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Estimating the causal tissues for complex traits and diseases.
Ongen, Halit; Brown, Andrew A; Delaneau, Olivier; Panousis, Nikolaos I; Nica, Alexandra C; Dermitzakis, Emmanouil T.
Afiliación
  • Ongen H; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland.
  • Brown AA; Institute for Genetics and Genomics in Geneva (iGE3), University of Geneva, Geneva, Switzerland.
  • Delaneau O; Swiss Institute of Bioinformatics, Geneva, Switzerland.
  • Panousis NI; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland.
  • Nica AC; Institute for Genetics and Genomics in Geneva (iGE3), University of Geneva, Geneva, Switzerland.
  • Dermitzakis ET; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland.
Nat Genet ; 49(12): 1676-1683, 2017 Dec.
Article en En | MEDLINE | ID: mdl-29058715
ABSTRACT
How to interpret the biological causes underlying the predisposing markers identified through genome-wide association studies (GWAS) remains an open question. One direct and powerful way to assess the genetic causality behind GWAS is through analysis of expression quantitative trait loci (eQTLs). Here we describe a new approach to estimate the tissues behind the genetic causality of a variety of GWAS traits, using the cis-eQTLs in 44 tissues from the Genotype-Tissue Expression (GTEx) Consortium. We have adapted the regulatory trait concordance (RTC) score to measure the probability of eQTLs being active in multiple tissues and to calculate the probability that a GWAS-associated variant and an eQTL tag the same functional effect. By normalizing the GWAS-eQTL probabilities by the tissue-sharing estimates for eQTLs, we generate relative tissue-causality profiles for GWAS traits. Our approach not only implicates the gene likely mediating individual GWAS signals, but also highlights tissues where the genetic causality for an individual trait is likely manifested.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Perfilación de la Expresión Génica / Sitios de Carácter Cuantitativo / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Perfilación de la Expresión Génica / Sitios de Carácter Cuantitativo / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Suiza