<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="A10-A12" accession="SRX1042376">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1042376</PRIMARY_ID>
      <SUBMITTER_ID namespace="CEBAS-CSIC">A10-A12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>COM-C: Compost made of pepper sludge, pepper wastes, garlic wastes, carrot wastes and vineyard pruning wastes in a open-air pile</TITLE>
    <STUDY_REF accession="SRP058843">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP058843</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA283180</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Variable regions V1 (175 bpinsert), V3 (259 bp insert), V6 (168 bp insert) and V1-V2 (416 bp insert) of the prokaryotic 16S rRNA gene were amplified from gDNA obtained from the isolates. Variable regions ITS5-ITS2 (306 bp insert) and ITS3-ITS4 (385 bp insert) of the eukaryotic 18S rRNA gene were amplified from gDNA obtained from the isolates.  PCR amplification products were used to create a library using the Ion Plus Fragment Library Kit (Cat. No. 4471252) with sample indexing using the Ion Xpress™ Barcode Adapter 1-96 Kit. Template preparation was performed using the Ion OneTouch™ 2 System and the Ion PGM™ Template OT2 400 Kit (Cat. No. 4479878). Sequencing was performed using the Ion PGM™ Sequencing 400 Kit (Cat. No. 4482002) on the Ion PGM™ System using the Ion 318™ Chip v2 (Cat. No. 4484355) with all barcoded samples on a single chip. Primary data analysis was performed with Torrent Suite™ Software v4.0.2.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS948645">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS948645</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN03743440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>A10-A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>0</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>Adapter</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>5</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent PGM</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
