Literature DB >> 26639010

Meta-Analysis of Rare Variant Association Tests in Multiethnic Populations.

Akweley Mensah-Ablorh1,2, Sara Lindstrom1,2, Christopher A Haiman3, Brian E Henderson3, Loic Le Marchand4, Seunngeun Lee5, Daniel O Stram3, A Heather Eliassen1,6, Alkes Price1,2,7, Peter Kraft1,2,7.   

Abstract

Several methods have been proposed to increase power in rare variant association testing by aggregating information from individual rare variants (MAF < 0.005). However, how to best combine rare variants across multiple ethnicities and the relative performance of designs using different ethnic sampling fractions remains unknown. In this study, we compare the performance of several statistical approaches for assessing rare variant associations across multiple ethnicities. We also explore how different ethnic sampling fractions perform, including single-ethnicity studies and studies that sample up to four ethnicities. We conducted simulations based on targeted sequencing data from 4,611 women in four ethnicities (African, European, Japanese American, and Latina). As with single-ethnicity studies, burden tests had greater power when all causal rare variants were deleterious, and variance component-based tests had greater power when some causal rare variants were deleterious and some were protective. Multiethnic studies had greater power than single-ethnicity studies at many loci, with inclusion of African Americans providing the largest impact. On average, studies including African Americans had as much as 20% greater power than equivalently sized studies without African Americans. This suggests that association studies between rare variants and complex disease should consider including subjects from multiple ethnicities, with preference given to genetically diverse groups.
© 2015 WILEY PERIODICALS, INC.

Entities:  

Keywords:  fine mapping; multiethnic meta-analysis; sequencing study design; statistical genetics; study subject selection

Mesh:

Year:  2015        PMID: 26639010      PMCID: PMC4968883          DOI: 10.1002/gepi.21939

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


  46 in total

1.  Pooled association tests for rare variants in exon-resequencing studies.

Authors:  Alkes L Price; Gregory V Kryukov; Paul I W de Bakker; Shaun M Purcell; Jeff Staples; Lee-Jen Wei; Shamil R Sunyaev
Journal:  Am J Hum Genet       Date:  2010-05-13       Impact factor: 11.025

2.  Detecting and describing heterogeneity in meta-analysis.

Authors:  R J Hardy; S G Thompson
Journal:  Stat Med       Date:  1998-04-30       Impact factor: 2.373

3.  Empirical power of very rare variants for common traits and disease: results from sanger sequencing 1998 individuals.

Authors:  Martin Ladouceur; Hou-Feng Zheng; Celia M T Greenwood; J Brent Richards
Journal:  Eur J Hum Genet       Date:  2013-01-16       Impact factor: 4.246

4.  Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability.

Authors:  Eileen Sproat Emison; Merce Garcia-Barcelo; Elizabeth A Grice; Francesca Lantieri; Jeanne Amiel; Grzegorz Burzynski; Raquel M Fernandez; Li Hao; Carl Kashuk; Kristen West; Xiaoping Miao; Paul K H Tam; Paola Griseri; Isabella Ceccherini; Anna Pelet; Anne-Sophie Jannot; Loic de Pontual; Alexandra Henrion-Caude; Stanislas Lyonnet; Joke B G M Verheij; Robert M W Hofstra; Guillermo Antiñolo; Salud Borrego; Andrew S McCallion; Aravinda Chakravarti
Journal:  Am J Hum Genet       Date:  2010-07-09       Impact factor: 11.025

5.  Caution in generalizing known genetic risk markers for breast cancer across all ethnic/racial populations.

Authors:  Fang Chen; Daniel O Stram; Loïc Le Marchand; Kristine R Monroe; Laurence N Kolonel; Brian E Henderson; Christopher A Haiman
Journal:  Eur J Hum Genet       Date:  2010-11-24       Impact factor: 4.246

6.  A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).

Authors:  Stephan Morgenthaler; William G Thilly
Journal:  Mutat Res       Date:  2006-11-13       Impact factor: 2.433

7.  Transethnic meta-analysis of genomewide association studies.

Authors:  Andrew P Morris
Journal:  Genet Epidemiol       Date:  2011-12       Impact factor: 2.135

8.  The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals.

Authors:  Martin Ladouceur; Zari Dastani; Yurii S Aulchenko; Celia M T Greenwood; J Brent Richards
Journal:  PLoS Genet       Date:  2012-02-02       Impact factor: 5.917

Review 9.  Exome sequencing and complex disease: practical aspects of rare variant association studies.

Authors:  Ron Do; Sekar Kathiresan; Gonçalo R Abecasis
Journal:  Hum Mol Genet       Date:  2012-09-13       Impact factor: 6.150

10.  Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.

Authors:  Wenqing Fu; Timothy D O'Connor; Goo Jun; Hyun Min Kang; Goncalo Abecasis; Suzanne M Leal; Stacey Gabriel; Mark J Rieder; David Altshuler; Jay Shendure; Deborah A Nickerson; Michael J Bamshad; Joshua M Akey
Journal:  Nature       Date:  2012-11-28       Impact factor: 49.962

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  5 in total

1.  Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.

Authors:  Antoine R Baldassari; Colleen M Sitlani; Heather M Highland; Dan E Arking; Steve Buyske; Dawood Darbar; Rahul Gondalia; Misa Graff; Xiuqing Guo; Susan R Heckbert; Lucia A Hindorff; Chani J Hodonsky; Yii-Der Ida Chen; Robert C Kaplan; Ulrike Peters; Wendy Post; Alex P Reiner; Jerome I Rotter; Ralph V Shohet; Amanda A Seyerle; Nona Sotoodehnia; Ran Tao; Kent D Taylor; Genevieve L Wojcik; Jie Yao; Eimear E Kenny; Henry J Lin; Elsayed Z Soliman; Eric A Whitsel; Kari E North; Charles Kooperberg; Christy L Avery
Journal:  Circ Genom Precis Med       Date:  2020-06-30

2.  Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities.

Authors:  Sara Lindström; Akweley Ablorh; Brad Chapman; Alexander Gusev; Gary Chen; Constance Turman; A Heather Eliassen; Alkes L Price; Brian E Henderson; Loic Le Marchand; Oliver Hofmann; Christopher A Haiman; Peter Kraft
Journal:  Breast Cancer Res       Date:  2016-11-05       Impact factor: 6.466

3.  Identification of a novel locus associated with skin colour in African-admixed populations.

Authors:  Natalia Hernandez-Pacheco; Carlos Flores; Santos Alonso; Celeste Eng; Angel C Y Mak; Scott Hunstman; Donglei Hu; Marquitta J White; Sam S Oh; Kelley Meade; Harold J Farber; Pedro C Avila; Denise Serebrisky; Shannon M Thyne; Emerita Brigino-Buenaventura; William Rodriguez-Cintron; Saunak Sen; Rajesh Kumar; Michael Lenoir; Jose R Rodriguez-Santana; Esteban G Burchard; Maria Pino-Yanes
Journal:  Sci Rep       Date:  2017-03-16       Impact factor: 4.379

4.  Polymorphism rs1801516 (G > A) in the ATM gene is not associated with overall cancer risk: an updated meta-analysis.

Authors:  Yueting Li; Pengxu Shi; Daqing Jiang
Journal:  J Int Med Res       Date:  2020-07       Impact factor: 1.671

5.  An adaptive test for meta-analysis of rare variant association studies.

Authors:  Tianzhong Yang; Junghi Kim; Chong Wu; Yiding Ma; Peng Wei; Wei Pan
Journal:  Genet Epidemiol       Date:  2019-12-12       Impact factor: 2.135

  5 in total

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