autism spectrum disorder bam genetic genomic life sciences vcf whole genome sequencing
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).
The dataset may be updated with additional or corrected data on a need-to-update basis.
Data use is subject to the access and publication polices of the iHART. More information on terms of use is available at iHART website
See all datasets managed by Stanford University.
iHART Whole Genome Sequencing Data Set was accessed on DATE
from https://registry.opendata.aws/ihart.
arn:aws:s3:::ihart-release
us-east-1
arn:aws:s3:::ihart-main
us-east-1
arn:aws:s3:::ihart-hg38
us-east-1
arn:aws:s3:::ihart-psp
us-east-1
arn:aws:s3:::ihart-brain
us-east-1