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Article: Improved estimation of functional enrichment in SNP heritability using feasible generalized least squares

TitleImproved estimation of functional enrichment in SNP heritability using feasible generalized least squares
Authors
Keywordscomplex human traits
functional enrichment
generalized LD score regression
GWAS summary statistics
partition heritability
Issue Date11-Apr-2024
PublisherElsevier
Citation
Human Genetics and Genomics Advances, 2024, v. 5, n. 2 How to Cite?
AbstractFunctional enrichment results typically implicate tissue or cell-type-specific biological pathways in disease pathogenesis and as therapeutic targets. We propose generalized linkage disequilibrium score regression (g-LDSC) that requires only genome-wide association studies (GWASs) summary-level data to estimate functional enrichment. The method adopts the same assumptions and regression model formulation as stratified linkage disequilibrium score regression (s-LDSC). Although s-LDSC only partially uses LD information, our method uses the whole LD matrix, which accounts for possible correlated error structure via a feasible generalized least-squares estimation. We demonstrate through simulation studies under various scenarios that g-LDSC provides more precise estimates of functional enrichment than s-LDSC, regardless of model misspecification. In an application to GWAS summary statistics of 15 traits from the UK Biobank, estimates of functional enrichment using g-LDSC were lower and more realistic than those obtained from s-LDSC. In addition, g-LDSC detected more significantly enriched functional annotations among 24 functional annotations for the 15 traits than s-LDSC (118 vs. 51).
Persistent Identifierhttp://hdl.handle.net/10722/345769

 

DC FieldValueLanguage
dc.contributor.authorXiong, Zewei-
dc.contributor.authorThach, Thuan Quoc-
dc.contributor.authorZhang, Yan Dora-
dc.contributor.authorSham, Pak Chung-
dc.date.accessioned2024-08-28T07:40:35Z-
dc.date.available2024-08-28T07:40:35Z-
dc.date.issued2024-04-11-
dc.identifier.citationHuman Genetics and Genomics Advances, 2024, v. 5, n. 2-
dc.identifier.urihttp://hdl.handle.net/10722/345769-
dc.description.abstractFunctional enrichment results typically implicate tissue or cell-type-specific biological pathways in disease pathogenesis and as therapeutic targets. We propose generalized linkage disequilibrium score regression (g-LDSC) that requires only genome-wide association studies (GWASs) summary-level data to estimate functional enrichment. The method adopts the same assumptions and regression model formulation as stratified linkage disequilibrium score regression (s-LDSC). Although s-LDSC only partially uses LD information, our method uses the whole LD matrix, which accounts for possible correlated error structure via a feasible generalized least-squares estimation. We demonstrate through simulation studies under various scenarios that g-LDSC provides more precise estimates of functional enrichment than s-LDSC, regardless of model misspecification. In an application to GWAS summary statistics of 15 traits from the UK Biobank, estimates of functional enrichment using g-LDSC were lower and more realistic than those obtained from s-LDSC. In addition, g-LDSC detected more significantly enriched functional annotations among 24 functional annotations for the 15 traits than s-LDSC (118 vs. 51).-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofHuman Genetics and Genomics Advances-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcomplex human traits-
dc.subjectfunctional enrichment-
dc.subjectgeneralized LD score regression-
dc.subjectGWAS summary statistics-
dc.subjectpartition heritability-
dc.titleImproved estimation of functional enrichment in SNP heritability using feasible generalized least squares-
dc.typeArticle-
dc.identifier.doi10.1016/j.xhgg.2024.100272-
dc.identifier.pmid38327050-
dc.identifier.scopuseid_2-s2.0-85185821870-
dc.identifier.volume5-
dc.identifier.issue2-
dc.identifier.eissn2666-2477-
dc.identifier.issnl2666-2477-

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