<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX3872563" alias="HGM_200">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3872563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3862042">HGM_200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HGM</TITLE>
    <STUDY_REF accession="SRP136936">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP136936</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA257563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Ion Proton shotgun sequencing   for library preparation clean genomic DNA (aprox. 1000 ng) were fragmented by 200-300 bp using Covaris S220 System (Covaris, Woburn, Massachusetts, USA). After that, Ion Xpress  Plus Fragment Library Kit (Life Technologies) was employed for barcode shotgun-library sample preparation. Emulsion PCR was performed using the One Touch system (Life Technologies). Beads were prepared using the One Touch 2 and Template Kit v2 Sequencing was performed by using Ion Proton 200 sequencing kit v2 on the P1 Ion chip. Raw data has been uploaded to NCBI SRA database</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3113988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3113988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06018827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HGM_200</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3872564" alias="HGM_56">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3872564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3862042">HGM_56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Hir_TrueMate_5_6</TITLE>
    <STUDY_REF accession="SRP136936">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP136936</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA257563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Ion Torrent mate-pair sequencing - mate-pair library with 3-6Kb fragment was prepared from a sample genomic DNA with reagent kits Ion TrueMate Library Reagents (Life Technologies). To conduct emulsion PCR, the Ion PGM  template OT2 400 kit (Life Technologies) was utilised. Sequencing was performed in accordance with manufacturer protocol for the genome analyser Ion Torrent PGM (Life Technologies) using an Ion 318 chip and Ion PGM  sequencing 400 kit v2 (Life Technologies). For separation non-mate reads and spliting true mate reads we use script  matePairingSplitReads.py</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3113988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3113988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06018827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HGM_56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent PGM</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3872565" alias="HGM_812">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3872565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3862042">HGM_812</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Hir</TITLE>
    <STUDY_REF accession="SRP136936">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP136936</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA257563</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina mate-pair sequencing - mate-pair library with 8-12Kb fragment was prepared from a sample genomic DNA with reagent kits Nextera Mate Pair library Sample Prep kit (Illumina) and TruSeq DNA Sample Prep kit (Illumina) in the protocols, recommended by the manufacturer. Sample was sequenced on the MiSeq platform (Illumina) using a 2   150 cycle MiSeq V2 reagent kit, following standard Illumina sequencing protocols. Demultiplexing was performed using bcl2fastq v2.17.1.14 Conversion Software (Illumina). Adaptor sequences were removed from reads during demultiplexing. For trimming and separation of single-end, paired-end, mate-pair reads we used NxTrim</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3113988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3113988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06018827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HGM_812</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
