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Shruti Paniwala1541 days ago
You can try the following --
1. gnomAD (https://gnomad.broadinstitute.org/)gnomAD v3, have 602M SNVs + 105M indels using whole-genome sequencing of 71,702 samples mapped to the GRCh38 build of the human reference genome.2. DiscoverEHR (http://www.discovehrshare.com/)exomes >50,000 MyCode® participants, have >4M rare SNV and indels
You can try the following --
1. gnomAD (https://gnomad.broadinstitute.org/)
gnomAD v3, have 602M SNVs + 105M indels using whole-genome sequencing of 71,702 samples mapped to the GRCh38 build of the human reference genome.
2. DiscoverEHR (http://www.discovehrshare.com/)
exomes >50,000 MyCode® participants, have >4M rare SNV and indels