SRX5554414 GSM3682499 SRP189095 SRS4518310 GSM3682499 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682499 GSM3682499 GEO Accession GSM3682499 SRX5554415 GSM3682500 SRP189095 SRS4518309 GSM3682500 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682500 GSM3682500 GEO Accession GSM3682500 SRX5554416 GSM3682501 SRP189095 SRS4518311 GSM3682501 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682501 GSM3682501 GEO Accession GSM3682501 SRX5554417 GSM3682502 SRP189095 SRS4518316 GSM3682502 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682502 GSM3682502 GEO Accession GSM3682502 SRX5554418 GSM3682503 SRP189095 SRS4518312 GSM3682503 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682503 GSM3682503 GEO Accession GSM3682503 SRX5554419 GSM3682504 SRP189095 SRS4518313 GSM3682504 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682504 GSM3682504 GEO Accession GSM3682504 SRX5554420 GSM3682505 SRP189095 SRS4518314 GSM3682505 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682505 GSM3682505 GEO Accession GSM3682505 SRX5554421 GSM3682506 SRP189095 SRS4518315 GSM3682506 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682506 GSM3682506 GEO Accession GSM3682506 SRX5554422 GSM3682507 SRP189095 SRS4518317 GSM3682507 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682507 GSM3682507 GEO Accession GSM3682507 SRX5554423 GSM3682508 SRP189095 SRS4518318 GSM3682508 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682508 GSM3682508 GEO Accession GSM3682508 SRX5554424 GSM3682509 SRP189095 SRS4518319 GSM3682509 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682509 GSM3682509 GEO Accession GSM3682509 SRX5554425 GSM3682510 SRP189095 SRS4518321 GSM3682510 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682510 GSM3682510 GEO Accession GSM3682510 SRX5554426 GSM3682511 SRP189095 SRS4518320 GSM3682511 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682511 GSM3682511 GEO Accession GSM3682511 SRX5554427 GSM3682512 SRP189095 SRS4518323 GSM3682512 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682512 GSM3682512 GEO Accession GSM3682512 SRX5554428 GSM3682513 SRP189095 SRS4518322 GSM3682513 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682513 GSM3682513 GEO Accession GSM3682513 SRX5554429 GSM3682514 SRP189095 SRS4518324 GSM3682514 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682514 GSM3682514 GEO Accession GSM3682514 SRX5554430 GSM3682515 SRP189095 SRS4518326 GSM3682515 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682515 GSM3682515 GEO Accession GSM3682515 SRX5554431 GSM3682516 SRP189095 SRS4518325 GSM3682516 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682516 GSM3682516 GEO Accession GSM3682516 SRX5554432 GSM3682517 SRP189095 SRS4518327 GSM3682517 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682517 GSM3682517 GEO Accession GSM3682517 SRX5554433 GSM3682518 SRP189095 SRS4518328 GSM3682518 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682518 GSM3682518 GEO Accession GSM3682518 SRX5554434 GSM3682519 SRP189095 SRS4518329 GSM3682519 RNA-Seq TRANSCRIPTOMIC cDNA Cell culture medium was removed, cells were washed with DPBS, TRIzol (Life Technologies) was added and cells were processed according to manufacturer's guidelines. Up to 4 µg of total RNA was used as an input for the Stranded mRNA-Seq Kit (KAPA). mRNA is captured using magnetic oligo-dT beads: while mRNA is retained, other RNA is washed away in two subsequent washes. mRNA fragments are fragmented and converted to cDNA, with dUTP incorporated in to the second cDNA strands. A-tailing, adapter ligation and enrichment is carried out, to obtain libraries. Enrichment of the libraries is achieved by using KAPA HiFi Hotstart Readymix. The strand marked with dUTP is not amplified, allowing strand specificity. Illumina HiSeq 2500 gds 303682519 GSM3682519 GEO Accession GSM3682519