SRX2993615 GSM2698982 SRP111462 SRS2345509 GSM2698982 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698982 GSM2698982 GEO Accession GSM2698982 SRX2993616 GSM2698983 SRP111462 SRS2345510 GSM2698983 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698983 GSM2698983 GEO Accession GSM2698983 SRX2993617 GSM2698984 SRP111462 SRS2345511 GSM2698984 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698984 GSM2698984 GEO Accession GSM2698984 SRX2993618 GSM2698985 SRP111462 SRS2345512 GSM2698985 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698985 GSM2698985 GEO Accession GSM2698985 SRX2993619 GSM2698986 SRP111462 SRS2345513 GSM2698986 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698986 GSM2698986 GEO Accession GSM2698986 SRX2993620 GSM2698987 SRP111462 SRS2345514 GSM2698987 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698987 GSM2698987 GEO Accession GSM2698987 SRX2993621 GSM2698988 SRP111462 SRS2345515 GSM2698988 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698988 GSM2698988 GEO Accession GSM2698988 SRX2993622 GSM2698989 SRP111462 SRS2345516 GSM2698989 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698989 GSM2698989 GEO Accession GSM2698989 SRX2993623 GSM2698990 SRP111462 SRS2345517 GSM2698990 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698990 GSM2698990 GEO Accession GSM2698990 SRX2993624 GSM2698991 SRP111462 SRS2345518 GSM2698991 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698991 GSM2698991 GEO Accession GSM2698991 SRX2993625 GSM2698992 SRP111462 SRS2345519 GSM2698992 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698992 GSM2698992 GEO Accession GSM2698992 SRX2993626 GSM2698993 SRP111462 SRS2345520 GSM2698993 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698993 GSM2698993 GEO Accession GSM2698993 SRX2993627 GSM2698994 SRP111462 SRS2345522 GSM2698994 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698994 GSM2698994 GEO Accession GSM2698994 SRX2993628 GSM2698995 SRP111462 SRS2345521 GSM2698995 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698995 GSM2698995 GEO Accession GSM2698995 SRX2993629 GSM2698996 SRP111462 SRS2345523 GSM2698996 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets were resuspended in TRIzol (Invitrogen) and total RNA was extracted using a Direct-zol RNA extraction kit (Zymo). RNA quantity was determined with Qubit fluorometry. RNA integrity was checked by a bioanalyzer and a Nanodrop spectrometer. Genewiz sequencing facilities performed rRNA removal, library construction, multiplexing and sequence the RNA with HiSeq2500, 2×100 Paired-End. RNA libraries were prepared for sequencing using standard Illumina protocols by Genewiz Sequencing Facilities. Illumina HiSeq 2500 gds 302698996 GSM2698996 GEO Accession GSM2698996