Source:http://linkedlifedata.com/resource/pubmed/id/11180446
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-2-22
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pubmed:abstractText |
We compare the statistical power of the transmission disequilibrium test (TDT) with that of two likelihood-based linkage tests, the classical LOD score and a modified LOD score in which a linkage disequilibrium (LD) parameter is incorporated into the likelihood (LD-LOD). We hypothesize that, when LD is present, the LD-LOD will have the greatest power of the three tests because the TDT breaks a multiplex pedigree into triads, and the LOD score has previously been shown to have lower power when LD is present but not accounted for. We test this hypothesis using a simulation study in which we generate affected sib-pair (ASP) pedigrees under a range of genetic models, varying the genotypic relative risk (GRR) from 6 to 16. Because the likelihood-based tests require that a genetic model be specified, we compare the tests under two scenarios. First, we assume the true genetic model in the analysis, and second, we compare the tests when the LD-LOD (LOD) is maximized over two wrong genetic models. For the generating models we considered, we find that the LD-LOD has greater power than the TDT even when the genetic models is mis-specified and the results corrected for multiple tests. Extreme differences occur under the multiplicative and dominant models, for which the difference in power is as high as 40% at complete LD. The LOD score provides the lowest power in the presence of LD for the range of GRR considered here.
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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 |
Feb
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pubmed:issn |
0741-0395
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2001 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
192-209
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:11180446-Adult,
pubmed-meshheading:11180446-Alleles,
pubmed-meshheading:11180446-Child,
pubmed-meshheading:11180446-Family,
pubmed-meshheading:11180446-Female,
pubmed-meshheading:11180446-Genetic Linkage,
pubmed-meshheading:11180446-Genetic Markers,
pubmed-meshheading:11180446-Genetic Techniques,
pubmed-meshheading:11180446-Genetics, Medical,
pubmed-meshheading:11180446-Humans,
pubmed-meshheading:11180446-Likelihood Functions,
pubmed-meshheading:11180446-Linkage Disequilibrium,
pubmed-meshheading:11180446-Lod Score,
pubmed-meshheading:11180446-Male,
pubmed-meshheading:11180446-Statistics as Topic
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pubmed:year |
2001
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pubmed:articleTitle |
Power comparisons between the TDT and two likelihood-based methods.
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pubmed:affiliation |
Department of Biostatistics, University of Iowa, Iowa City, Iowa, USA. slager@mayo.edu
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.
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