Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk

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 on consents should be directed to collections@sfari.org.


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