## Abstract Genotyping errors can create a problem for the analysis of case‐parents data because some families will exhibit genotypes that are inconsistent with Mendelian inheritance. The problem with correcting Mendelian inconsistent genotype errors by regenotyping or removing families in which th
Case-control association testing in the presence of unknown relationships
✍ Scribed by Yoonha Choi; Ellen M. Wijsman; Bruce S. Weir
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 298 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Genome‐wide association studies result in inflated false‐positive results when unrecognized cryptic relatedness exists. A number of methods have been proposed for testing association between markers and disease with a correction for known pedigree‐based relationships. However, in most case‐control studies, relationships are generally unknown, yet the design is predicated on the assumption of at least ancestral relatedness among cases. Here, we focus on adjusting cryptic relatedness when the genealogy of the sample is unknown, particularly in the context of samples from isolated populations where cryptic relatedness may be problematic. We estimate cryptic relatedness using maximum‐likelihood methods and use a corrected χ^2^ test with estimated kinship coefficients for testing in the context of unknown cryptic relatedness. Estimated kinship coefficients characterize precisely the relatedness between truly related people, but are biased for unrelated pairs. The proposed test substantially reduces spurious positive results, producing a uniform null distribution of P‐values. Especially with missing pedigree information, estimated kinship coefficients can still be used to correct non‐independence among individuals. The corrected test was applied to real data sets from genetic isolates and created a distribution of P‐value that was close to uniform. Thus, the proposed test corrects the non‐uniform distribution of P‐values obtained with the uncorrected test and illustrates the advantage of the approach on real data. Genet. Epidemiol. 33:668–678, 2009. © 2009 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
Genome-wide association studies typically test large numbers of genetic variants in association with trait values. It is well known that linkage disequilibrium (LD) between nearby markers tends to introduce correlation among association tests. Failure to properly adjust for multiple comparisons can
## Abstract Genome‐wide case‐control association study is gaining popularity, thanks to the rapid development of modern genotyping technology. In such studies, population stratification is a potential concern especially when the number of study subjects is large as it can lead to seriously inflated
## Abstract It has recently been shown that testing for association in the presence of linkage using a score test based on a gamma random effects (GRE) model is substantially more powerful than using the Family‐Based Association Test. A reason for the increased power lies in better specification of