Literature DB >> 20878716

CAPL: a novel association test using case-control and family data and accounting for population stratification.

Ren-Hua Chung1, Michael A Schmidt, Richard W Morris, Eden R Martin.   

Abstract

The recent successes of GWAS based on large sample sizes motivate combining independent datasets to obtain larger sample sizes and thereby increase statistical power. Analysis methods that can accommodate different study designs, such as family-based and case-control designs, are of general interest. However, population stratification can cause spurious association for population-based association analyses. For family-based association analysis that infers missing parental genotypes based on the allele frequencies estimated in the entire sample, the parental mating-type probabilities may not be correctly estimated in the presence of population stratification. Therefore, any approach to combining family and case-control data should also properly account for population stratification. Although several methods have been proposed to accommodate family-based and case-control data, all have restrictions. Most of them require sampling a homogeneous population, which may not be a reasonable assumption for data from a large consortium. One of the methods, FamCC, can account for population stratification and uses nuclear families with arbitrary number of siblings but requires parental genotype data, which are often unavailable for late-onset diseases. We extended the family-based test, Association in the Presence of Linkage (APL), to combine family and case-control data (CAPL). CAPL can accommodate case-control data and families with multiple affected siblings and missing parents in the presence of population stratification. We used simulations to demonstrate that CAPL is a valid test either in a homogeneous population or in the presence of population stratification. We also showed that CAPL can have more power than other methods that combine family and case-control data.
© 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20878716     DOI: 10.1002/gepi.20539

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


  11 in total

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3.  Case-sibling studies that acknowledge unstudied parents and permit the inclusion of unmatched individuals.

Authors:  Min Shi; David M Umbach; Clarice R Weinberg
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Review 4.  Population Stratification in Genetic Association Studies.

Authors:  Jacklyn N Hellwege; Jacob M Keaton; Ayush Giri; Xiaoyi Gao; Digna R Velez Edwards; Todd L Edwards
Journal:  Curr Protoc Hum Genet       Date:  2017-10-18

5.  CAPL: an efficient association software package using family and case-control data and accounting for population stratification.

Authors:  Ren-Hua Chung; Michael A Schmidt; Eden R Martin
Journal:  BMC Bioinformatics       Date:  2011-05-25       Impact factor: 3.307

6.  Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate.

Authors:  Ariadne Letra; Lorena Maili; John B Mulliken; Edward Buchanan; Susan H Blanton; Jacqueline T Hecht
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2014-08-27

7.  An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.

Authors:  Ren-Hua Chung; Deqiong Ma; Kai Wang; Dale J Hedges; James M Jaworski; John R Gilbert; Michael L Cuccaro; Harry H Wright; Ruth K Abramson; Ioanna Konidari; Patrice L Whitehead; Gerard D Schellenberg; Hakon Hakonarson; Jonathan L Haines; Margaret A Pericak-Vance; Eden R Martin
Journal:  Mol Autism       Date:  2011-11-04       Impact factor: 7.509

8.  Haplotype association analysis of combining unrelated case-control and triads with consideration of population stratification.

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9.  Family-based approaches: design, imputation, analysis, and beyond.

Authors:  Ellen M Wijsman
Journal:  BMC Genet       Date:  2016-02-03       Impact factor: 2.797

10.  A combined association test for rare variants using family and case-control data.

Authors:  Peng-Lin Lin; Wei-Yun Tsai; Ren-Hua Chung
Journal:  BMC Proc       Date:  2016-10-18
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