Whole-genome deep-learning analysis reveals causal role of noncoding mutations in autism

Explore the predicted effects of 127,140 autism proband mutations from Simons Simplex Collection whole genome sequencing data.

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The use of Simons Simplex Collection (and Simons VIP) data sets is limited to projects related to advancing the field of autism and related developmental disorder research. Questions regarding content should be directed to `collections@sfari.org`.