ArticleAmerican journal of human genetics2000
Power comparison of parametric and nonparametric linkage tests in small pedigrees.
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.
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Who cites it
8 citing papers in PubMed.
- Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance.Human genetics · 2013Trial
- Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder.Molecular autism · 2014Article
- Linkage of bipolar affective disorder on chromosome 8q24: follow-up and parametric analysis.Molecular psychiatry · 2004Article
- A survey of current software for linkage analysis.Human genomics · 2003Review
- The power and statistical behaviour of allele-sharing statistics when applied to models with two disease loci.Journal of genetics · 2002Article
- Statistics for nonparametric linkage analysis of X-linked traits in general pedigrees.American journal of human genetics · 2002Article
- A survey of affected-sibship statistics for nonparametric linkage analysis.American journal of human genetics · 2001Article
- A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6.Molecular psychiatry · 2000Article
Corrections and comments
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Authors and funding
4 authors.
Funding
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.
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