Maximum-likelihood estimation of gene location by linkage disequilibrium.
- 1 April 1994
- journal article
- Vol. 54 (4) , 705-14
Abstract
Linkage disequilibrium, D, between a polymorphic disease and mapped markers can, in principle, be used to help find the map position of the disease gene. Likelihoods are therefore derived for the value of D conditional on the observed number of haplotypes in the sample and on the population parameter Nc, where N is the effective population size and c the recombination fraction between the disease and marker loci. The likelihood is computed explicitly for the case of two loci with heterozygote superiority and, more generally, by computer simulations assuming a steady state of constant population size and selective pressures or neutrality. It is found that the likelihood is, in general, not very dependent on the degree of selection at the loci and is very flat. This suggests that precise information on map position will not be obtained from estimates of linkage disequilibrium.This publication has 9 references indexed in Scilit:
- Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in FinlandNature Genetics, 1992
- Expected behavior of conditional linkage disequilibrium.1992
- The Huntington's disease candidate region exhibits many different haplotypesNature Genetics, 1992
- The end in sight for Huntington disease?1991
- Variances and covariances of squared linkage disequilibria in finite populationsTheoretical Population Biology, 1988
- A candidate for the cystic fibrosis locus isolated by selection for methylation-free islandsNature, 1987
- Human Genetics: The Molecular ChallengePublished by Cold Spring Harbor Laboratory ,1986
- Correlation and probability methods for one and two lociTheoretical Population Biology, 1973