<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15220731" alias="GSM6125600_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15220731</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6125600_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6125600: K562 10ng heat_rep1; Homo sapiens; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP374506">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374506</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836767</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12955394">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12955394</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6125600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6125600</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>gDNA was extracted using Qiagen Dneasy Blood and Tissue kit. gDNA was fragmented using the LE220 Focused ultrasonicator (Covaris) and size selected for 100-200 bp fragments using BluePippin 2% agarose cassette (Sage Sciences). End repair and A-tailing using Kapa hyper prep kit and methylated Truseq nano adapters. Bisulfite conversion was done using Zymo EZ DNA Methylation-Gold kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15220732" alias="GSM6125601_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15220732</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6125601_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6125601: K562 10ng heat_rep2; Homo sapiens; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP374506">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374506</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836767</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12955395">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12955395</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6125601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6125601</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>gDNA was extracted using Qiagen Dneasy Blood and Tissue kit. gDNA was fragmented using the LE220 Focused ultrasonicator (Covaris) and size selected for 100-200 bp fragments using BluePippin 2% agarose cassette (Sage Sciences). End repair and A-tailing using Kapa hyper prep kit and methylated Truseq nano adapters. Bisulfite conversion was done using Zymo EZ DNA Methylation-Gold kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15220733" alias="GSM6125602_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15220733</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6125602_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6125602: K562 10ng 2 min heat; Homo sapiens; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP374506">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374506</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836767</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12955396">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12955396</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6125602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6125602</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>gDNA was extracted using Qiagen Dneasy Blood and Tissue kit. gDNA was fragmented using the LE220 Focused ultrasonicator (Covaris) and size selected for 100-200 bp fragments using BluePippin 2% agarose cassette (Sage Sciences). End repair and A-tailing using Kapa hyper prep kit and methylated Truseq nano adapters. Bisulfite conversion was done using Zymo EZ DNA Methylation-Gold kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15220734" alias="GSM6125603_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15220734</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6125603_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6125603: K562 10ng 5 min heat; Homo sapiens; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP374506">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374506</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836767</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12955397">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12955397</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6125603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6125603</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>gDNA was extracted using Qiagen Dneasy Blood and Tissue kit. gDNA was fragmented using the LE220 Focused ultrasonicator (Covaris) and size selected for 100-200 bp fragments using BluePippin 2% agarose cassette (Sage Sciences). End repair and A-tailing using Kapa hyper prep kit and methylated Truseq nano adapters. Bisulfite conversion was done using Zymo EZ DNA Methylation-Gold kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15220735" alias="GSM6125604_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15220735</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6125604_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6125604: K562 10ng 10 min heat; Homo sapiens; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP374506">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374506</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836767</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12955398">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12955398</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6125604</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6125604</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>gDNA was extracted using Qiagen Dneasy Blood and Tissue kit. gDNA was fragmented using the LE220 Focused ultrasonicator (Covaris) and size selected for 100-200 bp fragments using BluePippin 2% agarose cassette (Sage Sciences). End repair and A-tailing using Kapa hyper prep kit and methylated Truseq nano adapters. Bisulfite conversion was done using Zymo EZ DNA Methylation-Gold kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15220736" alias="GSM6125605_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15220736</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6125605_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6125605: K562 10ng 20 min heat; Homo sapiens; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP374506">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374506</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA836767</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12955399">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12955399</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6125605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6125605</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>gDNA was extracted using Qiagen Dneasy Blood and Tissue kit. gDNA was fragmented using the LE220 Focused ultrasonicator (Covaris) and size selected for 100-200 bp fragments using BluePippin 2% agarose cassette (Sage Sciences). End repair and A-tailing using Kapa hyper prep kit and methylated Truseq nano adapters. Bisulfite conversion was done using Zymo EZ DNA Methylation-Gold kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
