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. 2009 May;182(1):375-85.
doi: 10.1534/genetics.109.101501. Epub 2009 Mar 16.

Predicting quantitative traits with regression models for dense molecular markers and pedigree

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Predicting quantitative traits with regression models for dense molecular markers and pedigree

Gustavo de los Campos et al. Genetics. 2009 May.

Abstract

The availability of genomewide dense markers brings opportunities and challenges to breeding programs. An important question concerns the ways in which dense markers and pedigrees, together with phenotypic records, should be used to arrive at predictions of genetic values for complex traits. If a large number of markers are included in a regression model, marker-specific shrinkage of regression coefficients may be needed. For this reason, the Bayesian least absolute shrinkage and selection operator (LASSO) (BL) appears to be an interesting approach for fitting marker effects in a regression model. This article adapts the BL to arrive at a regression model where markers, pedigrees, and covariates other than markers are considered jointly. Connections between BL and other marker-based regression models are discussed, and the sensitivity of BL with respect to the choice of prior distributions assigned to key parameters is evaluated using simulation. The proposed model was fitted to two data sets from wheat and mouse populations, and evaluated using cross-validation methods. Results indicate that inclusion of markers in the regression further improved the predictive ability of models. An R program that implements the proposed model is freely available.

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Figures

F<sc>igure</sc> 1.—
Figure 1.—
Densities of a normal and of a double-exponential distribution (both with null mean and with unit variance).
F<sc>igure</sc> 2.—
Figure 2.—
Graphical representation of the hierarchical structure of the Bayesian LASSO (top) and Bayes A (bottom). In the Bayesian LASSO, the variances of the marker effects are formula image, formula image, with counterparts formula image in Bayes A.
F<sc>igure</sc> 3.—
Figure 3.—
Positions (chromosome and marker number) and effects of markers (there were 280 markers, with 270 with no effect).
F<sc>igure</sc> 4.—
Figure 4.—
Unnormalized density of the five priors evaluated in the MC study (BL1–BL4 use Gamma priors on formula image, and BL5 uses a prior for formula image based on a Beta distribution; the densities in this figure are the corresponding densities for formula image).
F<sc>igure</sc> 5.—
Figure 5.—
Absolute values of the posterior means of effects of allele substitution in a model including markers and pedigree information (P&M), by data set.
F<sc>igure</sc> 6.—
Figure 6.—
Predicted genetic value using markers and pedigree (P&M) vs. using pedigree only (P), by data set.

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