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  <EXPERIMENT alias="GSM2465795" accession="SRX2511763">
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      <PRIMARY_ID>SRX2511763</PRIMARY_ID>
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    </IDENTIFIERS>
    <TITLE>GSM2465795: BSseq_Col_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS1935456">
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          <PRIMARY_ID>SRS1935456</PRIMARY_ID>
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        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index ATCACG sequenced on 03/11/16 (40x40), 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX2511764</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465796</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465796: BSseq_Col_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS1935457">
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          <PRIMARY_ID>SRS1935457</PRIMARY_ID>
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        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index TTAGGC sequenced on 03/11/16 (40x40), 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_LINK>
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          <DB>gds</DB>
          <ID>302465796</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465797" accession="SRX2511765">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511765</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465797</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465797: BSseq_Cvi_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935458">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935458</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465797</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index CGATGT sequenced on 03/11/16 (40x40), 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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          <DB>gds</DB>
          <ID>302465797</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465797</VALUE>
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  <EXPERIMENT alias="GSM2465798" accession="SRX2511766">
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      <PRIMARY_ID>SRX2511766</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465798</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465798: BSseq_Cvi_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935459">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935459</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index GATCAG sequenced on 03/11/16 (40x40), 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465798</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM2465799" accession="SRX2511767">
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      <PRIMARY_ID>SRX2511767</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465799</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465799: BSseq_RIL8_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935460">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935460</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index TGACCA sequenced on 03/11/16 (40x40), 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465799</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465799</VALUE>
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  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465800" accession="SRX2511768">
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      <PRIMARY_ID>SRX2511768</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465800</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465800: BSseq_RIL8_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935461">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935461</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465800</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index TAGCTT sequenced on 03/11/16 (40x40), 03/31/16 (100x100), and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465800</ID>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM2465801" accession="SRX2511769">
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      <PRIMARY_ID>SRX2511769</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465801</SUBMITTER_ID>
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    <TITLE>GSM2465801: BSseq_RIL22_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935462">
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          <PRIMARY_ID>SRS1935462</PRIMARY_ID>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index ATCACG sequenced on 12/09/16.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
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  <EXPERIMENT alias="GSM2465802" accession="SRX2511770">
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      <PRIMARY_ID>SRX2511770</PRIMARY_ID>
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    <TITLE>GSM2465802: BSseq_RIL22_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935463">
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          <PRIMARY_ID>SRS1935463</PRIMARY_ID>
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        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index ACAGTG sequenced on 12/09/16.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465802</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465802</VALUE>
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  <EXPERIMENT alias="GSM2465803" accession="SRX2511771">
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      <PRIMARY_ID>SRX2511771</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465803</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465803: BSseq_RIL84_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935464">
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          <PRIMARY_ID>SRS1935464</PRIMARY_ID>
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        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index CGATGT sequenced on 12/09/16.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465803</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465803</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465804" accession="SRX2511772">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511772</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465804</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465804: BSseq_RIL84_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935465">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935465</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index GCCAAT sequenced on 12/09/16 .</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465804</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465804</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465805" accession="SRX2511773">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511773</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465805</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465805: BSseq_RIL124_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935466">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935466</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol sequenced on 10/03/14 with index GCCAAT.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465805</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465805</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465806" accession="SRX2511774">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511774</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465806</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465806: BSseq_RIL124_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935467">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935467</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol sequenced on 10/03/14 with index CTTGTA.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465806</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465806</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465807" accession="SRX2511775">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511775</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465807</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465807: BSseq_RIL242_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935468">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935468</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol sequenced on 10/03/14 with index TAGCTT.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465807</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465807</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465808" accession="SRX2511776">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511776</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465808</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465808: BSseq_RIL242_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935469">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935469</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol sequenced on 10/03/14 with index GGCTAC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465808</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465808</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465809" accession="SRX2511777">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511777</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465809</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465809: BSseq_RIL258_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935470</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index TTAGGC sequenced on 12/09/16.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465809</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465809</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465810" accession="SRX2511778">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511778</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465810</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465810: BSseq_RIL258_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935471</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index CAGATC sequenced on 12/09/16.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465810</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465810</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465811" accession="SRX2511779">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511779</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465811</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465811: BSseq_RIL303_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935472">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935472</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index CAGATC sequenced on 03/11/16 (40x 40), 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465811</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465811</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465812" accession="SRX2511780">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511780</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465812</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465812: BSseq_RIL303_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935473">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935473</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index GGCTAC sequenced on 03/11/16 (40x40) , 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465812</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465812</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465813" accession="SRX2511781">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511781</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465813</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465813: BSseq_RIL332_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935474">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935474</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index ACAGTG sequenced on 03/11/16 (40x40), 03/31/16 (100x100),and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465813</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465813</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465814" accession="SRX2511782">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511782</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465814</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465814: BSseq_RIL332_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935475">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935475</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index GCCAAT sequenced on 03/11/16 (40x40), 03/31/16 (100x100) and 04/13/16 (50x50).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465814</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465814</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465815" accession="SRX2511783">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511783</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465815</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465815: BSseq_RIL363_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935476">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935476</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index TGACCA sequenced on 12/09/16.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465815</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465815</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465816" accession="SRX2511784">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511784</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465816</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465816: BSseq_RIL363_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935477">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935477</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index ACTTGA sequenced on 12/09/16.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465816</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465816</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465817" accession="SRX2511785">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511785</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465817</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465817: BSseq_RIL495_rep1; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935478">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935478</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index ACTTGA sequenced on 03/11/16 (40x40) and 03/31/16 (100x100).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465817</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465817</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465818" accession="SRX2511786">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511786</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465818</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465818: BSseq_RIL495_rep2; Arabidopsis thaliana; Bisulfite-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935479</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For bisulfite sequencing, between 100 and 500ng DNA was bisulfite-converted using the MethylCode bisulfite conversion kit (Invitrogen). Libraries were prepared using the EpiGnome Methyl-seq kit from Epicentre (now the TruSeq DNA methylation kit from Illumina, cat no. EGMK81312), using all bisulfite-converted DNA. Reads were sequenced on an Illumina HiSeq 2000 to obtain 40x40, 50x50 and 100x100bp paired-end reads. Illumina TruSeq DNA methylation protocol with index CTTGTA sequenced on 03/11/16 (40x40) and 03/31/16 (100x100).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465818</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465818</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465819" accession="SRX2511787">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511787</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465819</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465819: RNAseq_col_rep1; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935480</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode TGACCA.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465819</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465819</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465820" accession="SRX2511788">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511788</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465820</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465820: RNAseq_col_rep2; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935481</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode CGATGT.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465820</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465820</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465821" accession="SRX2511789">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511789</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465821</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465821: RNAseq_col_rep3; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935482</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode CTTGTA.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465821</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465821</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465822" accession="SRX2511790">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511790</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465822</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465822: RNAseq_cvi_rep1; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935483">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935483</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode ACAGTG.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465822</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465822</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465823" accession="SRX2511791">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511791</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465823</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465823: RNAseq_cvi_rep2; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935484">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935484</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode AGTCAA.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465823</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465823</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465824" accession="SRX2511792">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511792</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465824</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465824: RNAseq_cvi_rep3; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935485">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935485</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode AGTTCC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465824</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465824</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465825" accession="SRX2511793">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511793</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465825</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465825: RNAseq_RIL124_rep1; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935486">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935486</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode GCCAAT.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465825</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465825</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465826" accession="SRX2511794">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511794</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465826</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465826: RNAseq_RIL124_rep2; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935487">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935487</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode ATGTCA.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465826</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465826</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465827" accession="SRX2511795">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511795</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465827</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465827: RNAseq_RIL124_rep3; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935488">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935488</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode CCGTCC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465827</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465827</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465828" accession="SRX2511796">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511796</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465828</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465828: RNAseq_RIL242_rep1; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935489">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935489</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode CAGATC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465828</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465828</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465829" accession="SRX2511797">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511797</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465829</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465829: RNAseq_RIL242_rep2; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935490">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935490</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode GTCCGC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465829</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465829</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2465830" accession="SRX2511798">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2511798</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2465830</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2465830: RNAseq_RIL242_rep3; Arabidopsis thaliana; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP097638" refname="GSE93968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP097638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1935491">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1935491</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2465830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Harvested leaf tissue was pulverized using the Qiagen TissueLyser II. For bisulfite-sequencing, DNA was extracted using the Qiagen DNeasy Plant Mini kit (cat. No. 69104). For RNA-seq, total RNA was isolated using the RNeasy plant mini kit (Qiagen, cat. no. 74903). For RNA-seq, libraries were constructed from 1ug RNA using the RNA TruSeq stranded library kit (Illumina, uses polyA selection) using 15 cycles of amplification. Reads were sequenced on an Illumina HiSeq2000 using a 40bp single-end protocol. Illumina TruSeq RNA stranded protocol sequenced on 07/24/2015 with barcode GTGAAA.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302465830</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2465830</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
