<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX3551114" alias="CP5781">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP5781</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>5781</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824503">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824503</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP5781</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551115" alias="CP5819">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP5819</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>5819</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824508">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824508</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP5819</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551116" alias="CP3453">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP3453</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>3453</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824504">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824504</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP3453</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551117" alias="CP3469">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP3469</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>3469</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824505">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824505</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP3469</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551118" alias="CP3403">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP3403</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>3403</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824507">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824507</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP3403</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551119" alias="CP3409">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP3409</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>3409</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824506">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824506</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP3409</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551120" alias="CP3376">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP3376</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>3376</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824509">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824509</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP3376</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551121" alias="CP3385">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP3385</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>3385</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824510">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824510</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP3385</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551122" alias="CP6535">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP6535</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>6535</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824511">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824511</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP6535</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551123" alias="CP7880">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP7880</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>7880</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824512">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP7880</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551124" alias="CP9852">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP9852</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9852</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824513">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP9852</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551125" alias="CP9725">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP9725</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9725</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824514">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP9725</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551126" alias="CP9854">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP9854</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9854</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824515">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824515</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP9854</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551127" alias="CP9683">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP9683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9683</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824517">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP9683</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551128" alias="CP9686">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP9686</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9686</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824516">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824516</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP9686</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551129" alias="CP8797">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP8797</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>8797</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824518">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP8797</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551130" alias="CP8804">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP8804</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>8804</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824520">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824520</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP8804</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551131" alias="CP9667">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP9667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9667</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824519">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP9667</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551132" alias="CP9679">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP9679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>9679</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824521">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824521</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP9679</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551133" alias="CP7885">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP7885</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>7885</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824522">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824522</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP7885</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551134" alias="CP7890">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP7890</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>7890</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824523">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824523</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP7890</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551135" alias="CP8084">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP8084</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>8084</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824524">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824524</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP8084</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3551136" alias="CP8789">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3551136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3314354">CP8789</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>8789</TITLE>
    <STUDY_REF accession="SRP128846">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP128846</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA419744</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Stool samples were homogenized in 1 mL of RNAlater. The NucliSens Magnetic Extraction kit and the QIAamp Stool DNA Miniprep Kit were used to extract nucleic acids from samples total nucleic acids and DNA  respectively. Total nucleic acids were initially treated with the TURBO DNA-free kit and purified using the RNeasy MinElute Cleanup kit. For removal of ribosomal RNA from plant  bacteria and mammalian host  prior to RNA library preparation  the total purified RNA was subjected to the ScriptSeq Complete Gold Kit: Epidemiology. The MiniElute PCR Purification Kit and the Agencourt AMPure XP System: PCR Purification kit were used to purify the PCR-amplified products whenever requested by the ScriptSeq kit protocol. DNA libraries were constructed using the DNA directly in Nextera DNA Sample Preparation kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2824525">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2824525</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08143638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>CP8789</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
