<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="EXP_At-R24_T6h_1574942447_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237461">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237461</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T6h_1574942447_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_R24_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5737001" refname="SAMPLE_At-R24_T6h_1574942447_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5737001</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T6h_1574942447_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-31_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T6h_1574942447_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237462">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237462</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T6h_1574942447_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_R24_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5737002" refname="SAMPLE_At-R24_T6h_1574942447_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5737002</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T6h_1574942447_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-15_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T6h_1574942447_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237463">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237463</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T6h_1574942447_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_R24_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5737003" refname="SAMPLE_At-R24_T6h_1574942447_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5737003</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T6h_1574942447_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-47_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T0_1574942446_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237464">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237464</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T0_1574942446_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_Col_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736998" refname="SAMPLE_At-Col_T0_1574942446_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736998</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T0_1574942446_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-17_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T0_1574942446_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237465">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237465</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T0_1574942446_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_Col_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736999" refname="SAMPLE_At-Col_T0_1574942446_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736999</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T0_1574942446_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-1_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T0_1574942446_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237466">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237466</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T0_1574942446_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_Col_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5737000" refname="SAMPLE_At-Col_T0_1574942446_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5737000</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T0_1574942446_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-33_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T3h_1574942446_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237467">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237467</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T3h_1574942446_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_R24_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736995" refname="SAMPLE_At-R24_T3h_1574942446_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736995</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T3h_1574942446_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-27_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T3h_1574942446_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237468">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237468</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T3h_1574942446_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_R24_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736996" refname="SAMPLE_At-R24_T3h_1574942446_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736996</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T3h_1574942446_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-11_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T3h_1574942446_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237469">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237469</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T3h_1574942446_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_R24_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736997" refname="SAMPLE_At-R24_T3h_1574942446_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736997</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T3h_1574942446_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-43_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T6h_1574942445_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237470">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237470</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T6h_1574942445_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_OE1_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736990" refname="SAMPLE_At-OE1_T6h_1574942445_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736990</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T6h_1574942445_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-32_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T6h_1574942445_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237471">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237471</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T6h_1574942445_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_OE1_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736991" refname="SAMPLE_At-OE1_T6h_1574942445_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736991</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T6h_1574942445_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-16_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T6h_1574942445_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237472">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237472</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T6h_1574942445_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_OE1_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736992" refname="SAMPLE_At-OE1_T6h_1574942445_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736992</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T6h_1574942445_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-48_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T6h_1574942445_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237473">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237473</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T6h_1574942445_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_Col_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736987" refname="SAMPLE_At-Col_T6h_1574942445_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736987</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T6h_1574942445_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-29_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T6h_1574942445_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237474">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237474</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T6h_1574942445_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_Col_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736988" refname="SAMPLE_At-Col_T6h_1574942445_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736988</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T6h_1574942445_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-13_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T6h_1574942445_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237475">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237475</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T6h_1574942445_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_Col_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736989" refname="SAMPLE_At-Col_T6h_1574942445_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736989</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T6h_1574942445_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-45_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T3h_1574942444_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237477">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237477</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T3h_1574942444_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_OE1_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736984" refname="SAMPLE_At-OE1_T3h_1574942444_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736984</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T3h_1574942444_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-28_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T3h_1574942444_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237478">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237478</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T3h_1574942444_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_OE1_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736985" refname="SAMPLE_At-OE1_T3h_1574942444_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736985</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T3h_1574942444_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-12_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T3h_1574942444_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237480">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237480</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T3h_1574942444_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_OE1_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736986" refname="SAMPLE_At-OE1_T3h_1574942444_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736986</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T3h_1574942444_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-44_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T0_1574942443_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237481">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237481</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T0_1574942443_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_OE1_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736980" refname="SAMPLE_At-OE1_T0_1574942443_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736980</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T0_1574942443_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-20_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T0_1574942443_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237482">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237482</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T0_1574942443_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_OE1_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736981" refname="SAMPLE_At-OE1_T0_1574942443_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736981</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T0_1574942443_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-4_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T0_1574942443_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237483">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237483</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T0_1574942443_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_OE1_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736983" refname="SAMPLE_At-OE1_T0_1574942443_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736983</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T0_1574942443_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-36_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T90mn_1574942443_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237484">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237484</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T90mn_1574942443_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_710_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736976" refname="SAMPLE_At-710_T90mn_1574942443_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736976</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T90mn_1574942443_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-22_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T90mn_1574942443_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237485">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237485</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T90mn_1574942443_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_710_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736978" refname="SAMPLE_At-710_T90mn_1574942443_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736978</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T90mn_1574942443_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-6_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T90mn_1574942443_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237486">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237486</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T90mn_1574942443_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_710_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736979" refname="SAMPLE_At-710_T90mn_1574942443_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736979</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T90mn_1574942443_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-38_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T3h_1574942442_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237487">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237487</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T3h_1574942442_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_710_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736973" refname="SAMPLE_At-710_T3h_1574942442_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736973</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T3h_1574942442_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-26_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T3h_1574942442_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237488">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237488</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T3h_1574942442_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_710_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736974" refname="SAMPLE_At-710_T3h_1574942442_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736974</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T3h_1574942442_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-10_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T3h_1574942442_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237489">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237489</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T3h_1574942442_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_710_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736975" refname="SAMPLE_At-710_T3h_1574942442_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736975</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T3h_1574942442_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-42_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T0_1574942440_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237490">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237490</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T0_1574942440_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_710_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736970" refname="SAMPLE_At-710_T0_1574942440_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736970</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T0_1574942440_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-18_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T0_1574942440_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237491">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237491</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T0_1574942440_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_710_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736971" refname="SAMPLE_At-710_T0_1574942440_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736971</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T0_1574942440_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-2_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T0_1574942440_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237492">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237492</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T0_1574942440_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_710_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736972" refname="SAMPLE_At-710_T0_1574942440_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736972</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T0_1574942440_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-34_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T6h_1574942440_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237493">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237493</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T6h_1574942440_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_710_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736967" refname="SAMPLE_At-710_T6h_1574942440_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736967</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T6h_1574942440_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-30_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T6h_1574942440_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237494">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237494</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T6h_1574942440_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_710_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736968" refname="SAMPLE_At-710_T6h_1574942440_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736968</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T6h_1574942440_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-14_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-710_T6h_1574942440_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237495">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237495</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-710_T6h_1574942440_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_710_T6h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736969" refname="SAMPLE_At-710_T6h_1574942440_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736969</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-710_T6h_1574942440_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-46_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T3h_1574942439_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237496">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237496</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T3h_1574942439_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_Col_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736964" refname="SAMPLE_At-Col_T3h_1574942439_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736964</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T3h_1574942439_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L005_HAM-25_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T3h_1574942439_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237497">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237497</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T3h_1574942439_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_Col_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736965" refname="SAMPLE_At-Col_T3h_1574942439_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736965</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T3h_1574942439_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L003_HAM-9_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T3h_1574942439_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237498">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237498</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T3h_1574942439_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_Col_T3h</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736966" refname="SAMPLE_At-Col_T3h_1574942439_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736966</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T3h_1574942439_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L007_HAM-41_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T0_1574942439_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237499">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237499</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T0_1574942439_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_R24_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736961" refname="SAMPLE_At-R24_T0_1574942439_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736961</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T0_1574942439_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-19_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T0_1574942439_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237500">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237500</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T0_1574942439_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_R24_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736962" refname="SAMPLE_At-R24_T0_1574942439_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736962</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T0_1574942439_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-3_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T0_1574942439_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237501">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237501</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T0_1574942439_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_R24_T0</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736963" refname="SAMPLE_At-R24_T0_1574942439_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736963</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T0_1574942439_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-35_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T90mn_1574942438_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237502">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237502</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T90mn_1574942438_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_Col_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736958" refname="SAMPLE_At-Col_T90mn_1574942438_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736958</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T90mn_1574942438_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-21_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T90mn_1574942438_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237503">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237503</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T90mn_1574942438_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_Col_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736959" refname="SAMPLE_At-Col_T90mn_1574942438_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736959</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T90mn_1574942438_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-5_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-Col_T90mn_1574942438_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237504">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237504</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-Col_T90mn_1574942438_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_Col_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736960" refname="SAMPLE_At-Col_T90mn_1574942438_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736960</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-Col_T90mn_1574942438_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-37_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T90mn_1574942438_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237505">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237505</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T90mn_1574942438_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_OE1_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736955" refname="SAMPLE_At-OE1_T90mn_1574942438_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736955</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T90mn_1574942438_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-24_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T90mn_1574942438_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237506">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237506</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T90mn_1574942438_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_OE1_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736956" refname="SAMPLE_At-OE1_T90mn_1574942438_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736956</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T90mn_1574942438_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-8_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-OE1_T90mn_1574942438_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237507">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237507</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-OE1_T90mn_1574942438_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_OE1_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736957" refname="SAMPLE_At-OE1_T90mn_1574942438_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736957</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-OE1_T90mn_1574942438_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-40_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T90mn_1574942437_sra_1" center_name="LIPM-INRA-CNRS" accession="SRX7237508">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237508</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T90mn_1574942437_sra_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR2_R24_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736952" refname="SAMPLE_At-R24_T90mn_1574942437_sra_1" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736952</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T90mn_1574942437_sra_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L004_HAM-23_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T90mn_1574942437_sra_2" center_name="LIPM-INRA-CNRS" accession="SRX7237509">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237509</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T90mn_1574942437_sra_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR1_R24_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736953" refname="SAMPLE_At-R24_T90mn_1574942437_sra_2" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736953</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T90mn_1574942437_sra_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L002_HAM-7_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="EXP_At-R24_T90mn_1574942437_sra_3" center_name="LIPM-INRA-CNRS" accession="SRX7237510">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7237510</PRIMARY_ID>
      <SUBMITTER_ID namespace="LIPM-INRA-CNRS">EXP_At-R24_T90mn_1574942437_sra_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>At-TR3_R24_T90mn</TITLE>
    <STUDY_REF accession="SRP233656" refname="QUANTIREX-RNASeq" refcenter="LIPM-INRA-CNRS">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP233656</PRIMARY_ID>
        <SUBMITTER_ID namespace="LIPM-INRA-CNRS">QUANTIREX-RNASeq</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5736954" refname="SAMPLE_At-R24_T90mn_1574942437_sra_3" refcenter="LIPM-INRA-CNRS">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5736954</PRIMARY_ID>
          <SUBMITTER_ID namespace="LIPM-INRA-CNRS">SAMPLE_At-R24_T90mn_1574942437_sra_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME/>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <!-- TODO: check the library selection. This value is under controled vocabulary (see SRA site fro more details) -->
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Illumina TruSeq SBS Kit v3</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>100</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>130717_SN365_A_L006_HAM-39_R1.fastq.gz</READ_LABEL>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <!-- TODO: modify the following ELEMENT nature according to your data. (Default is ILLUMINA). Then, modifiy the instrument model. Both are under a controled vocabulary (see SRA site fro more details) -->
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
