SRX5227237 GSM3554371 SRP176639 SRS4231142 GSM3554371 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554371 GSM3554371 GEO Accession GSM3554371 SRX5227238 GSM3554372 SRP176639 SRS4231141 GSM3554372 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554372 GSM3554372 GEO Accession GSM3554372 SRX5227239 GSM3554373 SRP176639 SRS4231144 GSM3554373 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554373 GSM3554373 GEO Accession GSM3554373 SRX5227240 GSM3554374 SRP176639 SRS4231143 GSM3554374 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554374 GSM3554374 GEO Accession GSM3554374 SRX5227241 GSM3554375 SRP176639 SRS4231146 GSM3554375 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554375 GSM3554375 GEO Accession GSM3554375 SRX5227242 GSM3554376 SRP176639 SRS4231145 GSM3554376 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554376 GSM3554376 GEO Accession GSM3554376 SRX5227243 GSM3554377 SRP176639 SRS4231147 GSM3554377 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554377 GSM3554377 GEO Accession GSM3554377 SRX5227244 GSM3554378 SRP176639 SRS4231148 GSM3554378 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554378 GSM3554378 GEO Accession GSM3554378 SRX5227245 GSM3554379 SRP176639 SRS4231149 GSM3554379 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554379 GSM3554379 GEO Accession GSM3554379 SRX5227246 GSM3554380 SRP176639 SRS4231150 GSM3554380 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554380 GSM3554380 GEO Accession GSM3554380 SRX5227247 GSM3554381 SRP176639 SRS4231151 GSM3554381 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554381 GSM3554381 GEO Accession GSM3554381 SRX5227248 GSM3554382 SRP176639 SRS4231152 GSM3554382 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554382 GSM3554382 GEO Accession GSM3554382 SRX5227249 GSM3554383 SRP176639 SRS4231153 GSM3554383 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554383 GSM3554383 GEO Accession GSM3554383 SRX5227250 GSM3554384 SRP176639 SRS4231154 GSM3554384 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554384 GSM3554384 GEO Accession GSM3554384 SRX5227251 GSM3554385 SRP176639 SRS4231155 GSM3554385 RNA-Seq TRANSCRIPTOMIC cDNA Cells were homogenized using a QiaShredder column (QIAGEN) and total RNA was purified using an RNeasy Mini kit (QIAGEN) followed by treatment with a DNase DNeasy kit (Thermo Fisher Scientific). Ribosomal RNA was removed from 1 ug total RNA using a Ribo-ZERO kit (Illumina-EpiCentre) then RNA libraries were prepared using standard Illumina techniques Illumina HiSeq 3000 gds 303554385 GSM3554385 GEO Accession GSM3554385