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        <URL_LINK>
          <LABEL>GEO Sample GSM1611699</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611699</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611699</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611699</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611700" accession="SRX878631" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878631</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611700</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611700: AS_Rad21_ChIPSeq WCE; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846532">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846532</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611700</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611700</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611700</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611700</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611700</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611701" accession="SRX878632" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878632</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611701</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611701: AS_Top2_ChIPSeq IP; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846531">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846531</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611701</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611701</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611701</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611701</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611701</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611702" accession="SRX878633" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878633</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611702</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611702: AS_Top2_ChIPSeq WCE; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846529">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846529</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611702</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611702</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611702</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611702</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611702</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611703" accession="SRX878634" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878634</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611703</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611703: HS_Cut14_ChIPSeq IP; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846528">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846528</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611703</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611703</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611703</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611703</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611703</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611704" accession="SRX878635" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878635</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611704</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611704: HS_Cut14_ChIPSeq WCE; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846530">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846530</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611704</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611704</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611704</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611704</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611704</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611705" accession="SRX878636" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878636</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611705</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611705: HS_Rad21_ChIPSeq IP; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846526">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846526</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611705</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611705</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611705</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611705</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611705</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611706" accession="SRX878637" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878637</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611706</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611706: HS_Rad21_ChIPSeq WCE; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846527">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846527</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611706</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611706</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611706</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611706</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611706</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611707" accession="SRX878638" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878638</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611707</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611707: HS_Top2_ChIPSeq IP; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846525">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846525</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611707</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611707</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611707</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611707</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611707</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1611708" accession="SRX878639" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX878639</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1611708</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1611708: HS_Top2_ChIPSeq WCE; Schizosaccharomyces pombe; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP055066" refname="GSE65956">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP055066</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS846524">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS846524</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1611708</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>Sonicated and cross-linked chromatin were prepared from S. pombe cell extracts (Nakazawa et al., 2008). DNA samples co-precipitated with anti-FLAG antibody were prepared along with input DNA (whole cell extract [WCE] DNA). Prepared DNA libraries were processed by single-end sequencing (36 bp) on the iIlumina Genome Analyzer GA IIx, according to the manufacturer’s instructions. ReferenceHiraoka et al., 1984 Cell 39, 349-358. Nakazawa et al., 2008 J Cell Biol 180, 1115-1131. Nakazawa et al., 2011 J Cell Sci 124, 1795-1807.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer IIx</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1611708</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611708</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301611708</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1611708</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
