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PMID: 9529345 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Genetic association mapping based on discordant sib pairs: the discordant-alleles test.

American journal of human genetics ·Vol. 62 ·No. 4 ·1998-04-00 ·Pages 950-61

Boehnke M, Langefeld CD

Abstract

Family-based tests of association provide the opportunity to test for an association between a disease and a genetic marker. Such tests avoid false-positive results produced by population stratification, so that evidence for association may be interpreted as evidence for linkage or causation. Several methods that use family-based controls have been proposed, including the haplotype relative risk, the transmission-disequilibrium test, and affected family-based controls. However, because these methods require genotypes on affected individuals and their parents, they are not ideally suited to the study of late-onset diseases. In this paper, we develop several family-based tests of association that use discordant sib pairs (DSPs) in which one sib is affected with a disease and the other sib is not. These tests are based on statistics that compare counts of alleles or genotypes or that test for symmetry in tables of alleles or genotypes. We describe the use of a permutation framework to assess the significance of these statistics. These DSP-based tests provide the same general advantages as parent-offspring trio-based tests, while being applicable to essentially any disease; they may also be tailored to particular hypotheses regarding the genetic model. We compare the statistical properties of our DSP-based tests by computer simulation and illustrate their use with an application to Alzheimer disease and the apolipoprotein E polymorphism. Our results suggest that the discordant-alleles test, which compares the numbers of nonmatching alleles in DSPs, is the most powerful of the tests we considered, for a wide class of disease models and marker types. Finally, we discuss advantages and disadvantages of the DSP design for genetic association mapping.

MeSH Terms
Alleles Alzheimer Disease/genetics Apolipoproteins E/genetics Chromosome Mapping/methods Computer Simulation Humans Models, Genetic
Chemicals
Apolipoproteins E
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Boehnke M
Department of Biostatistics, University of Michigan, Ann Arbor, MI USA. boehnke@umich.edu
Langefeld C D
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1998-04-00
Pages
950-61
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1377027
Subset
IM
Grants
NHGRI NIH HHS · HG00040 · United States
NHGRI NIH HHS · HG00376 · United States
NINDS NIH HHS · NS31153 · United States
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