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      <PRIMARY_ID>SRX5494875</PRIMARY_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494876</PRIMARY_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4464536</PRIMARY_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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        <PRIMARY_ID>SRP187941</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4464537</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-4-2</SUBMITTER_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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        <PRIMARY_ID>SRP187941</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4464538</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4464539</PRIMARY_ID>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494880</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-1-1</SUBMITTER_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
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      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4464540</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494881</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-1-2</SUBMITTER_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494882</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-2</SUBMITTER_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494885</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-3-2</SUBMITTER_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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          <SUBMITTER_ID namespace="pda|mismissing">S3-3-2</SUBMITTER_ID>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5494886</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-4</SUBMITTER_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4464546</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-4</SUBMITTER_ID>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX5494887</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-3</SUBMITTER_ID>
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    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
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      <IDENTIFIERS>
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        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464547">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464547</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-3</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494888" alias="Library-S3-3-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494888</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-3-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464548">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464548</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-3-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-3-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494889" alias="Library-S3-4-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494889</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-4-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464549">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464549</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-4-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-4-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494890" alias="Library-S3-4-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494890</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-4-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464550">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464550</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-4-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-4-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494891" alias="Library-S1-3-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494891</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-3-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464551">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464551</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-3-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-3-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494892" alias="Library-S1-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494892</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464552">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464552</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-4</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494893" alias="Library-S1-1-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494893</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-1-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464553">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464553</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-1-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-1-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494894" alias="Library-S1-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494894</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464554">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464554</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494895" alias="Library-S1-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494895</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464555">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464555</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494896" alias="Library-S1-1-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494896</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-1-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464556">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464556</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-1-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-1-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494897" alias="Library-S1-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494897</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464557">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464557</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-3</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494898" alias="Library-S1-3-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494898</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-3-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464558">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464558</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-3-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-3-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494899" alias="Library-S1-2-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494899</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-2-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464559">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464559</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-2-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-2-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494900" alias="Library-S1-2-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494900</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S1-2-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464560">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464560</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S1-2-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S1-2-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494901" alias="Library-S2-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494901</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464561">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464561</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S2-4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S2-4</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494902" alias="Library-S2-3-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494902</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-3-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464562">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464562</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S2-3-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S2-3-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494903" alias="Library-S2-4-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494903</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-4-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464563">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464563</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S2-4-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S2-4-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494904" alias="Library-S2-4-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494904</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S2-4-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464564">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464564</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S2-4-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S2-4-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494905" alias="Library-S3-1-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494905</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-1-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464565">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464565</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-1-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-1-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494906" alias="Library-S3-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494906</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464566">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464566</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494907" alias="Library-S3-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494907</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464567">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464567</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494908" alias="Library-S3-1-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494908</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-1-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464568</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-1-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-1-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494909" alias="Library-S3-2-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-2-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464569</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-2-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-2-2</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5494910" alias="Library-S3-2-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5494910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5293963">Library-S3-2-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16SrRNA sequencing of fecal sample</TITLE>
    <STUDY_REF accession="SRP187941">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP187941</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5293963">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA from samples was extracted using CTAB/SDS methodAll PCR reactions were carried out with Phusion High-Fidelity PCR MasterMix (New England Biolabs)Sequencing libraries were generated usingTruSeq DNA PCR-Free Sample Preparation Kit (Illumina, USA) following manufacturer's recommendations and index codes were added. The library quality was assessed on the Qubit@ 2.0 Fluorometer (Thermo Scientific) and Agilent Bioanalyzer 2100 system. At last, thelibrary was sequenced on an IlluminaHiSeq2500 platform and 250 bp paired-end reads were generated</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4464570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4464570</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|mismissing">S3-2-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Library-S3-2-1</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 HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
