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A unifying framework for joint trait analysis under a non-infinitesimal model.
Johnson, Ruth; Shi, Huwenbo; Pasaniuc, Bogdan; Sankararaman, Sriram.
Affiliation
  • Johnson R; Department of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA.
  • Shi H; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, USA.
  • Pasaniuc B; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, USA.
  • Sankararaman S; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Bioinformatics ; 34(13): i195-i201, 2018 07 01.
Article in En | MEDLINE | ID: mdl-29949958
Motivation: A large proportion of risk regions identified by genome-wide association studies (GWAS) are shared across multiple diseases and traits. Understanding whether this clustering is due to sharing of causal variants or chance colocalization can provide insights into shared etiology of complex traits and diseases. Results: In this work, we propose a flexible, unifying framework to quantify the overlap between a pair of traits called UNITY (Unifying Non-Infinitesimal Trait analYsis). We formulate a Bayesian generative model that relates the overlap between pairs of traits to GWAS summary statistic data under a non-infinitesimal genetic architecture underlying each trait. We propose a Metropolis-Hastings sampler to compute the posterior density of the genetic overlap parameters in this model. We validate our method through comprehensive simulations and analyze summary statistics from height and body mass index GWAS to show that it produces estimates consistent with the known genetic makeup of both traits. Availability and implementation: The UNITY software is made freely available to the research community at: https://github.com/bogdanlab/UNITY. Supplementary information: Supplementary data are available at Bioinformatics online.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Software / Models, Statistical / Polymorphism, Single Nucleotide / Genome-Wide Association Study Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Year: 2018 Type: Article

Full text: 1 Database: MEDLINE Main subject: Software / Models, Statistical / Polymorphism, Single Nucleotide / Genome-Wide Association Study Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Year: 2018 Type: Article