<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX11257111" alias="FMTDMSO1_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTDMSO1_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTDMSO1_1</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299284">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299284</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTDMSO1_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTDMSO1_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257112" alias="FMTDMSO1_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTDMSO1_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTDMSO1_2</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299287">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299287</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTDMSO1_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTDMSO1_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257113" alias="FMTDMSO1_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTDMSO1_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTDMSO1_3</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299283">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299283</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTDMSO1_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTDMSO1_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257114" alias="FMTDMSO1_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTDMSO1_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTDMSO1_4</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299288">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299288</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTDMSO1_4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTDMSO1_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257115" alias="FMTRTX1_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTRTX1_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTRTX1_1</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299286">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299286</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTRTX1_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTRTX1_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257116" alias="FMTRTX1_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTRTX1_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTRTX1_2</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299285">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299285</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTRTX1_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTRTX1_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257117" alias="FMTRTX1_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTRTX1_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTRTX1_3</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299289">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299289</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTRTX1_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTRTX1_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257118" alias="FMTRTX1_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">FMTRTX1_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample FMTRTX1_4</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299290">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299290</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">FMTRTX1_4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FMTRTX1_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257119" alias="DonorDMSO1_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorDMSO1_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorDMSO1_3</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299291">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299291</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorDMSO1_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorDMSO1_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257120" alias="DonorDMSO1_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorDMSO1_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorDMSO1_4</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299292">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299292</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorDMSO1_4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorDMSO1_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257121" alias="DonorDMSO1_5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorDMSO1_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorDMSO1_5</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299293">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299293</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorDMSO1_5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorDMSO1_5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257122" alias="DonorRTX1_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorRTX1_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorRTX1_1</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299294">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299294</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorRTX1_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorRTX1_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257123" alias="DonorRTX1_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorRTX1_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorRTX1_2</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299296">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299296</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorRTX1_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorRTX1_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257124" alias="DonorRTX1_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorRTX1_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorRTX1_3</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299295">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299295</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorRTX1_3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorRTX1_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257125" alias="DonorRTX1_4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorRTX1_4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorRTX1_4</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299297">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299297</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorRTX1_4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorRTX1_4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257126" alias="DonorRTX1_5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorRTX1_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorRTX1_5</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299298">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299298</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorRTX1_5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorRTX1_5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257127" alias="DonorDMSO1_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorDMSO1_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorDMSO1_1</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299299">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299299</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorDMSO1_1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorDMSO1_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX11257128" alias="DonorDMSO1_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX11257128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9924886">DonorDMSO1_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Fecal sample DonorDMSO1_2</TITLE>
    <STUDY_REF accession="SRP326003">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP326003</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB9924886">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Libraries were prepared according to the protocol of the Earth Microbiome Project (https://earthmicrobiome.org/protocols-and-standards/16s/). Amplicon libraries were washed using Beckman Coulter AMPure XP magnetic beads. Library quality and size verification was performed using a PerkinElmer LabChip GXII instrument with DNA 1K Reagent Kit (CLS760673). Library concentrations were quantified using Quant-iT dsDNA High Sensitivity Assay Kit using a Promega GloMax plate reader on a microplate (655087). Library molarity was calculated based on library peak size and concentration. Libraries were normalized to 2nM using the PerkinElmer Zephyr G3 NGS Workstation (133750) and pooled together using the same volume across all normalized libraries into a 1.5 ml Eppendorf DNA tube (022431021).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS9299300">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS9299300</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|grp2009@med.cornell.edu">DonorDMSO1_2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DonorDMSO1_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
