## Abstract Genome‐wide genetic association studies typically start with univariate statistical tests of each marker. In principle, this single‐SNP scanning is statistically straightforward—the testing is done with standard methods (e.g. χ^2^ tests, regression) that have been well studied for decad
The power of independent types of genetic information to detect association in a case-control study design
✍ Scribed by Sungho Won; Robert C. Elston
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 347 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
There have been many single nucleotide polymorphism‐based tests suggested for association analysis in a case‐control design. The possible evidence for association comprises three types of information: differences between cases and controls in allele frequencies, in parameters for Hardy Weinberg disequilibrium (HWD) and in parameters for linkage disequilibrium (LD). Here, first we find the pairwise covariances between statistics that measure these three types of information and show that the statistics are asymptotically trivariate normally distributed. Then we compare their power analytically to determine the most informative statistics according to the disease model. Our results show that differences in parameters for HWD are informative for dominant and recessive disease models, while differences in allele frequencies and in parameters for LD are generally informative except for rare recessive disease models. There is mutual independence of the statistics that detect these three differences under Hardy Weinberg equilibrium at the marker locus and linkage equilibrium between markers in the population. Knowing the pairwise covariances between the statistics makes it possible to define statistics that are mutually independent. This allows us to perform sequential analyses of the same data without the need to adjust significance levels for all the multiple analyses being performed on the same data set. As a result we can have improved flexible strategies to increase the power of genome‐wide association studies without requiring the collection of a new, independent sample. Genet. Epidemiol. 2008. © 2008 Wiley‐Liss, Inc.
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