SRX316179 ZN991 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453634 SAMN02213825 ZN991 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316180 ZN993 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453635 SAMN02213826 ZN993 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316181 ZN994 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453636 SAMN02213827 ZN994 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316182 ZN995 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453637 SAMN02213828 ZN995 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316183 ZN996 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453638 SAMN02213829 ZN996 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316184 ZN1048 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453639 SAMN02213830 ZN1048 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316185 ZN1083 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453640 SAMN02213831 ZN1083 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316186 ZN1084 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453641 SAMN02213832 ZN1084 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316187 GS28 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453642 SAMN02213833 GS28 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316188 GS29 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453643 SAMN02213834 GS29 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316189 ZN1040 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453644 SAMN02213835 ZN1040 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316190 ZN1041 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453645 SAMN02213836 ZN1041 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316191 ZN1042 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453646 SAMN02213837 ZN1042 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316192 ZN1043 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453647 SAMN02213838 ZN1043 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316193 ZN1044 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453648 SAMN02213839 ZN1044 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316194 ZN1045 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453649 SAMN02213840 ZN1045 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316195 ZN1046 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453650 SAMN02213841 ZN1046 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316196 ZN1085 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453651 SAMN02213842 ZN1085 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316197 ZN1086 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453652 SAMN02213843 ZN1086 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx SRX316198 ZN1047 SRP026359 PRJNA209572 dUTP method was used. Strand specificity is maintained by the incorporation of deoxy-UTP during the second strand cDNA synthesis and subsequent destruction of the uridine-containing strand during subsequent step of library construction. First-strand cDNA synthesis reaction was incubated at 25*C for 10 min, followed by 42*C for 1 h and inactivated by incubation at 70*C for 15 min. Double strand cDNAs were repaired with the DNA Terminator End Repair Kit. The Illumina PE Adapter was ligated to the ends of DNA fragments with the Quick Ligation Kit. Ligation product of 250-300 bp fragments was excised. The recovered fragment was digested at 37*C for 15 min with 2 units of Uracil-N- Glycosylase. The digested product was purified on a QIAQuick PCR column followed by 14 cycles of amplification using AccuPrime™ Pfx DNA Polymerase SRS453653 SAMN02213844 ZN1047 RNA-Seq TRANSCRIPTOMIC RANDOM 152 0 Application Read Forward 1 1 Application Read Reverse 77 Illumina Genome Analyzer IIx