- Research
- Open Access
Genome-assisted prediction of a quantitative trait measured in parents and progeny: application to food conversion rate in chickens
- Oscar González-Recio^{1}Email author,
- Daniel Gianola^{1, 2},
- Guilherme JM Rosa^{1},
- Kent A Weigel^{1} and
- Andreas Kranis^{3}
https://doi.org/10.1186/1297-9686-41-3
© González-Recio et al; licensee BioMed Central Ltd. 2009
- Received: 16 December 2008
- Accepted: 05 January 2009
- Published: 05 January 2009
Abstract
Accuracy of prediction of yet-to-be observed phenotypes for food conversion rate (FCR) in broilers was studied in a genome-assisted selection context. Data consisted of FCR measured on the progeny of 394 sires with SNP information. A Bayesian regression model (Bayes A) and a semi-parametric approach (Reproducing kernel Hilbert Spaces regression, RKHS) using all available SNPs (p = 3481) were compared with a standard linear model in which future performance was predicted using pedigree indexes in the absence of genomic data. The RKHS regression was also tested on several sets of pre-selected SNPs (p = 400) using alternative measures of the information gain provided by the SNPs. All analyses were performed using 333 genotyped sires as training set, and predictions were made on 61 birds as testing set, which were sons of sires in the training set. Accuracy of prediction was measured as the Spearman correlation (${\overline{r}}_{S}$) between observed and predicted phenotype, with its confidence interval assessed through a bootstrap approach. A large improvement of genome-assisted prediction (up to an almost 4-fold increase in accuracy) was found relative to pedigree index. Bayes A and RKHS regression were equally accurate (${\overline{r}}_{S}$ = 0.27) when all 3481 SNPs were included in the model. However, RKHS with 400 pre-selected informative SNPs was more accurate than Bayes A with all SNPs.
Keywords
- Information Gain
- Reproduce Kernel Hilbert Space
- Bandwidth Parameter
- Informative SNPs
- Bayesian Regression
Introduction
Genome-wide association studies of diseases and complex traits [1] have permeated into animal breeding, and genome-assisted selection has become a major focus of research [2, 3]. However, genome-based artificial selection poses several challenges. For instance, methods for prediction of genetic merit or phenotype using a large number of markers must be contrasted and improved. Also, biological and economical advantages of genome-assisted selection in a breeding program must be quantified (this second problem is not addressed herein).
A very important issue is how to deal with a much larger number of markers (p) than of individuals that are genotyped (n). Some proposals include treating marker effects as random, with shrinkage of estimates of non-informative markers to zero. This is done naturally in a Bayesian context, where all unknowns are treated as random variables (e.g., Gianola and Fernando, [4]). On the one hand, Bayesian regression methods, such as Bayes A and Bayes B [2], or the special case of Bayes A described by Xu [5] have recently gained attention. However, all of these procedures involve strong assumptions a priori. On the other hand, non-parametric methods have been suggested as an alternative for predicting genomic breeding values, because these methods may require weaker assumptions when modeling complex quantitative traits [6].
These non-parametric approaches have been applied to simulated [7] and field [8] data, and results seem promising. The simulations from Gianola et al. [7] involved 100 biallelic markers and additive × additive interactions between five pairs of loci. Gonzalez-Recio et al. [8] used 24 pre-selected SNPs from a filter and wrapper feature subset selection algorithm [9] in a reproducing kernel Hilbert spaces (RKHS) regression model. However, these non-parametric methods have not been tested yet using a large number of SNPs and field data. Inclusion of a large number of SNPs in these non-parametric models must be studied. Further, evaluating the accuracy of such methods in predicting phenotypes in future generations is a crucial issue in artificial selection programs.
Genomic information became available in animal breeding recently, and most research involving either the large p small n problem [10, 2] or the prediction of future generations [11, 12] has resorted to simulations. Arguably, assumptions built in simulations may fail to represent the true complexity of biological systems and, typically, simulations tend to favor some of the models under evaluation. Therefore, the extent to which simulation results hold with real data can be questioned.
The present paper uses field data from the Genomics Initiative Project at Aviagen Ltd. (Newbridge, UK). Food conversion rate (FCR) is one of the most economically important traits in the broiler industry, because it affects feeding and housing costs markedly. Genome-assisted selection programs may provide greater reliability of predictions of future performance, thus increasing profitability.
The objective of this study was to compare the ability of Bayes A regression and of semi-parametric (RKHS) regression to predict yet-to-be observed phenotypes, using field data on FCR in a two-generation setting.
Methods
Animal Care and Use Committee approval was not obtained for this study because the data were obtained from an existing database supplied by Aviagen Ltd. (Newbridge, UK).
In a nutshell, a one-fold cross-validation with a training set and a testing set was carried out, as the testing set included only sons of sires that were in the training test. Several statistical methods were used to predict the average phenotypes of offspring of animals in the testing set, i.e., first-generation performance. These included a standard genetic evaluation, which ignored SNP genotypes, and two methods that included all available SNPs (after editing) as predictors in the model. The latter methods, which included genomic information, were Bayesian regression and RKHS regression. In addition, the RKHS regression approach was fitted with 400 pre-selected SNPs, where pre-selection was based on information gain using alternative criteria. In this section, the data set employed, the pre-selection of SNPs, and the statistical methods that were applied are described.
Phenotypic Data
Data consisted of average FCR records for progeny of each of 394 sires from a commercial broiler line in the breeding program of Aviagen Ltd. Prior to the analyses, the individual bird FCR records were adjusted for environmental and mate effects, as described in Ye et al. [13]. In order to assess the reliability of genome-assisted evaluation, two data sets (training and testing) were constructed. The testing set included offspring from sires with records in the training set. Sires included in the testing set were required to have sires in the training set with progeny records, and needed to have more than 20 progenies with FCR records, to have a reliable mean phenotype. Sires in the training and testing sets had an average of 33 and 44 progeny, respectively. Family size (half sibs) in the training set ranged between 1 and 284, with the mean and median being 32 and 17, respectively. Sixty-one sires (15.5% of the total) were included in the testing set, whereas the remaining 333 sires were in the training set. Predictions were calculated from the training set, and the accuracy of predicting the mean progeny phenotype was assessed using sons in the testing set.
Genomic Data
Genotypes consisted of 4505 SNPs chosen from the 2.8 million SNPs identified in the sequencing project of the chicken genome [14]. A data file titled "Database of SNPs used in the Illumina Corp. chicken genotyping project" (downloadable from http://poultry.mph.msu.edu/resources/resources.htm) describes partially the panel used, and further details on the 6 K panel can be found in Andreescu et al. [15]. All SNPs with monomorphic genotypes or with minor allele frequencies less than 5% were excluded. After editing, genotypes consisted of 3481 of the initial 4505 SNPs.
where A is the set of all states that Y can take, and the logarithm is on base 2 to mimic bits of information. The above pertains to a discrete distribution since entropy is not well defined in the continuous case [17]. Here, Y refers to FCR phenotypes that were discretized by considering different number of classes of FCR and different cutpoints, as follows. First, two extreme FCR classes ("low" and "high") were set up using cutpoints corresponding to the α and (1-α) quantiles (α = 0.15, 0.20, 0.25, 0.35 and 0.40) of the FCR phenotypes for sires in the training set. Further, an additional "middle" class (FCR between percentiles 0.40 and 0.60) was included to enrich the discretized data. In total, information gain was calculated in ten subsets, corresponding to combinations of the five 'extreme' tail α-values, with or without the intermediate class.
where $\text{N}={N}_{k}^{L}+{N}_{k}^{M}+{N}_{k}^{H}$. Note that ${N}_{k}^{M}$ = 0 if a middle class was not included.
The 400 SNPs with largest information gain in each of the ten partitions were pre-selected to build up a 400-SNP genotype for each sire. Note that the choice of the 400 SNPs was arbitrary, but it roughly represents 10% of the initial SNPs.
Models
Let y (333 × 1) be the vector of mean adjusted FCR records for progeny of sires in the training set. Three different methods for prediction of genomic breeding values for FCR were used, as described next.
Standard genetic evaluation (E-BLUP)
A Bayesian equivalent of empirical best linear unbiased prediction of sires' transmitting abilities, as described by Henderson [18], was used. This method uses pedigree data as the only source of genetic information. The linear model was:
y = μ 1 + Zu + e
where, μ is an unknown mean; 1 is a vector of ones; u = {u_{ i }} is a vector of sire effects; u_{ i }is the effect of sire i in the pedigree (i = 1, 2, ..., 624) and Z is an incidence matrix of order 333 × 624 linking u to the observed data. A priori, the sire effects were assumed to be distributed as u ~N(0, A${\sigma}_{u}^{2}$), where A is the additive relationship matrix between sires, and ${\sigma}_{u}^{2}$ is the variance between sires. The residuals, e, were assumed to be distributed as N(0, R = N^{-1} ${\sigma}_{e}^{2}$), where N = {n_{ i }} is a diagonal matrix with elements n_{ i }representing the number of progeny of sire i and ${\sigma}_{e}^{2}$ is the residual variance. This dispersion structure for e weights the residuals according to the number of progeny each sire has [17, 19]. Independent scaled inverted chi-square prior distributions were assigned to the sire and residual variances as ${\sigma}_{u}^{2}~{\upsilon}_{u}{s}_{u}^{2}{\chi}_{{\upsilon}_{u}}^{-1}$ and ${\sigma}_{e}^{2}~{\upsilon}_{e}{s}_{e}^{2}{\chi}_{{\upsilon}_{e}}^{-1}$, respectively, where υ_{ u }= 5 and υ_{ e }= 3 correspond to the degrees of freedom, and ${s}_{u}^{2}$ = 0.1 and ${s}_{e}^{2}$ = 8.67 were the corresponding scale parameters. Sire merit (transmitting ability) was inferred using a Gibbs sampling algorithm.
Bayes A
Meuwissen et al. [2] have proposed a Bayesian model in which the additive effects of chromosome segments marked by SNPs follow a normal distribution with a segment-specific variance. These variances are assigned a common scaled inverted chi-square prior distribution. The model fitted in this study had the form:
y = μ 1 + Xb + e.
Here, y is a 333 × 1 vector of progeny means for adjusted FCR, μ is their mean value, and 1 is a column vector of ones; b = {b_{ s }} is a vector of 3481 × 1 SNP effects, and b_{ s }is the regression coefficient on the additive effect of SNP s (s = 1, 2, ..., 3481). Elements of the incidence matrix X, of order n × p (n = 333; p = 3481), were set up as for an additive model, with values -1, 0 or 1 for aa, Aa and AA, respectively. The b_{ s }effects were assumed normally and independently distributed a priori as N(0, ${\sigma}_{s}^{2}$), where ${\sigma}_{s}^{2}$ is an unknown variance specific to marker s. The prior distribution of each ${\sigma}_{s}^{2}$ was assumed to be χ^{-2}(υ, S) with υ = 4 and S = 0.01. The residuals (e) were assumed to be distributed as N(0, R), with R constructed as in the previous model.
Reproducing kernel Hilbert spaces regressions
A RKHS regression [20–22] is a semi-parametric approach that allows inference regarding functions, e.g., genomic breeding values, without making strong prior assumptions. As described in Gianola and van Kaam [6] and González-Recio et al. [8] in the context of genome-assisted selection, this model can be formulated as:
y = Xβ + K_{ h }α + e,
There are two key issues in the RKHS regression pertaining to the non-parametric term: choosing the matrix of kernels, and tuning the h and λ parameters. The matrix of kernels aims to measure "distances" between genotypes. This matrix K_{ h }had dimension 333 × 333, with rows in the form ${{k}^{\prime}}_{i}=\left\{{K}_{h}({x}_{i}-{x}_{j})\right\}$, j = 1, 2, ..., 333, where K_{ h }(x_{ i }- x_{ j }) is the kernel involving the genotypes of sires i and j. The kernel refers to any smooth function for distances between objects, such that K_{ h }(x_{ i }- x_{ j }) ≥ 0. Different types of kernels may be used [23]. A Gaussian kernel was chosen in this research, with form: ${K}_{h}({x}_{i}-{x}_{j})=\mathrm{exp}\left(-\frac{dist({x}_{i}-{x}_{j})}{h}\right)$, where dist(x_{ i }- x_{ j }) is a measurement of distance between genotypes of sires i and j, and h is a bandwidth parameter. The choice of h and of the measurement of distance between genotypes must be done cautiously. A generalized (direct) cross validation procedure was used to tune h, as described in Wahba et al. [24]. However, measuring distances between genotypes is less straightforward, because a large variety of criteria might be used for this purpose (e.g. Gianola et al. [7]; Gianola and van Kaam, [6]; Gonzalez-Recio et al., [8]).
Two substrings that differ from each other completely, corresponding to SNPs from loci 1–3, and 6–7
Substring 1 | Substring 2 | |
---|---|---|
Sire i | AABbCC | FFGg |
Sire j | AabbCc | ffgg |
where DA_{ k }is the number of different alleles in substring k. In the example, sires i and j differ in one allele at each SNP (AA vs Aa, Bb vs bb, and CC vs Cc) in substring 1. In substring 2, sires i and j differ in 2 alleles for the first SNP (FF vs ff) and in 1 allele for the second SNP (Gg vs gg). Here, the two substrings had distances DA_{1} = DA_{2} = 3.
A modification of this system was used for models in which SNPs were pre-selected using the information gain score. Here, the number of different alleles at each SNP was weighted by the information gain score at that locus. Therefore, the distance between two genotypes was calculated as: $dist({x}_{i}-{x}_{j})={\displaystyle \sum _{k=1}^{m}{\mathrm{log}}_{2}\left(1+{{w}^{\prime}}_{k}d{a}_{k}\right)}$, where w_{ k }and da_{ k }are column vectors with typical elements equal to the information gain score and the number of different alleles, respectively, for each SNP in substring k. This kernel weights dissimilarity between SNPs by the reduction in entropy. With this approach, the kernel matrix K is symmetric and positive definite, so it fulfills the requirements of a RKHS, and it can be viewed as a correlation matrix between genomic combinations.
In total, 11 RKHS regression analyses were performed: one including all 3481 SNPs; five (α = 0.15, 0.20, 0.25, 0.35 and 0.40) including 400 pre-selected SNPs using the information gain calculated using two ("low" and "high") classes to classify sires, and five (α = 0.15, 0.20, 0.25, 0.35 and 0.40) including 400 pre-selected SNPs with information gain calculated by classifying sires into three ("low", "medium" and "high") classes.
Posterior estimates from all models were obtained with a Gibbs sampling algorithm based on 150,000 iterations, discarding the first 50,000 as burn-in, and keeping all 100,000 subsequent samples for inferences.
Predictive ability
Progeny phenotypes in the testing set were predicted using the estimates obtained from the training set. First, using the training set with each model, inferences were made regarding the predicted transmitting ability for E- BLUP, prediction of SNPs coefficients for Bayes A, and prediction of non-parametric coefficients for RKHS regression. Phenotypes in the testing set were predicted as follows:
E-BLUP
Phenotypes were predicted using pedigree indexes via sire and maternal grandsire (information from maternal relatives was not included). The pedigree index for sire t in the testing set (PI_{ t }) was $P{I}_{t}={\scriptscriptstyle \raisebox{1ex}{$1$}\!\left/ \!\raisebox{-1ex}{$2$}\right.}PT{A}_{s}+{\scriptscriptstyle \raisebox{1ex}{$1$}\!\left/ \!\raisebox{-1ex}{$4$}\right.}PT{A}_{mgs}$, where PTA_{ s }and PTA_{ mgs }are the predicted transmitting abilities of the bird's sire and maternal grandsire, respectively.
Bayes A
The p = 3481 estimates of regressions coefficients corresponding to additive effects of the SNPs ($\widehat{b}$) from the training set were multiplied by their respective genotype codes (x_{ ts }= -1, 0 or 1 for aa, Aa or AA, respectively) for sire t in the testing set to obtain a predicted phenotype as ${\widehat{y}}_{t}=\widehat{\mu}+{\displaystyle \sum _{s=1}^{3481}{\widehat{b}}_{s}{x}_{ts}}$, where $\widehat{\mu}$ and ${\widehat{b}}_{s}$ are the posterior means of μ and b_{ s }, respectively.
Reproducing kernel Hilbert spaces regressions
where K* (h) is a matrix with dimension 61 × 333, and with rows of the form ${{k}^{\prime}}_{t}^{*}=\left\{{K}_{h}^{*}({x}_{t}-{x}_{j})\right\}$, j = 1, 2, ..., 333, where ${K}_{h}^{*}({x}_{t}-{x}_{j})$ is the kernel between the genotype of sire t in the testing set and sire j in the training set. The same bandwidth parameter that was tuned with the training set was used. The vector $\widehat{\alpha}$ represented the posterior means of the 333 non-parametric regression coefficients for sires in the training sample.
Typically, the objective of prediction in animal breeding is to rank candidates for selection, and to subsequently choose the highest-ranked candidates as parents of the next generation. Spearman correlations (r_{S}) were calculated between predicted and observed phenotypes of sires in the testing set for all methods. Confidence intervals of the correlation estimates were formed using bootstrapping [25, 26] for each method. Pairs, defined as the predicted phenotypes in the testing set and its corresponding observed (known) phenotype, were assumed to be from an independent and identically distributed population. Then, 10,000 pairs were drawn with replacement from the whole testing set, and the Spearman correlation was computed in each of the bootstrap samples.
Further, computing times for running the first 10,000 samples were tested for Bayes A and for RKHS regression using all 3481 SNPs in a HPxw6000 workstation with a 2.4 GHz × 2 processor and 2 Gb RAM. A Gauss-Seidel algorithm with residual updates [27] was used in the Bayes A method, as suggested by Legarra and Misztal [28]. The solving effect-by-effect strategy described in Misztal and Gianola [29] was adapted to compute the RKHS regressions.
Results and discussion
Mean adjusted FCR was 1.23 in the training set, with a standard deviation of 0.1. The posterior mean of heritability was 0.21 with the E-BLUP model. This estimate was similar to those reported by Gaya et al. [30] and Pym and Nicholls [31], but higher than that of Zhang et al. [32]. The posterior mean (standard deviation) of the residual variance was estimated at 1.17 (0.22) and 0.50 (0.12) with Bayes A and RKHS, respectively, using all 3481 SNPs in each case. Notably, analyses using RKHS regression on 400 pre-selected SNPs produced a slightly smaller posterior mean of the residual variance than analyses based on all 3481 SNPs.
Means, standard deviations (s.d.) and 95% confidence intervals (CI) of the Bootstrap distribution of Spearman correlations between predicted and observed phenotypes in the testing set
Whole genome methods | |||
---|---|---|---|
Method | Mean | s.d. | CI (95%) |
E-BLUP | 0.11 | 0.13 | (-0.13, 0.35) |
Bayes A | 0.27 | 0.12 | (0.04, 0.49) |
RKHS | 0.27 | 0.12 | (0.03, 0.50) |
Information gain using 2 classes (400 pre-selected SNPs) + RKHS | |||
Quantile | Mean | s.d. | CI (95%) |
0.15 | 0.33 | 0.12 | (0.09, 0.56) |
0.20 | 0.32 | 0.11 | (0.10, 0.53) |
0.25 | 0.36 | 0.11 | (0.13, 0.57) |
0.30 | 0.19 | 0.12 | (-0.05, 0.42) |
0.35 | 0.35 | 0.11 | (0.12,0.55) |
0.40 | 0.33 | 0.11 | (0.10, 0.53) |
Information gain using 3 classes (400 pre-selected SNPs) + RKHS | |||
Quantile | Mean | s.d. | CI (95%) |
0.15 | 0.32 | 0.11 | (0.10, 0.54) |
0.20 | 0.24 | 0.13 | (-0.01, 0.48) |
0.25 | 0.39 | 0.11 | (0.16, 0.59) |
0.30 | 0.19 | 0.12 | (-0.05, 0.42) |
0.35 | 0.20 | 0.12 | (-0.04, 0.43) |
0.40 | 0.16 | 0.12 | (-0.08, 0.40) |
RKHS regression with pre-selected SNPs was always more accurate than E-BLUP, and it was also more accurate than either whole-genome Bayes A or whole-genome RKHS in 7 out of 12 comparisons. However, the bootstrap confidence intervals overlapped to some extent. Analyses performed with SNPs that were pre-selected using only sires from the low and high classes tended to have better predictive abilities (${\overline{r}}_{S}$ > 0.33) than analyses that involved an additional middle class, except for the setting with α = 0.30 (${\overline{r}}_{S}$ = 0.19). Analyses that included SNPs that were pre-selected based on information gain from three classes (low, medium and high) were more variable, although confidence bands overlapped. Four out of six analyses produced poorer predictions than either Bayes A or RKHS using all 3481 SNPs. This is probably due to the lower information gain obtained when separating sires into 3 classes. However, SNPs that were pre-selected using 3 classes and α = 0.25 had the best predictive ability, with an almost 4-fold improvement in prediction accuracy relative to E-BLUP. Pre-selection of SNPs reduces noise when measuring genomic differences, because non-informative SNPs are not considered. Furthermore, with pre-selected SNPs, this kernel placed more weight on informative SNPs. Other methods of pre-selecting SNPs are available and should be tested as well. Among these, the least absolute shrinkage and selection operator (LASSO; [33]), or its Bayesian counterpart [34] are appealing and yield predicted genomic values directly.
Bayes A and RKHS regression using all SNPs had similar predictive ability, even though these methods are very different from each other. Bayesian regression shrinks weakly informative SNPs towards zero, whereas RKHS regression makes weaker a priori assumptions and focuses on prediction of outcomes. Bayes A is also highly dependent on the prior distribution assigned to the variances of regression coefficients. Different scale parameters and degrees of belief for the χ^{-2}(υ, S) distribution produced very different predictive abilities (only the best choice was shown in this study). The large p, small n, problem plays an important role in Bayes A, and posterior estimates are greatly affected by the choice of hyper-parameters in the prior distribution. Meuwissen et al. [2] chose their prior distribution for the variances of regression coefficients based on their simulation. This choice is not straightforward with real data. Hence, an extra layer is missing in the hierarchy of Bayes A. For example, markers on the same chromosome could be assigned the same prior variance, such that for chromosome j, the conditional posterior distribution of ${\sigma}_{j}^{2}$ would have p_{ j }+r degrees of freedom. The RKHS regression approach, on the other hand, is less dependent on priors, and it can also be implemented in a non-Bayesian manner. Nonetheless, two issues must be considered carefully in RKHS: the choice of the bandwidth parameter (h) and of the kernel (i.e., how to measure genomic differences). Generalized cross-validation or jackknife methods are broadly accepted for tuning smoothing parameters. In this study, the same bandwidth parameter was used in the training and testing sets, although tuning a specific parameter for each set is an option to be explored. However, measuring genomic differences (non-Euclidean distances) may be done in different ways, each yielding different predictive ability. The kernel described in this research performed best among several kernels that were tested. To be effective in prediction of phenotypes in future generations, a proper kernel function must be used. Furthermore, correct tuning of the smoothing parameter is needed. As knowledge on the genome increases, more suitable kernels may be designed. Since strong assumptions are used in parametric models (e.g., regarding dominance or epistasis), RKHS regression is expected to produce better predictions for complex traits because it may deal with crude, noisy, redundant and inconsistent information.
Computing times for the first 10,000 samples were 1398.6 and 110.88 CPU seconds for whole-genome Bayes A and whole-genome RKHS regression, respectively. Thus, the semi-parametric regression was 12.6 times faster, and computing time does not depend on the number of SNPs but, rather, on the number of animals that were genotyped. This is because the matrix of kernels is n × n, where n is the number of animals genotyped, irrespective of the number of SNPs. Computing time in Bayes A depends on the number of SNPs (or haplotypes) that are genotyped, because these influence the number of conditional distributions that must be sampled. Gibbs sampling may mix poorly, and methods including a Metropolis-Hastings step, such as Bayes B [2], might be prohibitive from a computational point of view when p is large. Further, convergence should be tested carefully in field data with Bayesian regression methods, as pointed out by ter Braak et al. [35].
Other authors have evaluated predictive ability of models including genomic information in different scenarios. Gonzalez-Recio et al. [8] analyzed a lowly heritable trait (chicken mortality) in a similar population using different parametric and non-parametric approaches. These authors found a higher predictive ability for RKHS regression than for other methods, including the Bayesian regression model proposed by Xu [5], which is similar to Bayes A. However, this study differed in some respects from the present research. For example, genomic differences between genotypes in the kernel utilized by Gonzalez-Recio et al. [8] were computed from only 24 pre-selected SNPs based on the filter-wrapper feature subset algorithm of Long et al. [9]. Also, predictive ability was assessed on current phenotypes, and not on phenotypes of future generations, as it was the case in the present study. Other authors using real data, such as a study in mice [36], found that methods incorporating genomic information produced more accurate phenotypic predictions than BLUP in a model with independent families.
Conclusion
This research indicated that prediction accuracy of genetic evaluations can be enhanced by incorporating genomic data into breeding programs for a moderate heritability trait, such as FCR in broilers. This is one of the most important traits in the broiler industry from an economical point of view, and genome-assisted selection may help increase profitability in breeding and commercial flocks [37]. Reproducing kernel Hilbert spaces regression can handle a large number of markers without making strong assumptions, and the tandem approach of pre-selection of SNPs for subsequent use in RKHS regression seems to be an appealing approach, as found in this study. Pre-selection may be useful in the development of assays with fewer number of SNPs. Pre-selection of SNPs may be performed from a large battery of SNPs, genotyped on a restricted number of sires with a large number of progeny. Genotyping of animals on a greater scale may become more affordable if a smaller number of informative SNPs is included on a chip. Subsequently, semi-parametric methods can be used in conjunction with these SNPs to predict future phenotypes with high accuracy.
Declarations
Acknowledgements
The authors wish to thank S Avendaño (Aviagen Ltd.) for providing the data and comments, and A Legarra for discussion on computing matters. The first author thanks the financial support from the Babcock Institute for International Dairy Research and Development at the University of Wisconsin-Madison. The Wisconsin Agriculture Experiment Station, grant NSF DMS-NSF DMS-044371 and Aviagen Limited are acknowledged for support to D Gianola. K Weigel acknowledges the National Association of Animal Breeders (Columbia, MO) for partial financial support.
Authors’ Affiliations
References
- Hirschhorn JL, Daly MJ: Genome wide association studies for common diseases and complex traits. Nat Rev Genet. 2005, 6: 95-108. 10.1038/nrg1521.View ArticlePubMedGoogle Scholar
- Meuwissen THE, Hayes BJ, Goddard ME: Prediction of total genetic value using genome-wide dense marker maps. Genetics. 2001, 157: 1819-1829.PubMed CentralPubMedGoogle Scholar
- Schaeffer LR: Strategy for applying genome-wide selection in dairy cattle. J Anim Breed Genet. 2006, 123 (4): 218-223. 10.1111/j.1439-0388.2006.00595.x.View ArticlePubMedGoogle Scholar
- Gianola D, Fernando RL: Bayesian methods in animal breeding theory. J Anim Sci. 1986, 63: 217-244.Google Scholar
- Xu S: Estimating polygenic effects using markers of the entire genome. Genetics. 2003, 163: 789-801.PubMed CentralPubMedGoogle Scholar
- Gianola D, van Kaam JBCHM: Reproducing kernel Hilbert spaces regression methods for genomic assisted prediction of quantitative traits. Genetics. 2008, 178: 2289-2303. 10.1534/genetics.107.084285.PubMed CentralView ArticlePubMedGoogle Scholar
- Gianola D, Fernando RL, Stella A: Genomic-Assisted prediction of genetic value with semiparametric procedures. Genetics. 2006, 173: 1761-1776. 10.1534/genetics.105.049510.PubMed CentralView ArticlePubMedGoogle Scholar
- González-Recio O, Gianola D, Long N, Weigel KA, Rosa GJM, Avendaño S: Nonparametric methods for incorporating genomic information into genetic evaluations: An application to mortality in broilers. Genetics. 2008, 178: 2305-2313. 10.1534/genetics.107.084293.PubMed CentralView ArticlePubMedGoogle Scholar
- Long N, Gianola D, Rosa GJM, Weigel K, Avendaño S: Machine learning classification procedure for selecting SNPs in genomic selection: Application to early mortality in broilers. J Anim Breed Genet. 2007, 124 (6): 377-389.View ArticlePubMedGoogle Scholar
- Fernando R, Habier D, Stricker C, Dekkers JCM, Totir LR: Genomic selection. Acta Agric Scand Sec A. 2007, 57: 192-195.Google Scholar
- Guillaume F, Fritz S, Boichard D, Druet T: Estimation by simulation of the efficiency of the French marker-assisted selection program in dairy cattle. Genet Sel Evol. 2008, 40: 91-102. 10.1051/gse:2007036.PubMed CentralPubMedGoogle Scholar
- Muir WM: Comparison of genomic and traditional BLUP-estimated breeding value accuracy and selection response under alternative trait and genomic parameters. J Anim Breed Genet. 2007, 124: 342-355.View ArticlePubMedGoogle Scholar
- Ye X, Avendaño S, Dekkers JCM, Lamont SJ: Association of twelve immune-related genes with performance of three broiler lines in two different hygiene environments. Poult Sci. 2006, 85: 1555-1569.View ArticlePubMedGoogle Scholar
- Wong GK, Liu B, Wang J, Zhang Y, Yang X, Zhang Z, Meng1 Q, Zhou J, Li D, Zhang J, Ni P, Li S, Ran L, Li H, Zhang J, Li R, Li S, Zheng H, Lin W, Li G, Wang X, Zhao W, Li J, Ye C, Dai M, Ruan J, Zhou Y, Li Y, He X, Zhang Y, Wang J, Huang X, Tong W, Chen J, Ye J, Chen C, Wei N, Li G, Dong L, Lan F, Sun Y, Zhang Z, Yang Z, Yu Y, Huang Y, He D, Xi Y, Wei D, Qi Q, Li W, Shi J, Wang M, Xie F, Wang J, Zhang X, Wang P, Zhao Y, Li N, Yang N, Dong W, Hu S, Zeng C, Zheng W, Hao B, Hillier LW, Yang SP, Warren WC, Wilson RK, Brandström M, Ellegren H, Crooijmans RPMA, Poel van der JJ, Bovenhuis H, Groenen MAM, Ovcharenko I, Gordon L, Stubbs L, Lucas S, Glavina T, Aerts A, Kaiser P, Rothwell L, Young JR, Rogers S, Walker BA, van Hateren A, Kaufman J, Bumstead N, Lamont SJ, Zhou H, Hocking PM, Morrice D, de Koning DJ, Law A, Bartley N, Burt DW, Hunt H, Cheng HH, Gunnarsson U, Wahlberg P, Andersson L, Kindlund E, Tammi MT, Andersson B, Webber C, Ponting CP, Overton IM, Boardman PE, Tang H, Hubbard SJ, Wilson SA, Yu J, Wang J, Yang HM: A genetic variation map for chicken with 2.8 single nucleotide polymorphism. Nature. 2004, 432: 717-722. 10.1038/nature03156.View ArticlePubMedGoogle Scholar
- Andreescu C, Avendano S, Brown S, Hassen A, Lamont SJ, Dekkers JCM: Linkage disequilibrium in related breeding lines of chickens. Genetics. 2007, 177: 2161-2169. 10.1534/genetics.107.082206.PubMed CentralView ArticlePubMedGoogle Scholar
- Ewens WJ, Grant GR: Statistical Methods in Bioinformatics: an introduction. 2005, New York: Springer-Verlag, 49-51.View ArticleGoogle Scholar
- Sorensen DA, Gianola D: Likelihood, Bayesian and MCMC methods in Quantitative Genetics. 2002, New York: Springer-Verlag, 588-595.View ArticleGoogle Scholar
- Henderson CR: Best linear unbiased estimation and prediction under a selection model. Biometrics. 1975, 31: 423-447. 10.2307/2529430.View ArticlePubMedGoogle Scholar
- Varona L, Sorensen DA, Thompson R: Analysis of litter size and average litter weight in pigs using a recursive model. Genetics. 2007, 177: 1791-1799. 10.1534/genetics.107.077818.PubMed CentralView ArticlePubMedGoogle Scholar
- Kimeldorf G, Wahba G: Some results on Tchebycheffian spline functions. J Math Anal Appl. 1971, 33: 82-95. 10.1016/0022-247X(71)90184-3.View ArticleGoogle Scholar
- Wahba G: Spline model for observational data. 1990, Philadelphia: Society for industrial and applied mathematicsView ArticleGoogle Scholar
- Wahba G: Support vector machines, reproducing kernel Hilbert space and randomized GACV. Advances in Kernel Methods—Support Vector Learning. Edited by: Scholkopf B, Burges C, Smola A. 1999, Cambridge: MIT Press, 68-88.Google Scholar
- Wasserman L: All of Non-parametric Statistics. 2006, New York: Springer, 55-56.Google Scholar
- Wahba G, Lin Y, Lee Y, Zhang H: Optimal properties and adaptive tuning of standard and non-standard support vector machines. Nonlinear estimation and classification. Edited by: Denison D, Hansen M, Holmes C, Mallick B, Yu B. 2002, New York: Springer, 125-143.Google Scholar
- Efron B: Bootstrap methods: another look at the Jackknife. Ann Stat. 1979, 7 (1): 1-26. 10.1214/aos/1176344552.View ArticleGoogle Scholar
- Efron B: Nonparametric estimates of standard error: The jackknife, the bootstrap and other methods. Biometrika. 1981, 68: 589-599. 10.1093/biomet/68.3.589.View ArticleGoogle Scholar
- Janss L, de Jong G: MCMC based estimations of variance components in a very large dairy cattle data set. Proceedings of the Computational Cattle Breeding '99 Workshop. 1999, Tuusula, Finland, 62-67.Google Scholar
- Legarra A, Misztal I: Technical note: Computing strategies in genome-wide selection. J Dairy Sci. 2008, 91: 360-366. 10.3168/jds.2007-0403.View ArticlePubMedGoogle Scholar
- Misztal I, Gianola D: Indirect solution of mixed model equations. J Dairy Sci. 1987, 70: 716-723.View ArticleGoogle Scholar
- Gaya LG, Ferraz JB, Rezende FM, Mourao GB, Mattos EC, Eler JP, Filho TM: Heritability and genetic correlation estimates for performance and carcass and body composition traits in a male broiler line. Poult Sci. 2006, 85: 837-843.View ArticlePubMedGoogle Scholar
- Pym RAE, Nicholls PJ: Selection for food conversion in broilers: Direct and correlated responses to selection for body-weight gain, food consumption and food conversion ratio. Br Poult Sci. 1979, 20 (1): 73-86. 10.1080/00071667908416551.View ArticleGoogle Scholar
- Zhang W, Aggrey SE, Pesti GM, Edwards HM, Bakalli RI: Genetics of phytate phosphorus bioavailability: heritability and genetic correlations with growth and feed utilization traits in a randombred chicken population. Poult Sci. 2003, 82: 1075-1079.View ArticlePubMedGoogle Scholar
- Tibshirani R: Regression shrinkage and selection via the Lasso. J Royal Stat Soc B. 1996, 58: 267-288.Google Scholar
- Park T, Casella G: The Bayesian Lasso. J Am Statist Assoc. 2008, 103: 681-686. 10.1198/016214508000000337.View ArticleGoogle Scholar
- ter Braak CJF, Boer MP, Bink MCAM: Extending Xu's Bayesian model for estimating polygenic effects using markers of the entire genome. Genetics. 2005, 170: 1435-1438. 10.1534/genetics.105.040469.PubMed CentralView ArticlePubMedGoogle Scholar
- Legarra A, Elsen JM, Manfredi E, Robert-Graniè C: Validation of genomic selection in an outbred mice population. Proceedings of the 58th Annual Meeting of European Association for Animal Production: 26–29 August 2007; Ireland, Dublin. 2007, session 18, abstract 1071Google Scholar
- Dekkers J: Commercial application of marker- and gene-assisted selection in livestock: Strategies and lessons. J Anim Sci. 2004, 82: E313-E328.PubMedGoogle Scholar
Copyright
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.