- Open Access
Effect of the prior distribution of SNP effects on the estimation of total breeding value
© Nadaf et al.; licensee BioMed Central Ltd. 2012
- Published: 21 May 2012
Five main methods, commonly applied in genomic selection, were used to estimate the GEBV on the 15th QTLMAS workshop dataset: GBLUP, LASSO, Bayes A and two Bayes B type of methods (BBn and BBt). GBLUP is a mixed model approach where GEBV are obtained using a relationship matrix calculated from the SNP genotypes. The remaining methods are regression-based approaches where the SNP effects are first estimated and, then GEBV are calculated given the individuals' genotypes.
The differences between the regression-based methods are in their prior distributions for the SNP effects. The prior distribution for LASSO is a Laplace distribution, for Bayes A is a scaled Student-t distribution, and the Bayes B type methods have a Spike and Slab prior where only a proportion (π) of SNP has an effect, following a given distribution. In this study, two different distributions were considered for the Bayes B type methods: (i) normal and (ii) scaled Student-t. They are referred here as the BBn and BBt methods, respectively. These prior distributions are defined by one or more parameters controlling their scale/rate (λ), shape (df) or proportion of SNP with effect (π). LASSO requires one (λ); two for Bayes A (λ, df) and Bayes Bn (λ, π); and three for Bayes Bt (λ, df, π). In this study, all parameters were estimated from the data. An extra scenario for Bayes A and BBt was included where df was not estimated but fixed to 4 (suffixed _4df). The implementation of GBLUP was done using ASREML, the heritability was also estimated from the data. All other methods were implemented using a MCMC approach.
All Bayes A and B methods showed accuracy (correlation between True and Estimated BV) as high as 0.94 except for BA_4df (r = 0.91). Compared to the traditional BLUP using pedigree information, these methods improved the accuracy between 50 and 55%. GBLUP and LASSO were less accurate (0.81 and 0.85 respectively) and the improvements were 34 and 40% compared to BLUP.
Results of all methods were consistent and the accuracies for GEBV ranged between 0.81 and 0.94. When all parameters were estimated the results were similar for the Bayes A and Bayes B methods. Results showed that Bayes A was more sensitive to the changes in the shape parameter, and the parameter changes led to change in the accuracy of GEBV. However BBt was more robust to the change in this parameter. This may be explained by the fact that BBt estimates one extra parameter and it can buffer against a non-proper shape parameter.
- Prior Distribution
- Genomic Selection
- Laplace Distribution
- Epistatic QTLs
- Allelic Substitution Effect
With the availability of cost-effective SNP chips, genomic selection is currently been applied in agricultural species, using different statistical approaches. SNP information can be used to estimate breeding values by using (i) a mixed model or (ii) a regression-based approach. For the first approach, the SNP genotypes are used to estimate the relationship matrix among individuals, which later is used in a BLUP analysis (GBLUP) to estimate genomic breeding values (GEBV). For the second approach, the effect of individual SNPs can be estimated using multiple regression, and then GEBV for each individual are calculated as the sum of the SNP effects given their genotypes. Estimated SNP effects may also be of value to be used as a criterion for QTL mapping. Examples of methods based on this approach include Bayes A, Bayes B  and LASSO . The main difference between these methods is their assumption on the prior distribution of the SNP effects. These distributions are defined by one or more parameters regulating their shapes and scales/rates and can be assumed known or, alternatively they can be estimated from the data itself.
The aim of this study was to compare the GEBV using different methods of genomic selection on the common dataset from the 2011 QTLMAS workshop. For the different methods, the values for the parameters regulating the prior distribution of the SNP effect were also estimated from the data.
The dataset used here was the one provided by the organisers of the 15th QTLMAS workshop. It consisted of 3220 individuals, all were genotyped for about 10000 SNP on five chromosomes of equal length (1 Morgan each). The pedigree included 20 half-sib and 200 full-sib families, each including 15 offspring. Eight QTLs were simulated to affect the quantitative trait, with the largest one on chromosome 1, 2 linked QTLs on chromosomes 2 and 3, 1 imprinting one on chromosome 4, and 2 epistatic QTLs on chromosome 5. Heritability of the trait was 0.3 and two third (n = 2000) of the offspring were phenotyped.
Mixed model based method: GBLUP
where g is the vector of random total genetic effect assumed to be normally distributed as N(0,Gσ2 g), with G being the realised relationship matrix calculated from SNP information , and σ2 g the variance of g. The GBLUP was implemented using ASREML , in a two-step approach where σ2 g was first estimated from the data and later used to calculate the GEBV.
where, n is total number of SNP, z i is the vector of genotypes at SNP i; βi indicates the allelic substitution effect for SNP i.
The difference between the regression-based methods lays on the assumption of the prior distributions for the SNP effects. For instance, the prior distribution for LASSO  is a Laplace distribution, for Bayes A  is a scaled Student-t distribution, and the Bayes B type methods have a Spike and Slab prior where a proportion (π) of SNP has an a non zero effect on the trait, and the remaining (1-π) SNP having no effect on the trait. For the SNP affecting the traits two different distributions were considered: (i) normal and (ii) scaled Student-t. Here, they are referred as the BBn and BBt methods, respectively. The BBn method has also been referred as Bayes C.
These prior distributions for SNP effects are described by one or more parameters which includes scale/rate (λ), shape (df) and/or proportion of SNP with effect (π). The prior distribution assumed with LASSO is defined by one parameter (λ); two for Bayes A (λ, df) and Bayes Bn (λ, π); and three for Bayes Bt (λ, df, π). In this study, all parameters were estimated from the data (suffixed _edf). An extra scenario for Bayes A and Bayes Bt was included where df was not estimated but fixed to 4 (suffixed _4df). The models were implemented under a Bayesian framework using Gibbs sampling. Bounded flat priors (between 0.5 and 9) were used for the estimation of df. The parameters π and σ2 SNP were estimated from data using flat priors. For each analysis, a MCMC chain was run and the first 10000 cycles were discarded as burn-in period. Following this, 10000 realisations were collected, each separated by 20 cycles between consecutive realisations (i.e. length of chain = 210,000 cycles). The posterior mean was used as the estimate for each parameter of interest. For the case of Bayes A and B where df was estimated, the chain was 5 times longer.
Variance explained by genomic information
where PEV is the Prediction Error Variance, and r is the accuracy of estimates. The explained additive genetic variance (σ2 g ) was obtained using the above equations, for regression-based methods and the corresponding heritability was reported.
QTL mapping analysis
Additionally to the GEBV, the regression-based methods also estimate the effects for each individual SNP used in the analysis. We compared these results with association and linkage analysis results, in order to assess its potential use as a criterion for QTL mapping.
Association analysis was performed using the GRAMMAR approach , which comprises two steps. First, phenotypes were adjusted for the polygenic effects and second, residuals were fitted against each SNP using additive model as implemented in GenABEL .
Accuracies and heritabilities estimated by all methods.
Previous studies reported in the literature, have shown a superiority of Bayes B method over Bayes A (e.g. ). The results obtained here showed that the superior performance of Bayes B over Bayes A disappears when the parameters of the prior distribution of the SNP effect are estimated from the data. In this study, the shape parameter df, for BB_edf and BA_edf were estimated to be around 1 for both methods (see Additional file 2). Fixing df to be 4, resulted in a slight reduction on the GEBV accuracy for Bayes A, but it has little impact on the accuracy of Bayes B. This would explain why previous studies have reported a better performance of Bayes B over Bayes A. An interesting result was on the estimation of the parameter π. The estimated value obtained with both BBn and BBt_4df was around 0.01, but for BBt this estimate was around 0.4. Surprisingly, this large difference in π had very small impact on the overall accuracy of the GEBV, suggesting the need of further study to refine the meaning of the π and its relationship with the true proportion of SNP, or QTL affecting the trait.
QTL mapping and association analysis
The dataset simulated includes 5 simple additive QTLs (one on chromosome 1, 2 on chromosome 2 and 2 on chromosome 3), one imprinted QTL (chromosome 4) and 2 QTLs with epistasis effect (on chromosome 5).
Good consistency was observed for the results of all applied methods. For this specific dataset, the accuracy of Bayes A and B type of methods were better than those of GBLUP and LASSO. When all parameters of the prior distribution were estimated with the data, the results of Bayes A and Bayes B were the same. Fixing the shape parameter with Bayes A have a slight decrease in the accuracy but little effect on Bayes B. These results are consistent with previous studies reporting a superiority of Bayes B over Bayes A when the parameters of the prior distribution are assumed known.
This article has been published as part of BMC Proceedings Volume 6 Supplement 2, 2012: Proceedings of the 15th European workshop on QTL mapping and marker assisted selection (QTL-MAS). The full contents of the supplement are available online at http://www.biomedcentral.com/bmcproc/supplements/6/S2.
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