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PMID: 8751872 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Genome scanning for linkage: an overview.

American journal of human genetics ·Vol. 59 ·No. 3 ·1996-09-00 ·Pages 704-16

Whittemore AS

Abstract

Several different methods for linkage analysis are shown to arise from a single likelihood function L for the observed allele-sharing data at multiple markers in a chromosomal region. These include classical parametric lod score methods, nonparametric or "model-free" affected pedigree-member (APM) methods, and the Gaussian process method. Setting the methods in the context of the likelihood function L clarifies their underlying assumptions. A test statistic derived from L, the efficient score statistic, is introduced. It is asymptotically equivalent to the lod score, but it can be easier to compute when the penetrances and frequencies of alleles of the trait gene are not known. APM test statistics and the Gaussian lod score are shown to be special cases of efficient score statistics. This unified framework facilitates exploration of a range of models for the effects of a putative trait-predisposing gene, and it facilitates sensitivity analyses to examine the consequences of model misspecification.

MeSH Terms
Female Genetic Linkage Genome, Human Humans Likelihood Functions Male Models, Genetic Multivariate Analysis Normal Distribution Pedigree Statistics, Nonparametric
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Whittemore A S
Department of Health Research and Policy, Stanford University School of Medicine, CA, USA. asw@osiris.stanford.edu
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17 references, click to expand
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1996-09-00
Pages
704-16
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1914900
Subset
IM
Grants
NCI NIH HHS · CA-R29-47448 · United States
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