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A Unified Approach for Quantifying, Testing and Correcting Population Stratification in Case-Control Association Studies
Author(s) -
Prakash Gorroochurn,
Susan E. Hodge,
Gary A. Heiman,
David A. Greenberg
Publication year - 2007
Publication title -
human heredity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.423
H-Index - 62
eISSN - 1423-0062
pISSN - 0001-5652
DOI - 10.1159/000102988
Subject(s) - population stratification , type i and type ii errors , null hypothesis , multiple comparisons problem , international hapmap project , statistical hypothesis testing , statistical power , context (archaeology) , statistics , population , genetic association , association (psychology) , computer science , computational biology , mathematics , biology , genetics , medicine , allele , psychology , genotype , paleontology , environmental health , gene , single nucleotide polymorphism , haplotype , psychotherapist
The HapMap project has given case-control association studies a unique opportunity to uncover the genetic basis of complex diseases. However, persistent issues in such studies remain the proper quantification of, testing for, and correction for population stratification (PS). In this paper, we present the first unified paradigm that addresses all three fundamental issues within one statistical framework. Our unified approach makes use of an omnibus quantity (delta), which can be estimated in a case-control study from suitable null loci. We show how this estimated value can be used to quantify PS, to statistically test for PS, and to correct for PS, all in the context of case-control studies. Moreover, we provide guidelines for interpreting values of delta in association studies (e.g., at alpha = 0.05, a delta of size 0.416 is small, a delta of size 0.653 is medium, and a delta of size 1.115 is large). A novel feature of our testing procedure is its ability to test for either strictly any PS or only 'practically important' PS. We also performed simulations to compare our correction procedure with Genomic Control (GC). Our results show that, unlike GC, it maintains good Type I error rates and power across all levels of PS.

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