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Comparison of Population-Based Association Study Methods Correcting for Population Stratification

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  • Feng Zhang
  • Yuping Wang
  • Hong-Wen Deng

Abstract

Population stratification can cause spurious associations in population–based association studies. Several statistical methods have been proposed to reduce the impact of population stratification on population–based association studies. We simulated a set of stratified populations based on the real haplotype data from the HapMap ENCODE project, and compared the relative power, type I error rates, accuracy and positive prediction value of four prevailing population–based association study methods: traditional case-control tests, structured association (SA), genomic control (GC) and principal components analysis (PCA) under various population stratification levels. Additionally, we evaluated the effects of sample sizes and frequencies of disease susceptible allele on the performance of the four analytical methods in the presence of population stratification. We found that the performance of PCA was very stable under various scenarios. Our comparison results suggest that SA and PCA have comparable performance, if sufficient ancestral informative markers are used in SA analysis. GC appeared to be strongly conservative in significantly stratified populations. It may be better to apply GC in the stratified populations with low stratification level. Our study intends to provide a practical guideline for researchers to select proper study methods and make appropriate inference of the results in population-based association studies.

Suggested Citation

  • Feng Zhang & Yuping Wang & Hong-Wen Deng, 2008. "Comparison of Population-Based Association Study Methods Correcting for Population Stratification," PLOS ONE, Public Library of Science, vol. 3(10), pages 1-7, October.
  • Handle: RePEc:plo:pone00:0003392
    DOI: 10.1371/journal.pone.0003392
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    References listed on IDEAS

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    1. B. Devlin & Kathryn Roeder, 1999. "Genomic Control for Association Studies," Biometrics, The International Biometric Society, vol. 55(4), pages 997-1004, December.
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    1. Marie-Claude Babron & Marie de Tayrac & Douglas N Rutledge & Eleftheria Zeggini & Emmanuelle Génin, 2012. "Rare and Low Frequency Variant Stratification in the UK Population: Description and Impact on Association Tests," PLOS ONE, Public Library of Science, vol. 7(10), pages 1-9, October.
    2. Arend Voorman & Thomas Lumley & Barbara McKnight & Kenneth Rice, 2011. "Behavior of QQ-Plots and Genomic Control in Studies of Gene-Environment Interaction," PLOS ONE, Public Library of Science, vol. 6(5), pages 1-7, May.
    3. Pornthep Sirimahachaiyakul & Ravi F Sood & Lara A Muffley & Max Seaton & Cheng-Ta Lin & Liang Qiao & Jeffrey S Armaly & Anne M Hocking & Nicole S Gibran, 2015. "Race Does Not Predict Melanocyte Heterogeneous Responses to Dermal Fibroblast-Derived Mediators," PLOS ONE, Public Library of Science, vol. 10(9), pages 1-15, September.

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