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One or more keywords matched the following properties of Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores.

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information resource reference LeMaster C, Schwendinger-Schreck C, Ge B, Cheung W, Johnston JJ, Pastinen T, Smail C. Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. medRxiv. 2024 Mar 18.
label Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores.

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  • Rare Diseases