<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY alias="WGS of autism trios" center_name="WENZHOU MEDICAL UNIVERSITY" broker_name="EBI" accession="ERP016377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERP016377</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject">PRJEB14713</EXTERNAL_ID>
      <SUBMITTER_ID namespace="WENZHOU MEDICAL UNIVERSITY">WGS of autism trios</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wenzhou Medical University">WGS of autism trios</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Whole-genome sequencing expands the mutational spectrum of autism with novel genes, causative CNVs and chromosomal rearrangements</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Identification of genomic variants from whole-genome sequencing dataset of 32 Chinese trios with autism, including de novo mutations (DNMs), inherited variants, copy number variants (CNVs) and genomic structural variants (SVs).</STUDY_ABSTRACT>
      <STUDY_DESCRIPTION>Identification of genomic variants from whole-genome sequencing dataset of 32 Chinese trios with autism, including de novo mutations (DNMs), inherited variants, copy number variants (CNVs) and genomic structural variants (SVs).</STUDY_DESCRIPTION>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
