<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX2880723" alias="NPC_3m6_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">NPC_3m6_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse NPC_3m6_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248585">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248585</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">NPC_3m6_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NPC_3m6_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880724" alias="NPC_12m5_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">NPC_12m5_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse NPC_12m5_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248586">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248586</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">NPC_12m5_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NPC_12m5_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880725" alias="Cereb_12m2_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_12m2_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_12m2_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248587">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248587</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_12m2_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_12m2_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880726" alias="Cereb_12m3_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_12m3_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_12m3_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248588">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248588</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_12m3_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_12m3_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880727" alias="Cereb_3m3_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_3m3_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_3m3_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248589">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248589</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_3m3_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_3m3_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880728" alias="Cereb_12m1_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_12m1_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_12m1_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248590">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248590</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_12m1_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_12m1_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880729" alias="Cereb_29m4_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_29m4_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_29m4_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248591">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248591</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_29m4_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_29m4_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880730" alias="NPC_3m5_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">NPC_3m5_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse NPC_3m5_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248592">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248592</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">NPC_3m5_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NPC_3m5_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880731" alias="Cereb_29m2_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_29m2_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_29m2_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248593">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248593</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_29m2_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_29m2_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880732" alias="Cereb_29m3_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_29m3_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_29m3_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248594">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248594</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_29m3_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_29m3_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880733" alias="OB_29m4_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_29m4_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_29m4_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248595">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248595</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_29m4_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_29m4_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880734" alias="OB_12m3_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_12m3_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_12m3_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248596">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248596</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_12m3_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_12m3_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880735" alias="OB_12m1_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_12m1_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_12m1_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248597">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248597</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_12m1_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_12m1_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880736" alias="3m4_heart_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">3m4_heart_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 3m4_heart_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248598">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248598</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">3m4_heart_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3m4_heart_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880737" alias="3m3_Liver_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">3m3_Liver_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 3m3_Liver_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248599">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248599</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">3m3_Liver_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3m3_Liver_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880738" alias="3m2_Liver_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">3m2_Liver_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 3m2_Liver_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248600">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248600</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">3m2_Liver_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3m2_Liver_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880739" alias="3m1_Liver_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">3m1_Liver_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 3m1_Liver_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248601">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248601</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">3m1_Liver_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3m1_Liver_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880740" alias="12m2_LiverRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">12m2_LiverRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 12m2_LiverRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248602">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248602</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">12m2_LiverRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12m2_LiverRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880741" alias="12m1_LiverRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">12m1_LiverRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 12m1_LiverRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248603">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248603</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">12m1_LiverRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12m1_LiverRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880742" alias="3m6_heart_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">3m6_heart_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 3m6_heart_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248604">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248604</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">3m6_heart_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3m6_heart_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880743" alias="3m5_heart_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">3m5_heart_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 3m5_heart_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248605">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248605</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">3m5_heart_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3m5_heart_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880744" alias="12m4_heartRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">12m4_heartRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 12m4_heartRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248606">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248606</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">12m4_heartRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12m4_heartRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880745" alias="12m3_LiverRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">12m3_LiverRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 12m3_LiverRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248607">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248607</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">12m3_LiverRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12m3_LiverRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880746" alias="29m6_heartRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">29m6_heartRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 29m6_heartRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248608">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248608</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">29m6_heartRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>29m6_heartRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880747" alias="29m5_heartRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">29m5_heartRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 29m5_heartRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248609">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248609</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">29m5_heartRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>29m5_heartRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880748" alias="29m4_heartRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">29m4_heartRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 29m4_heartRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248610">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248610</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">29m4_heartRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>29m4_heartRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880749" alias="29m3_LiverRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">29m3_LiverRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 29m3_LiverRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248611">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248611</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">29m3_LiverRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>29m3_LiverRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880750" alias="29m2_LiverRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">29m2_LiverRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 29m2_LiverRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248612">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248612</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">29m2_LiverRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>29m2_LiverRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880751" alias="29m1_LiverRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">29m1_LiverRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 29m1_LiverRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248613">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248613</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">29m1_LiverRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>29m1_LiverRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880752" alias="12m6_heartRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">12m6_heartRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 12m6_heartRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248614">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248614</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">12m6_heartRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12m6_heartRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880753" alias="12m5_heartRNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">12m5_heartRNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse 12m5_heartRNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248615">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248615</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">12m5_heartRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>12m5_heartRNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880754" alias="NPC_29m5_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">NPC_29m5_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse NPC_29m5_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248616">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248616</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">NPC_29m5_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NPC_29m5_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880755" alias="NPC_12m6_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">NPC_12m6_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse NPC_12m6_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248617">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248617</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">NPC_12m6_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NPC_12m6_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880756" alias="OB_3m1_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_3m1_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_3m1_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248618">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248618</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_3m1_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_3m1_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880757" alias="NPC_29m6_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">NPC_29m6_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse NPC_29m6_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248619">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248619</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">NPC_29m6_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NPC_29m6_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880758" alias="OB_3m3_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_3m3_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_3m3_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248620">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248620</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_3m3_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_3m3_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880759" alias="OB_3m2_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_3m2_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_3m2_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248621">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248621</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_3m2_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_3m2_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880760" alias="Cereb_3m2_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_3m2_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_3m2_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248622">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248622</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_3m2_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_3m2_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880761" alias="Cereb_3m1_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">Cereb_3m1_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse Cereb_3m1_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248623">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248623</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">Cereb_3m1_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cereb_3m1_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880762" alias="OB_29m3_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_29m3_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_29m3_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248624">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248624</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_29m3_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_29m3_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2880763" alias="OB_29m2_RNA">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2880763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2743758">OB_29m2_RNA</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of mouse OB_29m2_RNA</TITLE>
    <STUDY_REF accession="SRP057387">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP057387</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA281127</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>All tissue and cell samples were flash-frozen in liquid nitrogen until further processing. RNA was isolated using RNAeasy plus mini kit (Qiagen). 1ug of total RNA was combined to 2uL of a 1:100 dilution of ERCC RNA Spike in mix (Thermo-Fisher scientific) in nuclease-free water. The resulting mix was then subjected to rRNA depletion using the NEBNext rRNA Depletion Kit (New England Bioloabs). Strand specific RNA-seq libraries were then constructed using the SMARTer® Stranded RNA-Seq Kit (Clontech # 634836), according to the manufacturer’s protocol. Paired-end 75bp reads were generated on the Illumina NetxSeq 500 platform.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2248626">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2248626</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|berenicebenayoun">OB_29m2_RNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>OB_29m2_RNA</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
