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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX1736919" alias="P1_bacteria_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P1_bacteria_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>seq_bacteria_digester_341F-785R_P1_forward</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425539">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425539</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P1_bacteria_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1736920" alias="P2_bacteria_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P2_bacteria_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>seq_bacteria_digester_341F-785R_P2_forward</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425540">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425540</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915196</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P2_bacteria_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1736921" alias="P3_bacteria_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P3_bacteria_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>seq_bacteria_digester_341F-785R_P3_forward</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425541">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425541</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P3_bacteria_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1736922" alias="P4_bacteria_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P4_bacteria_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>seq_bacteria_digester_341F-785R_P4_forward</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425542">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425542</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P4_bacteria_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1736923" alias="P1_archaea_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P1_archaea_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P1_for</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425543">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425543</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P1_archaea_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1736924" alias="P2_archaea_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P2_archaea_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P2_for</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425544">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425544</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P2_archaea_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1736925" alias="P3_archaea_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P3_archaea_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P3_for</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425545">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425545</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P3_archaea_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1736926" alias="P4_archaea_forward">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1736926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">P4_archaea_forward</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P4_for</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425546">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425546</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P4_archaea_forward</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1747482" alias="archaea_reverse_P2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1747482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">archaea_reverse_P2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P2_rev</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425568">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425568</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>archaea_reverse_P2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1747483" alias="archaea_reverse_P3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1747483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">archaea_reverse_P3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P3_rev</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425569">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425569</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>archaea_reverse_P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1747484" alias="archaea_reverse_P4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1747484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">archaea_reverse_P4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P4_rev</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425570">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425570</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>archaea_reverse_P4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1747485" alias="archaea_reverse_P1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1747485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1489630">archaea_reverse_P1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>archaea-A340F-A915R__P1_rev</TITLE>
    <STUDY_REF accession="SRP074185">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP074185</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA318563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>About 20 ng of the amplicated sequences of each sample were pooled. For samples with low DNA yield up to 5 cycles were added. Ampliconpools were cleaned using Ampurebeads (Agencourt). Protein elimination and amplicon concentration were eliminated using MiElute columns (Qiagen). About 100 ng purified amplicons were used for the construction of the Illumina library using the Rapid DR Multiplex System 1-96 kit (NuGEN). Illumina librarys were size selected and sequenced using Illumina MiSeq Reagent Kits v3.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1425571">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1425571</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04915203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>archaea_reverse_P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
