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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX6935198" alias="GFGS_day_0_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_0_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 0 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465231">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886543</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_0_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935199" alias="GFGS_day_0_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_0_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 0 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465231">
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          <PRIMARY_ID>SRS5465231</PRIMARY_ID>
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        <LIBRARY_NAME>GFGS_day_0_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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  <EXPERIMENT accession="SRX6935200" alias="GFRS_day_0_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_0_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_0_rep2</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886546</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_0_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935201" alias="GFRS_day_0_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_0_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_0_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS5465232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886546</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_0_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935202" alias="GFRS_day_2_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_2_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_2_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886547</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_2_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935203" alias="GFRS_day_2_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_2_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_2_rep2</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886547</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_2_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935204" alias="GFRS_day_2_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_2_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_2_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886547</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_2_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935205" alias="GFRS_day_7_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_7_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_7_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS5465234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_7_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935206" alias="GFRS_day_7_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_7_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_7_rep2</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_7_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935207" alias="GFRS_day_7_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_7_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_7_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465234">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_7_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935208" alias="RFGS_day_0_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_0_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_0_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465235">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_0_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935209" alias="RFGS_day_0_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_0_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_0_rep2</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465235">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_0_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935210" alias="GFGS_day_0_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_0_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 0 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465231">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886543</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_0_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935211" alias="RFGS_day_0_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_0_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_0_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465235">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_0_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935212" alias="RFGS_day_2_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_2_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_2_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465236">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_2_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935213" alias="RFGS_day_2_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_2_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_2_rep2</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465236">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_2_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935214" alias="RFGS_day_2_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_2_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_2_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465236">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_2_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935215" alias="RFGS_day_7_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_7_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_7_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465237">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_7_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935216" alias="RFGS_day_7_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_7_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_7_rep2</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465237">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_7_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935217" alias="RFGS_day_7_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFGS_day_7_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFGS_day_7_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465237">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFGS_day_7_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935218" alias="RFRS_day_0_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_0_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_0_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465238">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_0_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935219" alias="RFRS_day_0_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_0_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_0_rep2</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465238">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_0_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935220" alias="RFRS_day_0_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_0_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_0_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465238">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_0_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935221" alias="GFGS_day_2_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_2_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 2 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465239">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886544</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_2_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935222" alias="RFRS_day_2_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_2_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_2_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465240">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_2_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935223" alias="RFRS_day_2_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_2_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_2_rep2</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465240">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_2_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935224" alias="RFRS_day_2_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_2_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_2_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465240">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_2_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935225" alias="RFRS_day_7_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_7_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_7_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465241">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_7_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935226" alias="RFRS_day_7_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_7_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_7_rep2</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465241">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_7_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935227" alias="RFRS_day_7_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">RFRS_day_7_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RFRS_day_7_rep3</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465241">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RFRS_day_7_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935228" alias="GFGS_day_2_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_2_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 2 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465239">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886544</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_2_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935229" alias="GFGS_day_2_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_2_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 2 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465239">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886544</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_2_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935230" alias="GFGS_day_7_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_7_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 7 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465242">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886545</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_7_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935231" alias="GFGS_day_7_rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_7_rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 7 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465242">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886545</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_7_rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935232" alias="GFGS_day_7_rep3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFGS_day_7_rep3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFGS dai 7 after inculation with Colletotrichum gloeosporioides</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465242">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886545</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFGS_day_7_rep3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6935233" alias="GFRS_day_0_rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6935233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6381674">GFRS_day_0_rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GFRS_day_0_rep1</TITLE>
    <STUDY_REF accession="SRP223935">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP223935</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA575336</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNA was extracted from the peel of the red and green sides of the red and green fruit inoculated with C. gloeosporioides, at the leading edge of the inoculation, before inoculation (0), and 2 and 7 dpi, as described previously (Djami-Tchatchou &amp; Straker, 2012) each treatment was consisted from 4 fruits, 2 inoculation spots for each side of the fruit, with three biological repeat. The RNA was subjected to deep sequencing TranSeq 3end sequencing method for 650bp single-end reading (Nancy and Stephen Grand Israel National Center, Weizmann Institute of Science, Israel) based on Tzfadia et al (2018).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5465232">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5465232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN12886546</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GFRS_day_0_rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
