Literature DB >> 20551674

Power of competing strategies of linkage analysis for complex traits.

Jianzhong Ma1, E Warwick Daw, Christopher I Amos.   

Abstract

Variance components (VC) and the Bayesian Markov chain Monte Carlo (MCMC) analysis are two of the widely used linkage analysis approaches to mapping genes for complex quantitative traits. Both approaches can handle extended pedigrees and multiple markers and do not require a prespecified genetic model. In this study, we used simulated data to compare the performance of these two approaches with the traditional parametric linkage analysis. Using simulated data sets without linkage between a quantitative trait and the markers, we estimated a critical value for various test scores used in VC or MCMC and the location (LOC) score at a fixed level of significance (5%). These critical values were then used to determine the power for the three methods for simulated data sets with linkage. We found that both the VC and MCMC approaches worked well, compared with the LOC score, when there was only one gene underlying the quantitative trait; however, VC had higher power than the other methods in a simulation study of a complex phenotype influenced by more than one gene. We also compared two implementations of MCMC analysis, finding interpretation of results using the log of placement score was more accurate for linkage inference than the Bayes factor but required much more intensive simulation studies. Copyright 2010 S. Karger AG, Basel.

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Mesh:

Year:  2010        PMID: 20551674      PMCID: PMC2912646          DOI: 10.1159/000288709

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  12 in total

1.  Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure.

Authors:  D B Allison; M C Neale; R Zannolli; N J Schork; C I Amos; J Blangero
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

2.  Genome scans for Q1 and Q2 on general population replicates using Loki.

Authors:  D Shmulewitz; S C Heath
Journal:  Genet Epidemiol       Date:  2001       Impact factor: 2.135

3.  A score for Bayesian genome screening.

Authors:  E Warwick Daw; Ellen M Wijsman; Elizabeth A Thompson
Journal:  Genet Epidemiol       Date:  2003-04       Impact factor: 2.135

4.  Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis.

Authors:  Robert P Igo; Ellen M Wijsman
Journal:  Genet Epidemiol       Date:  2008-02       Impact factor: 2.135

Review 5.  Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions.

Authors:  E M Wijsman; C I Amos
Journal:  Genet Epidemiol       Date:  1997       Impact factor: 2.135

6.  Multipoint quantitative-trait linkage analysis in general pedigrees.

Authors:  L Almasy; J Blangero
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

7.  Faster sequential genetic linkage computations.

Authors:  R W Cottingham; R M Idury; A A Schäffer
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

8.  Robust variance-components approach for assessing genetic linkage in pedigrees.

Authors:  C I Amos
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

9.  Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

Authors:  Nicola H Chapman; Robert P Igo; Jennifer B Thomson; Mark Matsushita; Zoran Brkanac; Ted Holzman; Virginia W Berninger; Ellen M Wijsman; Wendy H Raskind
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2004-11-15       Impact factor: 3.568

10.  Genetic Analysis Workshop 13: simulated longitudinal data on families for a system of oligogenic traits.

Authors:  E Warwick Daw; John Morrison; Xiaojun Zhou; Duncan C Thomas
Journal:  BMC Genet       Date:  2003-12-31       Impact factor: 2.797

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