<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2865021" accession="SRX3422663">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3422663</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865021</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865021: RNAseq_rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125646" refname="GSE107347">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125646</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2714314">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2714314</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865021</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>Total RNA was isolated with the Qiagen RNeasy Mini Kit according to the manufacturer's instructions. 10µg of the purified RNA was treated with Turbo DNase (Ambion) and then cleaned with RNeasy Mini Kit. DNase-treated RNA was resuspended in EB buffer (Qiagen). Total RNA-seq Illumina ScriptSeq with Complete Gold according to manufacturer's instructions</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>302865021</ID>
          <LABEL>GSM2865021</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865021</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2865022" accession="SRX3422664">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3422664</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865022</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865022: RNAseq_rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125646" refname="GSE107347">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125646</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2714315">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2714315</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865022</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>Total RNA was isolated with the Qiagen RNeasy Mini Kit according to the manufacturer's instructions. 10µg of the purified RNA was treated with Turbo DNase (Ambion) and then cleaned with RNeasy Mini Kit. DNase-treated RNA was resuspended in EB buffer (Qiagen). Total RNA-seq Illumina ScriptSeq with Complete Gold according to manufacturer's instructions</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>302865022</ID>
          <LABEL>GSM2865022</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865022</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2865023" accession="SRX3422665">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3422665</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865023</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865023: RNAseq_rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125646" refname="GSE107347">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125646</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2714316">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2714316</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865023</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>Total RNA was isolated with the Qiagen RNeasy Mini Kit according to the manufacturer's instructions. 10µg of the purified RNA was treated with Turbo DNase (Ambion) and then cleaned with RNeasy Mini Kit. DNase-treated RNA was resuspended in EB buffer (Qiagen). Total RNA-seq Illumina ScriptSeq with Complete Gold according to manufacturer's instructions</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>302865023</ID>
          <LABEL>GSM2865023</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865023</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
