Literature DB >> 27943406

Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data.

Hua Zhou1, John Blangero2, Thomas D Dyer2, Kei-Hang K Chan3,4, Kenneth Lange3,5,6, Eric M Sobel3.   

Abstract

Since most analysis software for genome-wide association studies (GWAS) currently exploit only unrelated individuals, there is a need for efficient applications that can handle general pedigree data or mixtures of both population and pedigree data. Even datasets thought to consist of only unrelated individuals may include cryptic relationships that can lead to false positives if not discovered and controlled for. In addition, family designs possess compelling advantages. They are better equipped to detect rare variants, control for population stratification, and facilitate the study of parent-of-origin effects. Pedigrees selected for extreme trait values often segregate a single gene with strong effect. Finally, many pedigrees are available as an important legacy from the era of linkage analysis. Unfortunately, pedigree likelihoods are notoriously hard to compute. In this paper, we reexamine the computational bottlenecks and implement ultra-fast pedigree-based GWAS analysis. Kinship coefficients can either be based on explicitly provided pedigrees or automatically estimated from dense markers. Our strategy (a) works for random sample data, pedigree data, or a mix of both; (b) entails no loss of power; (c) allows for any number of covariate adjustments, including correction for population stratification; (d) allows for testing SNPs under additive, dominant, and recessive models; and (e) accommodates both univariate and multivariate quantitative traits. On a typical personal computer (six CPU cores at 2.67 GHz), analyzing a univariate HDL (high-density lipoprotein) trait from the San Antonio Family Heart Study (935,392 SNPs on 1,388 individuals in 124 pedigrees) takes less than 2 min and 1.5 GB of memory. Complete multivariate QTL analysis of the three time-points of the longitudinal HDL multivariate trait takes less than 5 min and 1.5 GB of memory. The algorithm is implemented as the Ped-GWAS Analysis (Option 29) in the Mendel statistical genetics package, which is freely available for Macintosh, Linux, and Windows platforms from http://genetics.ucla.edu/software/mendel.
© 2016 WILEY PERIODICALS, INC.

Entities:  

Keywords:  fixed-effects models; genome-wide association study; kinship; multivariate traits; pedigree; score test

Mesh:

Year:  2016        PMID: 27943406      PMCID: PMC5340631          DOI: 10.1002/gepi.21988

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  43 in total

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Authors:  Christoph Lange; Nan M Laird
Journal:  Genet Epidemiol       Date:  2002-08       Impact factor: 2.135

2.  Family-based association studies for next-generation sequencing.

Authors:  Yun Zhu; Momiao Xiong
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3.  Improved linear mixed models for genome-wide association studies.

Authors:  Jennifer Listgarten; Christoph Lippert; Carl M Kadie; Robert I Davidson; Eleazar Eskin; David Heckerman
Journal:  Nat Methods       Date:  2012-05-30       Impact factor: 28.547

Review 4.  The pursuit of genome-wide association studies: where are we now?

Authors:  Chee Seng Ku; En Yun Loy; Yudi Pawitan; Kee Seng Chia
Journal:  J Hum Genet       Date:  2010-03-19       Impact factor: 3.172

5.  Association testing with Mendel.

Authors:  Kenneth Lange; Janet S Sinsheimer; Eric Sobel
Journal:  Genet Epidemiol       Date:  2005-07       Impact factor: 2.135

6.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Authors:  Lucia A Hindorff; Praveen Sethupathy; Heather A Junkins; Erin M Ramos; Jayashri P Mehta; Francis S Collins; Teri A Manolio
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

7.  Genome-wide association analysis by lasso penalized logistic regression.

Authors:  Tong Tong Wu; Yi Fang Chen; Trevor Hastie; Eric Sobel; Kenneth Lange
Journal:  Bioinformatics       Date:  2009-01-28       Impact factor: 6.937

8.  FaST linear mixed models for genome-wide association studies.

Authors:  Christoph Lippert; Jennifer Listgarten; Ying Liu; Carl M Kadie; Robert I Davidson; David Heckerman
Journal:  Nat Methods       Date:  2011-09-04       Impact factor: 28.547

9.  A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test.

Authors:  R S Spielman; W J Ewens
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

10.  Genetic and environmental contributions to cardiovascular risk factors in Mexican Americans. The San Antonio Family Heart Study.

Authors:  B D Mitchell; C M Kammerer; J Blangero; M C Mahaney; D L Rainwater; B Dyke; J E Hixson; R D Henkel; R M Sharp; A G Comuzzie; J L VandeBerg; M P Stern; J W MacCluer
Journal:  Circulation       Date:  1996-11-01       Impact factor: 29.690

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3.  Fast and flexible linear mixed models for genome-wide genetics.

Authors:  Daniel E Runcie; Lorin Crawford
Journal:  PLoS Genet       Date:  2019-02-08       Impact factor: 5.917

4.  The relevance of pedigrees in the conservation genomics era.

Authors:  Stephanie J Galla; Liz Brown; Yvette Couch-Lewis Ngāi Tahu Te Hapū O Ngāti Wheke Ngāti Waewae; Ilina Cubrinovska; Daryl Eason; Rebecca M Gooley; Jill A Hamilton; Julie A Heath; Samantha S Hauser; Emily K Latch; Marjorie D Matocq; Anne Richardson; Jana R Wold; Carolyn J Hogg; Anna W Santure; Tammy E Steeves
Journal:  Mol Ecol       Date:  2021-10-22       Impact factor: 6.622

5.  On the impact of relatedness on SNP association analysis.

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Journal:  BMC Genet       Date:  2017-12-06       Impact factor: 2.797

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