Evidence map›Paper›PMID 10762550›Full record

ArticleAmerican journal of human genetics2000

Power comparison of parametric and nonparametric linkage tests in small pedigrees.

P C Sham, M W Lin, J H Zhao, D Curtis

Abstract readComparative Study
In one paragraph

Article in American journal of human genetics, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

P C ShamDepartments of Psychiatry and Biostatistics and Computing, Institute of Psychiatry, London SE5 8AF, United Kingdom. p.sham@iop.kcl.ac.uk.
M W Lin
J H Zhao
D Curtis

Funding

VARIANCE COMPONENTS MODELS FOR MAPPING QTLSR01EY012562 · NEI · UNIVERSITY OF COLORADO AT BOULDER · PI HEWITT, JOHN K · 1999 to 2006
$2.1M
NEI NIH HHS EY12562
6 · The paper itself

Abstract

When the mode of inheritance of a disease is unknown, the LOD-score method of linkage analysis must take into account uncertainties in model parameters. We have previously proposed a parametric linkage test called "MFLOD," which does not require specification of disease model parameters. In the present study, we introduce two new model-free parametric linkage tests, known as "MLOD" and "MALOD." These tests are defined, respectively, as the LOD score and the admixture LOD score, maximized (subject to the same constraints as MFLOD) over disease-model parameters. We compared the power of these three parametric linkage tests and that of two nonparametric linkage tests, NPLall and NPLpairs, which are implemented in GENEHUNTER. With the use of small pedigrees and a fully informative marker, we found the powers of MLOD, NPLall, and NPLpairs to be almost equivalent to each other and not far below that of a LOD-score analysis performed under the assumption the correct genetic parameters. Thus, linkage analysis is not much hindered by uncertain mode of inheritance. The results also suggest that both parametric and nonparametric methods are suitable for linkage analysis of complex disorders in small pedigrees. However, whether these results apply to large pedigrees remains to be answered.

Indexed as

Models, GeneticChromosome MappingComputer SimulationFemaleGenetic Diseases, InbornGenetic MarkersHumansLod ScoreMalePedigreeReproducibility of ResultsSample SizeSoftwareStatistics, NonparametricGenetic Markers

Identifiers

PMID10762550
PMCPMC1378023

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