<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX19819268" alias="GSM7123833_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819268</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123833_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123833: HT1080 wild-type 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179603">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179603</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123833</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819269" alias="GSM7123834_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819269</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123834_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123834: HT1080 wild-type 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179604">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179604</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123834</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819270" alias="GSM7123835_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819270</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123835_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123835: HT1080 wild-type 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179605">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179605</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123835</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819271" alias="GSM7123836_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819271</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123836_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123836: HT1080 wild-type 4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179607">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179607</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123836</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819272" alias="GSM7123837_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819272</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123837_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123837: HT1080 KDAC6H216A 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179606">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179606</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123837</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819273" alias="GSM7123838_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819273</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123838_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123838: HT1080 KDAC6H216A 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179608">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179608</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123838</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819274" alias="GSM7123839_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819274</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123839_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123839: HT1080 KDAC6H216A 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179609">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179609</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123839</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819275" alias="GSM7123840_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819275</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123840_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123840: HT1080 KDAC6H216A 4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179610">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179610</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123840</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819276" alias="GSM7123841_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819276</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123841_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123841: HT1080 KDAC6H611A 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179611">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179611</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123841</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819277" alias="GSM7123842_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819277</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123842_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123842: HT1080 KDAC6H611A 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179612">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179612</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123842</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819278" alias="GSM7123843_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819278</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123843_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123843: HT1080 KDAC6H611A 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179613">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179613</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123843</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819279" alias="GSM7123844_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819279</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123844_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123844: HT1080 KDAC6H611A 4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179614">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179614</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123844</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819280" alias="GSM7123845_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819280</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123845_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123845: HT1080 KDAC8H143A 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179618">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179618</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123845</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819281" alias="GSM7123846_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819281</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123846_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123846: HT1080 KDAC8H143A 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179615">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179615</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123846</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819282" alias="GSM7123847_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819282</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123847_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123847: HT1080 KDAC8H143A 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179617">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179617</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123847</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819283" alias="GSM7123848_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819283</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123848_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123848: HT1080 KDAC8H143A 4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179616">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179616</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123848</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819284" alias="GSM7123849_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819284</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123849_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123849: HT1080 wild-type 1 µM tubastatin 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179620">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179620</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123849</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819285" alias="GSM7123850_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819285</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123850_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123850: HT1080 wild-type 1 µM tubastatin 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179619">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179619</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123850</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819286" alias="GSM7123851_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819286</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123851_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123851: HT1080 wild-type 1 µM tubastatin 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179621">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179621</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123851</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819287" alias="GSM7123852_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819287</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123852_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123852: HT1080 wild-type 5 µM PCI-34051 1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179622">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179622</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123852</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819288" alias="GSM7123853_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819288</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123853_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123853: HT1080 wild-type 5 µM PCI-34051 2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179623">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179623</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123853</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19819289" alias="GSM7123854_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19819289</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7123854_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7123854: HT1080 wild-type 5 µM PCI-34051 3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP430127">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP430127</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA950328</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17179624">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17179624</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7123854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7123854</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>3x10^6 cells were pelleted, resuspended in MEM with 5% glycerol, and frozen at -80 °C. Cells were shipped on dry ice, and total RNA extracted by Creative Genomics using a commercially available kit. Quality of RNA was verified using RNA Screen Tape (Agilent). RNA was rRNA-depleted using the Ribo-Zero plus kit (Illumina). Libraries were prepared using the PE150 platform (Illumina) following the manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
