Whole-genome sequencing expands the mutational spectrum of autism with novel genes, causative CNVs and chromosomal rearrangements
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https://www.omicsdi.org/dataset/eva/PRJEB14713
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资源简介：
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).
创建时间：
2016-07-06
