SRX9282845 MUC12134_Ms4a15_1 SRP287168 bp0 For library preparation, 1 g of total RNA per sample was used. RNA molecules were poly(A) selected, fragmented, and reverse transcribed with the Elute, Prime, Fragment Mix (EPF, Illumina). End repair, A-tailing, adaptor ligation, and library enrichment were performed as described in the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). RNA libraries were assessed for quality and quantity with the Agilent 2100 BioAnalyzer and the Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies). SRS7510737 MUC12134_Ms4a15_1 MUC12134_Ms4a15_1 RNA-Seq TRANSCRIPTOMIC RANDOM PCR Illumina HiSeq 4000 SRX9282846 MUC12135_Ms4a15_2 SRP287168 bp0 For library preparation, 1 g of total RNA per sample was used. RNA molecules were poly(A) selected, fragmented, and reverse transcribed with the Elute, Prime, Fragment Mix (EPF, Illumina). End repair, A-tailing, adaptor ligation, and library enrichment were performed as described in the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). RNA libraries were assessed for quality and quantity with the Agilent 2100 BioAnalyzer and the Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies). SRS7510738 MUC12135_Ms4a15_2 MUC12135_Ms4a15_2 RNA-Seq TRANSCRIPTOMIC RANDOM PCR Illumina HiSeq 4000 SRX9282847 MUC12136_Ms4a15_3 SRP287168 bp0 For library preparation, 1 g of total RNA per sample was used. RNA molecules were poly(A) selected, fragmented, and reverse transcribed with the Elute, Prime, Fragment Mix (EPF, Illumina). End repair, A-tailing, adaptor ligation, and library enrichment were performed as described in the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). RNA libraries were assessed for quality and quantity with the Agilent 2100 BioAnalyzer and the Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies). SRS7510739 MUC12136_Ms4a15_3 MUC12136_Ms4a15_3 RNA-Seq TRANSCRIPTOMIC RANDOM PCR Illumina HiSeq 4000 SRX9282848 MUC12137_control_1 SRP287168 bp0 For library preparation, 1 g of total RNA per sample was used. RNA molecules were poly(A) selected, fragmented, and reverse transcribed with the Elute, Prime, Fragment Mix (EPF, Illumina). End repair, A-tailing, adaptor ligation, and library enrichment were performed as described in the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). RNA libraries were assessed for quality and quantity with the Agilent 2100 BioAnalyzer and the Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies). SRS7510740 MUC12137_control_1 MUC12137_control_1 RNA-Seq TRANSCRIPTOMIC RANDOM PCR Illumina HiSeq 4000 SRX9282849 MUC12138_control_2 SRP287168 bp0 For library preparation, 1 g of total RNA per sample was used. RNA molecules were poly(A) selected, fragmented, and reverse transcribed with the Elute, Prime, Fragment Mix (EPF, Illumina). End repair, A-tailing, adaptor ligation, and library enrichment were performed as described in the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). RNA libraries were assessed for quality and quantity with the Agilent 2100 BioAnalyzer and the Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies). SRS7510741 MUC12138_control_2 MUC12138_control_2 RNA-Seq TRANSCRIPTOMIC RANDOM PCR Illumina HiSeq 4000 SRX9282850 MUC12139_control_3 SRP287168 bp0 For library preparation, 1 g of total RNA per sample was used. RNA molecules were poly(A) selected, fragmented, and reverse transcribed with the Elute, Prime, Fragment Mix (EPF, Illumina). End repair, A-tailing, adaptor ligation, and library enrichment were performed as described in the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). RNA libraries were assessed for quality and quantity with the Agilent 2100 BioAnalyzer and the Quant-iT PicoGreen dsDNA Assay Kit (Life Technologies). SRS7510742 MUC12139_control_3 MUC12139_control_3 RNA-Seq TRANSCRIPTOMIC RANDOM PCR Illumina HiSeq 4000