<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18290326" alias="BFNZWZ">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18290326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12260811">BFNZWZ</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitochondrion-Seq of Gonatopsis borealis musculsu: carcass</TITLE>
    <STUDY_REF accession="SRP408327">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408327</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12260811">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>1. With 1  G DNA initial quantity database;2. Covaris M220 ultrasound breaks DNA to 300~500bp;3. Leveling, adding A at 3 'end, and connecting index connector (TruSeq  Nano DNA Sample Prep Kit4. The library was enriched and 8 cycles were amplified by PCR;5. 2% agar gel to recover the target band (Certified Low Range Ultra Agarose);6. TBS380 (Picogreen) is quantitative, and the computer is mixed according to the data proportion;7. Carry out bridge PCR amplification on cBot solid phase carrier to generate clusters;8. Illumina NovaSeq sequencing platform for 2 * 150bp sequencing</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS15781975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15781975</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|dabai@orcid">Gonatopsis borealis</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>BFNZWZ</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 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
