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A Selection Operator for Summary Association Statistics Reveals Allelic Heterogeneity of Complex Traits.
Ning, Zheng; Lee, Youngjo; Joshi, Peter K; Wilson, James F; Pawitan, Yudi; Shen, Xia.
Afiliación
  • Ning Z; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Nobels väg 12A, SE-171 77 Stockholm, Sweden.
  • Lee Y; Department of Statistics, Seoul National University, Seoul 151747, South Korea.
  • Joshi PK; Center for Population Health Sciences, Usher Institute of Population Health Sciences and Informatics, Old Medical School, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, Scotland, United Kingdom.
  • Wilson JF; Center for Population Health Sciences, Usher Institute of Population Health Sciences and Informatics, Old Medical School, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, Scotland, United Kingdom; Medical Research Council Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine
  • Pawitan Y; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Nobels väg 12A, SE-171 77 Stockholm, Sweden.
  • Shen X; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Nobels väg 12A, SE-171 77 Stockholm, Sweden; Center for Population Health Sciences, Usher Institute of Population Health Sciences and Informatics, Old Medical School, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG
Am J Hum Genet ; 101(6): 903-912, 2017 Dec 07.
Article en En | MEDLINE | ID: mdl-29198721
ABSTRACT
In recent years, as a secondary analysis in genome-wide association studies (GWASs), conditional and joint multiple-SNP analysis (GCTA-COJO) has been successful in allowing the discovery of additional association signals within detected loci. This suggests that many loci mapped in GWASs harbor more than a single causal variant. In order to interpret the underlying mechanism regulating a complex trait of interest in each discovered locus, researchers must assess the magnitude of allelic heterogeneity within the locus. We developed a penalized selection operator for jointly analyzing multiple variants (SOJO) within each mapped locus on the basis of LASSO (least absolute shrinkage and selection operator) regression derived from summary association statistics. We found that, compared to stepwise conditional multiple-SNP analysis, SOJO provided better sensitivity and specificity in predicting the number of alleles associated with complex traits in each locus. SOJO suggested causal variants potentially missed by GCTA-COJO. Compared to using top variants from genome-wide significant loci in GWAS, using SOJO increased the proportion of variance prediction for height by 65% without additional discovery samples or additional loci in the genome. Our empirical results indicate that human height is not only a highly polygenic trait, but also has high allelic heterogeneity within its established hundreds of loci.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estatura / Herencia Multifactorial / Polimorfismo de Nucleótido Simple Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estatura / Herencia Multifactorial / Polimorfismo de Nucleótido Simple Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article País de afiliación: Suecia