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Whole-genome sequencing expands the mutational spectrum of autism with novel genes, causative CNVs and chromosomal rearrangements

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).

INSTRUMENT(S): Illumina HiSeq 2000

ORGANISM(S): Homo Sapiens

SUBMITTER: Wenzhou Medical University

PROVIDER: PRJEB14713 | EVA | 2016-07-06

REPOSITORIES: EVA

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