<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX5098734" alias="CMT3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5098734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4875101">CMT3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>VIGS of CMT3/3-2</TITLE>
    <STUDY_REF accession="SRP172578">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172578</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4875101">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation mix is added to fragments the mRNA. The cDNA is synthesized by using random Hexamer priming. The second-strand is generated to create double-strand cDNA . Purify the cDNA templates by the use of qiagen kit followed by end repair, poly A tailing and adaptor connection.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4109136">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4109136</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|sffuplant">TRV2-CMT3/3-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CMT3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5098735" alias="Ve">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5098735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4875101">Ve</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>VIGS of Ve</TITLE>
    <STUDY_REF accession="SRP172578">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172578</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4875101">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fragmentation mix is added to fragments the mRNA. The cDNA is synthesized by using random Hexamer priming. The second-strand is generated to create double-strand cDNA . Purify the cDNA templates by the use of qiagen kit followed by end repair, poly A tailing and adaptor connection.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4109137">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4109137</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|sffuplant">TRV2-Ve</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Ve</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RT-PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
