<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2495097" accession="SRX2574461">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2574461</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2495097</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2495097: no_tag(control)_1; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP100198">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP100198</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA375809</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1990230">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1990230</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06346012</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Using bead beater to lyse the cells, lysates were sonicated until chromatin is sheared to 200~400bp fragments (Diagenode Bioruptor Pico). Libraries of DNA were prepared using commercial high throughput library preparation kit (KAPA) according to the protocal.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent PGM</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302495097</ID>
          <LABEL>GSM2495097</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2495097</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2495098" accession="SRX2574462">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2574462</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2495098</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2495098: no_tag(control)_2; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP100198">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP100198</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA375809</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1990231">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1990231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06346011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Using bead beater to lyse the cells, lysates were sonicated until chromatin is sheared to 200~400bp fragments (Diagenode Bioruptor Pico). Libraries of DNA were prepared using commercial high throughput library preparation kit (KAPA) according to the protocal.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent PGM</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302495098</ID>
          <LABEL>GSM2495098</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2495098</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2495099" accession="SRX2574463">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2574463</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2495099</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2495099: ccp1-myc(test)_1; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP100198">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP100198</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA375809</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1990232">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1990232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06346010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Using bead beater to lyse the cells, lysates were sonicated until chromatin is sheared to 200~400bp fragments (Diagenode Bioruptor Pico). Libraries of DNA were prepared using commercial high throughput library preparation kit (KAPA) according to the protocal.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent PGM</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302495099</ID>
          <LABEL>GSM2495099</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2495099</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2495100" accession="SRX2574464">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2574464</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2495100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2495100: ccp1-myc(test)_2; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP100198">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP100198</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA375809</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1990233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1990233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06346009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Using bead beater to lyse the cells, lysates were sonicated until chromatin is sheared to 200~400bp fragments (Diagenode Bioruptor Pico). Libraries of DNA were prepared using commercial high throughput library preparation kit (KAPA) according to the protocal.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent PGM</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302495100</ID>
          <LABEL>GSM2495100</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2495100</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
