SRX5099519 GSM3502697 SRP172693 SRS4109854 GSM3502697 RNA-Seq TRANSCRIPTOMIC cDNA RNA isolation done as described in https://doi.org/10.1038/srep41114. rRNA was depleted using an Illumina Ribo-Zero rRNA removal kit (Bacteria; Illumina, San Diego, CA). RNA-seq libraries were constructed with a ScriptSeq RNA-seq library preparation kit (Illumina), pooled, and size selected (375 to 475 bp) with a Pippin Prep system (Sage Science, Beverley, MA). ; Libraries were sequenced on an Illumina MiSeq with 150 cycles kit (2 x 75 paired-end reads, single index) following the manufacturer's instructions Illumina MiSeq gds 303502697 GSM3502697 GEO Accession GSM3502697 SRX5099520 GSM3502698 SRP172693 SRS4109855 GSM3502698 RNA-Seq TRANSCRIPTOMIC cDNA RNA isolation done as described in https://doi.org/10.1038/srep41114. rRNA was depleted using an Illumina Ribo-Zero rRNA removal kit (Bacteria; Illumina, San Diego, CA). RNA-seq libraries were constructed with a ScriptSeq RNA-seq library preparation kit (Illumina), pooled, and size selected (375 to 475 bp) with a Pippin Prep system (Sage Science, Beverley, MA). ; Libraries were sequenced on an Illumina MiSeq with 150 cycles kit (2 x 75 paired-end reads, single index) following the manufacturer's instructions Illumina MiSeq gds 303502698 GSM3502698 GEO Accession GSM3502698 SRX5099521 GSM3502699 SRP172693 SRS4109856 GSM3502699 RNA-Seq TRANSCRIPTOMIC cDNA RNA isolation done as described in https://doi.org/10.1038/srep41114. rRNA was depleted using an Illumina Ribo-Zero rRNA removal kit (Bacteria; Illumina, San Diego, CA). RNA-seq libraries were constructed with a ScriptSeq RNA-seq library preparation kit (Illumina), pooled, and size selected (375 to 475 bp) with a Pippin Prep system (Sage Science, Beverley, MA). ; Libraries were sequenced on an Illumina MiSeq with 150 cycles kit (2 x 75 paired-end reads, single index) following the manufacturer's instructions Illumina MiSeq gds 303502699 GSM3502699 GEO Accession GSM3502699 SRX5099522 GSM3502700 SRP172693 SRS4109857 GSM3502700 RNA-Seq TRANSCRIPTOMIC cDNA RNA isolation done as described in https://doi.org/10.1038/srep41114. rRNA was depleted using an Illumina Ribo-Zero rRNA removal kit (Bacteria; Illumina, San Diego, CA). RNA-seq libraries were constructed with a ScriptSeq RNA-seq library preparation kit (Illumina), pooled, and size selected (375 to 475 bp) with a Pippin Prep system (Sage Science, Beverley, MA). ; Libraries were sequenced on an Illumina MiSeq with 150 cycles kit (2 x 75 paired-end reads, single index) following the manufacturer's instructions Illumina MiSeq gds 303502700 GSM3502700 GEO Accession GSM3502700 SRX5099523 GSM3502701 SRP172693 SRS4109858 GSM3502701 RNA-Seq TRANSCRIPTOMIC cDNA RNA isolation done as described in https://doi.org/10.1038/srep41114. rRNA was depleted using an Illumina Ribo-Zero rRNA removal kit (Bacteria; Illumina, San Diego, CA). RNA-seq libraries were constructed with a ScriptSeq RNA-seq library preparation kit (Illumina), pooled, and size selected (375 to 475 bp) with a Pippin Prep system (Sage Science, Beverley, MA). ; Libraries were sequenced on an Illumina MiSeq with 150 cycles kit (2 x 75 paired-end reads, single index) following the manufacturer's instructions Illumina MiSeq gds 303502701 GSM3502701 GEO Accession GSM3502701 SRX5099524 GSM3502702 SRP172693 SRS4109859 GSM3502702 RNA-Seq TRANSCRIPTOMIC cDNA RNA isolation done as described in https://doi.org/10.1038/srep41114. rRNA was depleted using an Illumina Ribo-Zero rRNA removal kit (Bacteria; Illumina, San Diego, CA). RNA-seq libraries were constructed with a ScriptSeq RNA-seq library preparation kit (Illumina), pooled, and size selected (375 to 475 bp) with a Pippin Prep system (Sage Science, Beverley, MA). ; Libraries were sequenced on an Illumina MiSeq with 150 cycles kit (2 x 75 paired-end reads, single index) following the manufacturer's instructions Illumina MiSeq gds 303502702 GSM3502702 GEO Accession GSM3502702