TY - JOUR
T1 - Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components
AU - Pratt, Stephen C.
AU - Daly, Mark J.
AU - Kruglyak, Leonid
N1 - Funding Information:
We thank Mike Boehnke, Richard Watanabe, Jerry Lanchbury, and anonymous referees for helpful feedback. This work was supported in part by grants from the National Human Genome Research Institute and the National Institute of Mental Health. L.K. is a James S. McDonnell Centennial Fellow.
PY - 2000
Y1 - 2000
N2 - Methods based on variance components are powerful tools for linkage analysis of quantitative traits, because they allow simultaneous consideration of all pedigree members. The central idea is to identify loci making a significant contribution to the population variance of a trait, by use of allele-sharing probabilities derived from genotyped marker loci. The technique is only as powerful as the methods used to infer these probabilities, but, to date, no implementation has made full use of the inheritance information in mapping data. Here we present a new implementation that uses an exact multipoint algorithm to extract the full probability distribution of allele sharing at every point in a mapped region. At each locus in the region, the program fits a model that partitions total phenotypic variance into components due to environmental factors, a major gene at the locus, and other unlinked genes. Numerical methods are used to derive maximum-likelihood estimates of the variance components, under the assumption of multivariate normality. A likelihood-ratio test is then applied to detect any significant effect of the hypothesized major gene. Simulations show the method to have greater power than does traditional sib-pair analysis. The method is freely available in a new release of the software package GENEHUNTER.
AB - Methods based on variance components are powerful tools for linkage analysis of quantitative traits, because they allow simultaneous consideration of all pedigree members. The central idea is to identify loci making a significant contribution to the population variance of a trait, by use of allele-sharing probabilities derived from genotyped marker loci. The technique is only as powerful as the methods used to infer these probabilities, but, to date, no implementation has made full use of the inheritance information in mapping data. Here we present a new implementation that uses an exact multipoint algorithm to extract the full probability distribution of allele sharing at every point in a mapped region. At each locus in the region, the program fits a model that partitions total phenotypic variance into components due to environmental factors, a major gene at the locus, and other unlinked genes. Numerical methods are used to derive maximum-likelihood estimates of the variance components, under the assumption of multivariate normality. A likelihood-ratio test is then applied to detect any significant effect of the hypothesized major gene. Simulations show the method to have greater power than does traditional sib-pair analysis. The method is freely available in a new release of the software package GENEHUNTER.
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U2 - 10.1086/302830
DO - 10.1086/302830
M3 - Article
C2 - 10712227
AN - SCOPUS:0033928381
SN - 0002-9297
VL - 66
SP - 1153
EP - 1157
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 3
ER -