<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX13126302" alias="GSM5688949_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126302</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688949_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688949: BCL7-siNTC-Cont-A; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061180">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061180</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688949</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126303" alias="GSM5688950_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126303</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688950_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688950: BCL7-siNTC-Cont-B; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061179">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061179</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688950</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126304" alias="GSM5688951_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126304</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688951_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688951: BCL7-siNTC-Cont-C; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061183">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061183</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688951</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126305" alias="GSM5688952_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126305</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688952_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688952: BCL7-siNTC-Dox-A; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061181">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061181</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688952</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126306" alias="GSM5688953_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126306</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688953_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688953: BCL7-siNTC-Dox-B; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061182">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061182</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688953</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126307" alias="GSM5688954_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126307</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688954_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688954: BCL7-siNTC-Dox-C; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061184">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061184</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688954</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126308" alias="GSM5688955_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126308</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688955_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688955: BCL7-siABC-Cont-A; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061185">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061185</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688955</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126309" alias="GSM5688956_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126309</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688956_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688956: BCL7-siABC-Cont-B; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061186">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061186</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688956</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126310" alias="GSM5688957_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126310</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688957_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688957: BCL7-siABC-Cont-C; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061190">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061190</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688957</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126311" alias="GSM5688958_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126311</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688958_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688958: BCL7-siABC-Dox-A; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061188">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061188</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688958</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126312" alias="GSM5688959_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126312</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688959_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688959: BCL7-siABC-Dox-B; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061187">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061187</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688959</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX13126313" alias="GSM5688960_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX13126313</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5688960_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5688960: BCL7-siABC-Dox-C; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP345839">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP345839</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA780002</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS11061189">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS11061189</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5688960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5688960</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>All RNA was produced using TRIzol (Invitrogen) followed by the RNeasy Mini Kit (Qiagen) and treated with DNaseI (Qiagen). All libraries were sequenced 75x75 base pairs, paired-end on Illumina NextSeq 500. Libraries were generated using the TruSeq RNA Sample Prep Kit v2 according to manufacturer's instructions (Illumina).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
