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Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies.
Salehi Nowbandegani, Pouria; Wohns, Anthony Wilder; Ballard, Jenna L; Lander, Eric S; Bloemendal, Alex; Neale, Benjamin M; O'Connor, Luke J.
Afiliación
  • Salehi Nowbandegani P; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. psalehin@broadinstitute.org.
  • Wohns AW; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. psalehin@broadinstitute.org.
  • Ballard JL; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. awohns@broadinstitute.org.
  • Lander ES; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. awohns@broadinstitute.org.
  • Bloemendal A; Stanford University School of Medicine, Stanford, CA, USA. awohns@broadinstitute.org.
  • Neale BM; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • O'Connor LJ; Graduate Group in Genomics and Computational Biology, University of Pennsylvania, Philadelphia, PA, USA.
Nat Genet ; 55(9): 1494-1502, 2023 09.
Article en En | MEDLINE | ID: mdl-37640881
ABSTRACT
Linkage disequilibrium (LD) is the correlation among nearby genetic variants. In genetic association studies, LD is often modeled using large correlation matrices, but this approach is inefficient, especially in ancestrally diverse studies. In the present study, we introduce LD graphical models (LDGMs), which are an extremely sparse and efficient representation of LD. LDGMs are derived from genome-wide genealogies; statistical relationships among alleles in the LDGM correspond to genealogical relationships among haplotypes. We published LDGMs and ancestry-specific LDGM precision matrices for 18 million common variants (minor allele frequency >1%) in five ancestry groups, validated their accuracy and demonstrated order-of-magnitude improvements in runtime for commonly used LD matrix computations. We implemented an extremely fast multiancestry polygenic prediction method, BLUPx-ldgm, which performs better than a similar method based on the reference LD correlation matrix. LDGMs will enable sophisticated methods that scale to ancestrally diverse genetic association data across millions of variants and individuals.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Desequilibrio de Ligamiento Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Desequilibrio de Ligamiento Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos