scholarly journals Genome-enabled prediction of meat and carcass traits using Bayesian regression, single-step genomic best linear unbiased prediction and blending methods in Nelore cattle

animal ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 100006
Author(s):  
F.B. Lopes ◽  
F. Baldi ◽  
T.L. Passafaro ◽  
L.C. Brunes ◽  
M.F.O. Costa ◽  
...  
Genes ◽  
2020 ◽  
Vol 11 (9) ◽  
pp. 1013
Author(s):  
Bryan Irvine Lopez ◽  
Seung-Hwan Lee ◽  
Jong-Eun Park ◽  
Dong-Hyun Shin ◽  
Jae-Don Oh ◽  
...  

The authors wish to make the following corrections to this paper [...]


Genes ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 266
Author(s):  
Hossein Mehrban ◽  
Masoumeh Naserkheil ◽  
Deuk Hwan Lee ◽  
Chungil Cho ◽  
Taejeong Choi ◽  
...  

The weighted single-step genomic best linear unbiased prediction (GBLUP) method has been proposed to exploit information from genotyped and non-genotyped relatives, allowing the use of weights for single-nucleotide polymorphism in the construction of the genomic relationship matrix. The purpose of this study was to investigate the accuracy of genetic prediction using the following single-trait best linear unbiased prediction methods in Hanwoo beef cattle: pedigree-based (PBLUP), un-weighted (ssGBLUP), and weighted (WssGBLUP) single-step genomic methods. We also assessed the impact of alternative single and window weighting methods according to their effects on the traits of interest. The data was comprised of 15,796 phenotypic records for yearling weight (YW) and 5622 records for carcass traits (backfat thickness: BFT, carcass weight: CW, eye muscle area: EMA, and marbling score: MS). Also, the genotypic data included 6616 animals for YW and 5134 for carcass traits on the 43,950 single-nucleotide polymorphisms. The ssGBLUP showed significant improvement in genomic prediction accuracy for carcass traits (71%) and yearling weight (99%) compared to the pedigree-based method. The window weighting procedures performed better than single SNP weighting for CW (11%), EMA (11%), MS (3%), and YW (6%), whereas no gain in accuracy was observed for BFT. Besides, the improvement in accuracy between window WssGBLUP and the un-weighted method was low for BFT and MS, while for CW, EMA, and YW resulted in a gain of 22%, 15%, and 20%, respectively, which indicates the presence of relevant quantitative trait loci for these traits. These findings indicate that WssGBLUP is an appropriate method for traits with a large quantitative trait loci effect.


2018 ◽  
Vol 135 (4) ◽  
pp. 251-262 ◽  
Author(s):  
Jeremy T. Howard ◽  
Tom A. Rathje ◽  
Caitlyn E. Bruns ◽  
Danielle F. Wilson-Wells ◽  
Stephen D. Kachman ◽  
...  

Animals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 569
Author(s):  
Chen Wei ◽  
Hanpeng Luo ◽  
Bingru Zhao ◽  
Kechuan Tian ◽  
Xixia Huang ◽  
...  

Genomic evaluations are a method for improving the accuracy of breeding value estimation. This study aimed to compare estimates of genetic parameters and the accuracy of breeding values for wool traits in Merino sheep between pedigree-based best linear unbiased prediction (PBLUP) and single-step genomic best linear unbiased prediction (ssGBLUP) using Bayesian inference. Data were collected from 28,391 yearlings of Chinese Merino sheep (classified in 1992–2018) at the Xinjiang Gonaisi Fine Wool Sheep-Breeding Farm, China. Subjectively-assessed wool traits, namely, spinning count (SC), crimp definition (CRIM), oil (OIL), and body size (BS), and objectively-measured traits, namely, fleece length (FL), greasy fleece weight (GFW), mean fiber diameter (MFD), crimp number (CN), and body weight pre-shearing (BWPS), were analyzed. The estimates of heritability for wool traits were low to moderate. The largest h2 values were observed for FL (0.277) and MFD (0.290) with ssGBLUP. The heritabilities estimated for wool traits with ssGBLUP were slightly higher than those obtained with PBLUP. The accuracies of breeding values were low to moderate, ranging from 0.362 to 0.573 for the whole population and from 0.318 to 0.676 for the genotyped subpopulation. The correlation between the estimated breeding values (EBVs) and genomic EBVs (GEBVs) ranged from 0.717 to 0.862 for the whole population, and the relative increase in accuracy when comparing EBVs with GEBVs ranged from 0.372% to 7.486% for these traits. However, in the genotyped population, the rank correlation between the estimates obtained with PBLUP and ssGBLUP was reduced to 0.525 to 0.769, with increases in average accuracy of 3.016% to 11.736% for the GEBVs in relation to the EBVs. Thus, genomic information could allow us to more accurately estimate the relationships between animals and improve estimates of heritability and the accuracy of breeding values by ssGBLUP.


2020 ◽  
Vol 98 (6) ◽  
Author(s):  
Johnna L Baller ◽  
Stephen D Kachman ◽  
Larry A Kuehn ◽  
Matthew L Spangler

Abstract Economically relevant traits are routinely collected within the commercial segments of the beef industry but are rarely included in genetic evaluations because of unknown pedigrees. Individual relationships could be resurrected with genomics, but this would be costly; therefore, pooling DNA and phenotypic data provide a cost-effective solution. Pedigree, phenotypic, and genomic data were simulated for a beef cattle population consisting of 15 generations. Genotypes mimicked a 50k marker panel (841 quantitative trait loci were located across the genome, approximately once per 3 Mb) and the phenotype was moderately heritable. Individuals from generation 15 were included in pools (observed genotype and phenotype were mean values of a group). Estimated breeding values (EBV) were generated from a single-step genomic best linear unbiased prediction model. The effects of pooling strategy (random and minimizing or uniformly maximizing phenotypic variation within pools), pool size (1, 2, 10, 20, 50, 100, or no data from generation 15), and generational gaps of genotyping on EBV accuracy (correlation of EBV with true breeding values) were quantified. Greatest EBV accuracies of sires and dams were observed when there was no gap between genotyped parents and pooled offspring. The EBV accuracies resulting from pools were usually greater than no data from generation 15 regardless of sire or dam genotyping. Minimizing phenotypic variation increased EBV accuracy by 8% and 9% over random pooling and uniformly maximizing phenotypic variation, respectively. A pool size of 2 was the only scenario that did not significantly decrease EBV accuracy compared with individual data when pools were formed randomly or by uniformly maximizing phenotypic variation (P > 0.05). Pool sizes of 2, 10, 20, or 50 did not generally lead to statistical differences in EBV accuracy than individual data when pools were constructed to minimize phenotypic variation (P > 0.05). Largest numerical increases in EBV accuracy resulting from pooling compared with no data from generation 15 were seen with sires with prior low EBV accuracy (those born in generation 14). Pooling of any size led to larger EBV accuracies of the pools than individual data when minimizing phenotypic variation. Resulting EBV for the pools could be used to inform management decisions of those pools. Pooled genotyping to garner commercial-level phenotypes for genetic evaluations seems plausible although differences exist depending on pool size and pool formation strategy.


2020 ◽  
Vol 98 (12) ◽  
Author(s):  
Ignacy Misztal ◽  
Shogo Tsuruta ◽  
Ivan Pocrnic ◽  
Daniela Lourenco

Abstract Single-step genomic best linear unbiased prediction with the Algorithm for Proven and Young (APY) is a popular method for large-scale genomic evaluations. With the APY algorithm, animals are designated as core or noncore, and the computing resources to create the inverse of the genomic relationship matrix (GRM) are reduced by inverting only a portion of that matrix for core animals. However, using different core sets of the same size causes fluctuations in genomic estimated breeding values (GEBVs) up to one additive standard deviation without affecting prediction accuracy. About 2% of the variation in the GRM is noise. In the recursion formula for APY, the error term modeling the noise is different for every set of core animals, creating changes in breeding values. While average changes are small, and correlations between breeding values estimated with different core animals are close to 1.0, based on the normal distribution theory, outliers can be several times bigger than the average. Tests included commercial datasets from beef and dairy cattle and from pigs. Beyond a certain number of core animals, the prediction accuracy did not improve, but fluctuations decreased with more animals. Fluctuations were much smaller than the possible changes based on prediction error variance. GEBVs change over time even for animals with no new data as genomic relationships ties all the genotyped animals, causing reranking of top animals. In contrast, changes in nongenomic models without new data are small. Also, GEBV can change due to details in the model, such as redefinition of contemporary groups or unknown parent groups. In particular, increasing the fraction of blending of the GRM with a pedigree relationship matrix from 5% to 20% caused changes in GEBV up to 0.45 SD, with a correlation of GEBV > 0.99. Fluctuations in genomic predictions are part of genomic evaluation models and are also present without the APY algorithm when genomic evaluations are computed with updated data. The best approach to reduce the impact of fluctuations in genomic evaluations is to make selection decisions not on individual animals with limited individual accuracy but on groups of animals with high average accuracy.


Author(s):  
Egill Gautason ◽  
Goutam Sahana ◽  
Guosheng Su ◽  
Baldur Helgi Benjamínsson ◽  
Guðmundur Jóhannesson ◽  
...  

Abstract Icelandic Cattle is a local dairy cattle breed in Iceland. With about 26,000 breeding females, it is by far the largest among the indigenous Nordic cattle breeds. The objective of this study was to investigate the feasibility of genomic selection in Icelandic Cattle. Pedigree-based best linear unbiased prediction (PBLUP) and single-step genomic best linear unbiased prediction (ssGBLUP) were compared. Accuracy, bias, and dispersion of estimated breeding values (EBV) for milk yield (MY), fat yield (FY), protein yield (PY), and somatic cell score (SCS) were estimated in a cross validation-based design. Accuracy (r) was estimated by the correlation between EBV and corrected phenotype in a validation set. The accuracy (r) of predictions using ssGBLUP increased by 13, 23, 19 and 20 percentage points for MY, FY, PY, and SCS for genotyped animals, compared to PBLUP. The accuracy of non-genotyped animals was not improved for MY and PY, but increased by 0.9 and 3.5 percentage points for FY and SCS. We used the linear regression (LR) method to quantify relative improvements in accuracy, bias (∆), and dispersion (b) of EBV. Using the LR method, the relative improvements in accuracy of validation from PBLUP to ssGBLUP were 43%, 60%, 50%, and 48% for genotyped animals for MY, FY, PY, and SCS. Single-step GBLUP EBV were less underestimated (∆), and less over-dispersed (b) than PBLUP EBV for FY and PY. Pedigree-based BLUP EBV were close to unbiased for MY and SCS. Single-step GBLUP underestimated MY EBV but overestimated SCS EBV. Based on the average accuracy of 0.45 for ssGBLUP EBV obtained in this study, selection intensities according to the breeding scheme of Icelandic Cattle, and assuming a generation interval of 2.0 years for sires of bulls, sires of dams and dams of bulls, genetic gain in Icelandic Cattle could be increased by about 50% relative to the current breeding scheme.


Sign in / Sign up

Export Citation Format

Share Document