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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS17238967</PRIMARY_ID>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX19884773</PRIMARY_ID>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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        <PRIMARY_ID>SRP431114</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS17238968</PRIMARY_ID>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX19884774</PRIMARY_ID>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX19884775</PRIMARY_ID>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX19884776</PRIMARY_ID>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX19884777</PRIMARY_ID>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX19884778</PRIMARY_ID>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
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      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX19884781</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">O_20D_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238978">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238978</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">O_20D_R3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>O_20D_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884784" alias="O_45D_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">O_45D_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238979">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238979</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">O_45D_R1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>O_45D_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884785" alias="O_45D_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">O_45D_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238980">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238980</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">O_45D_R2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>O_45D_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884786" alias="O_45D_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">O_45D_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238981">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238981</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">O_45D_R3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>O_45D_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884787" alias="M_7D_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">M_7D_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238982">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238982</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">M_7D_R1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>M_7D_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884788" alias="M_7D_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">M_7D_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238983">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238983</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">M_7D_R2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>M_7D_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884789" alias="M_7D_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">M_7D_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238984">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238984</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">M_7D_R3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>M_7D_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884790" alias="M_20D_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">M_20D_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238985">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238985</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">M_20D_R1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>M_20D_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884791" alias="M_20D_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">M_20D_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238986">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238986</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">M_20D_R2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>M_20D_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884792" alias="M_20D_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">M_20D_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238987">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238987</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">M_20D_R3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>M_20D_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX19884793" alias="M_45D_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX19884793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB13022759">M_45D_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Dendrobium officinale under water stress</TITLE>
    <STUDY_REF accession="SRP431114">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP431114</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB13022759">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total RNAs were extracted from Dendrobium officinale stem under water stress. After removing genomic DNA using DNase I (Takara), mRNAs were obtained using olio (dT) beads and broken into short fragments, followed with cDNA synthesis. Paired-end sequencing was conducted on HiSeq X Ten platform (Illumina, CA, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS17238988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17238988</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|huangzhang8899@orcid">M_45D_R1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>M_45D_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
