SRX3450336 GSM2877308 SRP126244 SRS2739269 GSM2877308 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877308 GSM2877308 GEO Accession GSM2877308 SRX3450337 GSM2877309 SRP126244 SRS2739270 GSM2877309 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877309 GSM2877309 GEO Accession GSM2877309 SRX3450338 GSM2877310 SRP126244 SRS2739271 GSM2877310 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877310 GSM2877310 GEO Accession GSM2877310 SRX3450339 GSM2877311 SRP126244 SRS2739272 GSM2877311 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877311 GSM2877311 GEO Accession GSM2877311 SRX3450340 GSM2877312 SRP126244 SRS2739273 GSM2877312 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877312 GSM2877312 GEO Accession GSM2877312 SRX3450341 GSM2877313 SRP126244 SRS2739274 GSM2877313 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877313 GSM2877313 GEO Accession GSM2877313 SRX3450342 GSM2877314 SRP126244 SRS2739275 GSM2877314 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877314 GSM2877314 GEO Accession GSM2877314 SRX3450343 GSM2877315 SRP126244 SRS2739276 GSM2877315 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877315 GSM2877315 GEO Accession GSM2877315 SRX3450344 GSM2877316 SRP126244 SRS2739277 GSM2877316 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 2500 gds 302877316 GSM2877316 GEO Accession GSM2877316 SRX3450345 GSM2877317 SRP126244 SRS2739278 GSM2877317 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877317 GSM2877317 GEO Accession GSM2877317 SRX3450346 GSM2877318 SRP126244 SRS2739279 GSM2877318 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877318 GSM2877318 GEO Accession GSM2877318 SRX3450347 GSM2877319 SRP126244 SRS2739280 GSM2877319 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877319 GSM2877319 GEO Accession GSM2877319 SRX3450348 GSM2877320 SRP126244 SRS2739281 GSM2877320 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877320 GSM2877320 GEO Accession GSM2877320 SRX3450349 GSM2877321 SRP126244 SRS2739282 GSM2877321 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877321 GSM2877321 GEO Accession GSM2877321 SRX3450350 GSM2877322 SRP126244 SRS2739283 GSM2877322 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877322 GSM2877322 GEO Accession GSM2877322 SRX3450351 GSM2877323 SRP126244 SRS2739284 GSM2877323 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877323 GSM2877323 GEO Accession GSM2877323 SRX3450352 GSM2877324 SRP126244 SRS2739286 GSM2877324 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877324 GSM2877324 GEO Accession GSM2877324 SRX3450353 GSM2877325 SRP126244 SRS2739285 GSM2877325 RNA-Seq TRANSCRIPTOMIC cDNA RNeasy Mini Kit (Qiagen) was used to isolate RNA from cell pellets Ribosomal RNA was removed by poly-A selection using Oligo-dT beads. mRNA was then fragmented and reverse transcribed to yield double stranded cDNA using random hexamers. cDNA was blunt ended, had an A base added to the 3' ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 12 cycles using primers incorporating unique index tags. Illumina HiSeq 3000 gds 302877325 GSM2877325 GEO Accession GSM2877325