Totir Liviu R, Fernando Rohan L, Dekkers Jack C M, Fernández Soledad A, Guldbrandtsen Bernt
Department of Animal Science, Iowa State University, Ames, IA 50011, USA.
Genet Sel Evol. 2004 Jan-Feb;36(1):29-48. doi: 10.1186/1297-9686-36-1-29.
Under additive inheritance, the Henderson mixed model equations (HMME) provide an efficient approach to obtaining genetic evaluations by marker assisted best linear unbiased prediction (MABLUP) given pedigree relationships, trait and marker data. For large pedigrees with many missing markers, however, it is not feasible to calculate the exact gametic variance covariance matrix required to construct HMME. The objective of this study was to investigate the consequences of using approximate gametic variance covariance matrices on response to selection by MABLUP. Two methods were used to generate approximate variance covariance matrices. The first method (Method A) completely discards the marker information for individuals with an unknown linkage phase between two flanking markers. The second method (Method B) makes use of the marker information at only the most polymorphic marker locus for individuals with an unknown linkage phase. Data sets were simulated with and without missing marker data for flanking markers with 2, 4, 6, 8 or 12 alleles. Several missing marker data patterns were considered. The genetic variability explained by marked quantitative trait loci (MQTL) was modeled with one or two MQTL of equal effect. Response to selection by MABLUP using Method A or Method B were compared with that obtained by MABLUP using the exact genetic variance covariance matrix, which was estimated using 15,000 samples from the conditional distribution of genotypic values given the observed marker data. For the simulated conditions, the superiority of MABLUP over BLUP based only on pedigree relationships and trait data varied between 0.1% and 13.5% for Method A, between 1.7% and 23.8% for Method B, and between 7.6% and 28.9% for the exact method. The relative performance of the methods under investigation was not affected by the number of MQTL in the model.
在加性遗传模型下,亨德森混合模型方程(HMME)提供了一种有效的方法,可在已知系谱关系、性状和标记数据的情况下,通过标记辅助最佳线性无偏预测(MABLUP)获得遗传评估。然而,对于具有许多缺失标记的大型系谱,计算构建HMME所需的精确配子方差协方差矩阵是不可行的。本研究的目的是调查使用近似配子方差协方差矩阵对MABLUP选择响应的影响。使用两种方法生成近似方差协方差矩阵。第一种方法(方法A)完全舍弃两个侧翼标记之间连锁相未知的个体的标记信息。第二种方法(方法B)仅利用连锁相未知的个体在最具多态性的标记位点上的标记信息。针对侧翼标记有2、4、6、8或12个等位基因的情况,模拟了有无缺失标记数据的数据集。考虑了几种缺失标记数据模式。由标记数量性状位点(MQTL)解释的遗传变异性用一个或两个效应相等的MQTL进行建模。将使用方法A或方法B的MABLUP选择响应与使用精确遗传方差协方差矩阵的MABLUP选择响应进行比较,精确遗传方差协方差矩阵是根据给定观测标记数据的基因型值的条件分布,利用15,000个样本估计得到的。对于模拟条件,MABLUP相对于仅基于系谱关系和性状数据的BLUP的优势,方法A在0.1%至13.5%之间,方法B在1.7%至23.8%之间,精确方法在7.6%至28.9%之间。所研究方法的相对性能不受模型中MQTL数量的影响。