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Using genomic annotations increases statistical power to detect eGenes

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dc.contributor.authorDuong, Dat-
dc.contributor.authorZou, Jennifer-
dc.contributor.authorHormozdiari, Farhad-
dc.contributor.authorSul, Jae Hoon-
dc.contributor.authorErnst, Jason-
dc.contributor.authorHan, Buhm-
dc.contributor.authorEskin, Eleazar-
dc.date.accessioned2023-04-26T05:09:40Z-
dc.date.available2023-04-26T05:09:40Z-
dc.date.created2023-04-21-
dc.date.created2023-04-21-
dc.date.created2023-04-21-
dc.date.issued2016-06-
dc.identifier.citationBioinformatics, Vol.32 No.12, pp.156-163-
dc.identifier.issn1367-4803-
dc.identifier.urihttps://hdl.handle.net/10371/191581-
dc.description.abstractMotivation: Expression quantitative trait loci (eQTLs) are genetic variants that affect gene expression. In eQTL studies, one important task is to find eGenes or genes whose expressions are associated with at least one eQTL. The standard statistical method to determine whether a gene is an eGene requires association testing at all nearby variants and the permutation test to correct for multiple testing. The standard method however does not consider genomic annotation of the variants. In practice, variants near gene transcription start sites (TSSs) or certain histone modifications are likely to regulate gene expression. In this article, we introduce a novel eGene detection method that considers this empirical evidence and thereby increases the statistical power. Results: We applied our method to the liver Genotype-Tissue Expression (GTEx) data using distance from TSSs, DNase hypersensitivity sites, and six histone modifications as the genomic annotations for the variants. Each of these annotations helped us detected more candidate eGenes. Distance from TSS appears to be the most important annotation; specifically, using this annotation, our method discovered 50% more candidate eGenes than the standard permutation method.-
dc.language영어-
dc.publisherOxford University Press-
dc.titleUsing genomic annotations increases statistical power to detect eGenes-
dc.typeArticle-
dc.identifier.doi10.1093/bioinformatics/btw272-
dc.citation.journaltitleBioinformatics-
dc.identifier.wosid000379734300018-
dc.identifier.scopusid2-s2.0-84976491372-
dc.citation.endpage163-
dc.citation.number12-
dc.citation.startpage156-
dc.citation.volume32-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorHan, Buhm-
dc.type.docTypeArticle; Proceedings Paper-
dc.description.journalClass1-
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  • College of Medicine
  • Department of Medicine
Research Area Bioinformatics, Genomics, Statistical Genetics

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