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Calculation of multipoint likelihoods using flanking marker data: a simulation study.

Andrew W George·LaVonne A Mangin·Christopher W Bartlett·Mark W Logue·Alberto M Segre·Veronica J Vieland
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Abstract

The calculation of multipoint likelihoods is computationally challenging, with the exact calculation of multipoint probabilities only possible on small pedigrees with many markers or large pedigrees with few markers. This paper explores the utility of calculating multipoint likelihoods using data on markers flanking a hypothesized position of the trait locus. The calculation of such likelihoods is often feasible, even on large pedigrees with missing data and complex structures. Performance characteristics of the flanking marker procedure are assessed through the calculation of multipoint heterogeneity LOD scores on data simulated for Genetic Analysis Workshop 14 (GAW14). Analysis is restricted to data on the Aipotu population on chromosomes 1, 3, and 4, where chromosomes 1 and 3 are known to contain disease loci. The flanking marker procedure performs well, even when missing data and genotyping errors are introduced.

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Chromosome MappingChromosomes, Human, Pair 1Computer SimulationDatabases, GeneticGenetic HeterogeneityGenetic LinkageGenetic MarkersGenotypeHumansLikelihood FunctionsLod ScoreQuantitative Trait LociSoftwareJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, U.S. Gov't, Non-P.H.S.

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Andrew W George, LaVonne A Mangin, Christopher W Bartlett, Mark W Logue, Alberto M Segre, Veronica J Vieland. 2005-12-30. Calculation of multipoint likelihoods using flanking marker data: a simulation study.. https://doi.org/10.1186/1471-2156-6-s1-s44

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