<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX10904697" alias="28627">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10904697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9594187">28627</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Short read sequencing of gDNA from D. vanus Ben 133T culture</TITLE>
    <STUDY_REF accession="SRP320034">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP320034</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA635277</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA Library preparation was performed using a modified version of the Illumina TruSeq DNA Sample Preparation protocol. We then performed a MiSeq sequencing run with a read length of 301 bp (paired--end) or a HiSeq2500 sequencing run with a read length of 251 bp (paired-end) as specified above.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8996854">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8996854</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|akrithika">DVBen114T_gDNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>28627</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX10904698" alias="DVBen114T_gDNA_MinION">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10904698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB9594187">DVBen114T_gDNA_MinION</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>MinION sequencing of gDNA from D. vanus Ben 133T culture</TITLE>
    <STUDY_REF accession="SRP320034">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP320034</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA635277</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Nanopore sequencing was performed on a MinION Mk1B instrument (Oxford Nanopore Technologies) using a SpotON FLO MIN106 flowcells and R9.4 chemistry. Data acquisition was performed using MinKNOW software, without live basecalling, running on a HP ProDesk 600G2 computer (64--bit, 16 GB RAM, 2 Tb SSD HD; Windows 10).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS8996854">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8996854</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|akrithika">DVBen114T_gDNA</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DVBen114T_gDNA_MinION</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <OXFORD_NANOPORE>
        <INSTRUMENT_MODEL>MinION</INSTRUMENT_MODEL>
      </OXFORD_NANOPORE>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
