<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX22499175" alias="MYB5oe3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22499175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13967864">MYB5oe3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>MpRR-MYB5 overexpressor 3</TITLE>
    <STUDY_REF accession="SRP471380">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471380</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039314</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from 3-4 two-week old gemmae, using the RNeasy Plant kit (#74903, Qiagen) according to the manufacturers protocol (RLT buffer supplemented with beta-merchaptoethanol was used) and residual genomic DNA was removed using the Turbo DNA-free kit (# AM1907, Invitrogen) according to the manufacturers instructions.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19511994">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19511994</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|efrangedakis@orcid">MpRR-MYB5 OE 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MYB5oe3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22499176" alias="MYB5oe10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22499176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13967864">MYB5oe10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>MpRR-MYB5 overexpressor 10</TITLE>
    <STUDY_REF accession="SRP471380">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471380</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039314</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from 3-4 two-week old gemmae, using the RNeasy Plant kit (#74903, Qiagen) according to the manufacturers protocol (RLT buffer supplemented with beta-merchaptoethanol was used) and residual genomic DNA was removed using the Turbo DNA-free kit (# AM1907, Invitrogen) according to the manufacturers instructions.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19511995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19511995</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|efrangedakis@orcid">MpRR-MYB5 OE 10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MYB5oe10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22499177" alias="MYB5oea">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22499177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13967864">MYB5oea</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>MpRR-MYB5 overexpressor a</TITLE>
    <STUDY_REF accession="SRP471380">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471380</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039314</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from 3-4 two-week old gemmae, using the RNeasy Plant kit (#74903, Qiagen) according to the manufacturers protocol (RLT buffer supplemented with beta-merchaptoethanol was used) and residual genomic DNA was removed using the Turbo DNA-free kit (# AM1907, Invitrogen) according to the manufacturers instructions.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19511996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19511996</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|efrangedakis@orcid">MpRR-MYB5 OE A</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MYB5oea</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22499178" alias="MYB2oe1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22499178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13967864">MYB2oe1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>MpRR-MYB2 overexpressor 1</TITLE>
    <STUDY_REF accession="SRP471380">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471380</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039314</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from 3-4 two-week old gemmae, using the RNeasy Plant kit (#74903, Qiagen) according to the manufacturers protocol (RLT buffer supplemented with beta-merchaptoethanol was used) and residual genomic DNA was removed using the Turbo DNA-free kit (# AM1907, Invitrogen) according to the manufacturers instructions.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19511997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19511997</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|efrangedakis@orcid">MpRR-MYB2 OE 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MYB2oe1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22499179" alias="MYB2oe2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22499179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13967864">MYB2oe2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>MpRR-MYB2 overexpressor 2</TITLE>
    <STUDY_REF accession="SRP471380">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471380</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039314</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from 3-4 two-week old gemmae, using the RNeasy Plant kit (#74903, Qiagen) according to the manufacturers protocol (RLT buffer supplemented with beta-merchaptoethanol was used) and residual genomic DNA was removed using the Turbo DNA-free kit (# AM1907, Invitrogen) according to the manufacturers instructions.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19511998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19511998</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|efrangedakis@orcid">MpRR-MYB2 OE 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MYB2oe2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22499180" alias="MYB2oe3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22499180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13967864">MYB2oe3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>MpRR-MYB2 overexpressor 3</TITLE>
    <STUDY_REF accession="SRP471380">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP471380</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1039314</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from 3-4 two-week old gemmae, using the RNeasy Plant kit (#74903, Qiagen) according to the manufacturers protocol (RLT buffer supplemented with beta-merchaptoethanol was used) and residual genomic DNA was removed using the Turbo DNA-free kit (# AM1907, Invitrogen) according to the manufacturers instructions.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19511999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19511999</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|efrangedakis@orcid">MpRR-MYB2 OE 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>MYB2oe3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
