<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2590110" accession="SRX2766767">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2766767</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2590110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2590110: RNA-seq siNC, si Negative control; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP105333" refname="GSE98273">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105333</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2150896">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2150896</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2590110</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 RNAs were extracted as described previously (Mizutani et al., 2011, J Biol Chem). Libraries were prepared using  Dynabeads mRNA DIRECT Purification Kit (Life Technologies) and Ion Total RNA-seq kit v2 (Thermo Scientific). Sequencing was performed as described (Sakurai et al., 2016, Oncogene).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302590110</ID>
          <LABEL>GSM2590110</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2590110</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2590111" accession="SRX2766768">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2766768</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2590111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2590111: RNA-seq, si ZEB1-1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP105333" refname="GSE98273">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105333</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2150897">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2150897</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2590111</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 RNAs were extracted as described previously (Mizutani et al., 2011, J Biol Chem). Libraries were prepared using  Dynabeads mRNA DIRECT Purification Kit (Life Technologies) and Ion Total RNA-seq kit v2 (Thermo Scientific). Sequencing was performed as described (Sakurai et al., 2016, Oncogene).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302590111</ID>
          <LABEL>GSM2590111</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2590111</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2590112" accession="SRX2766769">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2766769</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2590112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2590112: RNA-seq, si ZEB1-2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP105333" refname="GSE98273">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105333</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2150898">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2150898</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2590112</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 RNAs were extracted as described previously (Mizutani et al., 2011, J Biol Chem). Libraries were prepared using  Dynabeads mRNA DIRECT Purification Kit (Life Technologies) and Ion Total RNA-seq kit v2 (Thermo Scientific). Sequencing was performed as described (Sakurai et al., 2016, Oncogene).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302590112</ID>
          <LABEL>GSM2590112</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2590112</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2590113" accession="SRX2766770">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2766770</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2590113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2590113: RNA-seq, si ZEB2-1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP105333" refname="GSE98273">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105333</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2150899">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2150899</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2590113</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 RNAs were extracted as described previously (Mizutani et al., 2011, J Biol Chem). Libraries were prepared using  Dynabeads mRNA DIRECT Purification Kit (Life Technologies) and Ion Total RNA-seq kit v2 (Thermo Scientific). Sequencing was performed as described (Sakurai et al., 2016, Oncogene).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302590113</ID>
          <LABEL>GSM2590113</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2590113</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2590114" accession="SRX2766771">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2766771</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2590114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2590114: RNA-seq, si ZEB2-2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP105333" refname="GSE98273">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105333</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2150900">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2150900</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2590114</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 RNAs were extracted as described previously (Mizutani et al., 2011, J Biol Chem). Libraries were prepared using  Dynabeads mRNA DIRECT Purification Kit (Life Technologies) and Ion Total RNA-seq kit v2 (Thermo Scientific). Sequencing was performed as described (Sakurai et al., 2016, Oncogene).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302590114</ID>
          <LABEL>GSM2590114</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2590114</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
