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Refining Mendelian disease analysis via detection of clinically relevant repeat variants

assignment_turned_inproject14 Sep 2018(Started)-30 Jun 2022(Ended)Closed

Funder: National Institutes of HealthProject code: 1R01HG010149-01

Funded under: NATIONAL HUMAN GENOME RESEARCH INSTITUTE Funder Contribution: 570,000 USD

Refining Mendelian disease analysis via detection of clinically relevant repeat variants

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Refining Mendelian disease analysis via detection of clinically relevant repeat variants

Refining Mendelian disease analysis via detection of clinically relevant repeat variants

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