ArticleAmerican journal of human genetics2007
Simultaneously correcting for population stratification and for genotyping error in case-control association studies.
Article in American journal of human genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Assessing the joint effect of population stratification and sample selection in studies of gene-gene (environment) interactions.BMC genetics · 2012Article
- Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.Human heredity · 2012Article
- Accounting for population stratification in practice: a comparison of the main strategies dedicated to genome-wide association studies.PloS one · 2011Article
- A novel tool for individual haplotype inference using mixed data.Journal of biomedical science · 2009Article
- Power comparisons between similarity-based multilocus association methods, logistic regression, and score tests for haplotypes.Genetic epidemiology · 2009Article
- Tracing sub-structure in the European American population with PCA-informative markers.PLoS genetics · 2008Article
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In population-based case-control association studies, the regular chi (2) test is often used to investigate association between a candidate locus and disease. However, it is well known that this test may be biased in the presence of population stratification and/or genotyping error. Unlike some other biases, this bias will not go away with increasing sample size. On the contrary, the false-positive rate will be much larger when the sample size is increased. The usual family-based designs are robust against population stratification, but they are sensitive to genotype error. In this article, we propose a novel method of simultaneously correcting for the bias arising from population stratification and/or for the genotyping error in case-control studies. The appropriate corrections depend on sample odds ratios of the standard 2x3 tables of genotype by case and control from null loci. Therefore, the test is simple to apply. The corrected test is robust against misspecification of the genetic model. If the null hypothesis of no association is rejected, the corrections can be further used to estimate the effect of the genetic factor. We considered a simulation study to investigate the performance of the new method, using parameter values similar to those found in real-data examples. The results show that the corrected test approximately maintains the expected type I error rate under various simulation conditions. It also improves the power of the association test in the presence of population stratification and/or genotyping error. The discrepancy in power between the tests with correction and those without correction tends to be more extreme as the magnitude of the bias becomes larger. Therefore, the bias-correction method proposed in this article should be useful for the genetic analysis of complex traits.
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