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    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/34J male mouse</TITLE>
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    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/36J male mouse</TITLE>
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      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt32 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786735">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786735</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTFZ_1.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FZ_1.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040125" alias="FZ_2.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">FZ_2.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/38J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt34 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786736">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786736</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTFZ_2.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FZ_2.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040126" alias="FZ_3.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">FZ_3.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/40J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt36 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786737">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786737</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTFZ_3.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FZ_3.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040127" alias="FZ_4.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">FZ_4.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/42J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt38 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786738">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786738</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTFZ_4.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FZ_4.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040128" alias="FZ_5.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">FZ_5.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/44J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt40 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786739">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786739</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTFZ_5.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>FZ_5.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040129" alias="Con_3.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">Con_3.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/10J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt6 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786740">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786740</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTCon_3.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Con_3.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040130" alias="DH_1.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">DH_1.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/46J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt42 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786741">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786741</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTDH_1.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DH_1.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040131" alias="DH_2.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">DH_2.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/48J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt44 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786742">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786742</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTDH_2.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DH_2.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040132" alias="DH_3.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">DH_3.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/50J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt46 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786743">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786743</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTDH_3.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DH_3.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040133" alias="DH_4.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">DH_4.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/52J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt48 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786744">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786744</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTDH_4.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DH_4.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040134" alias="DH_5.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">DH_5.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/54J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt50 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786745">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786745</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTDH_5.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DH_5.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040135" alias="HQ_1.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HQ_1.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/56J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt52 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786746">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786746</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHQ_1.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HQ_1.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040136" alias="HQ_2.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HQ_2.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/58J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt54 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786747">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786747</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHQ_2.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HQ_2.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15040137" alias="HQ_3.1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HQ_3.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/60J male mouse</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt56 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786748</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHQ_3.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HQ_3.1</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HQ_4.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/62J male mouse</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt58 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786749">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786749</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHQ_4.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HQ_4.1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HQ_5.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/64J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt60 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786750">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786750</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHQ_5.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HQ_5.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">Con_4.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/12J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt8 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786751">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786751</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTCon_4.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Con_4.1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HL_1.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/66J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt62 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786752">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786752</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHL_1.1.fq</SUBMITTER_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HL_2.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/68J male mouse</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt64 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786753">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786753</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHL_2.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HL_2.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HL_3.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/70J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt66 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786754">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786754</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHL_3.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HL_4.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/72J male mouse</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt68 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786755">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786755</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHL_4.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
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        <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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">HL_5.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/74J male mouse</TITLE>
    <STUDY_REF accession="SRP372719">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt70 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786756">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786756</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTHL_5.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX15040146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11383374">Con_5.1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16s rDNA sequencing of cecal contents: five weeks C57BL/14J male mouse</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP372719</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11383374">bp0</SUBMITTER_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fecal DNA was isolated using the Qiagen QIAamp DNA Stool Mini Kit (Qiagen, Dusseldorf, Germany). Illumina sequencing was done based on published methods. The V3V4 region of the 16S ribosomal RNA gene was amplified and sequenced. Sequence reads were analyzed using QIIME software 1.9.1. Functional profiles of microbial communities for 16S rRNA sequencing were predicted using PICRUSt10 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS12786757">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12786757</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|libinbing">LTCon_5.1.fq</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Con_5.1</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 HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
