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      <PRIMARY_ID>SRX7194604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
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        <PRIMARY_ID>SRP173131</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX7194606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc1-1</SUBMITTER_ID>
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    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS5700469</PRIMARY_ID>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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  <EXPERIMENT accession="SRX7194607" alias="AsymCxAc1-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc1-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS5700469</PRIMARY_ID>
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        <LIBRARY_NAME>AsymCxAc1-4</LIBRARY_NAME>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX7194608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc1-6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS5700469</PRIMARY_ID>
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        <LIBRARY_NAME>AsymCxAc1-6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX7194609" alias="AsymCxAc1-8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc1-8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS5700469</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>SRX7194610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc6-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
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        <PRIMARY_ID>SRP173131</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700470</PRIMARY_ID>
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        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc6-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700470</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX7194612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc6-5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc6-6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700470</PRIMARY_ID>
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        </IDENTIFIERS>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxAc6-8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5700470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700470</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">[A]C6</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxAc6-8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194615" alias="AsymCxc1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxc1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700471</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">Control</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxc1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194617" alias="AsymCxc2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxc2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5700471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700471</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">Control</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxc2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194618" alias="AsymCxc4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxc4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5700471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700471</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">Control</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxc4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194619" alias="AsymCxc5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxc5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5700471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700471</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">Control</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxc5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194620" alias="AsymCxc6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxc6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5700471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700471</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">Control</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxc6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194621" alias="AsymCxc7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxc7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5700471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5700471</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">Control</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxc7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194622" alias="AsymCxc8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxc8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxc8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194623" alias="AsymCxCa-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194624" alias="AsymCxCa-5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194625" alias="AsymCxCa-6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194626" alias="AsymCxCa-7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194627" alias="AsymCxCa-8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194628" alias="AsymCxCa-9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX7194629" alias="AsymCxCa-10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7194629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB6586446">AsymCxCa-10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s amplicon of Nasonia vitripennis, adult female</TITLE>
    <STUDY_REF accession="SRP173131">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP173131</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA509675</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Prior to extraction, each individual was put in 1.5 ml tube and rinsed with 1ml 70% ETOH once, 1ml 10% bleach once, and finally sterile water 1ml twice. Then sampleswere frozen in liquid nitrogen with additional mechanical homogenization. All samples were processed for DNA extraction using the DNeasy Blood &amp; Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturers instructions. Samples were then quantified using the dsDNA HS Assay kit on the Qubit 2.0 Fluorometer (Life Technologies).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4133257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4133257</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|peter123">ATZ</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AsymCxCa-10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
