SRX2214375 GSM2338054 SRP090904 SRS1730563 GSM2338054 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338054 GEO Accession GSM2338054 SRX2214376 GSM2338055 SRP090904 SRS1730564 GSM2338055 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338055 GEO Accession GSM2338055 SRX2214377 GSM2338056 SRP090904 SRS1730565 GSM2338056 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338056 GEO Accession GSM2338056 SRX2214378 GSM2338057 SRP090904 SRS1730566 GSM2338057 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338057 GEO Accession GSM2338057 SRX2214379 GSM2338058 SRP090904 SRS1730567 GSM2338058 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338058 GEO Accession GSM2338058 SRX2214380 GSM2338059 SRP090904 SRS1730568 GSM2338059 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338059 GEO Accession GSM2338059 SRX2214381 GSM2338060 SRP090904 SRS1730569 GSM2338060 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338060 GEO Accession GSM2338060 SRX2214382 GSM2338061 SRP090904 SRS1730570 GSM2338061 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated using the RNeasy Mini Kit (Quiagen) Total RNA was quantified using both the NanoDrop to assess sample contamination by proteins or carryover reagents from RNA isolation, and the Qubit fluorometer (Invitrogen). Samples were then qualified using the Bioanalyzer that analyzes the integrity of the total RNA by measuring the ratio between the 18S and 28S ribosomal peaks. Libraries were constructed using SMARTer Ultra Low Input RNA v3 kit (Clontech), indexed using Nextera indices (Illumina). Final libraries were again quantitated with the Qubit fluorometer and checked for size via the Fragment Analyzer. Libraries were diluted to 4nM and pooled in equal volumes for denaturation, hybridization, and sequencing on an Illumina NextSeq 500 (Illumina) with single end 75bp sequencing chemistry. NextSeq 500 gds 302338061 GEO Accession GSM2338061