<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2871664" accession="SRX3436269">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436269</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871664</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871664: Control replicate 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125994" refname="GSE107578">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125994</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727234">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727234</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871664</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells using Trizol reagent by following the manufactorers guidelines. Purified RNA was treated with DNAse I to remove contaminating genomic DNA and then purified again using Qiagen minelute RNA-purification columns before library construction. TruSeq Stranded mRNA with Ribo-Zero human/mouse/rat assay (Illumina) following the manufacturers protocol</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>302871664</ID>
          <LABEL>GSM2871664</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871664</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871665" accession="SRX3436270">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436270</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871665: Control replicate 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125994" refname="GSE107578">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125994</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727233</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871665</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells using Trizol reagent by following the manufactorers guidelines. Purified RNA was treated with DNAse I to remove contaminating genomic DNA and then purified again using Qiagen minelute RNA-purification columns before library construction. TruSeq Stranded mRNA with Ribo-Zero human/mouse/rat assay (Illumina) following the manufacturers protocol</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>302871665</ID>
          <LABEL>GSM2871665</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871665</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871666" accession="SRX3436271">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436271</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871666: Mybl2 overexpression replicate 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125994" refname="GSE107578">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125994</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727235">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727235</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871666</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells using Trizol reagent by following the manufactorers guidelines. Purified RNA was treated with DNAse I to remove contaminating genomic DNA and then purified again using Qiagen minelute RNA-purification columns before library construction. TruSeq Stranded mRNA with Ribo-Zero human/mouse/rat assay (Illumina) following the manufacturers protocol</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>302871666</ID>
          <LABEL>GSM2871666</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871666</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871667" accession="SRX3436272">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436272</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871667: Mybl2 overexpression replicate 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125994" refname="GSE107578">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125994</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727236">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727236</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871667</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells using Trizol reagent by following the manufactorers guidelines. Purified RNA was treated with DNAse I to remove contaminating genomic DNA and then purified again using Qiagen minelute RNA-purification columns before library construction. TruSeq Stranded mRNA with Ribo-Zero human/mouse/rat assay (Illumina) following the manufacturers protocol</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>302871667</ID>
          <LABEL>GSM2871667</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871667</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
