Mapping quantitative trait loci for binary traits using a heterogeneous residual variance model: an application to Marek's disease susceptibility in chickens

被引:23
作者
Xu, SZ [1 ]
Yonash, N
Vallejo, RL
Cheng, HH
机构
[1] Univ Calif Riverside, Dept Bot & Plant Sci, Riverside, CA 92521 USA
[2] USDA ARS, Avian Dis & Oncol Lab, E Lansing, MI 48823 USA
[3] NIAAA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
关键词
chicken; fisher-scoring; Marek's disease; maximum likelihood; QTL; threshold trait;
D O I
10.1023/A:1003522902078
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A typical problem in mapping quantitative trait loci (QTLs) comes from missing QTL genotype. A routine method for parameter estimation involving missing data is the mixture model maximum likelihood method. We developed an alternative QTL mapping method that describes a mixture of several distributions by a single model with a heterogeneous residual variance. The two methods produce similar results, but the heterogeneous residual Variance method is computationally much faster than the mixture model approach. In addition, the new method can automatically generate sampling variances of the estimated parameters. We derive the new method in the context of QTL mapping for binary traits in a F-2 population. Using the heterogeneous residual variance model, we identified a QTL on chromosome IV that controls Marek's disease susceptibility in chickens. The QTL alone explains 7.2% of the total disease variation.
引用
收藏
页码:171 / 178
页数:8
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