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Multitrait Fine Mapping of Quantitative Trait Loci Using Combined Linkage Disequilibria and Linkage Analysis
Author(s) -
Mogens Sandø Lund,
Peter Sørensen,
Bernt Guldbrandtsen,
Daniel Sørensen
Publication year - 2003
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/163.1.405
Subject(s) - quantitative trait locus , linkage disequilibrium , biology , family based qtl mapping , genetics , linkage (software) , identity by descent , inclusive composite interval mapping , genetic linkage , haplotype , association mapping , allele , trait , evolutionary biology , gene mapping , gene , chromosome , single nucleotide polymorphism , genotype , computer science , programming language
A novel multitrait fine-mapping method is presented. The method is implemented by a model that treats QTL effects as random variables. The covariance matrix of allelic effects is proportional to the IBD matrix, where each element is the probability that a pair of alleles is identical by descent, given marker information and QTL position. These probabilities are calculated on the basis of similarities of marker haplotypes of individuals of the first generation of genotyped individuals, using “gene dropping” (linkage disequilibrium) and transmission of markers from genotyped parents to genotyped offspring (linkage). A small simulation study based on a granddaughter design was carried out to illustrate that the method provides accurate estimates of QTL position. Results from the simulation also indicate that it is possible to distinguish between a model postulating one pleiotropic QTL affecting two traits vs. one postulating two closely linked loci, each affecting one of the traits.

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