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      <PRIMARY_ID>SRX3040882</PRIMARY_ID>
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    <TITLE>GSM2719015: embryonic stem cells 1; Mus musculus; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS2388999">
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          <PRIMARY_ID>SRS2388999</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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          <ID>302719015</ID>
          <LABEL>GSM2719015</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX3040883</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719016</SUBMITTER_ID>
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    <TITLE>GSM2719016: embryonic stem cells 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS2389000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389000</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
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          <DB>gds</DB>
          <ID>302719016</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM2719017" accession="SRX3040885">
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      <PRIMARY_ID>SRX3040885</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719017</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719017: embryonic stem cells  3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389002</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719017</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719017</ID>
          <LABEL>GSM2719017</LABEL>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719017</VALUE>
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  <EXPERIMENT alias="GSM2719018" accession="SRX3040886">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040886</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719018</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719018: embryonic stem cells 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389003</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719018</EXTERNAL_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719018</ID>
          <LABEL>GSM2719018</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719018</VALUE>
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  <EXPERIMENT alias="GSM2719019" accession="SRX3040887">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040887</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719019</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719019: dermal fibroblasts 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389004</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719019</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719019</ID>
          <LABEL>GSM2719019</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719019</VALUE>
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  <EXPERIMENT alias="GSM2719020" accession="SRX3040888">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040888</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719020</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719020: dermal fibroblasts 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389005</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719020</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719020</ID>
          <LABEL>GSM2719020</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719020</VALUE>
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  <EXPERIMENT alias="GSM2719021" accession="SRX3040889">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040889</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719021</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719021: dermal fibroblasts 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389006</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719021</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719021</ID>
          <LABEL>GSM2719021</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719021</VALUE>
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      <PRIMARY_ID>SRX3040890</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719022</SUBMITTER_ID>
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    <TITLE>GSM2719022: dermal fibroblasts 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719022</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719022</ID>
          <LABEL>GSM2719022</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719022</VALUE>
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  <EXPERIMENT alias="GSM2719023" accession="SRX3040891">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040891</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719023</SUBMITTER_ID>
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    <TITLE>GSM2719023: heart PDGFRalpha 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719023</ID>
          <LABEL>GSM2719023</LABEL>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719023</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719024" accession="SRX3040892">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040892</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719024</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719024: heart PDGFRalpha 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719024</ID>
          <LABEL>GSM2719024</LABEL>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719024</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719025" accession="SRX3040893">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040893</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719025</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719025: heart PDGFRalpha 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719025</ID>
          <LABEL>GSM2719025</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719025</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719026" accession="SRX3040894">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040894</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719026</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719026: heart PDGFRalpha 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719026</ID>
          <LABEL>GSM2719026</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719026</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719027" accession="SRX3040895">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040895</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719027</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719027: mesenchymal stem cells 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719027</ID>
          <LABEL>GSM2719027</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719027</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719028" accession="SRX3040896">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040896</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719028</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719028: mesenchymal stem cells 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719028</ID>
          <LABEL>GSM2719028</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719028</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719029" accession="SRX3040897">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040897</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719029</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719029: mesenchymal stem cells 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719029</ID>
          <LABEL>GSM2719029</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719029</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719030" accession="SRX3040898">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040898</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719030</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719030: mesenchymal stem cells 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719030</ID>
          <LABEL>GSM2719030</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719030</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719031" accession="SRX3040899">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040899</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719031</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719031: skeletal muscle PDGFRalpha cells 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389016</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719031</ID>
          <LABEL>GSM2719031</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719031</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719032" accession="SRX3040900">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040900</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719032</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719032: skeletal muscle PDGFRalpha cells 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389017</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719032</ID>
          <LABEL>GSM2719032</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719032</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719033" accession="SRX3040901">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040901</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719033</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719033: skeletal muscle PDGFRalpha cells 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389018</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719033</ID>
          <LABEL>GSM2719033</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719033</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2719034" accession="SRX3040902">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3040902</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2719034</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2719034: skeletal muscle PDGFRalpha cells 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP113644" refname="GSE101930">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP113644</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2389019">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2389019</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2719034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA-Seq and bioinformatic analysis were performed at the Institute for Genomics and Multiscale Biology at the Icahn School of Medicine at Mount Sinai. As an initial step, Qubit QC values were evaluated and a cut-off of above 500ng total was applied. Libraries from the SPIA amplified cDNA as described above were made using the Ultralow DR library kit (NuGEN) according to manufacturer’s instructions. High-throughput RNAseq was performed using a HiSeq 2500 (Illumina) with reads between 7- 20 million among the different samples.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302719034</ID>
          <LABEL>GSM2719034</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2719034</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
