<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX12775771" alias="Strain m25">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12775771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB10570303">Strain m25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Lutispora sp. strain m25</TITLE>
    <STUDY_REF accession="SRP343143">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP343143</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA772957</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Genomic DNA libraries are prepared using the Nextera XT Library Prep Kit (Illumina, San Diego, USA) following the manufacturers protocol with the following modifications: input DNA is increased 2-fold, and PCR elongation time is increased to 45 s. DNA quantification and library preparation are carried out on a Hamilton Microlab STAR automated liquid handling system (Hamilton Bonaduz AG, Switzerland). Pooled libraries are quantified using the Kapa Biosystems Library Quantification Kit for Illumina. Libraries are sequenced using Illumina sequencers (HiSeq/NovaSeq) using a 250bp paired end protocol.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS10721150">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10721150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN22425435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Strain m25</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
