Literature DB >> 26680660

Genetic Variant Selection: Learning Across Traits and Sites.

Laurel Stell1, Chiara Sabatti2.   

Abstract

We consider resequencing studies of associated loci and the problem of prioritizing sequence variants for functional follow-up. Working within the multivariate linear regression framework helps us to account for the joint effects of multiple genes; and adopting a Bayesian approach leads to posterior probabilities that coherently incorporate all information about the variants' function. We describe two novel prior distributions that facilitate learning the role of each variable site by borrowing evidence across phenotypes and across mutations in the same gene. We illustrate their potential advantages with simulations and reanalyzing a data set of sequencing variants.
Copyright © 2016 by the Genetics Society of America.

Keywords:  Bayesian variant selection; fine mapping; pleiotropy; rare variants

Mesh:

Year:  2015        PMID: 26680660      PMCID: PMC4788227          DOI: 10.1534/genetics.115.184572

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  31 in total

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2.  Incorporating model uncertainty in detecting rare variants: the Bayesian risk index.

Authors:  Melanie A Quintana; Jonine L Berstein; Duncan C Thomas; David V Conti
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3.  Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics.

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Journal:  Genetics       Date:  2015-05-06       Impact factor: 4.562

4.  Penalized multimarker vs. single-marker regression methods for genome-wide association studies of quantitative traits.

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5.  Identifying causal variants at loci with multiple signals of association.

Authors:  Farhad Hormozdiari; Emrah Kostem; Eun Yong Kang; Bogdan Pasaniuc; Eleazar Eskin
Journal:  Genetics       Date:  2014-08-07       Impact factor: 4.562

6.  Incorporating prior biologic information for high-dimensional rare variant association studies.

Authors:  Melanie A Quintana; Fredrick R Schumacher; Graham Casey; Jonine L Bernstein; Li Li; David V Conti
Journal:  Hum Hered       Date:  2013-04-11       Impact factor: 0.444

7.  Finite adaptation and multistep moves in the metropolis-hastings algorithm for variable selection in genome-wide association analysis.

Authors:  Tomi Peltola; Pekka Marttinen; Aki Vehtari
Journal:  PLoS One       Date:  2012-11-15       Impact factor: 3.240

8.  Reprioritizing genetic associations in hit regions using LASSO-based resample model averaging.

Authors:  William Valdar; Jeremy Sabourin; Andrew Nobel; Christopher C Holmes
Journal:  Genet Epidemiol       Date:  2012-04-30       Impact factor: 2.135

9.  Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification.

Authors:  Laura L Faye; Mitchell J Machiela; Peter Kraft; Shelley B Bull; Lei Sun
Journal:  PLoS Genet       Date:  2013-08-08       Impact factor: 5.917

10.  A unified framework for association analysis with multiple related phenotypes.

Authors:  Matthew Stephens
Journal:  PLoS One       Date:  2013-07-05       Impact factor: 3.240

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  2 in total

1.  MULTILAYER KNOCKOFF FILTER: CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS.

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2.  Controlling the Rate of GWAS False Discoveries.

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Journal:  Genetics       Date:  2016-10-26       Impact factor: 4.562

  2 in total

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