Source:http://linkedlifedata.com/resource/pubmed/id/12508255
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
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| pubmed:dateCreated |
2002-12-31
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| pubmed:abstractText |
Although genetic association studies using unrelated individuals may be subject to bias caused by population stratification, alternative methods that are robust to population stratification such as family-based association designs may be less powerful. Recently, various statistical methods robust to population stratification were proposed for association studies, using unrelated individuals to identify associations between candidate markers and traits of interest (both qualitative and quantitative). Here, we propose a semiparametric test for association (SPTA). SPTA controls for population stratification through a set of genomic markers by first deriving a genetic background variable for each sampled individual through his/her genotypes at a series of independent markers, and then modeling the relationship between trait values, genotypic scores at the candidate marker, and genetic background variables through a semiparametric model. We assume that the exact form of relationship between the trait value and the genetic background variable is unknown and estimated through smoothing techniques. We evaluate the performance of SPTA through simulations both with discrete subpopulation models and with continuous admixture population models. The simulation results suggest that our procedure has a correct type I error rate in the presence of population stratification and is more powerful than statistical association tests for family-based association designs in all the cases considered. Moreover, SPTA is more powerful than the Quantitative Similarity-Based Association Test (QSAT) developed by us under continuous admixture populations, and the number of independent markers needed by SPTA to control for population stratification is substantially fewer than that required by QSAT.
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| pubmed:grant | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:month |
Jan
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| pubmed:issn |
0741-0395
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| pubmed:author | |
| pubmed:copyrightInfo |
Copyright 2003 Wiley-Liss, Inc.
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| pubmed:issnType |
Print
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| pubmed:volume |
24
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
44-56
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| pubmed:dateRevised |
2008-11-21
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| pubmed:meshHeading |
pubmed-meshheading:12508255-Analysis of Variance,
pubmed-meshheading:12508255-Bias (Epidemiology),
pubmed-meshheading:12508255-Factor Analysis, Statistical,
pubmed-meshheading:12508255-Genetic Markers,
pubmed-meshheading:12508255-Genetic Variation,
pubmed-meshheading:12508255-Genetics, Population,
pubmed-meshheading:12508255-Genotype,
pubmed-meshheading:12508255-Humans,
pubmed-meshheading:12508255-Least-Squares Analysis,
pubmed-meshheading:12508255-Linear Models,
pubmed-meshheading:12508255-Models, Genetic,
pubmed-meshheading:12508255-Pedigree,
pubmed-meshheading:12508255-Quantitative Trait, Heritable,
pubmed-meshheading:12508255-Regression Analysis,
pubmed-meshheading:12508255-Statistics, Nonparametric
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| pubmed:year |
2003
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| pubmed:articleTitle |
On a semiparametric test to detect associations between quantitative traits and candidate genes using unrelated individuals.
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| pubmed:affiliation |
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Connecticut 06520-8034, USA.
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| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Validation Studies
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