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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18376981" alias="GSM6755718_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376981</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755718_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755718: carnation petal, full blooming, rep1, Input [In-E0h-1]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863054">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863054</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755718</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755718</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376982" alias="GSM6755719_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376982</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755719_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755719: carnation petal, full blooming, rep2, Input [In-E0h-2]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863055">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863055</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755719</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755719</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376983" alias="GSM6755720_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376983</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755720_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755720: carnation petal, full blooming, rep3, Input [In-E0h-3]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863056">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863056</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755720</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755720</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376984" alias="GSM6755721_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376984</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755721_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755721: carnation petal, ethylene treatment, 4h, rep1, Input [In-E4h-1]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863057">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863057</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755721</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755721</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376985" alias="GSM6755722_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376985</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755722_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755722: carnation petal, ethylene treatment, 4h, rep2, Input [In-E4h-2]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863058">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863058</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755722</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755722</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376986" alias="GSM6755723_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376986</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755723_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755723: carnation petal, ethylene treatment, 4h, rep3, Input [In-E4h-3]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863059">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863059</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755723</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376987" alias="GSM6755724_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376987</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755724_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755724: carnation petal, ethylene treatment, 24h, rep1, Input [In-E24h-1]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863060">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863060</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755724</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755724</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376988" alias="GSM6755725_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376988</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755725_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755725: carnation petal, ethylene treatment, 24h, rep2, Input [In-E24h-2]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863061">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863061</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755725</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376989" alias="GSM6755726_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376989</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755726_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755726: carnation petal, ethylene treatment, 24h, rep3, Input [In-E24h-3]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863062">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863062</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755726</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376990" alias="GSM6755727_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376990</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755727_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755727: carnation petal, full blooming, rep1, IP [IP-E0h-1]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863063">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863063</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755727</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755727</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376991" alias="GSM6755728_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376991</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755728_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755728: carnation petal, full blooming, rep2, IP [IP-E0h-2]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863064">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863064</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755728</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755728</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376992" alias="GSM6755729_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376992</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755729_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755729: carnation petal, full blooming, rep3, IP [IP-E0h-3]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863065">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863065</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755729</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376993" alias="GSM6755730_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376993</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755730_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755730: carnation petal, ethylene treatment, 4h, rep1, IP [IP-E4h-1]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863066">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863066</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755730</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755730</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376994" alias="GSM6755731_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376994</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755731_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755731: carnation petal, ethylene treatment, 4h, rep2, IP [IP-E4h-2]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863067">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863067</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755731</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755731</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376995" alias="GSM6755732_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376995</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755732_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755732: carnation petal, ethylene treatment, 4h, rep3, IP [IP-E4h-3]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863068">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863068</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755732</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376996" alias="GSM6755733_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376996</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755733_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755733: carnation petal, ethylene treatment, 24h, rep1, IP [IP-E24h-1]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863069">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863069</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755733</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755733</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376997" alias="GSM6755734_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376997</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755734_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755734: carnation petal, ethylene treatment, 24h, rep2, IP [IP-E24h-2]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863070">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863070</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755734</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755734</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18376998" alias="GSM6755735_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18376998</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6755735_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6755735: carnation petal, ethylene treatment, 24h, rep3, IP [IP-E24h-3]; Dianthus caryophyllus; ChIP-Seq</TITLE>
    <STUDY_REF accession="SRP409758">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409758</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905358</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15863071">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15863071</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6755735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6755735</LIBRARY_NAME>
        <LIBRARY_STRATEGY>ChIP-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>ChIP</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>petals were fixed with 1% formaldehyde for 30 minutes and sonicated into DNA fragments. 6% of the sonicated chromatin was saved as the input. The left samples were subsequently incubated with 2 µl of antibodies of anti-H3K4me3 (abcam ab8580) overnight at 4°C with gentle agitation. Immunoprecipitated DNA was used to construct sequencing libraries following the protocol provided by the I NEXTFLEX ChIP-Seq Library Prep Kit for Illumina Sequencing（NOVA-5143-02，Bioo Scientific） and sequenced on Illumina NovaSeq 6000 with PE 150 method.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
