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      <PRIMARY_ID>SRX2007061</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2263691</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2263691: H3K36me3-ChIP 25°C biological replicate C; Arabidopsis thaliana; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP081052">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP081052</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA338073</EXTERNAL_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1605899">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1605899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05520837</EXTERNAL_ID>
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      </SAMPLE_DESCRIPTOR>
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        <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 each sample, 0.5 g of plant material were used for each biological replicate. Material was collected at from plant growing at 16 °C, as well as at 1 day after the plants were moved to 25°C (5-6 h after lights on). Using jeweler's forceps, leaves were removed to obtain SAM enriched tissue. ChIP experiments were performed following a previously published protocol (Kaufmann et al., Nature Protocols 2010). After the preclearing step the sample was split, one aliquot was incubated with anti-H3K36me3 antibody (ab9050, abcam)and the other with anti-H3 antibody (ab1791, abcam). Samples were prepared for Illumina sequencing using the ThruPLEX DNA-seq Kit (Cat. No: R400429) from Rubicon Genomics according to the manufacturer's protocol.</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>302263691</ID>
          <LABEL>GSM2263691</LABEL>
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      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2263691</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2263692" accession="SRX2007062">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2007062</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2263692</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2263692: H3K36me3-ChIP 25°C biological replicate D; Arabidopsis thaliana; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP081052">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP081052</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA338073</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1605900">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1605900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05520836</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 each sample, 0.5 g of plant material were used for each biological replicate. Material was collected at from plant growing at 16 °C, as well as at 1 day after the plants were moved to 25°C (5-6 h after lights on). Using jeweler's forceps, leaves were removed to obtain SAM enriched tissue. ChIP experiments were performed following a previously published protocol (Kaufmann et al., Nature Protocols 2010). After the preclearing step the sample was split, one aliquot was incubated with anti-H3K36me3 antibody (ab9050, abcam)and the other with anti-H3 antibody (ab1791, abcam). Samples were prepared for Illumina sequencing using the ThruPLEX DNA-seq Kit (Cat. No: R400429) from Rubicon Genomics according to the manufacturer's protocol.</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>302263692</ID>
          <LABEL>GSM2263692</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2263692</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2263693" accession="SRX2007063">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2007063</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2263693</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2263693: H3-ChIP 25°C biological replicate A; Arabidopsis thaliana; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP081052">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP081052</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA338073</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1605901">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1605901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05520835</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 each sample, 0.5 g of plant material were used for each biological replicate. Material was collected at from plant growing at 16 °C, as well as at 1 day after the plants were moved to 25°C (5-6 h after lights on). Using jeweler's forceps, leaves were removed to obtain SAM enriched tissue. ChIP experiments were performed following a previously published protocol (Kaufmann et al., Nature Protocols 2010). After the preclearing step the sample was split, one aliquot was incubated with anti-H3K36me3 antibody (ab9050, abcam)and the other with anti-H3 antibody (ab1791, abcam). Samples were prepared for Illumina sequencing using the ThruPLEX DNA-seq Kit (Cat. No: R400429) from Rubicon Genomics according to the manufacturer's protocol.</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>302263693</ID>
          <LABEL>GSM2263693</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2263693</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2263694" accession="SRX2007064">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2007064</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2263694</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2263694: H3-ChIP 25°C biological replicate B; Arabidopsis thaliana; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP081052">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP081052</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA338073</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1605902">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1605902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05520834</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 each sample, 0.5 g of plant material were used for each biological replicate. Material was collected at from plant growing at 16 °C, as well as at 1 day after the plants were moved to 25°C (5-6 h after lights on). Using jeweler's forceps, leaves were removed to obtain SAM enriched tissue. ChIP experiments were performed following a previously published protocol (Kaufmann et al., Nature Protocols 2010). After the preclearing step the sample was split, one aliquot was incubated with anti-H3K36me3 antibody (ab9050, abcam)and the other with anti-H3 antibody (ab1791, abcam). Samples were prepared for Illumina sequencing using the ThruPLEX DNA-seq Kit (Cat. No: R400429) from Rubicon Genomics according to the manufacturer's protocol.</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>302263694</ID>
          <LABEL>GSM2263694</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2263694</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2263695" accession="SRX2007065">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2007065</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2263695</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2263695: H3-ChIP 25°C biological replicate C; Arabidopsis thaliana; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP081052">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP081052</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA338073</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1605903">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1605903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05520833</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 each sample, 0.5 g of plant material were used for each biological replicate. Material was collected at from plant growing at 16 °C, as well as at 1 day after the plants were moved to 25°C (5-6 h after lights on). Using jeweler's forceps, leaves were removed to obtain SAM enriched tissue. ChIP experiments were performed following a previously published protocol (Kaufmann et al., Nature Protocols 2010). After the preclearing step the sample was split, one aliquot was incubated with anti-H3K36me3 antibody (ab9050, abcam)and the other with anti-H3 antibody (ab1791, abcam). Samples were prepared for Illumina sequencing using the ThruPLEX DNA-seq Kit (Cat. No: R400429) from Rubicon Genomics according to the manufacturer's protocol.</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>302263695</ID>
          <LABEL>GSM2263695</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2263695</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
