iHART Whole Genome Sequencing Data Set

Description

iHART is the Hartwell Foundation’s Autism Research and Technology Initiative. This release contains whole genome data from over 1000 families with 2 or more children with autism, of which biomaterials were provided by the Autism Genetic Resource Exchange (AGRE).

Update Frequency

The dataset may be updated with additional or corrected data on a need-to-update basis.

License

Data use is subject to the access and publication polices of the iHART. More information on terms of use is available at iHART website

Documentation

http://www.ihart.org/data

Contact

ihart2-org@stanford.edu

How to Cite

iHART Whole Genome Sequencing Data Set was accessed on DATE from https://registry.opendata.aws/ihart.

Usage Examples

Publications

• Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks by Ruzzo et al. (2020)