A statistical model that uses an iterative maximum likelihood estimation procedure is proposed for measuring and testing the association between polymorhphic genetic markers and quantitative traits in human pedigrees, after adjusting for covariates such as age and sex. The model allows the quantitat
Statistical validity for testing associations between genetic markers and quantitative traits in family data
β Scribed by Todd G. Nick; Varghese George; Robert C. Elston; Alexander F. Wilson
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 943 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
β¦ Synopsis
In genetic analysis it is often of interest to analyze associations between traits of unknown genetic etiology and genetic markers from pedigree data. Statistical methods that assume independence of pedigree members cannot be used because they disregard the statistical dependencies of members in a pedigree. For quantitative traits, a regression model proposed by George and Elston [Genet Epidemiol4: 193-201, 19871 uses an asymptotic likelihood ratio test and incorporates a correlation structure that allows for statistical dependence among the pedigree members. The statistical validity of this test is assessed for finite samples by measuring the discrepancy between the empirical and theoretical chi-square distributions. The variance of the mean of the dependent variable is determined to be related to this discrepancy and can be used to determine whether a pedigree structure is large enough for making valid statistical inferences on the basis of the asymptotic test. A multigenerational pedigree of 200 or so individuals should in many cases be sufficient for valid results when using the asymptotic likelihood ratio test for the association between markers and continuous traits. o 1995 Wiley-Liss, Inc.
π SIMILAR VOLUMES
## Abstract The optimal method for considering different genetic models in association studies is not clear. We compared analytical strategies that use different genetic models to analyze genotypeβphenotype information from association studies of quantitative traits in unrelated individuals. We cre
## Abstract Genetic association studies are generally performed either by examining differences in the genotype distribution between individuals or by testing for preferential allele transmission within families. In the absence of population stratification bias (PSB), integrated analyses of individ
## Abstract Index cases from a clinically relevant cohort of 102 Spanish families with at least 3 cases of breast and/or ovarian cancer (at least 1 case diagnosed before age 50) in the same lineage were screened for germline mutations in the entire coding sequence and intron boundaries of the breas