## Abstract Varianceβcomponents (VC) linkage analysis is a powerful modelβfree method for assessing linkage, but the distribution of VC logarithm of the odds ratio (LOD) scores may deviate substantially from the assumed asymptotic distribution. Typically, the null distribution of the VCβLOD score a
MCMC segregation and linkage analysis
β Scribed by S.C. Heath; G.L. Snow; E.A. Thompson; C. Tseng; E.M. Wijsman
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 47 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0741-0395
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β¦ Synopsis
Our objective was to infer the genetic model for the quantitative traits using a variety of methods developed in our group. Only a single data set was analyzed in any one analysis, although some comparison between data sets was made. In addition, the simulated model was not known during the course of the analysis. Basic modeling and segregation analyses for the five quantitative traits was followed by several simple genome scans to indicate areas of interest. A Markov chain Monte Carlo (MCMC) multipoint quantitative trait locus (QTL) mapping approach was then used to estimate the posterior probabilities of linkage of QTL to each chromosome simultaneously with trait model parameters, and to further localize the genes. Comparisons between the nuclear family and pedigree data sets indicated a greater power for QTL detection and mapping with the pedigree data sets. Even with the pedigree data, however, precise localization of the QTL did not appear to be possible using single replicate data sets. Two of the three genes with effects on trait Q1 were detected by the MCMC method.
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Data simulated for Genetic Analysis Workshop I1 were analyzed using PAP. Segregation analysis showed a simple recessive mode of inheritance for data set 2 while no conclusions could be made about the mode of inheritance for data set 3 . Pairwise linkage analysis suggested three linkage groups, but
A combined segregation, linkage, and association analysis using the program COMBIN was performed on the simulated pedigree data prepared for the Second Genetic Analysis Workshop. The model used in COMBIN is described and the presented results illustrate its effectiveness in the analysis of such data