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    <TITLE>GSM3963011: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_3K_rep1; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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      <PRIMARY_ID>SRX6488011</PRIMARY_ID>
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    <TITLE>GSM3963012: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_3K_rep2; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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      <PRIMARY_ID>SRX6488012</PRIMARY_ID>
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    <TITLE>GSM3963013: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_4K_rep1; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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        <PRIMARY_ID>SRP215947</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
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          <PRIMARY_ID>SRS5136818</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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          <DB>gds</DB>
          <ID>303963013</ID>
          <LABEL>GSM3963013</LABEL>
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      <PRIMARY_ID>SRX6488013</PRIMARY_ID>
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    <TITLE>GSM3963014: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_4K_rep2; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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        <PRIMARY_ID>SRP215947</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
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          <PRIMARY_ID>SRS5136819</PRIMARY_ID>
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        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
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          <SINGLE/>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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          <ID>303963014</ID>
          <LABEL>GSM3963014</LABEL>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX6488014</PRIMARY_ID>
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    <TITLE>GSM3963015: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_5K_rep1; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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        <PRIMARY_ID>SRP215947</PRIMARY_ID>
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        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX6488015</PRIMARY_ID>
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    <TITLE>GSM3963016: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_5K_rep2; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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        <PRIMARY_ID>SRP215947</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
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          <PRIMARY_ID>SRS5136821</PRIMARY_ID>
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        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX6488016</PRIMARY_ID>
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    <TITLE>GSM3963017: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_rep1; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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        <PRIMARY_ID>SRP215947</PRIMARY_ID>
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          <PRIMARY_ID>SRS5136822</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX6488017</PRIMARY_ID>
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    <TITLE>GSM3963018: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_Caulobacter_crescentus_ParB_rep2; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <PRIMARY_ID>SRX6488018</PRIMARY_ID>
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    <TITLE>GSM3963019: LeLab_ChIP_seq_MT148_vanA_Pvan_1xFLAG_yfp_rep1; Caulobacter vibrioides NA1000; ChIP-Seq</TITLE>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136824">
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          <PRIMARY_ID>SRS5136824</PRIMARY_ID>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
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        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM3963020" accession="SRX6488019">
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      <PRIMARY_ID>SRX6488019</PRIMARY_ID>
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    <TITLE>GSM3963020: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Bacillus_subtilis_ParB; Escherichia coli; ChIP-Seq</TITLE>
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        <PRIMARY_ID>SRP215947</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136825">
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          <PRIMARY_ID>SRS5136825</PRIMARY_ID>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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          <DB>gds</DB>
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  <EXPERIMENT alias="GSM3963021" accession="SRX6488020">
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      <PRIMARY_ID>SRX6488020</PRIMARY_ID>
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    <TITLE>GSM3963021: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Caulobacter_crescentus_ParB; Escherichia coli; ChIP-Seq</TITLE>
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        <PRIMARY_ID>SRP215947</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136826">
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          <PRIMARY_ID>SRS5136826</PRIMARY_ID>
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      <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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963021</ID>
          <LABEL>GSM3963021</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963021</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963022" accession="SRX6488021">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488021</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963022</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963022: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Dechloromonas_aromatica_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136827">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136827</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963022</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963022</ID>
          <LABEL>GSM3963022</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963022</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963023" accession="SRX6488022">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488022</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963023</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963023: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Helicobacter_pylori_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136828">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136828</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963023</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963023</ID>
          <LABEL>GSM3963023</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963023</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963024" accession="SRX6488023">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488023</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963024</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963024: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Lawsonia_intracellularis_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136829">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136829</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963024</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963024</ID>
          <LABEL>GSM3963024</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963024</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963025" accession="SRX6488024">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488024</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963025</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963025: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Moorella_thermoacetica_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136830">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136830</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963025</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963025</ID>
          <LABEL>GSM3963025</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963025</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963026" accession="SRX6488025">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488025</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963026</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963026: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Myxococcus_xanthus_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136831">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136831</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963026</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963026</ID>
          <LABEL>GSM3963026</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963026</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963027" accession="SRX6488026">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488026</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963027</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963027: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Pseudomonas_aeruginosa_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136832">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136832</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963027</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963027</ID>
          <LABEL>GSM3963027</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963027</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963028" accession="SRX6488027">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488027</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963028</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963028: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Thermus_thermophilus_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136833">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136833</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963028</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963028</ID>
          <LABEL>GSM3963028</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963028</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963029" accession="SRX6488028">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488028</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963029</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963029: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_Xanthomonas_campestris_ParB; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136834">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136834</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963029</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963029</ID>
          <LABEL>GSM3963029</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963029</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963030" accession="SRX6488029">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488029</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963030</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963030: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_chimera_A_rep1; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136835">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136835</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963030</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963030</ID>
          <LABEL>GSM3963030</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963030</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963031" accession="SRX6488030">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488030</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963031</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963031: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_chimera_A_rep2; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136836">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136836</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963031</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963031</ID>
          <LABEL>GSM3963031</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963031</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963032" accession="SRX6488031">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488031</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963032</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963032: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_chimera_B_rep1; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136837">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136837</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963032</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963032</ID>
          <LABEL>GSM3963032</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963032</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963033" accession="SRX6488032">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488032</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963033</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963033: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_chimera_B_rep2; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136838">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136838</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963033</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963033</ID>
          <LABEL>GSM3963033</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963033</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963034" accession="SRX6488033">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488033</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963034</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963034: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_Chimera_C_rep1; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136839">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136839</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963034</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963034</ID>
          <LABEL>GSM3963034</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963034</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963035" accession="SRX6488034">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488034</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963035</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963035: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_Chimera_C_rep2; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136840">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136840</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963035</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963035</ID>
          <LABEL>GSM3963035</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963035</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963036" accession="SRX6488035">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488035</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963036</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963036: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_chimera_D_rep1; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136841">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136841</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963036</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963036</ID>
          <LABEL>GSM3963036</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963036</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3963037" accession="SRX6488036">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6488036</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3963037</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3963037: LeLab_ChIP_seq_TLE3002_pUT18C_1xFLAG_ParB_chimera_D_rep2; Escherichia coli; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP215947" refname="GSE134665">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP215947</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5136842">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5136842</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3963037</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>For ChIP-seq, DNA was isolated using Qiagen PCR purification columns. For ChIP-seq libraries, a standard library construction procedure (using NEBNext® Ultra™ II DNA Library Prep Kit for Illumina sequencing) was employed.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303963037</ID>
          <LABEL>GSM3963037</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3963037</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
