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    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4515807</PRIMARY_ID>
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        <LIBRARY_NAME>Nijm_AspF_V157-80</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550261" alias="Nijm_AspF_V157-60">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
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        <PRIMARY_ID>SRP189042</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515808</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-60</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>Nijm_AspF_V157-60</LIBRARY_NAME>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550262" alias="Nijm_AspF_V157-61">
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      <PRIMARY_ID>SRX5550262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-61</SUBMITTER_ID>
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    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515809</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-61</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V157-61</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550263" alias="Nijm_AspF_V157-62">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515810">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515810</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-62</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <LIBRARY_NAME>Nijm_AspF_V157-62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550264" alias="Nijm_AspF_V157-59">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515811">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515811</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-59</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V157-59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550265" alias="Nijm_AspF_V157-39">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515812">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515812</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-39</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V157-39</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550266" alias="Nijm_AspF_V157-40">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515813">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515813</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-40</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V157-40</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550267" alias="Nijm_AspF_V157-47">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515814">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515814</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-47</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V157-47</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550268" alias="Nijm_AspF_V157-48">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V157-48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515815</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V157-48</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V157-48</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V130-15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515816</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V130-15</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V130-15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550270" alias="Nijm_AspF_V130-14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V130-14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515817">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515817</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V130-14</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V130-14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550271" alias="Nijm_AspF_V130-18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V130-18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515818">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515818</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V130-18</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V130-18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5550272" alias="Nijm_AspF_V130-54">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5550272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5344940">Nijm_AspF_V130-54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Raw whole genome sequence of Aspergillus fumigatus isolated from a patient.</TITLE>
    <STUDY_REF accession="SRP189042">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP189042</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5344940">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Fungal mass was suspended in TE buffer (pH 8, 1% SDS, 2% Triton X100, 100mM NaCl). The suspension was shaken for 30 min at 70 C. DNA was extracted using phenol/chloroform extraction and purified using the QIAamp DNA Blood Mini kit (Qiagen, Germany). A fragmented genomic DNA library was prepared using a Nextera XT DNA sample preparation kit (Illumina, USA). Subsequent sequencing was conducted in a paired end 2150 bp mode using an Illumina NextSeq 500 machine (Illumina, USA).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4515819">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4515819</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|eballard1234">V130-54</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Nijm_AspF_V130-54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
