM1904072 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904072 GEO Accession GSM1904072 SRX1310967 GSM1904073 SRP064574 SRS1103580 GSM1904073 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904073 GEO Accession GSM1904073 SRX1310968 GSM1904074 SRP064574 SRS1103581 GSM1904074 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904074 GEO Accession GSM1904074 SRX1310969 GSM1904075 SRP064574 SRS1103579 GSM1904075 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904075 GEO Accession GSM1904075 SRX1310970 GSM1904076 SRP064574 SRS1103578 GSM1904076 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904076 GEO Accession GSM1904076 SRX1310971 GSM1904077 SRP064574 SRS1103577 GSM1904077 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904077 GEO Accession GSM1904077 SRX1310972 GSM1904078 SRP064574 SRS1103576 GSM1904078 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904078 GEO Accession GSM1904078 SRX1310973 GSM1904079 SRP064574 SRS1103575 GSM1904079 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904079 GEO Accession GSM1904079 SRX1310974 GSM1904080 SRP064574 SRS1103573 GSM1904080 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904080 GEO Accession GSM1904080 SRX1310975 GSM1904081 SRP064574 SRS1103574 GSM1904081 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904081 GEO Accession GSM1904081 SRX1310976 GSM1904082 SRP064574 SRS1103572 GSM1904082 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904082 GEO Accession GSM1904082 SRX1310977 GSM1904083 SRP064574 SRS1103571 GSM1904083 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904083 GEO Accession GSM1904083 SRX1310978 GSM1904084 SRP064574 SRS1103569 GSM1904084 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted using Qiagen RNEasy Mini Kit Protocol Library construction and sequencing was performed by Bejing Genomics Institute (http://www.genomics.cn/en/index) The total RNA samples are first treated with DNase I. Then the mRNA is enriched by using the oligo(dT) magnetic beads (for eukaryotes) or by removing rRNAs from the total RNA (for prokaryotes). Mixed with the fragmentation buffer, the mRNA is fragmented into short fragments. Then the first strand of cDNA is synthesized by using random hexamer-primer. Buffer, dNTPs, RNase H and DNA polymerase I are added to synthesize the second strand. The double strand cDNA is purified with magnetic beads. End reparation and 3'-end single nucleotide A (adenine) addition is then performed. Finally, sequencing adaptors are ligated to the fragments. The fragments are enriched by PCR amplification. During the QC step, Agilent 2100 Bioanaylzer and ABI StepOnePlus Real-Time PCR System are used to qualify and quantify of the sample library. Illumina HiSeq 2000 gds 301904084 GEO Accession GSM1904084