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    <TITLE>RNA-Seq of Allobates femoralis: adult male skin</TITLE>
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        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102744" alias="H4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">H4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Pristimantis toftae: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112948">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102745" alias="H3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">H3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Pristimantis toftae: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112949">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527514</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102746" alias="H10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">H10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Pristimantis toftae: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112950">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102747" alias="I6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">I6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112951">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102748" alias="I5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">I5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112952">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527511</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>I5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102749" alias="I2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">I2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112953">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527510</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102750" alias="I1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">I1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112954">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>I1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102751" alias="G9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112955">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102752" alias="G8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112956">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102753" alias="H2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">H2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult female liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112957">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102754" alias="H1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">H1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult female skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112958">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102755" alias="G5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112959">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102756" alias="G10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112960">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102757" alias="G7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112961">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102758" alias="G6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Scinax ruber: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112962">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527531</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102759" alias="E3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">E3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102760" alias="E4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">E4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112964">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102761" alias="J3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Pristimantis toftae: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112965">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102762" alias="J4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Pristimantis toftae: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112966">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102763" alias="C5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">C5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112967">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102764" alias="C6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">C6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112968">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102765" alias="C7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">C7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112969">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102766" alias="C8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">C8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112970">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102767" alias="D1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">D1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112973">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102768" alias="D2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">D2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ranitomeya sirensis: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112971">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102769" alias="J6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ameerega petersi: adult female liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112972">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102770" alias="J7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ameerega petersi: adult female skin</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX5102771" alias="J2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ameerega petersi: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112975</PRIMARY_ID>
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        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102772" alias="J5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ameerega petersi: adult female skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112977">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102773" alias="F3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">F3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102774" alias="F4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">F4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102775" alias="J8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ameerega petersi: adult female liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102776" alias="J9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">J9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Ameerega petersi: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102777" alias="G2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male liver</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112981">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5102778" alias="G1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5102778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881828">G1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Amazophrynella minuta: adult male skin</TITLE>
    <STUDY_REF accession="SRP172775">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172775</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA430346</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Total mRNA was extracted from the samples using the QIAGEN miRNAeasy kit. Quantity and quality of the extracted total mRNA was assessed with the NanoDrop ND-1000 spectrophotometer (Thermo Scientific) and Experion Labchip electrophoresis (BIORAD). Illumina Tru-Seq libraries for polyA-tail mRNA were prepared following manufacturers guidelines. Raw reads were processed for quality, read size and read number using FastQC v0.11.2 (Babraham Bioinformatics) and Trimmomatic (Bolger et al. 2014) including adapter trimming.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4112982">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4112982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN10527508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
