Literature DB >> 24248908

Robust rare variant association testing for quantitative traits in samples with related individuals.

Duo Jiang1, Mary Sara McPeek.   

Abstract

The recent development of high-throughput sequencing technologies calls for powerful statistical tests to detect rare genetic variants associated with complex human traits. Sampling related individuals in sequencing studies offers advantages over sampling unrelated individuals only, including improved protection against sequencing error, the ability to use imputation to make more efficient use of sequence data, and the possibility of power boost due to more observed copies of extremely rare alleles among relatives. With related individuals, familial correlation needs to be accounted for to ensure correct control over type I error and to improve power. Recognizing the limitations of existing rare-variant association tests for family data, we propose MONSTER (Minimum P-value Optimized Nuisance parameter Score Test Extended to Relatives), a robust rare-variant association test, which generalizes the SKAT-O method for independent samples. MONSTER uses a mixed effects model that accounts for covariates and additive polygenic effects. To obtain a powerful test, MONSTER adaptively adjusts to the unknown configuration of effects of rare-variant sites. MONSTER also offers an analytical way of assessing P-values, which is desirable because permutation is not straightforward to conduct in related samples. In simulation studies, we demonstrate that MONSTER effectively accounts for family structure, is computationally efficient and compares very favorably, in terms of power, to previously proposed tests that allow related individuals. We apply MONSTER to an analysis of high-density lipoprotein cholesterol in the Framingham Heart Study, where we are able to replicate association with three genes.
© 2013 WILEY PERIODICALS, INC.

Entities:  

Keywords:  MONSTER; association mapping; family data; mixed effects; sequence

Mesh:

Substances:

Year:  2013        PMID: 24248908      PMCID: PMC4510991          DOI: 10.1002/gepi.21775

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


  30 in total

1.  BLUP genotype imputation for case-control association testing with related individuals and missing data.

Authors:  Mary Sara McPeek
Journal:  J Comput Biol       Date:  2012-06       Impact factor: 1.479

2.  Optimal tests for rare variant effects in sequencing association studies.

Authors:  Seunggeun Lee; Michael C Wu; Xihong Lin
Journal:  Biostatistics       Date:  2012-06-14       Impact factor: 5.899

3.  Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data.

Authors:  Daniel J Schaid; Shannon K McDonnell; Jason P Sinnwell; Stephen N Thibodeau
Journal:  Genet Epidemiol       Date:  2013-05-05       Impact factor: 2.135

4.  Family-based association tests for sequence data, and comparisons with population-based association tests.

Authors:  Iuliana Ionita-Laza; Seunggeun Lee; Vladimir Makarov; Joseph D Buxbaum; Xihong Lin
Journal:  Eur J Hum Genet       Date:  2013-02-06       Impact factor: 4.246

5.  MASTOR: mixed-model association mapping of quantitative traits in samples with related individuals.

Authors:  Johanna Jakobsdottir; Mary Sara McPeek
Journal:  Am J Hum Genet       Date:  2013-05-02       Impact factor: 11.025

6.  Population-based and family-based designs to analyze rare variants in complex diseases.

Authors:  Rémi Kazma; Julia N Bailey
Journal:  Genet Epidemiol       Date:  2011       Impact factor: 2.135

7.  Accurate imputation of rare and common variants in a founder population from a small number of sequenced individuals.

Authors:  Lawrence H Uricchio; Jessica X Chong; Kevin D Ross; Carole Ober; Dan L Nicolae
Journal:  Genet Epidemiol       Date:  2012-03-28       Impact factor: 2.135

8.  SNP set association analysis for familial data.

Authors:  Elizabeth D Schifano; Michael P Epstein; Lawrence F Bielak; Min A Jhun; Sharon L R Kardia; Patricia A Peyser; Xihong Lin
Journal:  Genet Epidemiol       Date:  2012-09-11       Impact factor: 2.135

9.  Sequence kernel association test for quantitative traits in family samples.

Authors:  Han Chen; James B Meigs; Josée Dupuis
Journal:  Genet Epidemiol       Date:  2012-12-26       Impact factor: 2.135

10.  Joint rare variant association test of the average and individual effects for sequencing studies.

Authors:  Yuanjia Wang; Yin-Hsiu Chen; Qiong Yang
Journal:  PLoS One       Date:  2012-03-16       Impact factor: 3.240

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  30 in total

1.  ADAPTIVE-WEIGHT BURDEN TEST FOR ASSOCIATIONS BETWEEN QUANTITATIVE TRAITS AND GENOTYPE DATA WITH COMPLEX CORRELATIONS.

Authors:  Xiaowei Wu; Ting Guan; Dajiang J Liu; Luis G León Novelo; Dipankar Bandyopadhyay
Journal:  Ann Appl Stat       Date:  2018-09-11       Impact factor: 2.083

2.  A statistical approach for rare-variant association testing in affected sibships.

Authors:  Michael P Epstein; Richard Duncan; Erin B Ware; Min A Jhun; Lawrence F Bielak; Wei Zhao; Jennifer A Smith; Patricia A Peyser; Sharon L R Kardia; Glen A Satten
Journal:  Am J Hum Genet       Date:  2015-03-19       Impact factor: 11.025

3.  On Efficient and Accurate Calculation of Significance P-Values for Sequence Kernel Association Testing of Variant Set.

Authors:  Baolin Wu; Weihua Guan; James S Pankow
Journal:  Ann Hum Genet       Date:  2016-01-12       Impact factor: 1.670

4.  Flexible and robust methods for rare-variant testing of quantitative traits in trios and nuclear families.

Authors:  Yunxuan Jiang; Karen N Conneely; Michael P Epstein
Journal:  Genet Epidemiol       Date:  2014-07-14       Impact factor: 2.135

5.  Rare variant association test in family-based sequencing studies.

Authors:  Xuefeng Wang; Zhenyu Zhang; Nathan Morris; Tianxi Cai; Seunggeun Lee; Chaolong Wang; Timothy W Yu; Christopher A Walsh; Xihong Lin
Journal:  Brief Bioinform       Date:  2017-11-01       Impact factor: 11.622

6.  Longitudinal SNP-set association analysis of quantitative phenotypes.

Authors:  Zhong Wang; Ke Xu; Xinyu Zhang; Xiaowei Wu; Zuoheng Wang
Journal:  Genet Epidemiol       Date:  2016-11-09       Impact factor: 2.135

7.  Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees.

Authors:  Mohamad Saad; Ellen M Wijsman
Journal:  Genet Epidemiol       Date:  2014-08-01       Impact factor: 2.135

Review 8.  Statistical methods for genome-wide and sequencing association studies of complex traits in related samples.

Authors:  Timothy A Thornton
Journal:  Curr Protoc Hum Genet       Date:  2015-01-20

9.  Parameter Expanded Algorithms for Bayesian Latent Variable Modeling of Genetic Pleiotropy Data.

Authors:  Lizhen Xu; Radu V Craiu; Lei Sun; Andrew D Paterson
Journal:  J Comput Graph Stat       Date:  2016-05-10       Impact factor: 2.302

Review 10.  Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.

Authors:  Roseann E Peterson; Karoline Kuchenbaecker; Raymond K Walters; Chia-Yen Chen; Alice B Popejoy; Sathish Periyasamy; Max Lam; Conrad Iyegbe; Rona J Strawbridge; Leslie Brick; Caitlin E Carey; Alicia R Martin; Jacquelyn L Meyers; Jinni Su; Junfang Chen; Alexis C Edwards; Allan Kalungi; Nastassja Koen; Lerato Majara; Emanuel Schwarz; Jordan W Smoller; Eli A Stahl; Patrick F Sullivan; Evangelos Vassos; Bryan Mowry; Miguel L Prieto; Alfredo Cuellar-Barboza; Tim B Bigdeli; Howard J Edenberg; Hailiang Huang; Laramie E Duncan
Journal:  Cell       Date:  2019-10-10       Impact factor: 41.582

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