SRX7182934 GSM4177569 SRP230626 SRS5689163 GSM4177569 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177569 GSM4177569 GEO Accession GSM4177569 SRX7182935 GSM4177570 SRP230626 SRS5689164 GSM4177570 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177570 GSM4177570 GEO Accession GSM4177570 SRX7182936 GSM4177572 SRP230626 SRS5689165 GSM4177572 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177572 GSM4177572 GEO Accession GSM4177572 SRX7182937 GSM4177573 SRP230626 SRS5689166 GSM4177573 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177573 GSM4177573 GEO Accession GSM4177573 SRX7182938 GSM4177575 SRP230626 SRS5689167 GSM4177575 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177575 GSM4177575 GEO Accession GSM4177575 SRX7182939 GSM4177577 SRP230626 SRS5689168 GSM4177577 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177577 GSM4177577 GEO Accession GSM4177577 SRX7182940 GSM4177578 SRP230626 SRS5689169 GSM4177578 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177578 GSM4177578 GEO Accession GSM4177578 SRX7182941 GSM4177580 SRP230626 SRS5689170 GSM4177580 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177580 GSM4177580 GEO Accession GSM4177580 SRX7182942 GSM4177581 SRP230626 SRS5689171 GSM4177581 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177581 GSM4177581 GEO Accession GSM4177581 SRX7182943 GSM4177583 SRP230626 SRS5689172 GSM4177583 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177583 GSM4177583 GEO Accession GSM4177583 SRX7182944 GSM4177584 SRP230626 SRS5689173 GSM4177584 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177584 GSM4177584 GEO Accession GSM4177584 SRX7182945 GSM4177586 SRP230626 SRS5689174 GSM4177586 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177586 GSM4177586 GEO Accession GSM4177586 SRX7182946 GSM4177587 SRP230626 SRS5689175 GSM4177587 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177587 GSM4177587 GEO Accession GSM4177587 SRX7182947 GSM4177589 SRP230626 SRS5689176 GSM4177589 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177589 GSM4177589 GEO Accession GSM4177589 SRX7182948 GSM4177590 SRP230626 SRS5689177 GSM4177590 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177590 GSM4177590 GEO Accession GSM4177590 SRX7182949 GSM4177592 SRP230626 SRS5689178 GSM4177592 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177592 GSM4177592 GEO Accession GSM4177592 SRX7182950 GSM4177594 SRP230626 SRS5689179 GSM4177594 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177594 GSM4177594 GEO Accession GSM4177594 SRX7182951 GSM4177595 SRP230626 SRS5689180 GSM4177595 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177595 GSM4177595 GEO Accession GSM4177595 SRX7182952 GSM4177597 SRP230626 SRS5689181 GSM4177597 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177597 GSM4177597 GEO Accession GSM4177597 SRX7182953 GSM4177598 SRP230626 SRS5689182 GSM4177598 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177598 GSM4177598 GEO Accession GSM4177598 SRX7182954 GSM4177600 SRP230626 SRS5689183 GSM4177600 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177600 GSM4177600 GEO Accession GSM4177600 SRX7182955 GSM4177601 SRP230626 SRS5689184 GSM4177601 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177601 GSM4177601 GEO Accession GSM4177601 SRX7182956 GSM4177603 SRP230626 SRS5689185 GSM4177603 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177603 GSM4177603 GEO Accession GSM4177603 SRX7182957 GSM4177604 SRP230626 SRS5689186 GSM4177604 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177604 GSM4177604 GEO Accession GSM4177604 SRX7182958 GSM4177606 SRP230626 SRS5689187 GSM4177606 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177606 GSM4177606 GEO Accession GSM4177606 SRX7182959 GSM4177608 SRP230626 SRS5689188 GSM4177608 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177608 GSM4177608 GEO Accession GSM4177608 SRX7182960 GSM4177609 SRP230626 SRS5689189 GSM4177609 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177609 GSM4177609 GEO Accession GSM4177609 SRX7182961 GSM4177611 SRP230626 SRS5689190 GSM4177611 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177611 GSM4177611 GEO Accession GSM4177611 SRX7182962 GSM4177612 SRP230626 SRS5689191 GSM4177612 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177612 GSM4177612 GEO Accession GSM4177612 SRX7182963 GSM4177614 SRP230626 SRS5689192 GSM4177614 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177614 GSM4177614 GEO Accession GSM4177614 SRX7182964 GSM4177615 SRP230626 SRS5689193 GSM4177615 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177615 GSM4177615 GEO Accession GSM4177615 SRX7182965 GSM4177617 SRP230626 SRS5689194 GSM4177617 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177617 GSM4177617 GEO Accession GSM4177617 SRX7182966 GSM4177618 SRP230626 SRS5689195 GSM4177618 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177618 GSM4177618 GEO Accession GSM4177618 SRX7182967 GSM4177620 SRP230626 SRS5689196 GSM4177620 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177620 GSM4177620 GEO Accession GSM4177620 SRX7182968 GSM4177621 SRP230626 SRS5689197 GSM4177621 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177621 GSM4177621 GEO Accession GSM4177621 SRX7182969 GSM4177623 SRP230626 SRS5689198 GSM4177623 RNA-Seq TRANSCRIPTOMIC cDNA Cells were pelleted and lysate with TRI-Reagent, followed by Direct-zol RNA kit for RNA isolation. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 4000 gds 304177623 GSM4177623 GEO Accession GSM4177623