Abstract

BackgroundMost genomic predictions use a unique population that is split into a training and a validation set. However, genomic prediction using genetically heterogeneous training sets could provide more flexibility when constructing the training sets in small populations. The aim of our study was to investigate the potential of genomic prediction of feed efficiency related traits using training sets that combine animals from two different, but genetically-related lines. We compared realized prediction accuracy and prediction bias for different training set compositions for five production traits.ResultsGenomic breeding values (GEBV) were predicted using the single-step genomic best linear unbiased prediction method in six scenarios applied iteratively to two genetically-related lines (i.e. 12 scenarios). The objective for all scenarios was to predict GEBV of pigs in the last three generations (~ 400 pigs, G7 to G9) of a given line. For each line, a control scenario was set up with a training set that included only animals from that line (target line). For all traits, adding more animals from the other line to the training set did not increase prediction accuracy compared to the control scenario. A small decrease in prediction accuracies was found for average daily gain, backfat thickness, and daily feed intake as the number of animals from the target line decreased in the training set. Including more animals from the other line did not decrease prediction accuracy for feed conversion ratio and residual feed intake, which were both highly affected by selection within lines. However, prediction biases were systematic for these cases and might be reduced with bivariate analyses.ConclusionsOur results show that genomic prediction using a training set that includes animals from genetically-related lines can be as accurate as genomic prediction using a training set from the target population. With combined reference sets, accuracy increased for traits that were highly affected by selection. Our results provide insights into the design of reference populations, especially to initiate genomic selection in small-sized lines, for which the number of historical samples is small and that are developed simultaneously. This applies especially to poultry and pig breeding and to other crossbreeding schemes.

Highlights

  • Most genomic predictions use a unique population that is split into a training and a validation set.genomic prediction using genetically heterogeneous training sets could provide more flexibility when constructing the training sets in small populations

  • A small decrease in prediction accuracies was found for average daily gain, backfat thickness, and daily feed intake as the number of animals from the target line decreased in the training set

  • Our results showed that Genomic breeding values (GEBV) were more biased for traits that were more affected by selection, especially when early generations of the target line were not included in the training set

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Summary

Introduction

Most genomic predictions use a unique population that is split into a training and a validation set.genomic prediction using genetically heterogeneous training sets could provide more flexibility when constructing the training sets in small populations. The aim of our study was to investigate the potential of genomic prediction of feed efficiency related traits using training sets that combine animals from two different, but geneticallyrelated lines. Selection of animals based on FCR can be accompanied by undesirable correlated responses in other traits such as appetite [5, 6], whereas selection for RFI is almost independent of these traits since RFI is feed intake adjusted for production trait by linear regression. Due to the high cost of measuring daily feed intake (DFI), and RFI and FCR [7], fewer phenotypic records are available, which reduces the accuracy of selection. Genomic selection has the potential to improve pig feed efficiency in some populations [8, 9]. The number of animals in the reference population has been shown to affect the accuracy of genomic predictions [14]

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