Comparison of significance level at the true location using two linkage approaches: LODPAL and GENEFINDER

被引:2
作者
Hsu, FC
Hetmanski, JB
Li, L
Markakis, D
Jacobs, K
Shugart, YY [1 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21218 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Publ Hlth Sci, Biostat Sect, Winston Salem, NC 27103 USA
[3] Case Western Reserve Univ, Dept Epidemiol & Biostat, Div Genet Epidemiol, Cleveland, OH 44106 USA
[4] OPAL Grp, Div Stat Genet & Bioinformat, Cleveland, OH USA
关键词
D O I
10.1186/1471-2156-4-S1-S46
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: We compare two new software packages for linkage analysis, LODPAL and GENEFINDER. Both allow for covariate adjustment. Replicates 1 to 3 of Genetic Analysis Workshop 13 simulated data sets were used for the analyses. We described the results of searching for evidence of loci contributing to a simulated quantitative trait related to systolic blood pressure (SBP). Individuals with SBP greater than 130 mm Hg were defined as affected individuals, and all others as unaffected. Total cholesterol was treated as a covariate. Results: Using LODPAL, the power of detecting one of the three major genes related to SBP is 44.4% when a LOD score of 1 is used as the cut- off point. The power of GENEFINDER is lower than that of LODPAL. It is 22.2%. Conclusions: Based on the limited comparison, LODPAL provided the more reasonable power to detect linkage compared to GENEFINDER. After adjusting for the total cholesterol covariate, the current version of both programs appeared to give a high number of false positives.
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页数:6
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