Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies.

Journal article

We present a Bayesian, Markov-chain Monte Carlo method for fine-scale linkage-disequilibrium gene mapping using high-density marker maps. The method explicitly models the genealogy underlying a sample of case chromosomes in the vicinity of a putative disease locus, in contrast with the assumption of a star-shaped tree made by many existing multipoint methods. Within this modeling framework, we can allow for missing marker information and for uncertainty about the true underlying genealogy and the makeup of ancestral marker haplotypes. A crucial advantage of our method is the incorporation of the shattered coalescent model for genealogies, allowing for multiple founding mutations at the disease locus and for sporadic cases of disease. Output from the method includes approximate posterior distributions of the location of the disease locus and population-marker haplotype proportions. In addition, output from the algorithm is used to construct a cladogram to represent genetic heterogeneity at the disease locus, highlighting clusters of case chromosomes sharing the same mutation. We present detailed simulations to provide evidence of improvements over existing methodology. Furthermore, inferences about the location of the disease locus are shown to remain robust to modeling assumptions.

Authors: Morris, A; Whittaker, J; Balding, D

• Publication status: Published
• Journal: American journal of human genetics
• Volume: 70
• Issue: 3
• Pages: 686-707
• Publication date: 2002-03-01
• DOI: 10.1086/339271
• EISSN: 1537-6605
• ISSN: 0002-9297
• Language: English
• Keywords: Mutation; Female; Alleles; Case-Control Studies; Chromosome Mapping; Sequence Deletion; Humans; Probability; Genetic Heterogeneity; Genetic Markers; Models, Genetic; Cystic Fibrosis; Pedigree; Markov Chains; Linkage Disequilibrium; Cystic Fibrosis Transmembrane Conductance Regulator; Computer Simulation; Algorithms; Haplotypes; Recombination, Genetic; Phylogeny; Monte Carlo Method; Bayes Theorem; Bias (Epidemiology); Male