SRX2007780 GSM2264684 SRP081095 SRS1606337 GSM2264684 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264684 GEO Accession GSM2264684 SRX2007781 GSM2264685 SRP081095 SRS1606338 GSM2264685 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264685 GEO Accession GSM2264685 SRX2007782 GSM2264686 SRP081095 SRS1606339 GSM2264686 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264686 GEO Accession GSM2264686 SRX2007783 GSM2264687 SRP081095 SRS1606340 GSM2264687 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264687 GEO Accession GSM2264687 SRX2007784 GSM2264688 SRP081095 SRS1606341 GSM2264688 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264688 GEO Accession GSM2264688 SRX2007785 GSM2264689 SRP081095 SRS1606342 GSM2264689 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264689 GEO Accession GSM2264689 SRX2007786 GSM2264690 SRP081095 SRS1606343 GSM2264690 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264690 GEO Accession GSM2264690 SRX2007787 GSM2264691 SRP081095 SRS1606344 GSM2264691 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264691 GEO Accession GSM2264691 SRX2007788 GSM2264692 SRP081095 SRS1606345 GSM2264692 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264692 GEO Accession GSM2264692 SRX2007789 GSM2264693 SRP081095 SRS1606346 GSM2264693 RNA-Seq TRANSCRIPTOMIC cDNA RNA was prepared according to the Illumina TruSeq Stranded mRNA Library Prep Kit protocol following addition of 10uL of 1:100 dilution of ERCC92 Mix 1 (Ambion/Life) to each cell pellet as an external spike-in control. Total RNA was DNase treated, and purified with Qiagen RNeasy columns.  Ribosomal RNA was depleted using an Illumina Yeast RiboZero rRNA depletion kit (MRZY1306) RNA fragmentation and priming with Illumina TruSeq Stranded mRNA library synthesis (CAT RS-122-2101). All protocols were performed according to manufacturer’s directions. Single read sequencing was completed on the Illumina HiSeq2500 platform with Version 4 reagents at the Donnelly Sequencing Centre. Single-end reads of 51 bp in length were acquired with a total of 240-250 million reads per lane. Illumina HiSeq 2500 gds 302264693 GEO Accession GSM2264693