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PMID: 16934005 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Regional admixture mapping and structured association testing: conceptual unification and an extensible general linear model.

PLoS genetics ·Vol. 2 ·No. 8 ·2006-08-25 ·Pages e137

Redden DT, Divers J, Vaughan LK, Tiwari HK, Beasley TM, Fernández JR, Kimberly RP, Feng R, Padilla MA, Liu N, Miller MB, Allison DB

Abstract

Individual genetic admixture estimates, determined both across the genome and at specific genomic regions, have been proposed for use in identifying specific genomic regions harboring loci influencing phenotypes in regional admixture mapping (RAM). Estimates of individual ancestry can be used in structured association tests (SAT) to reduce confounding induced by various forms of population substructure. Although presented as two distinct approaches, we provide a conceptual framework in which both RAM and SAT are special cases of a more general linear model. We clarify which variables are sufficient to condition upon in order to prevent spurious associations and also provide a simple closed form "semiparametric" method of evaluating the reliability of individual admixture estimates. An estimate of the reliability of individual admixture estimates is required to make an inherent errors-in-variables problem tractable. Casting RAM and SAT methods as a general linear model offers enormous flexibility enabling application to a rich set of phenotypes, populations, covariates, and situations, including interaction terms and multilocus models. This approach should allow far wider use of RAM and SAT, often using standard software, in addressing admixture as either a confounder of association studies or a tool for finding loci influencing complex phenotypes in species as diverse as plants, humans, and nonhuman animals.

MeSH Terms
Computer Simulation Female Genetics, Population/methods Humans Linear Models Linkage Disequilibrium Male Models, Genetic Phenotype Quantitative Trait Loci Software
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Redden David T
Department of Biostatistics, Section on Statistical Genetics, University of Alabama at Birmingham, Birmingham, Alabama, United States of America. [email protected]
Divers Jasmin
Vaughan Laura Kelly
Tiwari Hemant K
Beasley T Mark
Fernández José R
Kimberly Robert P
Feng Rui
Padilla Miguel A
Liu Nianjun
Miller Michael B
Allison David B
Conflict of Interest

Competing interests. The authors have declared that no competing interests exist.

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Article Info
Journal
PLoS genetics
Abbr.
PLoS Genet
ISSN
1553-7404
Published
2006-08-25
Epub
2006-00-18
Pages
e137
Language
English
Region
United States
NLM ID
101239074
PMCID
PMC1557785
Subset
IM
Grants
NIAMS NIH HHS · AR049084 · United States
NIAMS NIH HHS · T32 AR007450 · United States
NCRR NIH HHS · M01-RR-00032 · United States
NIDDK NIH HHS · R01 DK067426 · United States
NIDDK NIH HHS · R01 DK051684 · United States
NCRR NIH HHS · RR11811 · United States
NIEHS NIH HHS · ES09912 · United States
NIAMS NIH HHS · AR007450 · United States
NIDDK NIH HHS · DK49779-03 · United States
NIDDK NIH HHS · DK062817 · United States
NIAMS NIH HHS · P30 AR048311 · United States
NIDDK NIH HHS · DK056336 · United States
NHLBI NIH HHS · HL072757 · United States
NIDDK NIH HHS · DK51684-01 · United States
NCRR NIH HHS · M01 RR000032 · United States
NIEHS NIH HHS · R01 ES009912 · United States
NCI NIH HHS · U54 CA100949 · United States
NIDDK NIH HHS · P30 DK056336 · United States
NIDDK NIH HHS · DK067426 · United States
NCI NIH HHS · CA100949 · United States
NIAMS NIH HHS · AR048311 · United States
NHLBI NIH HHS · T32 HL072757 · United States
NIDDK NIH HHS · K25 DK062817 · United States
NIAMS NIH HHS · P01 AR049084 · United States
NIDDK NIH HHS · R01 DK049779 · United States
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