<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM4091099" accession="SRX6891047">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891047</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091099</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091099: STAT5_KO_AB10_1_S45; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424026">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424026</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091099</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091099</ID>
          <LABEL>GSM4091099</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091099</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091100" accession="SRX6891048">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891048</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091100: STAT5_KO_AB10_2_S31; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424027">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424027</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091100</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091100</ID>
          <LABEL>GSM4091100</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091100</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091101" accession="SRX6891049">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891049</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091101: STAT5_KO_AB10_3_S35; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424028">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424028</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091101</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091101</ID>
          <LABEL>GSM4091101</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091101</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091102" accession="SRX6891050">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891050</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091102: STAT5_KO_AB10_4_S53; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424029">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424029</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091102</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091102</ID>
          <LABEL>GSM4091102</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091102</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091103" accession="SRX6891051">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891051</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091103: STAT5_KO_AB10_5_S46; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424030">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424030</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091103</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091103</ID>
          <LABEL>GSM4091103</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091103</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091104" accession="SRX6891052">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891052</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091104: STAT5_KO_AB10_6_S46; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424031">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424031</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091104</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091104</ID>
          <LABEL>GSM4091104</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091104</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091105" accession="SRX6891053">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891053</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091105: STAT5_KO_AB10_7_S38; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424032">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424032</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091105</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091105</ID>
          <LABEL>GSM4091105</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091105</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091106" accession="SRX6891054">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891054</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091106: STAT5_KO_AB17_1_S48; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424033">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424033</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091106</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091106</ID>
          <LABEL>GSM4091106</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091106</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091107" accession="SRX6891055">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891055</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091107: STAT5_KO_AB17_2_S42; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424034">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424034</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091107</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091107</ID>
          <LABEL>GSM4091107</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091107</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091108" accession="SRX6891056">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891056</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091108: STAT5_KO_AB17_3_S43; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424035">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424035</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091108</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091108</ID>
          <LABEL>GSM4091108</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091108</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091109" accession="SRX6891057">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891057</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091109: STAT5_KO_AB17_4_S31; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424036">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424036</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091109</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091109</ID>
          <LABEL>GSM4091109</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091109</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091110" accession="SRX6891058">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891058</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091110: STAT5_KO_AB17_5_S50; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424037">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424037</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091110</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091110</ID>
          <LABEL>GSM4091110</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091110</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091111" accession="SRX6891059">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891059</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091111: STAT5_KO_AB17_6_S44; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424038">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424038</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091111</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091111</ID>
          <LABEL>GSM4091111</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091111</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091112" accession="SRX6891060">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891060</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091112: STAT5_KO_AB17_7_S30; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424039">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424039</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091112</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091112</ID>
          <LABEL>GSM4091112</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091112</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091113" accession="SRX6891061">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891061</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091113: STAT5_KO_AB1_1_S39; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424040">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424040</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091113</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091113</ID>
          <LABEL>GSM4091113</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091113</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091114" accession="SRX6891062">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891062</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091114: STAT5_KO_AB1_2_S47; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424041">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424041</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091114</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091114</ID>
          <LABEL>GSM4091114</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091114</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091115" accession="SRX6891063">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891063</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091115: STAT5_KO_AB1_3_S54; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424042">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424042</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091115</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091115</ID>
          <LABEL>GSM4091115</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091115</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091116" accession="SRX6891064">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891064</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091116: STAT5_KO_AB1_4_S34; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424043">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424043</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091116</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091116</ID>
          <LABEL>GSM4091116</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091116</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091117" accession="SRX6891065">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891065</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091117: STAT5_KO_AB1_5_S41; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424044">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424044</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091117</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091117</ID>
          <LABEL>GSM4091117</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091117</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091118" accession="SRX6891066">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891066</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091118: STAT5_KO_AB1_6_S39; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424045">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424045</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091118</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091118</ID>
          <LABEL>GSM4091118</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091118</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091119" accession="SRX6891067">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891067</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091119: STAT5_KO_AB1_7_S21; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424046">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424046</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091119</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091119</ID>
          <LABEL>GSM4091119</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091119</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091120" accession="SRX6891068">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891068</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091120: STAT5_KO_AB22_1_S44; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424047">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424047</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091120</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091120</ID>
          <LABEL>GSM4091120</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091120</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091121" accession="SRX6891069">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891069</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091121: STAT5_KO_AB22_2_S47; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424048">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424048</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091121</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091121</ID>
          <LABEL>GSM4091121</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091121</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091122" accession="SRX6891070">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891070</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091122: STAT5_KO_AB22_3_S52; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424049">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424049</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091122</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091122</ID>
          <LABEL>GSM4091122</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091122</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091147" accession="SRX6891071">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891071</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091147: Scramble_S1_7_S27; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424050">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424050</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091147</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091147</ID>
          <LABEL>GSM4091147</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091147</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091148" accession="SRX6891072">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891072</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091148: Scramble_S2_1_S25; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424051">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424051</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091148</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091148</ID>
          <LABEL>GSM4091148</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091148</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091149" accession="SRX6891073">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891073</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091149: Scramble_S2_2_S23; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424052">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424052</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091149</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091149</ID>
          <LABEL>GSM4091149</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091149</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091150" accession="SRX6891074">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891074</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091150: Scramble_S2_3_S26; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424053">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424053</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091150</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091150</ID>
          <LABEL>GSM4091150</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091150</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091151" accession="SRX6891075">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891075</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091151: Scramble_S2_4_S36; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424054">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424054</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091151</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091151</ID>
          <LABEL>GSM4091151</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091151</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091152" accession="SRX6891076">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891076</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091152: Scramble_S2_5_S30; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424055">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424055</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091152</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091152</ID>
          <LABEL>GSM4091152</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091152</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091153" accession="SRX6891077">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891077</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091153: Scramble_S2_6_S35; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424056">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424056</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091153</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091153</ID>
          <LABEL>GSM4091153</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091153</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091154" accession="SRX6891078">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891078</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091154: Scramble_S2_7_S40; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424057">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424057</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091154</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091154</ID>
          <LABEL>GSM4091154</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091154</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091123" accession="SRX6891079">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891079</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091123: STAT5_KO_AB22_4_S51; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424058">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424058</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091123</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091123</ID>
          <LABEL>GSM4091123</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091123</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091124" accession="SRX6891080">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891080</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091124: STAT5_KO_AB22_5_S37; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424059">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424059</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091124</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091124</ID>
          <LABEL>GSM4091124</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091124</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091125" accession="SRX6891081">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891081</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091125: STAT5_KO_AB22_6_S49; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424060">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424060</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091125</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091125</ID>
          <LABEL>GSM4091125</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091125</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091126" accession="SRX6891082">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891082</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091126: STAT5_KO_AB22_7_S55; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424061">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424061</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091126</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091126</ID>
          <LABEL>GSM4091126</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091126</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091127" accession="SRX6891083">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891083</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091127: Scramble_S18_1_S43; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424062">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424062</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091127</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091127</ID>
          <LABEL>GSM4091127</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091127</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091128" accession="SRX6891084">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891084</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091128: Scramble_S18_2_S30; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424063">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424063</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091128</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091128</ID>
          <LABEL>GSM4091128</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091128</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091129" accession="SRX6891085">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891085</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091129: Scramble_S18_3_S36; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424064">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424064</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091129</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091129</ID>
          <LABEL>GSM4091129</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091129</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091130" accession="SRX6891086">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891086</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091130: Scramble_S18_4_S28; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424065">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424065</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091130</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091130</ID>
          <LABEL>GSM4091130</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091130</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091131" accession="SRX6891087">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891087</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091131: Scramble_S18_5_S48; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424066">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424066</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091131</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091131</ID>
          <LABEL>GSM4091131</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091131</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091132" accession="SRX6891088">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891088</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091132: Scramble_S18_6_S34; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424067">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424067</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091132</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091132</ID>
          <LABEL>GSM4091132</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091132</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091133" accession="SRX6891089">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891089</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091133: Scramble_S18_7_S42; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424068">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424068</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091133</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091133</ID>
          <LABEL>GSM4091133</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091133</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091134" accession="SRX6891090">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891090</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091134: Scramble_S19_1_S40; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424069">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424069</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091134</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091134</ID>
          <LABEL>GSM4091134</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091134</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091135" accession="SRX6891091">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891091</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091135: Scramble_S19_2_S38; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424070">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424070</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091135</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091135</ID>
          <LABEL>GSM4091135</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091135</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091136" accession="SRX6891092">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891092</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091136: Scramble_S19_3_S33; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424071">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424071</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091136</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091136</ID>
          <LABEL>GSM4091136</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091136</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091137" accession="SRX6891093">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891093</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091137: Scramble_S19_4_S29; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424072">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424072</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091137</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091137</ID>
          <LABEL>GSM4091137</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091137</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091138" accession="SRX6891094">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891094</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091138: Scramble_S19_5_S45; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424073">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424073</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091138</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091138</ID>
          <LABEL>GSM4091138</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091138</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091139" accession="SRX6891095">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891095</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091139: Scramble_S19_6_S41; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424074">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424074</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091139</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091139</ID>
          <LABEL>GSM4091139</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091139</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091140" accession="SRX6891096">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891096</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091140: Scramble_S19_7_S37; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424075">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424075</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091140</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091140</ID>
          <LABEL>GSM4091140</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091140</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091141" accession="SRX6891097">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891097</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091141: Scramble_S1_1_S33; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424076">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424076</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091141</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091141</ID>
          <LABEL>GSM4091141</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091141</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091142" accession="SRX6891098">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891098</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091142: Scramble_S1_2_S32; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424077">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424077</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091142</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091142</ID>
          <LABEL>GSM4091142</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091142</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091143" accession="SRX6891099">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891099</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091143: Scramble_S1_3_S32; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424078">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424078</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091143</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091143</ID>
          <LABEL>GSM4091143</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091143</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091144" accession="SRX6891100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891100</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091144: Scramble_S1_4_S31; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424079">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424079</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091144</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091144</ID>
          <LABEL>GSM4091144</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091144</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091145" accession="SRX6891101">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891101</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091145: Scramble_S1_5_S22; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424080">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424080</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091145</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091145</ID>
          <LABEL>GSM4091145</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091145</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4091146" accession="SRX6891102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6891102</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4091146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4091146: Scramble_S1_6_S24; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP223020" refname="GSE137893">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223020</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5424081">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5424081</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4091146</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 prepared using Trizol based extraction. Samples were purified and concentrated using the RNeasy Mini Kit. RNA concentration was determined using a NanoDrop spectrophotometer. RNA quality was assessed using an Agilent 2200 Bioanalyzer. Libraries were prepared using the TruSeq RNA Exome RNA kit. Libraries were sequenced on a NextSeq 500 using 150bp paired-end chemistry.</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>304091146</ID>
          <LABEL>GSM4091146</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4091146</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
