SRX1066094 GSM1715787 SRP059670 SRS966010 GSM1715787 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715787 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715787 gds 301715787 GEO Accession GSM1715787 SRX1066095 GSM1715788 SRP059670 SRS966009 GSM1715788 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715788 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715788 gds 301715788 GEO Accession GSM1715788 SRX1066096 GSM1715789 SRP059670 SRS966008 GSM1715789 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715789 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715789 gds 301715789 GEO Accession GSM1715789 SRX1066097 GSM1715790 SRP059670 SRS966006 GSM1715790 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715790 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715790 gds 301715790 GEO Accession GSM1715790 SRX1066098 GSM1715791 SRP059670 SRS966005 GSM1715791 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715791 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715791 gds 301715791 GEO Accession GSM1715791 SRX1066099 GSM1715792 SRP059670 SRS966004 GSM1715792 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715792 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715792 gds 301715792 GEO Accession GSM1715792 SRX1066100 GSM1715793 SRP059670 SRS966003 GSM1715793 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715793 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715793 gds 301715793 GEO Accession GSM1715793 SRX1066101 GSM1715794 SRP059670 SRS966002 GSM1715794 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715794 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715794 gds 301715794 GEO Accession GSM1715794 SRX1066102 GSM1715795 SRP059670 SRS966001 GSM1715795 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715795 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715795 gds 301715795 GEO Accession GSM1715795 SRX1066103 GSM1715796 SRP059670 SRS966000 GSM1715796 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715796 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715796 gds 301715796 GEO Accession GSM1715796 SRX1066104 GSM1715797 SRP059670 SRS965999 GSM1715797 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715797 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715797 gds 301715797 GEO Accession GSM1715797 SRX1066105 GSM1715798 SRP059670 SRS965998 GSM1715798 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715798 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715798 gds 301715798 GEO Accession GSM1715798 SRX1066106 GSM1715799 SRP059670 SRS965997 GSM1715799 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715799 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715799 gds 301715799 GEO Accession GSM1715799 SRX1066107 GSM1715800 SRP059670 SRS965996 GSM1715800 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715800 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715800 gds 301715800 GEO Accession GSM1715800 SRX1066108 GSM1715801 SRP059670 SRS965995 GSM1715801 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715801 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715801 gds 301715801 GEO Accession GSM1715801 SRX1066109 GSM1715802 SRP059670 SRS965994 GSM1715802 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715802 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715802 gds 301715802 GEO Accession GSM1715802 SRX1066110 GSM1715803 SRP059670 SRS965993 GSM1715803 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715803 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715803 gds 301715803 GEO Accession GSM1715803 SRX1066111 GSM1715804 SRP059670 SRS965992 GSM1715804 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715804 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715804 gds 301715804 GEO Accession GSM1715804 SRX1066112 GSM1715805 SRP059670 SRS965991 GSM1715805 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715805 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715805 gds 301715805 GEO Accession GSM1715805 SRX1066113 GSM1715806 SRP059670 SRS965990 GSM1715806 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715806 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715806 gds 301715806 GEO Accession GSM1715806 SRX1066114 GSM1715807 SRP059670 SRS965989 GSM1715807 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715807 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715807 gds 301715807 GEO Accession GSM1715807 SRX1066115 GSM1715808 SRP059670 SRS965988 GSM1715808 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715808 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715808 gds 301715808 GEO Accession GSM1715808 SRX1066116 GSM1715809 SRP059670 SRS965987 GSM1715809 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715809 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715809 gds 301715809 GEO Accession GSM1715809 SRX1066117 GSM1715810 SRP059670 SRS965986 GSM1715810 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715810 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715810 gds 301715810 GEO Accession GSM1715810 SRX1066118 GSM1715811 SRP059670 SRS965985 GSM1715811 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715811 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715811 gds 301715811 GEO Accession GSM1715811 SRX1066119 GSM1715812 SRP059670 SRS965984 GSM1715812 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715812 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715812 gds 301715812 GEO Accession GSM1715812 SRX1066120 GSM1715813 SRP059670 SRS965983 GSM1715813 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715813 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715813 gds 301715813 GEO Accession GSM1715813 SRX1066121 GSM1715814 SRP059670 SRS965982 GSM1715814 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715814 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715814 gds 301715814 GEO Accession GSM1715814 SRX1066122 GSM1715815 SRP059670 SRS965981 GSM1715815 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715815 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715815 gds 301715815 GEO Accession GSM1715815 SRX1066123 GSM1715816 SRP059670 SRS965980 GSM1715816 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715816 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715816 gds 301715816 GEO Accession GSM1715816 SRX1066124 GSM1715817 SRP059670 SRS965979 GSM1715817 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715817 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715817 gds 301715817 GEO Accession GSM1715817 SRX1066125 GSM1715818 SRP059670 SRS965978 GSM1715818 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715818 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715818 gds 301715818 GEO Accession GSM1715818 SRX1066126 GSM1715819 SRP059670 SRS965977 GSM1715819 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715819 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715819 gds 301715819 GEO Accession GSM1715819 SRX1066127 GSM1715820 SRP059670 SRS965976 GSM1715820 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715820 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715820 gds 301715820 GEO Accession GSM1715820 SRX1066128 GSM1715821 SRP059670 SRS965975 GSM1715821 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715821 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715821 gds 301715821 GEO Accession GSM1715821 SRX1066129 GSM1715822 SRP059670 SRS965974 GSM1715822 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715822 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715822 gds 301715822 GEO Accession GSM1715822 SRX1066130 GSM1715823 SRP059670 SRS965973 GSM1715823 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715823 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715823 gds 301715823 GEO Accession GSM1715823 SRX1066131 GSM1715824 SRP059670 SRS965972 GSM1715824 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715824 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715824 gds 301715824 GEO Accession GSM1715824 SRX1066132 GSM1715825 SRP059670 SRS965971 GSM1715825 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715825 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715825 gds 301715825 GEO Accession GSM1715825 SRX1066133 GSM1715826 SRP059670 SRS965970 GSM1715826 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715826 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715826 gds 301715826 GEO Accession GSM1715826 SRX1066134 GSM1715827 SRP059670 SRS965969 GSM1715827 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715827 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715827 gds 301715827 GEO Accession GSM1715827 SRX1066135 GSM1715828 SRP059670 SRS965968 GSM1715828 RNA-Seq TRANSCRIPTOMIC cDNA Cell lysates for RNA extraction were harvested using Trizol reagent (Life Technologies) followed by chloroform extraction, isopropanol precipitation and resuspension in Tris-HCL pH 8.0. cDNA libraries for RNA-sequencing were prepared with poly-A purified mRNAs and the TruSeq™ Stranded mRNA LT Sample Prep Kit (Illumina) according to the manufacturers protocol . We generated ~734 million 101x2 bp paired-end and ~335 million 101 bp single-end RNA-seq reads on a HiSeq 2000 sequencer. cDNA libraries for sequencing were prepared using the Illumina True-seq Stranded mRNA kit and protocol. Illumina HiSeq 2000 GEO Sample GSM1715828 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1715828 gds 301715828 GEO Accession GSM1715828