SRX7202564 GSM4189039 SRP231449 SRS5707798 GSM4189039 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189039 GSM4189039 GEO Accession GSM4189039 SRX7202565 GSM4189040 SRP231449 SRS5707799 GSM4189040 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189040 GSM4189040 GEO Accession GSM4189040 SRX7202566 GSM4189041 SRP231449 SRS5707800 GSM4189041 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189041 GSM4189041 GEO Accession GSM4189041 SRX7202567 GSM4189042 SRP231449 SRS5707801 GSM4189042 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189042 GSM4189042 GEO Accession GSM4189042 SRX7202568 GSM4189043 SRP231449 SRS5707802 GSM4189043 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189043 GSM4189043 GEO Accession GSM4189043 SRX7202569 GSM4189044 SRP231449 SRS5707803 GSM4189044 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189044 GSM4189044 GEO Accession GSM4189044 SRX7202570 GSM4189045 SRP231449 SRS5707804 GSM4189045 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189045 GSM4189045 GEO Accession GSM4189045 SRX7202571 GSM4189046 SRP231449 SRS5707805 GSM4189046 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189046 GSM4189046 GEO Accession GSM4189046 SRX7202572 GSM4189047 SRP231449 SRS5707806 GSM4189047 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189047 GSM4189047 GEO Accession GSM4189047 SRX7202573 GSM4189048 SRP231449 SRS5707807 GSM4189048 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189048 GSM4189048 GEO Accession GSM4189048 SRX7202574 GSM4189049 SRP231449 SRS5707808 GSM4189049 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189049 GSM4189049 GEO Accession GSM4189049 SRX7202575 GSM4189050 SRP231449 SRS5707809 GSM4189050 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189050 GSM4189050 GEO Accession GSM4189050 SRX7202576 GSM4189051 SRP231449 SRS5707810 GSM4189051 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189051 GSM4189051 GEO Accession GSM4189051 SRX7202577 GSM4189052 SRP231449 SRS5707811 GSM4189052 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189052 GSM4189052 GEO Accession GSM4189052 SRX7202578 GSM4189053 SRP231449 SRS5707812 GSM4189053 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189053 GSM4189053 GEO Accession GSM4189053 SRX7202579 GSM4189054 SRP231449 SRS5707813 GSM4189054 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189054 GSM4189054 GEO Accession GSM4189054 SRX7202580 GSM4189055 SRP231449 SRS5707814 GSM4189055 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189055 GSM4189055 GEO Accession GSM4189055 SRX7202581 GSM4189056 SRP231449 SRS5707815 GSM4189056 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189056 GSM4189056 GEO Accession GSM4189056 SRX7202582 GSM4189057 SRP231449 SRS5707816 GSM4189057 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189057 GSM4189057 GEO Accession GSM4189057 SRX7202583 GSM4189058 SRP231449 SRS5707817 GSM4189058 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA from culture cells was extracted using Trizol reagents (Life Technologies) following the manufacturer's instructions. Total mRNA was prepared from 1 mg total RNA using poly(A) mRNA magnetic isolation reagents (NEB) and fragmented at 94 °C for 15 min. RNA was then reverse-transcribed into cDNA with random primers. After end repairing and A-tailing, cDNA was ligated with adapters and amplified by PCR with Illumina sequencing primers. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 304189058 GSM4189058 GEO Accession GSM4189058