๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Mixture models for linkage analysis of affected sibling pairs and covariates

โœ Scribed by B. Devlin; Bobby L. Jones; Silviu-Alin Bacanu; Kathryn Roeder


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
70 KB
Volume
22
Category
Article
ISSN
0741-0395

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

To determine the genetic etiology of complex diseases, a common study design is to recruit affected sib/relative pairs (ASP/ARP) and evaluate their genomeโ€wide distribution of identical by descent (IBD) sharing using a set of highly polymorphic markers. Other attributes or environmental exposures of the ASP/ARP, which are thought to affect liability to disease, are sometimes collected. Conceivably, these covariates could refine the linkage analysis. Most published methods for ASP/ARP linkage with covariates can be conceptualized as logistic models in which IBD status of the ASP is predicted by pairโ€specific covariates. We develop a different approach to the problem of ASP analysis in the presence of covariates, one that extends naturally to ARP under certain conditions. For ASP linkage analysis, we formulate a mixture model in which a disease mutation is segregating in only a fraction ฮฑ of the sibships, with 1 โ€“ ฮฑ sibships being unlinked. Covariate information is used to predict membership within groups; in this report, the two groups correspond to the linked and unlinked sibships. For an ASP with covariate(s) Z = z and multilocus genotype X = x, the mixture model is ฮฑ(z)g(x; ฮป) + [1 โ€“ ฮฑ(z)]g~0~(x), in which g~0~(x) follows the distribution of genotypes under the null IBD distribution and g(x; ฮป) allows for increased IBD sharing. Two mixture models are developed. The preโ€clustering model uses covariate information to form probabilistic clusters and then tests for excess IBD sharing independent of the covariates. The Covโ€IBD model determines probabilistic group membership by joint consideration of covariate and IBD values. Simulations show that incorporating covariates into linkage analysis can enhance power substantially. A feature of our conceptualization of ASP linkage analysis, with covariates, is that it is apparent how data analysis might evaluate covariates prior to the linkage analysis, thus avoiding the loss of power described by Leal and Ott [2000] when data are stratified. Genet. Epidemiol. 22:52โ€“65, 2002. ยฉ 2002 Wileyโ€Liss, Inc.


๐Ÿ“œ SIMILAR VOLUMES


โ€œMixture models for linkage analysis of
โœ Jane M. Olson ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 74 KB

2002] propose a mixture representation of the affected sib pair (ASP) likelihood ratio that allows inclusion of covariates. They correctly point out that the primary purpose of covariates in linkage models is to allow for locus heterogeneity. They show using simulations the considerable increase in

Interpreting analyses of continuous cova
โœ Silke Schmidt; Xuejun Qin; Michael A. Schmidt; Eden R. Martin; Elizabeth R. Haus ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 192 KB ๐Ÿ‘ 1 views

## Abstract Datasets collected for linkage analyses of complex human diseases often include a number of clinical or environmental covariates. In this study, we evaluated the performance of three linkage analysis methods when the relationship between continuous covariates and disease risk or linkage

Comprehensive linkage and linkage hetero
โœ Tiffany A. Greenwood; Ondrej Libiger; Sharon Kardia; Craig Hanis; Alanna C. Morr ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 255 KB

## Abstract Linkage analyses of complex, multifactorial traits and diseases, such as essential hypertension, have been difficult to interpret and reconcile. Many published studies provide evidence suggesting that different genes and genomic regions influence hypertension, but knowing which of these

Mixture models for cancer survival analy
โœ R. De Angelis; R. Capocaccia; T. Hakulinen; B. Soderman; A. Verdecchia ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 140 KB ๐Ÿ‘ 2 views

The interest in estimating the probability of cure has been increasing in cancer survival analysis as the curability of many cancer diseases is becoming a reality. Mixture survival models provide a way of modelling time to death when cure is possible, simultaneously estimating death hazard of fatal