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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706309">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023427</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g0M_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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            <READ_INDEX>1</READ_INDEX>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706892" center_name="University of Utah" alias="g1A1_PE150_Original">
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      <PRIMARY_ID>SRX706892</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A1_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A1</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023428</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g1A1_PE150_Original</LIBRARY_NAME>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_TYPE>Primer</READ_TYPE>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706893" center_name="University of Utah" alias="g1A2_PE150_Original">
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      <PRIMARY_ID>SRX706893</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A2_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A2</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023429</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g1A2_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
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            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX706894</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A3_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A3</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023430</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g1A3_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX706895</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A4_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A4</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023431</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX706896</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A5_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A5</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023432</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
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            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706897" center_name="University of Utah" alias="g1B1_PE150_Original">
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      <PRIMARY_ID>SRX706897</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1B1_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1B1</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706898" center_name="University of Utah" alias="g1B2_PE150_Original">
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      <PRIMARY_ID>SRX706898</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1B2_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1B2</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023434</EXTERNAL_ID>
        </IDENTIFIERS>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        </SPOT_DECODE_SPEC>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706906" center_name="University of Utah" alias="g1C5_PE150_Original">
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      <PRIMARY_ID>SRX706906</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1C5_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1C5</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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            <READ_INDEX>1</READ_INDEX>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706907" center_name="University of Utah" alias="g1D1_PE150_Original">
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      <PRIMARY_ID>SRX706907</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D1_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1D1</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023443</EXTERNAL_ID>
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          <READ_SPEC>
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            <READ_INDEX>3</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX706908</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D2_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1D2</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023444</EXTERNAL_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706909</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023445</EXTERNAL_ID>
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          <READ_SPEC>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706910</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D4_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023446</EXTERNAL_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX706911</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D5_PE150_Original</SUBMITTER_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <EXTERNAL_ID namespace="BioSample">SAMN03023447</EXTERNAL_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX706912</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A10_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023448</EXTERNAL_ID>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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        <TAG>16S forward primer</TAG>
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      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706913" center_name="University of Utah" alias="g2A6_PE150_Original">
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      <PRIMARY_ID>SRX706913</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A6_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <READ_SPEC>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX706914</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A7_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX706915</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A8_PE150_Original</SUBMITTER_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX706916</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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          <READ_SPEC>
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          <READ_SPEC>
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      <EXPERIMENT_ATTRIBUTE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706345</PRIMARY_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
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      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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      <PRIMARY_ID>SRX706928</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D6_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX706929</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D7_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2D7</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706348</PRIMARY_ID>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX706930</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706931</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D9_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706932</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <READ_SPEC>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706933</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706353</PRIMARY_ID>
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          <READ_SPEC>
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          <READ_SPEC>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706934</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023470</EXTERNAL_ID>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706949" center_name="University of Utah" alias="g3D14_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706949</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3D14_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3D14</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706368">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>g3D14_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_INDEX>0</READ_INDEX>
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            <READ_TYPE>Primer</READ_TYPE>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706950" center_name="University of Utah" alias="g3D15_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706950</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3D15_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3D15</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706365">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>g3D15_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706951" center_name="University of Utah" alias="g4A16_PE150_Original">
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      <PRIMARY_ID>SRX706951</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A16_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A16</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023487</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g4A16_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_INDEX>1</READ_INDEX>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX706952</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A17_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A17</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023488</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX706953</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A18_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A18</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023489</EXTERNAL_ID>
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        <LIBRARY_NAME>g4A18_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706954" center_name="University of Utah" alias="g4A19_PE150_Original">
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      <PRIMARY_ID>SRX706954</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A19_PE150_Original</SUBMITTER_ID>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023490</EXTERNAL_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706955" center_name="University of Utah" alias="g4A20_PE150_Original">
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      <PRIMARY_ID>SRX706955</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A20_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A20</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023491</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g4A20_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706382">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4C19_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706964" center_name="University of Utah" alias="g4C20_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706964</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4C20_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4C20</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706381">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4C20_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706965" center_name="University of Utah" alias="g4D16_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706965</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D16_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D16</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706383">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D16_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706966" center_name="University of Utah" alias="g4D17_PE150_Original">
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      <PRIMARY_ID>SRX706966</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D17_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D17</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706384">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>g4D17_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706967" center_name="University of Utah" alias="g4D18_PE150_Original">
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      <PRIMARY_ID>SRX706967</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D18_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D18</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706385">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023503</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g4D18_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706968" center_name="University of Utah" alias="g4D19_PE150_Original">
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      <PRIMARY_ID>SRX706968</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D19_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D19</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023504</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g4D19_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706969" center_name="University of Utah" alias="g4D20_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706969</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D20_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D20</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706386">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D20_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706970" center_name="University of Utah" alias="g5A22_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706970</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5A22_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5A22</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706389">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
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        <TAG>16S forward primer</TAG>
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    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706971" center_name="University of Utah" alias="g5A23_PE150_Original">
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      <PRIMARY_ID>SRX706971</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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            <READ_INDEX>3</READ_INDEX>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX706972</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706387</PRIMARY_ID>
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      <PRIMARY_ID>SRX706973</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <TAG>16S forward primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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          <READ_SPEC>
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          <READ_SPEC>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706977</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706978" center_name="University of Utah" alias="g5C21_PE150_Original">
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      <PRIMARY_ID>SRX706978</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C21_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023515</EXTERNAL_ID>
        </IDENTIFIERS>
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            <READ_INDEX>1</READ_INDEX>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706979" center_name="University of Utah" alias="g5C22_PE150_Original">
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      <PRIMARY_ID>SRX706979</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C22_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5C22</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023516</EXTERNAL_ID>
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            <READ_INDEX>1</READ_INDEX>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX706980</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C23_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706396</PRIMARY_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX706981</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C24_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023518</EXTERNAL_ID>
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            <READ_CLASS>Application Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706982</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C25_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023519</EXTERNAL_ID>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX706983</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D21_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023520</EXTERNAL_ID>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX706984</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D22_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023521</EXTERNAL_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
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      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
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    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706985" center_name="University of Utah" alias="g5D23_PE150_Original">
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      <PRIMARY_ID>SRX706985</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D23_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D23</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706405">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>g5D23_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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        <SPOT_DECODE_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706986" center_name="University of Utah" alias="g5D24_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706986</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D24_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D24</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706404">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5D24_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706987" center_name="University of Utah" alias="g5D25_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706987</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D25_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D25</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706403">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023524</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g5D25_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706988" center_name="University of Utah" alias="g6A26_PE150_Original">
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      <PRIMARY_ID>SRX706988</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A26_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6A26</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023525</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g6A26_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706989" center_name="University of Utah" alias="g6A27_PE150_Original">
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      <PRIMARY_ID>SRX706989</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A27_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6A27</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023526</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g6A27_PE150_Original</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX706990" center_name="University of Utah" alias="g6A28_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706990</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A28_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6A28</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023527</EXTERNAL_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706991" center_name="University of Utah" alias="g6A29_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX706991</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A29_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6A29</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023528</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6A29_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX706992" center_name="University of Utah" alias="g6A30_PE150_Original">
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX706994</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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        <TAG>16S forward primer</TAG>
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        <TAG>16S forward primer</TAG>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706417">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6B31_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707000" center_name="University of Utah" alias="g6C26_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707000</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C26_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C26</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706418">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023537</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C26_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707001" center_name="University of Utah" alias="g6C27_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707001</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C27_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C27</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706422">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023538</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C27_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
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            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707002" center_name="University of Utah" alias="g6C28_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707002</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C28_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C28</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706420">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023539</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C28_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707003" center_name="University of Utah" alias="g6C29_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707003</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C29_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C29</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706423">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023540</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C29_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707004" center_name="University of Utah" alias="g6C30_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707004</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C30_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C30</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706419">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023541</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C30_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707005" center_name="University of Utah" alias="g6D26_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707005</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D26_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D26</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706421">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023542</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6D26_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>394</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>19</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>148</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>164</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707006" center_name="University of Utah" alias="g6D27_PE150_Original">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707006</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D27_PE150_Original</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D27</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706425">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023543</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6D27_PE150_Original</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
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          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        </SPOT_DECODE_SPEC>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707007" center_name="University of Utah" alias="g6D28_PE150_Original">
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      <PRIMARY_ID>SRX707007</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D28_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706424</PRIMARY_ID>
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            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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  </EXPERIMENT>
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      <PRIMARY_ID>SRX707008</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D29_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706426</PRIMARY_ID>
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          <READ_SPEC>
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      <EXPERIMENT_ATTRIBUTE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707009</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D30_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706427</PRIMARY_ID>
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        </IDENTIFIERS>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707010</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D31_PE150_Original</SUBMITTER_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <EXTERNAL_ID namespace="BioSample">SAMN03023547</EXTERNAL_ID>
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            <READ_CLASS>Application Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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  <EXPERIMENT accession="SRX707011" center_name="University of Utah" alias="s1Ab_PE150_Original">
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      <PRIMARY_ID>SRX707011</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s1Ab_PE150_Original</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank bottom with 4dpf fish: Sample s1Ab</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023563</EXTERNAL_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707012</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s1Bb_PE150_Original</SUBMITTER_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706430</PRIMARY_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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            <READ_CLASS>Application Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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  <EXPERIMENT accession="SRX707013" center_name="University of Utah" alias="s1Cb_PE150_Original">
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      <PRIMARY_ID>SRX707013</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s1Cb_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023565</EXTERNAL_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Primer</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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  </EXPERIMENT>
  <EXPERIMENT accession="SRX707014" center_name="University of Utah" alias="s1Db_PE150_Original">
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      <PRIMARY_ID>SRX707014</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <PRIMARY_ID>SRX707015</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s2Ab_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707016</PRIMARY_ID>
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      <PRIMARY_ID>SRX707018</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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        <TAG>16S forward primer</TAG>
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  </EXPERIMENT>
  <EXPERIMENT accession="SRX707021" center_name="University of Utah" alias="s6Db_PE150_Original">
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      <PRIMARY_ID>SRX707021</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <PRIMARY_ID>SRX707022</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w0EM1_PE150_Original</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX707023</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <PRIMARY_ID>SRX707024</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX707026</PRIMARY_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX707036</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706454</PRIMARY_ID>
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          <READ_SPEC>
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            <READ_CLASS>Technical Read</READ_CLASS>
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          <READ_SPEC>
            <READ_INDEX>3</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707037</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">f2.1_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf food sample: Sample f2.1</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706251</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707038</PRIMARY_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf food sample: Sample f2.2</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707039</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706303</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707040</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">f6.1_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707041</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707042</PRIMARY_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf food sample: Sample f6.3</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707043</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g0F_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 320dpf adult female parent intestine: Sample g0F</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706307">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g0F_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707044" center_name="University of Utah" alias="g0M_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707044</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g0M_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 320dpf adult male parent intestine: Sample g0M</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706309">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g0M_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707045" center_name="University of Utah" alias="g1A1_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707045</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A1_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A1</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706310">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1A1_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707046" center_name="University of Utah" alias="g1A2_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707046</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A2_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A2</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706311">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1A2_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707047" center_name="University of Utah" alias="g1A3_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707047</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A3_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A3</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706313">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1A3_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707048" center_name="University of Utah" alias="g1A4_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707048</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A4_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A4</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706319">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1A4_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707049" center_name="University of Utah" alias="g1A5_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707049</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1A5_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1A5</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706318">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1A5_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707050" center_name="University of Utah" alias="g1B1_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707050</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1B1_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1B1</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706316">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1B1_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707051" center_name="University of Utah" alias="g1B2_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707051</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1B2_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1B2</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706312">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1B2_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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            <READ_CLASS>Application Read</READ_CLASS>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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      <PRIMARY_ID>SRX707052</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1B3_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706315</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707053</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1B4_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706314</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
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            <READ_TYPE>Reverse</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707054</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1B5_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1B5</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023437</EXTERNAL_ID>
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        <LIBRARY_NAME>g1B5_PE150_Reseq</LIBRARY_NAME>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707055</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1C1_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1C1</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706320</PRIMARY_ID>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707056</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1C2_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1C2</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023439</EXTERNAL_ID>
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            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707057</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1C3_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706322</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707058</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1C4_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706321</PRIMARY_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707059</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1C5_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1C5</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023442</EXTERNAL_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_INDEX>0</READ_INDEX>
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            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707060" center_name="University of Utah" alias="g1D1_PE150_Reseq">
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      <PRIMARY_ID>SRX707060</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D1_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1D1</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706328">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023443</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g1D1_PE150_Reseq</LIBRARY_NAME>
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          <PAIRED/>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX707061</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D2_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1D2</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706324">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023444</EXTERNAL_ID>
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        <LIBRARY_NAME>g1D2_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707062" center_name="University of Utah" alias="g1D3_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707062</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D3_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1D3</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706325">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023445</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g1D3_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
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          <PAIRED/>
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      <SPOT_DESCRIPTOR>
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            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707063" center_name="University of Utah" alias="g1D4_PE150_Reseq">
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      <PRIMARY_ID>SRX707063</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D4_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1D4</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706333">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023446</EXTERNAL_ID>
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        <LIBRARY_NAME>g1D4_PE150_Reseq</LIBRARY_NAME>
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      <SPOT_DESCRIPTOR>
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            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX707064</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g1D5_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 4dpf intestine: Sample g1D5</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706327">
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          <EXTERNAL_ID namespace="BioSample">SAMN03023447</EXTERNAL_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707065</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A10_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2A10</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023448</EXTERNAL_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707066</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A6_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2A6</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706331</PRIMARY_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707067</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A7_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2A7</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023450</EXTERNAL_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707068</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A8_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2A8</TITLE>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707069</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2A9_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2A9</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706335</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707070</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2B10_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2B10</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023453</EXTERNAL_ID>
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        <LIBRARY_NAME>g2B10_PE150_Reseq</LIBRARY_NAME>
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            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707071</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2B6_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2B6</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707072</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2B7_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2B7</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707073</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2B8_PE150_Reseq</SUBMITTER_ID>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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          <READ_SPEC>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707074</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2B9_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707075</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2C10_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2C10</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706342</PRIMARY_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707076</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2C6_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2C6</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023459</EXTERNAL_ID>
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        <LIBRARY_NAME>g2C6_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707077" center_name="University of Utah" alias="g2C7_PE150_Reseq">
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      <PRIMARY_ID>SRX707077</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2C7_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2C7</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706343">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023460</EXTERNAL_ID>
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            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707078</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2C8_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2C8</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706341</PRIMARY_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707079</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2C9_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2C9</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023462</EXTERNAL_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707080</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D10_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2D10</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707081</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D6_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2D6</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707082</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D7_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2D7</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707083</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D8_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2D8</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707084</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2D9_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2D9</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706347</PRIMARY_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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      <PRIMARY_ID>SRX707085</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A11_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3A11</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706351">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023468</EXTERNAL_ID>
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        <LIBRARY_NAME>g3A11_PE150_Reseq</LIBRARY_NAME>
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            <READ_INDEX>1</READ_INDEX>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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      <PRIMARY_ID>SRX707086</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A12_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3A12</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023469</EXTERNAL_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707087</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A13_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3A13</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023470</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3A13_PE150_Reseq</LIBRARY_NAME>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707088</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A14_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3A14</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023471</EXTERNAL_ID>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707089</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A15_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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          <EXTERNAL_ID namespace="BioSample">SAMN03023472</EXTERNAL_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707090</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3B11_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707091</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3B12_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707092</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3B13_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3B13</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023475</EXTERNAL_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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            <READ_INDEX>0</READ_INDEX>
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            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707093</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3B14_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3B14</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706357">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023476</EXTERNAL_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>g3B14_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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            <BASE_COORD>146</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707094" center_name="University of Utah" alias="g3B15_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707094</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3B15_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3B15</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706360">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023477</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3B15_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707095" center_name="University of Utah" alias="g3C11_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707095</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3C11_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3C11</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706359">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3C11_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
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            <READ_INDEX>0</READ_INDEX>
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            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707096" center_name="University of Utah" alias="g3C12_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707096</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3C12_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3C12</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706363">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3C12_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
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      <SPOT_DESCRIPTOR>
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            <READ_INDEX>0</READ_INDEX>
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            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX707097</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3C13_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3C13</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706361">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023480</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3C13_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707098" center_name="University of Utah" alias="g3C14_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707098</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3C14_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3C14</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706366">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023481</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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        </SPOT_DECODE_SPEC>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX707099</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3C15_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3C15</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023482</EXTERNAL_ID>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX707100</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3D12_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3D12</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706362">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023483</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3D12_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707101" center_name="University of Utah" alias="g3D13_PE150_Reseq">
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      <PRIMARY_ID>SRX707101</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3D13_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3D13</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706367">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3D13_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707102" center_name="University of Utah" alias="g3D14_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707102</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3D14_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3D14</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706368">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3D14_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707103" center_name="University of Utah" alias="g3D15_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707103</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3D15_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3D15</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706365">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3D15_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707104" center_name="University of Utah" alias="g4A16_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707104</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A16_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A16</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706369">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4A16_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707105" center_name="University of Utah" alias="g4A17_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707105</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A17_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A17</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706371">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4A17_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707106" center_name="University of Utah" alias="g4A18_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707106</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A18_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A18</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706370">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4A18_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707107" center_name="University of Utah" alias="g4A19_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707107</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A19_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A19</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706372">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4A19_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707108" center_name="University of Utah" alias="g4A20_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707108</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A20_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A20</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706375">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4A20_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707109" center_name="University of Utah" alias="g4B17_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707109</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B17_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B17</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706373">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B17_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707110" center_name="University of Utah" alias="g4B18_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707110</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B18_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B18</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706374">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023493</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B18_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707111" center_name="University of Utah" alias="g4B19_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707111</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B19_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B19</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706376">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B19_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707112" center_name="University of Utah" alias="g4B20_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707112</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B20_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B20</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706379">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B20_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707113" center_name="University of Utah" alias="g4C16_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707113</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4C16_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4C16</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706378">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4C16_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707114" center_name="University of Utah" alias="g4C17_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707114</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4C17_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4C17</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706377">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4C17_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707115" center_name="University of Utah" alias="g4C18_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707115</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4C18_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4C18</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706380">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023498</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4C18_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707116" center_name="University of Utah" alias="g4C19_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707116</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4C19_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4C19</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706382">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4C19_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707117" center_name="University of Utah" alias="g4C20_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707117</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4C20_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4C20</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4C20_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707118" center_name="University of Utah" alias="g4D16_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707118</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D16_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D16</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706383">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>g4D16_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707119" center_name="University of Utah" alias="g4D17_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707119</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D17_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D17</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706384">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D17_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707120" center_name="University of Utah" alias="g4D18_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707120</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D18_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D18</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706385">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D18_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707121" center_name="University of Utah" alias="g4D19_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707121</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D19_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D19</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706388">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D19_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707122" center_name="University of Utah" alias="g4D20_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707122</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D20_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D20</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706386">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D20_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707123" center_name="University of Utah" alias="g5A22_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707123</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5A22_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5A22</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706389">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5A22_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707124" center_name="University of Utah" alias="g5A23_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707124</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5A23_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5A23</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706390">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5A23_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707125" center_name="University of Utah" alias="g5A25_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707125</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5A25_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5A25</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5A25_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707126" center_name="University of Utah" alias="g5B21_PE150_Reseq">
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      <PRIMARY_ID>SRX707126</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5B21_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5B21</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707127</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706392</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707128</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5B23_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023512</EXTERNAL_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707129</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5B24_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX707130</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707132</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C22_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707133</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C23_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707134</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C24_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707135" center_name="University of Utah" alias="g5C25_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707135</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5C25_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5C25</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706400">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5C25_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707136" center_name="University of Utah" alias="g5D21_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707136</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D21_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D21</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706401">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5D21_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707137" center_name="University of Utah" alias="g5D22_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707137</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D22_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D22</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706402">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5D22_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707138" center_name="University of Utah" alias="g5D23_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707138</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D23_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D23</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706405">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5D23_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707139" center_name="University of Utah" alias="g5D24_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707139</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D24_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D24</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706404">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5D24_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707140" center_name="University of Utah" alias="g5D25_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707140</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5D25_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5D25</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706403">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5D25_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707141" center_name="University of Utah" alias="g6A26_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707141</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A26_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6A26</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706409">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6A26_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707142" center_name="University of Utah" alias="g6A27_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707142</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A27_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6A27</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706406">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6A27_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
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    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707143</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A28_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707144</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A29_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS706410</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
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        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707145</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A30_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706408</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707146</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6A31_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6A31</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706412</PRIMARY_ID>
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          <READ_SPEC>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707147</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6B26_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706415</PRIMARY_ID>
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            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707148</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6B27_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6B27</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707149</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6B28_PE150_Reseq</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707150</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6B29_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6B29</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707151</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6B30_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6B30</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>g6B30_PE150_Reseq</LIBRARY_NAME>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707152" center_name="University of Utah" alias="g6B31_PE150_Reseq">
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      <PRIMARY_ID>SRX707152</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6B31_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6B31</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023536</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6B31_PE150_Reseq</LIBRARY_NAME>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707153" center_name="University of Utah" alias="g6C26_PE150_Reseq">
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      <PRIMARY_ID>SRX707153</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C26_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C26</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706418">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023537</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C26_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707154" center_name="University of Utah" alias="g6C27_PE150_Reseq">
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      <PRIMARY_ID>SRX707154</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C27_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C27</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706422">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023538</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C27_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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            <READ_TYPE>Forward</READ_TYPE>
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          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX707155</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C28_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C28</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706420">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023539</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C28_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707156</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C29_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C29</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706423">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023540</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C29_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707157</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C30_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C30</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706419">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023541</EXTERNAL_ID>
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        <LIBRARY_NAME>g6C30_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707158" center_name="University of Utah" alias="g6D26_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707158</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D26_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D26</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706421">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023542</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6D26_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707159" center_name="University of Utah" alias="g6D27_PE150_Reseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707159</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D27_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D27</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706425">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023543</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6D27_PE150_Reseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707160" center_name="University of Utah" alias="g6D28_PE150_Reseq">
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      <PRIMARY_ID>SRX707160</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D28_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D28</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023544</EXTERNAL_ID>
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        <LIBRARY_NAME>g6D28_PE150_Reseq</LIBRARY_NAME>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707161</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D29_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D29</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706426</PRIMARY_ID>
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        <LIBRARY_NAME>g6D29_PE150_Reseq</LIBRARY_NAME>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      </SPOT_DESCRIPTOR>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707162</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D30_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D30</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023546</EXTERNAL_ID>
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        <LIBRARY_NAME>g6D30_PE150_Reseq</LIBRARY_NAME>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707163" center_name="University of Utah" alias="g6D31_PE150_Reseq">
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      <PRIMARY_ID>SRX707163</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D31_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D31</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023547</EXTERNAL_ID>
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        <LIBRARY_NAME>g6D31_PE150_Reseq</LIBRARY_NAME>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707164</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s1Ab_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank bottom with 4dpf fish: Sample s1Ab</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023563</EXTERNAL_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707165</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s1Bb_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank bottom with 4dpf fish: Sample s1Bb</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023564</EXTERNAL_ID>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707166</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s1Cb_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank bottom with 4dpf fish: Sample s1Cb</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706432</PRIMARY_ID>
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      <SPOT_DESCRIPTOR>
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            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
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      <PRIMARY_ID>SRX707167</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">s1Db_PE150_Reseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank bottom with 4dpf fish: Sample s1Db</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023566</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      <EXPERIMENT_ATTRIBUTE>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX707177</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX707178</PRIMARY_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX707179</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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        <TAG>16S forward primer</TAG>
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      <PRIMARY_ID>SRX707180</PRIMARY_ID>
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            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707185" center_name="University of Utah" alias="w2C_PE150_Reseq">
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      <PRIMARY_ID>SRX707185</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w2C_PE150_Reseq</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank water with 10dpf fish: Sample w2C</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706450</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707186</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w2D_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706451</PRIMARY_ID>
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        <LIBRARY_NAME>w2D_PE150_Reseq</LIBRARY_NAME>
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            <READ_INDEX>1</READ_INDEX>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707187</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w6A_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707188</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w6B_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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      <PRIMARY_ID>SRX707189</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w6C_PE150_Reseq</SUBMITTER_ID>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707190</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">f6.1_PE150_Seq3</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf food sample: Sample f6.1</TITLE>
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        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023582</EXTERNAL_ID>
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          <READ_SPEC>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>SRX707191</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g0M_PE150_Seq3</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 320dpf adult male parent intestine: Sample g0M</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706309</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="SRX707192" center_name="University of Utah" alias="g2C9_PE150_Seq3">
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      <PRIMARY_ID>SRX707192</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g2C9_PE150_Seq3</SUBMITTER_ID>
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    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 10dpf intestine: Sample g2C9</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS706344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023462</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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      <SPOT_DESCRIPTOR>
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            <READ_INDEX>0</READ_INDEX>
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            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707193" center_name="University of Utah" alias="g3A13_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707193</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A13_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3A13</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706350">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3A13_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707194" center_name="University of Utah" alias="g3A14_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707194</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A14_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3A14</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706356">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3A14_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707195" center_name="University of Utah" alias="g3A15_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707195</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3A15_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3A15</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706352">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3A15_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707196" center_name="University of Utah" alias="g3C14_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707196</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3C14_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3C14</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706366">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3C14_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707197" center_name="University of Utah" alias="g3D12_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707197</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g3D12_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 21dpf intestine: Sample g3D12</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706362">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g3D12_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707198" center_name="University of Utah" alias="g4A20_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707198</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4A20_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4A20</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706375">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4A20_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707199" center_name="University of Utah" alias="g4B17_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707199</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B17_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B17</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706373">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B17_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707200" center_name="University of Utah" alias="g4B18_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707200</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B18_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B18</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706374">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023493</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B18_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707201" center_name="University of Utah" alias="g4B19_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707201</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B19_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B19</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706376">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B19_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707202" center_name="University of Utah" alias="g4B20_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707202</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4B20_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4B20</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706379">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4B20_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707203" center_name="University of Utah" alias="g4D19_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707203</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D19_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D19</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706388">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D19_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707204" center_name="University of Utah" alias="g4D20_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707204</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g4D20_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 28dpf intestine: Sample g4D20</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706386">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g4D20_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707205" center_name="University of Utah" alias="g5A22_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707205</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5A22_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5A22</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706389">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5A22_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707206" center_name="University of Utah" alias="g5A25_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707206</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g5A25_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 35dpf intestine: Sample g5A25</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706387">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g5A25_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707207" center_name="University of Utah" alias="g6C26_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707207</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C26_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C26</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706418">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023537</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C26_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707208" center_name="University of Utah" alias="g6C27_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707208</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C27_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C27</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706422">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023538</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C27_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707209" center_name="University of Utah" alias="g6C30_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707209</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6C30_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6C30</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706419">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023541</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6C30_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707210" center_name="University of Utah" alias="g6D26_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707210</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D26_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D26</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706421">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023542</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6D26_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707211" center_name="University of Utah" alias="g6D31_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707211</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g6D31_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 75dpf intestine: Sample g6D31</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706428">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023547</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g6D31_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707212" center_name="University of Utah" alias="g9B2_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707212</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9B2_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9B2</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706457">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9B2_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707213" center_name="University of Utah" alias="g9B3_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707213</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9B3_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9B3</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706456">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9B3_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707214" center_name="University of Utah" alias="g9B4_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707214</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9B4_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9B4</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706455">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9B4_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707215" center_name="University of Utah" alias="g9B5_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707215</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9B5_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9B5</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706459">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9B5_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707216" center_name="University of Utah" alias="g9B6_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707216</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9B6_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9B6</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706462">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9B6_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707217" center_name="University of Utah" alias="g9C1_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707217</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9C1_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9C1</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706461">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706461</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9C1_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707218" center_name="University of Utah" alias="g9C3_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707218</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9C3_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9C3</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706458">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9C3_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707219" center_name="University of Utah" alias="g9C4_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707219</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9C4_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9C4</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706460">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023555</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9C4_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707220" center_name="University of Utah" alias="g9C5_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707220</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9C5_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9C5</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706467">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023556</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9C5_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707221" center_name="University of Utah" alias="g9C6_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707221</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9C6_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9C6</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706464">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023557</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9C6_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707222" center_name="University of Utah" alias="g9D1_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707222</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9D1_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9D1</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706466">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023558</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9D1_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707223" center_name="University of Utah" alias="g9D2_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707223</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9D2_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9D2</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706463">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023559</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9D2_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707224" center_name="University of Utah" alias="g9D4_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707224</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9D4_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9D4</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706465">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023560</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9D4_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707225" center_name="University of Utah" alias="g9D5_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707225</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9D5_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9D5</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706468">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023561</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9D5_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707226" center_name="University of Utah" alias="g9D6_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707226</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">g9D6_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: 380dpf intestine: Sample g9D6</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706469">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023562</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>g9D6_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
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            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707227" center_name="University of Utah" alias="w6A_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707227</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w6A_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank water with 75dpf fish: Sample w6A</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706452">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>w6A_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707228" center_name="University of Utah" alias="w6B_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707228</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w6B_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank water with 75dpf fish: Sample w6B</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706453">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>w6B_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX707229" center_name="University of Utah" alias="w6C_PE150_Seq3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX707229</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Utah">w6C_PE150_Seq3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene sequencing of Zebrafish gut microbiota: Tank water with 75dpf fish: Sample w6C</TITLE>
    <STUDY_REF accession="SRP047327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP047327</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA260461</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>2 rounds of PCR from template was used to amplify the 16S rRNA gene and add Illumina adapter sequences and dual-indexed barcodes.  Barcodes removed from SRA submission, while primer sequences targeting 16S remain.  NOTE: Read 1 is from "reverse" primer relative to 16S rRNA gene, while read 2 is from "forward" direction of 16S.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS706454">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS706454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03023590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>w6C_PE150_Seq3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>290</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>146</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S reverse primer</TAG>
        <VALUE>TACNVGGGTATCTAATCC</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>16S forward primer</TAG>
        <VALUE>GTGCCAGCMGCCGCGG</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
