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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>SRX3637661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">CY.13</SUBMITTER_ID>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637663</PRIMARY_ID>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904098</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_02</SUBMITTER_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.01</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904099</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_01</SUBMITTER_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IB.18</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904100</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IB_18</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
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        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IB.17</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904104</PRIMARY_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637667</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637668</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637669</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX3637670</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637673</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.14</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904109</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_ST_14</SUBMITTER_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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      <PRIMARY_ID>SRX3637675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.11</SUBMITTER_ID>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.12</SUBMITTER_ID>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.17</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.18</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904113</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_ST_18</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
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        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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      <PRIMARY_ID>SRX3637679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904115</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_ST_15</SUBMITTER_ID>
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        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.16</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IB.15</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637682</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX3637683</PRIMARY_ID>
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      <PRIMARY_ID>SRX3637684</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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      <PRIMARY_ID>SRX3637685</PRIMARY_ID>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <PRIMARY_ID>SRX3637686</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637687</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904122</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IB_07</SUBMITTER_ID>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IB.08</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904123</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IB_08</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
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        </LIBRARY_LAYOUT>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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    </PLATFORM>
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      <PRIMARY_ID>SRX3637689</PRIMARY_ID>
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      <PRIMARY_ID>SRX3637690</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637691</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">CO.01</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904127</PRIMARY_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">AQ.12</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">AQ.11</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637695</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX3637696</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX3637698</PRIMARY_ID>
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      <PRIMARY_ID>SRX3637702</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904138</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_ST_01</SUBMITTER_ID>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.04</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.03</SUBMITTER_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.06</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904141</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_ST_06</SUBMITTER_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.05</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904142</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_ST_05</SUBMITTER_ID>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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    </PLATFORM>
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      <PRIMARY_ID>SRX3637707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.08</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904143</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_ST_08</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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    </PLATFORM>
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      <PRIMARY_ID>SRX3637708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.07</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS2904144</PRIMARY_ID>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.10</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">ST.09</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637711</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <PRIMARY_ID>SRX3637712</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX3637713</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637714</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_AQ_03</SUBMITTER_ID>
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    <PLATFORM>
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        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637715</PRIMARY_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904151</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_AQ_06</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX3637716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">AQ.05</SUBMITTER_ID>
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    <TITLE>sponge metagenome</TITLE>
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        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904152</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_AQ_05</SUBMITTER_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AQ.05</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="SRX3637717" alias="AQ.08">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">AQ.08</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904176">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904176</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_AQ_08</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AQ.08</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="SRX3637718" alias="AQ.07">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">AQ.07</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904153">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904153</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_AQ_07</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AQ.07</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="SRX3637719" alias="AQ.10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">AQ.10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904154">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904154</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_AQ_10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AQ.10</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="SRX3637720" alias="AQ.09">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">AQ.09</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904155">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904155</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_AQ_09</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AQ.09</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="SRX3637721" alias="IR.11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904156">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904156</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_11</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.11</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="SRX3637722" alias="IR.12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904157">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904157</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_12</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.12</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="SRX3637723" alias="IR.09">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.09</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904158">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904158</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_09</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.09</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="SRX3637724" alias="IR.10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904159">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904159</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.10</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="SRX3637725" alias="IR.15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904160">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904160</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_15</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.15</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="SRX3637726" alias="IR.16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904161">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904161</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_16</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.16</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="SRX3637727" alias="IR.13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904162">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904162</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_13</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.13</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="SRX3637728" alias="IR.14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904163">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904163</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_14</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.14</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="SRX3637729" alias="IR.17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904165">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904165</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_17</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>IR.17</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="SRX3637730" alias="IR.18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3637730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3594162">IR.18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>sponge metagenome</TITLE>
    <STUDY_REF accession="SRP131926">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131926</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA432116</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>The V1-V3 region of the 16S rRNA gene was amplified using primers 27F (Lane 1991) and 519R (Lane et al. 1993) and libraries were prepared with the Illumina TruSeq preparation protocol, followed by Illumina MiSeq 2 x300 bp sequencing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2904166">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2904166</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|bettinaglasl">SpongeMicrobiomeStability_IR_18</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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      <PRIMARY_ID>SRX3637731</PRIMARY_ID>
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