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  <EXPERIMENT alias="GSM2793733" accession="SRX3216751">
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      <PRIMARY_ID>SRX3216751</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793733</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793733: WT iPSCs siC; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
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      <SAMPLE_DESCRIPTOR accession="SRS2541826">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541826</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793733</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793733</ID>
          <LABEL>GSM2793733</LABEL>
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        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM2793734" accession="SRX3216752">
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      <PRIMARY_ID>SRX3216752</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793734</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793734: WT iPSCs siDnmt3a; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS2541827">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541827</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793734</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>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793734</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM2793735" accession="SRX3216753">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3216753</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793735</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793735: WT iPSCs si Dnmt3b; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2541828">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541828</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793735</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>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793735</ID>
          <LABEL>GSM2793735</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2793735</VALUE>
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  <EXPERIMENT alias="GSM2793736" accession="SRX3216754">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3216754</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793736</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793736: WT iPSCs si Dnmt3a and Dnmt3b; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2541829">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541829</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793736</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>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793736</ID>
          <LABEL>GSM2793736</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2793736</VALUE>
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  <EXPERIMENT alias="GSM2793737" accession="SRX3216755">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3216755</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793737</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793737: miR-203 tKI iPSCs (induced with dox) clon1; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2541830">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541830</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793737</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>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793737</ID>
          <LABEL>GSM2793737</LABEL>
        </XREF_LINK>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2793737</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2793738" accession="SRX3216756">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3216756</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793738</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793738: miR-203 KI iPSCs (not induced) clon1; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2541831">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541831</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793738</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>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793738</ID>
          <LABEL>GSM2793738</LABEL>
        </XREF_LINK>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2793738</VALUE>
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  </EXPERIMENT>
  <EXPERIMENT alias="GSM2793739" accession="SRX3216757">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3216757</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793739</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793739: miR-203 tKI iPSCs (induced with dox) clon2; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2541832">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541832</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793739</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>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793739</ID>
          <LABEL>GSM2793739</LABEL>
        </XREF_LINK>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2793739</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2793740" accession="SRX3216758">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3216758</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2793740</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2793740: miR-203 KI iPSCs (not induced) clon2; Mus musculus; ssRNA-seq</TITLE>
    <STUDY_REF accession="SRP118884" refname="GSE104250">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP118884</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2541833">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2541833</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2793740</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>miRVana RNA isolation Kit form Thermo Fisher Scientific 1 µg of total RNA  was extracted. Sample RNA Integrity Numbers were in the range 9.1 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fraction was purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" kit (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by PCR with Illumina PE primers (8 cycles). The resulting purified cDNA library was applied to an Illumina flow cell for cluster generation and sequenced on an Illumina HiSeq2500 by following manufacturer's protocols.</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>302793740</ID>
          <LABEL>GSM2793740</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2793740</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
