<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX2930851" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-1" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930851</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930852" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-2" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930852</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874271">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930853" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-3" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930853</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930854" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-4" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930854</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930855" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-5" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930855</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930856" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-6" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930856</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930857" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-7" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930857</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930858" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-8" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930858</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930859" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-9" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930859</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930860" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-10" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930860</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930861" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-11" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930861</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930862" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-12" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930862</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930863" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-13" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930863</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930864" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-14" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930864</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874283">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930865" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-15" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930865</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930866" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-16" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930866</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874285">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930867" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-17" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930867</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874286">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874286</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930868" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-18" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930868</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874287">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874287</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930869" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-19" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930869</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874288">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930870" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-20" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930870</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930871" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-21" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930871</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_25</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930872" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-22" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930872</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874291">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_26</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930873" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-23" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930873</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_27</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930874" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-24" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930874</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_28</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930875" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-25" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930875</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:625-25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_29</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930876" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-26" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930876</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_30</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930877" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-27" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930877</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_31</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930878" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-28" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930878</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874297">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_32</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930879" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-29" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930879</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_33</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930880" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-30" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930880</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_34</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930881" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-31" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930881</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_36</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930882" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-32" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930882</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_38</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930883" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-33" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930883</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_39</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930884" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-34" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930884</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_40</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930885" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-35" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930885</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_41</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930886" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-36" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930886</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_43</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930887" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-37" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930887</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_44</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930888" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-38" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930888</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_45</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930889" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-39" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930889</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_46</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930890" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-40" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930890</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_47</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930891" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-41" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930891</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_48</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930892" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-42" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930892</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_51</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930893" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-43" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930893</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_52</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930894" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-44" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930894</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_53</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930895" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-45" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930895</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930896" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-46" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930896</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_55</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930897" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-47" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930897</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930898" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-48" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930898</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874317">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_57</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930899" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-49" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930899</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_58</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930900" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-50" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930900</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930901" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-51" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930901</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_60</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930902" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-52" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930902</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930903" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-53" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930903</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_65</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930904" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-54" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930904</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_67</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930905" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-55" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930905</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_68</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930906" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-56" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930906</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_69</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930907" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-57" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930907</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:626-57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_70</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930908" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-58" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930908</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874327">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_71</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930909" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-59" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930909</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_73</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930910" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-60" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930910</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_74</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930911" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-61" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930911</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_75</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930912" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-62" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930912</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_76</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930913" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-63" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930913</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_77</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930914" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-64" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930914</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_78</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930915" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-65" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930915</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_79</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930916" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-66" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930916</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_80</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930917" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-67" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930917</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_81</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930918" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-68" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930918</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_82</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930919" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-69" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930919</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_83</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930920" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-70" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930920</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_84</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930921" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-71" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930921</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_85</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930922" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-72" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930922</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_86</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930923" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-73" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930923</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_87</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930924" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-74" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930924</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_90</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930925" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-75" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930925</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_92</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930926" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-76" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930926</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_93</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930927" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-77" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930927</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_94</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930928" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-78" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930928</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_95</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930929" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-79" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930929</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_96</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930930" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-80" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930930</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_97</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930931" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-81" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930931</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_98</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930932" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-82" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930932</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_99</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930933" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-83" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930933</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930934" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-84" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930934</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930935" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-85" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930935</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930936" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-86" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930936</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_103</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930937" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-87" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930937</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930938" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-88" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930938</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_105</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930939" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-89" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930939</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:627-89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_106</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930940" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-90" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930940</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063193</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_107</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930941" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-91" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930941</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_108</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930942" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-92" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930942</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_110</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930943" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-93" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930943</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063196</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_111</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930944" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-94" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930944</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_112</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930945" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-95" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930945</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930946" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-96" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930946</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063199</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930947" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-97" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930947</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930948" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-98" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930948</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930949" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-99" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930949</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930950" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-100" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930950</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_118</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930951" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-101" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930951</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_119</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930952" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-102" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930952</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_121</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930953" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-103" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930953</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_122</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930954" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-104" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930954</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_123</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930955" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-105" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930955</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930956" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-106" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930956</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_126</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930957" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-107" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930957</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_127</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930958" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-108" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930958</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_128</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930959" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-109" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930959</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063212</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_130</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930960" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-110" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930960</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_131</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930961" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-111" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930961</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063214</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_132</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930962" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-112" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930962</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_133</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930963" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-113" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930963</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_134</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930964" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-114" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930964</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_135</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930965" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-115" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930965</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_136</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930966" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-116" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930966</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930967" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-117" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930967</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063220</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_138</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930968" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-118" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930968</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063221</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_139</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930969" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-119" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930969</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063222</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_140</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930970" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-120" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930970</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_141</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930971" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-121" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930971</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:628-121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_143</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930972" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-122" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930972</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_144</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930973" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-123" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930973</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874392">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063226</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_146</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930974" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-124" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930974</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_147</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930975" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-125" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930975</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_148</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930976" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-126" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930976</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063229</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_150</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930977" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-127" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930977</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_151</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930978" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-128" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930978</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_152</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930979" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-129" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930979</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_153</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930980" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-130" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930980</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_155</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930981" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-131" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930981</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_156</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930982" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-132" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930982</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_157</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930983" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-133" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930983</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874402">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063236</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_158</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930984" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-134" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930984</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063237</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_159</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930985" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-135" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930985</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930986" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-136" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930986</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874405">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_162</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930987" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-137" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930987</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874406">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063240</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_163</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930988" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-138" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930988</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874407">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_164</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930989" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-139" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930989</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063242</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_165</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930990" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-140" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930990</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063243</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_166</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930991" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-141" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930991</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063244</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_167</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930992" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-142" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930992</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_168</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930993" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-143" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930993</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063246</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_169</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930994" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-144" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930994</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063247</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_170</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930995" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-145" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930995</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_171</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930996" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-146" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930996</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063249</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930997" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-147" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930997</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063250</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_173</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930998" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-148" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930998</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_174</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2930999" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-149" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2930999</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063252</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_175</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931000" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-150" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931000</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063253</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_176</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931001" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-151" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931001</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_177</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931002" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-152" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931002</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063255</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_178</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931003" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-153" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931003</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063256</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_179</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931004" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-154" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931004</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:629-154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_181</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931005" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-155" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931005</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_182</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931006" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-156" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931006</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_183</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931007" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-157" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931007</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_184</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931008" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-158" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931008</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_185</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931009" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-159" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931009</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_186</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931010" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-160" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931010</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_187</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931011" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-161" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931011</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_188</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931012" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-162" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931012</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_189</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931013" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-163" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931013</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_190</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931014" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-164" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931014</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063267</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_191</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931015" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-165" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931015</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_192</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931016" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-166" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931016</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_193</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931017" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-167" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931017</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_194</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931018" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-168" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931018</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_195</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931019" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-169" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931019</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063272</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_196</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931020" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-170" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931020</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_197</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931021" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-171" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931021</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_198</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931022" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-172" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931022</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874441">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_199</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931023" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-173" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931023</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_200</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931024" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-174" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931024</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874443">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063277</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_201</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931025" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-175" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931025</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874444">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_202</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931026" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-176" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931026</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063279</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_203</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931027" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-177" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931027</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874446">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063280</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_205</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931028" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-178" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931028</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874447">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_206</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931029" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-179" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931029</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874448">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_207</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931030" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-180" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931030</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874449">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_208</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931031" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-181" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931031</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063284</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_209</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931032" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-182" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931032</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_210</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931033" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-183" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931033</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_211</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931034" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-184" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931034</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874453">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_212</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931035" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-185" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931035</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874454">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063288</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_213</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931036" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-186" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931036</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063289</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_214</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931037" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-187" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931037</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:630-187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063290</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_215</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931038" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:631-188" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931038</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:631-188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_216</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX2931039" alias="ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:631-189" center_name="Institute of Population Genetics, Vetmeduni Vienna">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2931039</PRIMARY_ID>
      <SUBMITTER_ID namespace="Institute of Population Genetics, Vetmeduni Vienna">ena-EXPERIMENT-Institute of Population Genetics, Vetmeduni Vienna-21-11-2018-13:00:56:631-189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP111789">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP111789</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB29483</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Goal was to set up a mutliplexed library with mutliplex haplotypes which have then been extracted here.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS2874458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS2874458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5063292</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Dsim_Fl_BASE_Iso_217</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="260"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>150 ng start material, fragmented with Covaris S2, Library Prep Kit was NEBNext Ultra II DNA Library Prep Kit (E7645), with size selected via AMPure XP beads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
