<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX4717082" alias="H10Y">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H10Y</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Isochrysis sp. SAG 927-3</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802722">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802722</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H10Y_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H10Y</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717083" alias="H15Y">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H15Y</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Coccolithophora sp. SAG 912-1</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802723">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802723</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H15Y_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H15Y</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717084" alias="H01Y">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H01Y</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Prymnesium saltans SAG 18.97</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802724">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802724</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H01Y_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H01Y</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717085" alias="H02Y">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H02Y</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Apistonema sp. SAG 126.79</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802725">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802725</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H02Y_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H02Y</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717086" alias="C09C">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">C09C</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Cryptomonas baltica SAG 18.80</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802726">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802726</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">C09C_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C09C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717087" alias="C13C">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">C13C</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Pyrenomonas helgolandii SAG 28.87</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802727">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802727</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">C13C_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C13C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717088" alias="H07P">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H07P</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Diacronema lutheri SAG 926-1</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802728">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802728</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H07P_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H07P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717089" alias="H09Y">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H09Y</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Cricosphaera carterae SAG 944-1</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802729">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802729</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H09Y_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H09Y</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717090" alias="H03Y">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H03Y</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Prymnesium parvum SAG 127.79</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802730">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802730</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H03Y_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H03Y</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717091" alias="H05Y">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">H05Y</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Isochrysis sp. SAG 927-2</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802731">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802731</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">H05Y_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H05Y</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717092" alias="A01A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A01A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Chromera velia CCAP 1602/1</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802732">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802732</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A01A_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A01A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717093" alias="A02A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A02A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Chromera velia CCAP 1602/2</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802733">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802733</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A02A_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A02A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717094" alias="A03A">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A03A</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Vitrella brassicaformis CCMP 3155</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802734">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802734</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A03A_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A03A</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717095" alias="A06D">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A06D</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Amphidinium carterae SAG 37.80</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802737">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802737</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A06D_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A06D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717096" alias="A07D">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A07D</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Amphidinium klebsii SAG 36.80</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802735">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802735</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A07D_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A07D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717097" alias="A08D">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A08D</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Prorocentrum cassubicum SAG 40.80</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802736">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802736</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A08D_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A08D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717098" alias="A09D">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A09D</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Amphidinium hoefleri SAG 35.80</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802739">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802739</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A09D_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A09D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717099" alias="A11D">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A11D</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Prorocentrum micans SAG 2018</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802738">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802738</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A11D_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A11D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717100" alias="A13D">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">A13D</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Prorocentrum micans SAG 29.97</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802797">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802797</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">A13D_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A13D</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717101" alias="C05C">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">C05C</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Pyrenomonas salina SAG 2002</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802740">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802740</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">C05C_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>C05C</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717102" alias="S12B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">S12B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Stephanopyxis turris SAG 2019</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802741">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802741</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">S12B_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>S12B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717103" alias="S04B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">S04B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Navicula salinicola SAG 40.96</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802742">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802742</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">S04B_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>S04B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717104" alias="S03B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">S03B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Phaeodactylum tricornutum SAG 1090-1a</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802744">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802744</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">S03B_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>S03B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717105" alias="S02B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">S02B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Skeletonema marinoi SAG 19.99</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802743">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802743</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">S02B_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>S02B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4717106" alias="S01B">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4717106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4533189">S01B</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S rRNA gene amplicon based analysis of the bacterial community associated with Nitzschia frustulum SAG 1052-2</TITLE>
    <STUDY_REF accession="SRP162141">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP162141</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4533189">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Metagenomic DNA was extracted from algal culture. Subsequently the16S rRNA was amplified. All samples were amplified in triplicate purified and pooled in equal amounts. Sequences were determined using a 454 GS FLX Titanium (Roche).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3802745">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3802745</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|g2l_goettingen">S01B_16SrRNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>S01B</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <LS454>
        <INSTRUMENT_MODEL>454 GS FLX Titanium</INSTRUMENT_MODEL>
      </LS454>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
