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Gene- and pathway-based association tests for multiple traits with GWAS summary statistics

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dc.contributor.authorKwak, I.-Y.-
dc.contributor.authorPan, W.-
dc.date.accessioned2023-03-08T16:12:11Z-
dc.date.available2023-03-08T16:12:11Z-
dc.date.issued2017-
dc.identifier.issn1367-4803-
dc.identifier.issn1367-4811-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/64066-
dc.description.abstractTo identify novel genetic variants associated with complex traits and to shed new insights on underlying biology, in addition to the most popular single SNP-single trait association analysis, it would be useful to explore multiple correlated (intermediate) traits at the gene- or pathway-level by mining existing single GWAS or meta-analyzed GWAS data. For this purpose, we present an adaptive gene-based test and a pathway-based test for association analysis of multiple traits with GWAS summary statistics. The proposed tests are adaptive at both the SNP- and trait-levels; that is, they account for possibly varying association patterns (e.g. signal sparsity levels) across SNPs and traits, thus maintaining high power across a wide range of situations. Furthermore, the proposed methods are general: they can be applied to mixed types of traits, and to Z-statistics or P-values as summary statistics obtained from either a single GWAS or a meta-analysis of multiple GWAS. Our numerical studies with simulated and real data demonstrated the promising performance of the proposed methods. © The Author 2016. Published by Oxford University Press. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherOxford University Press-
dc.titleGene- and pathway-based association tests for multiple traits with GWAS summary statistics-
dc.typeArticle-
dc.identifier.doi10.1093/bioinformatics/btw577-
dc.identifier.bibliographicCitationBioinformatics, v.33, no.1, pp 64 - 71-
dc.description.isOpenAccessY-
dc.identifier.scopusid2-s2.0-85014858664-
dc.citation.endPage71-
dc.citation.number1-
dc.citation.startPage64-
dc.citation.titleBioinformatics-
dc.citation.volume33-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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