Publications by authors named "Pascal Duenk"

Heat stress in broilers is a pressing issue in the changing climate. Data on broiler behavior might be useful for early detection of heat stress and subsequent intervention, and may provide potential indicators for heat tolerance that can be used in broiler breeding programs. Here, we used bird location data collected in a previous study during which broilers were inadvertently exposed to high ambient temperatures due to a local heat wave.

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Background: In genomic prediction, it is common to centre the genotypes of single nucleotide polymorphisms based on the allele frequencies in the current population, rather than those in the base generation. The mean breeding value of non-genotyped animals is conditional on the mean performance of genotyped relatives, but can be corrected by fitting the mean performance of genotyped individuals as a fixed regression. The associated covariate vector has been referred to as a 'J-factor', which if fitted as a fixed effect can improve the accuracy and dispersion bias of sire genomic estimated breeding values (GEBV).

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Background: The genetic correlation between purebred (PB) and crossbred (CB) performances ([Formula: see text]) partially determines the response in CB when selection is on PB performance in the parental lines. An earlier study has derived expressions for an upper and lower bound of [Formula: see text], using the variance components of the parental purebred lines, including e.g.

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Breeding programs aiming to improve the performance of crossbreds may benefit from genomic prediction of crossbred (CB) performance for purebred (PB) selection candidates. In this review, we compared genomic prediction strategies that differed in 1) the genomic prediction model used or 2) the data used in the reference population. We found 27 unique studies, two of which used deterministic simulation, 11 used stochastic simulation, and 14 real data.

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Background: The genetic correlation between purebred and crossbred performance ([Formula: see text]) is an important parameter in pig and poultry breeding, because response to selection in crossbred performance depends on the value of [Formula: see text] when selection is based on purebred (PB) performance. The value of [Formula: see text] can be substantially lower than 1, which is partly due to differences in allele frequencies between parental lines when non-additive genetic effects are present. This relationship between [Formula: see text] and parental allele frequencies suggests that [Formula: see text] can be expressed as a function of genetic parameters for the trait in the parental lines.

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Background: Estimating the genetic component of a complex phenotype is a complicated problem, mainly because there are many allele effects to estimate from a limited number of phenotypes. In spite of this difficulty, linear methods with variable selection have been able to give good predictions of additive effects of individuals. However, prediction of non-additive genetic effects is challenging with the usual prediction methods.

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Current artificial insemination (AI) laboratory practices assess semen quality of each boar ejaculate to decide which ones to process into AI doses. This decision is aided with two, world-wide used, motility parameters that come available through computer assisted semen analysis (CASA). This decision process, however, still results in AI doses with variable and sometimes suboptimal fertility outcomes (e.

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Average effects of alleles can show considerable differences between populations. The magnitude of these differences can be measured by the additive genetic correlation between populations ([Formula: see text]). This [Formula: see text] can be lower than one due to the presence of non-additive genetic effects together with differences in allele frequencies between populations.

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Following publication of original article [1], we noticed that there was an error: Eq. (3) on page 5 is the genomic relationship matrix that.

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Background: Pig and poultry breeding programs aim at improving crossbred (CB) performance. Selection response may be suboptimal if only purebred (PB) performance is used to compute genomic estimated breeding values (GEBV) because the genetic correlation between PB and CB performance ([Formula: see text]) is often lower than 1. Thus, it may be beneficial to use information on both PB and CB performance.

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Background: In pig and poultry breeding programs, the breeding goal is to improve crossbred (CB) performance, whereas selection in the purebred (PB) lines is often based on PB performance. Thus, response to selection may be suboptimal, because the genetic correlation between PB and CB performance ([Formula: see text]) is generally lower than 1. Accurate estimates of the [Formula: see text] are needed, so that breeders can decide if they should collect data from CB animals.

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Background: Generally, populations differ in terms of environmental and genetic factors, which can create differences in allele substitution effects between populations. Therefore, a single genotype may have different additive genetic values in different populations. The correlation between the two additive genetic values of a single genotype in two populations is known as the additive genetic correlation between populations and thus, can differ from 1.

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In quantitative genetics, the average effect at a single locus can be estimated by an additive (A) model, or an additive plus dominance (AD) model. In the presence of dominance, the AD-model is expected to be more accurate, because the A-model falsely assumes that residuals are independent and identically distributed. Our objective was to investigate the accuracy of an estimated average effect ([Formula: see text]) in the presence of dominance, using either a single locus A-model or AD-model.

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