<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18321286" alias="GSM6743978_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321286</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743978_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743978: HCT116 cells, ovControl-1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903397</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811575">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811575</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were removed, and RNA was harvested using Trizol reagent. Intact mRNA was isolated from total RNA samples using an Arraystar Seq-StarTM poly(A) mRNA Isolation Kit (Aksomics, Shanghai, China). A KAPA Stranded mRNA-seq Kit (F. Hoffmann-La Roche Ltd, Grenzacherstrasse, Basel, Switzerland) was used to create RNA-seq libraries. The prepared libraries were diluted to a final concentration of 8 pmol/L, and clusters were generated on an Illumina cBot using a HiSeq 3000/4000 PE Cluster Kit (#PE-410-1001, Illumina), followed by sequencing on an Illumina HiSeq 2500.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18321287" alias="GSM6743979_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321287</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743979_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743979: HCT116 cells, ovControl-2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903397</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811576">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811576</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were removed, and RNA was harvested using Trizol reagent. Intact mRNA was isolated from total RNA samples using an Arraystar Seq-StarTM poly(A) mRNA Isolation Kit (Aksomics, Shanghai, China). A KAPA Stranded mRNA-seq Kit (F. Hoffmann-La Roche Ltd, Grenzacherstrasse, Basel, Switzerland) was used to create RNA-seq libraries. The prepared libraries were diluted to a final concentration of 8 pmol/L, and clusters were generated on an Illumina cBot using a HiSeq 3000/4000 PE Cluster Kit (#PE-410-1001, Illumina), followed by sequencing on an Illumina HiSeq 2500.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18321288" alias="GSM6743980_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321288</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743980_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743980: HCT116 cells, ovControl-3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903397</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811577">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811577</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were removed, and RNA was harvested using Trizol reagent. Intact mRNA was isolated from total RNA samples using an Arraystar Seq-StarTM poly(A) mRNA Isolation Kit (Aksomics, Shanghai, China). A KAPA Stranded mRNA-seq Kit (F. Hoffmann-La Roche Ltd, Grenzacherstrasse, Basel, Switzerland) was used to create RNA-seq libraries. The prepared libraries were diluted to a final concentration of 8 pmol/L, and clusters were generated on an Illumina cBot using a HiSeq 3000/4000 PE Cluster Kit (#PE-410-1001, Illumina), followed by sequencing on an Illumina HiSeq 2500.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18321289" alias="GSM6743981_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321289</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743981_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743981: HCT116 cells, ov-PBX1-1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903397</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811578">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811578</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were removed, and RNA was harvested using Trizol reagent. Intact mRNA was isolated from total RNA samples using an Arraystar Seq-StarTM poly(A) mRNA Isolation Kit (Aksomics, Shanghai, China). A KAPA Stranded mRNA-seq Kit (F. Hoffmann-La Roche Ltd, Grenzacherstrasse, Basel, Switzerland) was used to create RNA-seq libraries. The prepared libraries were diluted to a final concentration of 8 pmol/L, and clusters were generated on an Illumina cBot using a HiSeq 3000/4000 PE Cluster Kit (#PE-410-1001, Illumina), followed by sequencing on an Illumina HiSeq 2500.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18321290" alias="GSM6743982_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321290</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743982_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743982: HCT116 cells, ov-PBX1-2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903397</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811579">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811579</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were removed, and RNA was harvested using Trizol reagent. Intact mRNA was isolated from total RNA samples using an Arraystar Seq-StarTM poly(A) mRNA Isolation Kit (Aksomics, Shanghai, China). A KAPA Stranded mRNA-seq Kit (F. Hoffmann-La Roche Ltd, Grenzacherstrasse, Basel, Switzerland) was used to create RNA-seq libraries. The prepared libraries were diluted to a final concentration of 8 pmol/L, and clusters were generated on an Illumina cBot using a HiSeq 3000/4000 PE Cluster Kit (#PE-410-1001, Illumina), followed by sequencing on an Illumina HiSeq 2500.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18321291" alias="GSM6743983_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18321291</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6743983_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6743983: HCT116 cells, ov-PBX1-3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903397</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15811580">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15811580</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6743983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6743983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were removed, and RNA was harvested using Trizol reagent. Intact mRNA was isolated from total RNA samples using an Arraystar Seq-StarTM poly(A) mRNA Isolation Kit (Aksomics, Shanghai, China). A KAPA Stranded mRNA-seq Kit (F. Hoffmann-La Roche Ltd, Grenzacherstrasse, Basel, Switzerland) was used to create RNA-seq libraries. The prepared libraries were diluted to a final concentration of 8 pmol/L, and clusters were generated on an Illumina cBot using a HiSeq 3000/4000 PE Cluster Kit (#PE-410-1001, Illumina), followed by sequencing on an Illumina HiSeq 2500.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
