Leibniz Institute for Farm Animal Biology, Research Unit Genetics and Biometry, 18196 Dummerstorf, Germany.
Genetics. 2011 Jan;187(1):261-70. doi: 10.1534/genetics.110.122333. Epub 2010 Oct 18.
Methodology for mapping quantitative trait loci (QTL) has focused primarily on treating the QTL as a fixed effect. These methods differ from the usual models of genetic variation that treat genetic effects as random. Computationally expensive methods that allow QTL to be treated as random have been explicitly developed for additive genetic and dominance effects. By extending these methods with a variance component method (VCM), multiple QTL can be mapped. We focused on an F(2) crossbred population derived from inbred lines and estimated effects for each individual and their corresponding marker-derived genetic covariances. We present extensions to pairwise epistatic effects, which are computationally intensive because a great many individual effects must be estimated. But by replacing individual genetic effects with average genetic effects for each marker class, genetic covariances are approximated. This substantially reduces the computational burden by reducing the dimensions of covariance matrices of genetic effects, resulting in a remarkable gain in the speed of estimating the variance components and evaluating the residual log-likelihood. Preliminary results from simulations indicate competitiveness of the reduced model with multiple-interval mapping, regression interval mapping, and VCM with individual genetic effects in its estimated QTL positions and experimental power.
定位数量性状基因座 (QTL) 的方法主要侧重于将 QTL 视为固定效应。这些方法与通常将遗传效应视为随机的遗传变异模型不同。已经明确开发了计算成本高的方法,允许将 QTL 视为随机效应,这些方法适用于加性遗传和显性效应。通过使用方差分量法 (VCM) 扩展这些方法,可以定位多个 QTL。我们专注于从近交系衍生的 F2 杂交群体,并估计每个个体及其相应标记衍生遗传协方差的效应。我们提出了扩展的成对上位性效应,这些效应计算量很大,因为必须估计大量的个体效应。但是,通过用每个标记类的平均遗传效应替换个体遗传效应,可以近似遗传协方差。这通过减少遗传效应协方差矩阵的维数,显著降低了计算负担,从而显著提高了估计方差分量和评估剩余对数似然的速度。来自模拟的初步结果表明,该简化模型在估计的 QTL 位置和实验能力方面具有竞争力,与多区间映射、回归区间映射和具有个体遗传效应的 VCM 相比。