SRX3778517 GSM3035973 SRP134265 SRS3032359 GSM3035973 RNA-Seq TRANSCRIPTOMIC cDNA Cells (10^7) were lysed and RNA was extracted according to manufacturer's protocol (Qiagen RNeasy Mini kit). Total RNA was fractionated by size using ethanol concentration manipulations. The large RNA fraction (>200 nt) was fragmented prior to library construction. Ribosomal RNA was reduced by duplex specific nuclease (DSN) following limited hybridizations of both fractions and then amplified to add barcodes for multiplexing on the Illumina HiSeq2000 platform. Illumina HiSeq 2000 gds 303035973 GSM3035973 GEO Accession GSM3035973 SRX3778518 GSM3035974 SRP134265 SRS3032361 GSM3035974 RNA-Seq TRANSCRIPTOMIC cDNA Cells (10^7) were lysed and RNA was extracted according to manufacturer's protocol (Qiagen RNeasy Mini kit). Total RNA was fractionated by size using ethanol concentration manipulations. The large RNA fraction (>200 nt) was fragmented prior to library construction. Ribosomal RNA was reduced by duplex specific nuclease (DSN) following limited hybridizations of both fractions and then amplified to add barcodes for multiplexing on the Illumina HiSeq2000 platform. Illumina HiSeq 2000 gds 303035974 GSM3035974 GEO Accession GSM3035974 SRX3778519 GSM3035975 SRP134265 SRS3032360 GSM3035975 RNA-Seq TRANSCRIPTOMIC cDNA Cells (10^7) were lysed and RNA was extracted according to manufacturer's protocol (Qiagen RNeasy Mini kit). Total RNA was fractionated by size using ethanol concentration manipulations. The large RNA fraction (>200 nt) was fragmented prior to library construction. Ribosomal RNA was reduced by duplex specific nuclease (DSN) following limited hybridizations of both fractions and then amplified to add barcodes for multiplexing on the Illumina HiSeq2000 platform. Illumina HiSeq 2000 gds 303035975 GSM3035975 GEO Accession GSM3035975 SRX3778520 GSM3035976 SRP134265 SRS3032363 GSM3035976 RNA-Seq TRANSCRIPTOMIC cDNA Cells (10^7) were lysed and RNA was extracted according to manufacturer's protocol (Qiagen RNeasy Mini kit). Total RNA was fractionated by size using ethanol concentration manipulations. The large RNA fraction (>200 nt) was fragmented prior to library construction. Ribosomal RNA was reduced by duplex specific nuclease (DSN) following limited hybridizations of both fractions and then amplified to add barcodes for multiplexing on the Illumina HiSeq2000 platform. Illumina HiSeq 2000 gds 303035976 GSM3035976 GEO Accession GSM3035976