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PMID: 10436380 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Multipoint linkage analysis. A cautionary note.

Human heredity ·Vol. 49 ·No. 4 ·1999-07-00 ·Pages 194-6

Halpern J, Whittemore AS

Abstract

Multipoint linkage analysis is commonly used to evaluate linkage of a disease to multiple markers in a small region. Multipoint analysis is particularly powerful when the IBD relations of family members at the trait locus are ambiguous. The increased power arises because, unlike single-marker analyses, multipoint analysis uses haplotype information from several markers to infer the IBD relations. We wish to temper this advantage with a cautionary note: multipoint analysis is sensitive to power loss due to misspecification of intermarker distances. Such misspecification is especially problematic when dealing with closely spaced markers. We present computer simulations comparing the power of single-point and multipoint analyses, both when IBD relations are ambiguous, and when the intermarker distances are misspecified. We conclude that when evaluating markers in a small region to confirm or refute previous findings, a situation in which p values of modest statistical significance are important, single marker analyses may provide more reliable measures of the strength of support for linkage than multipoint statistics.

MeSH Terms
Computer Simulation Genetic Linkage Genetic Markers Humans Male Models, Genetic Models, Statistical Polymorphism, Genetic Prostatic Neoplasms/genetics
Chemicals
Genetic Markers
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Halpern J
Department of Health Research and Policy, Stanford University School of Medicine, Stanford, CA 94305-5405, USA.
Whittemore A S
Article Info
Journal
Human heredity
Abbr.
Hum Hered
ISSN
0001-5652
Published
1999-07-00
Pages
194-6
Language
English
Region
Switzerland
NLM ID
0200525
Subset
IM
Grants
PHS HHS · R35-47448 · United States
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