Phenotypic data on BW and breast meat area were available on up to 287,614 broilers. A total of 4,113 birds were genotyped for 57,636 SNP. Data were analyzed by a single-step genomic BLUP (ssGBLUP), which accounts for all phenotypic, pedigree, and genomic information. The genomic relationship matrix (G) in ssGBLUP was constructed using either equal (0.5; GEq) or current (GC) allele frequencies, and with all SNP or with SNP with minor allele frequencies (MAF) below multiple thresholds (0.1, 0.2, 0.3, and 0.4) ignored. Additionally, a pedigree-based relationship matrix for genotyped birds (A(22)) was available. The matrices and their inverses were compared with regard to average diagonal (AvgD) and off-diagonal (AvgOff) elements. In A(22), AvgD was 1.004 and AvgOff was 0.014. In GEq, both averages decreased with the increasing thresholds for MAF, with AvgD decreasing from 1.373 to 1.020 and AvgOff decreasing from 0.722 to 0.025. In GC, AvgD was approximately 1.01 and AvgOff was 0 for all MAF. For inverses of the relationship matrices, all AvgOff were close to 0; AvgD was 2.375 in A(22), varied from 11.563 to 12.943 for GEq, and increased from 8.675 to 12.859 for GC as the threshold for MAF increased. Predictive ability with all GEq and GC was similar except that at MAF = 0.4, they declined by 0.01 for BW and improved by 0.01 for breast meat area. Compared with BLUP, EBV in the ssGBLUP were, on average, increased by up to 1 additive SD greater with GEq and decreased by 2 additive SD less with GC. Genotyped animals were biased upward with GEq and downward with GC. The biases and differences in EBV could be controlled by adding a constant to GC; they were eliminated with a constant of 0.014, which corresponds to AvgOff in A(22). Unbiased evaluation in the ssGBLUP may be obtained with GC scaled to be compatible with A(22). The reduction of SNP with small MAF has a small effect on the real accuracy, but it may falsely increase the estimated accuracies by inversion.
Data of broiler chickens for 2 pure lines across 3 generations were used for genomic evaluation. A complete population (full data set; FDS) consisted of 183,784 and 164,246 broilers for the 2 lines. The genotyped subsets (SUB) consisted of 3,284 and 3,098 broilers with 57,636 SNP. Genotyped animals were preselected based on more than 20 traits with different index applied to each line. Three traits were analyzed: BW at 6 wk (BW6), ultrasound measurement of breast meat (BM), and leg score (LS) coded 1 = no and 2 = yes for leg defect. Some phenotypes were missing for BM. The training population consisted of the first 2 generations including all animals in FDS or only genotyped animals in SUB. The validation data set contained only genotyped animals in the third generation. Genetic evaluations were performed using 3 approaches: 1) phenotypic BLUP, 2) extending BLUP methodologies to utilize pedigree and genomic information in a single step (ssGBLUP), and 3) Bayes A. Whereas BLUP and ssGBLUP utilized all phenotypic data, Bayes A could use only those of the genotyped subset. Heritabilities were 0.17 to 0.20 for BW6, 0.30 to 0.35 for BM, and 0.09 to 0.11 for LS. The average accuracies of the validation population with BLUP for BW6, BM, and LS were 0.46, 0.30, and <0 with SUB and 0.51, 0.34, and 0.28 with FDS. With ssGBLUP, those accuracies were 0.60, 0.34, and 0.06 with SUB and 0.61, 0.40, and 0.37 with FDS, respectively. With Bayes A, the accuracies were 0.60, 0.36, and 0.09 with SUB. With SUB, Bayes A and ssGBLUP had similar accuracies. For traits of high heritability, the accuracy of Bayes A/SUB and ssGBLUP/FDS were similar, and up to 50% better than BLUP/FDS. However, with low heritability, ssGBLUP/FDS was 4 to 6 times more accurate than Bayes A/SUB and 50% better than BLUP/FDS. An optimal genomic evaluation would be multi-trait and involve all traits and records on which selection is based.
Newman, S.; and Van Vleck, L. Dale, "Estimation of genetic parameters for average daily gain using models with competition effects" (2008). Faculty Papers and Publications in Animal Science. 452. http://digitalcommons.unl.edu/animalscifacpub/452 ABSTRACT: Components of variance for ADG with models including competition effects were estimated from data provided by the Pig Improvement Company on 11,235 pigs from 4 selected lines of swine. Fifteen pigs with average age of 71 d were randomly assigned to a pen by line and sex and taken off test after approximately 89 d (off-test BW ranged from 61 to 158 kg). Models included fixed effects of line, sex, and contemporary group and initial test age as a covariate, with random direct genetic, competition (genetic and environmental), pen, litter, and residual effects. With the full model, variances attributable to direct, directcompetition, genetic competition, and litter (co)variance components could be partitioned; genetic competition variance was small but statistically significantly different from zero. Variances attributable to environmental competition, pen, and residual effects could not be partitioned, but combinations of these environmental variances were estimable. Variances could be partitioned with either pen effects or environmental competition effects in the model. Environmental competition effects seemed to be the source of variance associated with pens. With pen as a fixed effect and without environmental competition effects in the model, genetic components of variance could not be partitioned, but combinations of genetic (co)variances were estimable. With both pen and environmental competition effects ignored, estimates of direct-competition and genetic competition (co)variance components were greatly inflated. With competition (genetic and environmental) effects ignored, the estimate of pen variance increased by 39%, with little change in estimates of direct genetic or residual variance. When both pen and competition (genetic and environmental) effects were dropped from the model, variance attributable to direct genetic effects was inflated. Estimates of variance attributable to competition effects were small in this study. Including environmental competition effects as permanent environmental effects in the model did not change estimates of genetic (co)variances. We concluded that including either pen effects or environmental competition effects as random effects in the model avoids bias in estimates of genetic variances but that including pen effects is much easier.
Combining purebreed and crossbreed information is beneficial for genetic evaluation of some livestock species. Genetic evaluations can use relationships based on genomic information, relying on allele frequencies that are breed specific. Single-step genomic BLUP (ssGBLUP) does not account for different allele frequencies, which could limit the genetic gain in crossbreed evaluations. In this study, we tested the performance of different breed-specific genomic relationship matrices () in ssGBLUP for crossbreed evaluations; we also tested the importance of genotyping crossbred animals. Genotypes were available for purebreeds (AA and BB) and crossbreeds (F) in simulated and real pig populations. The number of genotyped animals was, on average, 4,315 for the simulated population and 15,798 for the real population. Cross-validation was performed on 1,200 and 3,117 F animals in the simulated and real populations, respectively. Simulated scenarios were under no artificial selection, mass selection, or BLUP selection. Two genomic relationship matrices were constructed based on breed-specific allele frequencies: 1) , a genomic relationship matrix centered by breed-specific allele frequencies, and 2) , a genomic relationship matrix centered and scaled by breed-specific allele frequencies. All (the across-breed genomic relationship matrix), , and were also tuned to account for selective genotyping. Using breed-specific allele frequencies reduced the number of negative relationships between 2 purebreeds, pulling the average closer to 0, as in the pedigree-based relationship matrix. For simulated populations that included mass selection, genomic EBV (GEBV) in F, when using and , were, on average, 10% more accurate than ; however, after tuning to account for selective genotyping, provided the same accuracy as for breed-specific genomic relationship matrices. For the real population, accuracies for litter size in F were 0.62 for , , and , and tuning had no impact on accuracy, except for , which was 1 percentage point less accurate. Accuracy of GEBV for number of stillborns in F1 was 0.5 for all tested genomic relationship matrices with no changes after tuning. We observed that genotyping F increased accuracies of GEBV for the same animals by up to 39% compared with having genotypes for only AA and BB. In crossbreed evaluations, accounting for breed-specific allele frequencies promoted changes in G that were not influential enough to improve accuracy of GEBV. Therefore, the best performance of ssGBLUP for crossbreed evaluations requires genotypes for pure- and crossbreeds and no breed-specific adjustments in the realized relationship matrix.
Background: The coupling of appropriate sequencing strategies and imputation methods is critical for assembling large whole-genome sequence datasets from livestock populations for research and breeding. In this paper, we describe and validate the coupling of a sequencing strategy with the imputation method hybrid peeling in real animal breeding settings. Methods:We used data from four pig populations of different size (18,349 to 107,815 individuals) that were widely genotyped at densities between 15,000 and 75,000 markers genome-wide. Around 2% of the individuals in each population were sequenced (most of them at 1× or 2× and 37-92 individuals per population, totalling 284, at 15-30×). We imputed whole-genome sequence data with hybrid peeling. We evaluated the imputation accuracy by removing the sequence data of the 284 individuals with high coverage, using a leave-one-out design. We simulated data that mimicked the sequencing strategy used in the real populations to quantify the factors that affected the individualwise and variant-wise imputation accuracies using regression trees.Results: Imputation accuracy was high for the majority of individuals in all four populations (median individual-wise dosage correlation: 0.97). Imputation accuracy was lower for individuals in the earliest generations of each population than for the rest, due to the lack of marker array data for themselves and their ancestors. The main factors that determined the individual-wise imputation accuracy were the genotyping status, the availability of marker array data for immediate ancestors, and the degree of connectedness to the rest of the population, but sequencing coverage of the relatives had no effect. The main factors that determined variant-wise imputation accuracy were the minor allele frequency and the number of individuals with sequencing coverage at each variant site. Results were validated with the empirical observations. Conclusions:We demonstrate that the coupling of an appropriate sequencing strategy and hybrid peeling is a powerful strategy for generating whole-genome sequence data with high accuracy in large pedigreed populations where only a small fraction of individuals (2%) had been sequenced, mostly at low coverage. This is a critical step for the successful implementation of whole-genome sequence data for genomic prediction and fine-mapping of causal variants.© The Author(s) 2020. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article' s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article'
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