Azevedo Camila Ferreira, de Resende Marcos Deon Vilela, E Silva Fabyano Fonseca, Viana José Marcelo Soriano, Valente Magno Sávio Ferreira, Resende Márcio Fernando Ribeiro, Muñoz Patricio
Department of Statistics, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
Embrapa Forestry, Colombo, Paraná, Brazil.
BMC Genet. 2015 Aug 25;16:105. doi: 10.1186/s12863-015-0264-2.
A complete approach for genome-wide selection (GWS) involves reliable statistical genetics models and methods. Reports on this topic are common for additive genetic models but not for additive-dominance models. The objective of this paper was (i) to compare the performance of 10 additive-dominance predictive models (including current models and proposed modifications), fitted using Bayesian, Lasso and Ridge regression approaches; and (ii) to decompose genomic heritability and accuracy in terms of three quantitative genetic information sources, namely, linkage disequilibrium (LD), co-segregation (CS) and pedigree relationships or family structure (PR). The simulation study considered two broad sense heritability levels (0.30 and 0.50, associated with narrow sense heritabilities of 0.20 and 0.35, respectively) and two genetic architectures for traits (the first consisting of small gene effects and the second consisting of a mixed inheritance model with five major genes).
G-REML/G-BLUP and a modified Bayesian/Lasso (called BayesAB or t-BLASSO) method performed best in the prediction of genomic breeding as well as the total genotypic values of individuals in all four scenarios (two heritabilities x two genetic architectures). The BayesAB-type method showed a better ability to recover the dominance variance/additive variance ratio. Decomposition of genomic heritability and accuracy revealed the following descending importance order of information: LD, CS and PR not captured by markers, the last two being very close.
Amongst the 10 models/methods evaluated, the G-BLUP, BAYESAB (-2,8) and BAYESAB (4,6) methods presented the best results and were found to be adequate for accurately predicting genomic breeding and total genotypic values as well as for estimating additive and dominance in additive-dominance genomic models.
全基因组选择(GWS)的完整方法涉及可靠的统计遗传学模型和方法。关于这个主题的报告在加性遗传模型中很常见,但在加性-显性模型中却不多见。本文的目的是:(i)比较使用贝叶斯、套索和岭回归方法拟合的10种加性-显性预测模型(包括当前模型和提出的改进模型)的性能;(ii)根据三种数量遗传信息来源,即连锁不平衡(LD)、共分离(CS)以及系谱关系或家族结构(PR),对基因组遗传力和准确性进行分解。模拟研究考虑了两个广义遗传力水平(0.30和0.50,分别对应狭义遗传力0.20和0.35)以及两种性状的遗传结构(第一种由小基因效应组成,第二种由包含五个主基因的混合遗传模型组成)。
G-REML/G-BLUP和一种改进的贝叶斯/套索方法(称为BayesAB或t-BLASSO)在所有四种情景(两种遗传力×两种遗传结构)下对基因组育种以及个体的总基因型值的预测中表现最佳。BayesAB型方法显示出更好的恢复显性方差/加性方差比率的能力。基因组遗传力和准确性的分解揭示了信息的重要性顺序如下:LD、未被标记捕获的CS和PR,后两者非常接近。
在评估的10种模型/方法中,G-BLUP、BAYESAB(-2,8)和BAYESAB(4,6)方法呈现出最佳结果,并且被发现足以准确预测基因组育种和总基因型值,以及估计加性-显性基因组模型中的加性和显性效应。