Literature DB >> 8213819

Two-locus models of disease: comparison of likelihood and nonparametric linkage methods.

L R Goldin1, D E Weeks.   

Abstract

The power to detect linkage for likelihood and nonparametric (Haseman-Elston, affected-sib-pair, and affected-pedigree-member) methods is compared for the case of a common, dichotomous trait resulting from the segregation of two loci. Pedigree data for several two-locus epistatic and heterogeneity models have been simulated, with one of the loci linked to a marker locus. Replicate samples of 20 three-generation pedigrees (16 individuals/pedigree) were simulated and then ascertained for having at least 6 affected individuals. The power of linkage detection calculated under the correct two-locus model is only slightly higher than that under a single locus model with reduced penetrance. As expected, the nonparametric linkage methods have somewhat lower power than does the lod-score method, the difference depending on the mode of transmission of the linked locus. Thus, for many pedigree linkage studies, the lod-score method will have the best power. However, this conclusion depends on how many times the lod score will be calculated for a given marker. The Haseman-Elston method would likely be preferable to calculating lod scores under a large number of genetic models (i.e., varying both the mode of transmission and the penetrances), since such an analysis requires an increase in the critical value of the lod criterion. The power of the affected-pedigree-member method is lower than the other methods, which can be shown to be largely due to the fact that marker genotypes for unaffected individuals are not used.

Mesh:

Year:  1993        PMID: 8213819      PMCID: PMC1682376     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  17 in total

1.  Linkage strategies for genetically complex traits. I. Multilocus models.

Authors:  N Risch
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

2.  Power of the linkage test for a heterogeneous disorder due to two independent inherited causes: a simulation study.

Authors:  M Martinez; L R Goldin
Journal:  Genet Epidemiol       Date:  1990       Impact factor: 2.135

3.  Robust methods for the detection of genetic linkage for quantitative data from pedigrees.

Authors:  C I Amos; R C Elston
Journal:  Genet Epidemiol       Date:  1989       Impact factor: 2.135

4.  The affected-pedigree-member method of linkage analysis.

Authors:  D E Weeks; K Lange
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

5.  Effects of misspecifying genetic parameters in lod score analysis.

Authors:  F Clerget-Darpoux; C Bonaïti-Pellié; J Hochez
Journal:  Biometrics       Date:  1986-06       Impact factor: 2.571

6.  A comparison of sib-pair linkage tests for disease susceptibility loci.

Authors:  W C Blackwelder; R C Elston
Journal:  Genet Epidemiol       Date:  1985       Impact factor: 2.135

7.  Linkage between quantitative trait and marker loci: methods using all relative pairs.

Authors:  J M Olson; E M Wijsman
Journal:  Genet Epidemiol       Date:  1993       Impact factor: 2.135

8.  On the lod score method in linkage analysis.

Authors:  J Chotai
Journal:  Ann Hum Genet       Date:  1984-10       Impact factor: 1.670

9.  The investigation of linkage between a quantitative trait and a marker locus.

Authors:  J K Haseman; R C Elston
Journal:  Behav Genet       Date:  1972-03       Impact factor: 2.805

10.  A family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands.

Authors:  E S Gershon; J Hamovit; J J Guroff; E Dibble; J F Leckman; W Sceery; S D Targum; J I Nurnberger; L R Goldin; W E Bunney
Journal:  Arch Gen Psychiatry       Date:  1982-10
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  19 in total

1.  Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases.

Authors:  P C Abreu; D A Greenberg; S E Hodge
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

Review 2.  Genetic analyses of schizophrenia.

Authors:  C N Pato; K M Schindler; M T Pato
Journal:  Curr Psychiatry Rep       Date:  2000-04       Impact factor: 5.285

3.  Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization.

Authors:  K Strauch; R Fimmers; T Kurz; K A Deichmann; T F Wienker; M P Baur
Journal:  Am J Hum Genet       Date:  2000-05-04       Impact factor: 11.025

4.  Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations.

Authors:  K A Goddard; P J Hopkins; J M Hall; J S Witte
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

5.  HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity.

Authors:  Susan E Hodge; Veronica J Vieland; David A Greenberg
Journal:  Am J Hum Genet       Date:  2002-02       Impact factor: 11.025

6.  The power and statistical behaviour of allele-sharing statistics when applied to models with two disease loci.

Authors:  Yin Y Shugart; Bing-Jian Feng; Andrew Collins
Journal:  J Genet       Date:  2002-12       Impact factor: 1.166

7.  Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

Authors:  L L Field; B J Kaplan
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

8.  Affecteds-only linkage methods are not a panacea.

Authors:  D A Greenberg; S E Hodge; V J Vieland; M A Spence
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

9.  Nonparametric simulation-based statistics for detecting linkage in general pedigrees.

Authors:  S Davis; M Schroeder; L R Goldin; D E Weeks
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

10.  Further evidence for the increased power of LOD scores compared with nonparametric methods.

Authors:  M Durner; V J Vieland; D A Greenberg
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

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