<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX23826647" alias="Not provided">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX23826647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14164074">Not provided</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>mitogenome of Vulpes rueppellii</TITLE>
    <STUDY_REF accession="SRP493174">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP493174</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14164074">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA was randomly sheared into short fragments, size selected to ca. 350 base pairs (bp), A-tailed, ligated to Illumina adapters (5'-AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCGTAT-CATT-3' and 5'-GATCGGAAGAGCACACGTCTGAACTCCAGTCACGGATGACTATC-TCGTATGCCGTCTTCTGCTTG-3'), PCR-amplified, and purified. After subsequent quantification and checks for fragment size distribution using Qubit, real-time PCR and a bioanalyzer, the library was sequenced on an Illumina Novaseq instrument using paired-end reads (2x 151 bp).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS20648725">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS20648725</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|alibasuony">375</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Not provided</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</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 NovaSeq X</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
