scholarly journals Genomic Predictions For Fillet Yield And Firmness In Rainbow Trout Using Reduced-Density SNP Panels

2020 ◽  
Author(s):  
Rafet Al-Tobasei ◽  
Ali R. Ali ◽  
Andre L. S. Garcia ◽  
Daniela Lourenco ◽  
Tim Leeds ◽  
...  

Abstract Background One of the most important goals for the rainbow trout aquaculture industry is to improve fillet yield and fillet quality. Previously, we showed that a 50K transcribed-SNP chip can be used to detect quantitative trait loci (QTL) associated with fillet yield and fillet firmness. In this study, data from 1,568 fish genotyped for the 50K transcribed-SNP chip and ~774 fish phenotyped for fillet yield and fillet firmness were used in a single-step genomic BLUP (ssGBLUP) model to compute the genomic estimated breeding values (GEBV). In addition, pedigree-based best linear unbiased prediction (PBLUP) was used to calculate traditional, family-based estimated breeding values (EBV). Results The genomic predictions outperformed the traditional EBV by 35% for fillet yield and 42% for fillet firmness. The predictive ability for fillet yield and fillet firmness was 0.19 - 0.20 with PBLUP, and 0.27 with ssGBLUP. Additionally, reducing SNP panel densities indicated that using 500 – 800 SNPs in genomic predictions still provides predictive abilities higher than PBLUP. Conclusion These results suggest that genomic evaluation is a feasible strategy to identify and select fish with superior genetic merit within rainbow trout families, even with low-density SNP panels.

2020 ◽  
Author(s):  
Rafet Al-Tobasei ◽  
Ali R. Ali ◽  
Andre L. S. Garcia ◽  
Daniela Lourenco ◽  
Tim Leeds ◽  
...  

Abstract BackgroundOne of the most important goals for the rainbow trout aquaculture industry is to improve fillet yield and fillet quality. Previously, we showed that a 50K transcribed-SNP chip can be used to detect quantitative trait loci (QTL) associated with fillet yield and fillet firmness. In this study, data from 1,568 fish genotyped for the 50K transcribed-SNP chip and ~774 fish phenotyped for fillet yield and fillet firmness were used in a single-step genomic BLUP (ssGBLUP) model to compute the genomic estimated breeding values (GEBV). In addition, pedigree-based best linear unbiased prediction (PBLUP) was used to calculate traditional, family-based estimated breeding values (EBV). ResultsThe genomic predictions outperformed the traditional EBV by 35% for fillet yield and 42% for fillet firmness. The predictive ability for fillet yield and fillet firmness was 0.19 - 0.20 with PBLUP, and 0.27 with ssGBLUP. Additionally, reducing SNP panel densities indicated that using 500 – 800 SNPs in genomic predictions still provides predictive abilities higher than PBLUP. ConclusionThese results suggest that genomic evaluation is a feasible strategy to identify and select fish with superior genetic merit within rainbow trout families, even with low-density SNP panels.


BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Rafet Al-Tobasei ◽  
Ali Ali ◽  
Andre L. S. Garcia ◽  
Daniela Lourenco ◽  
Tim Leeds ◽  
...  

Abstract Background One of the most important goals for the rainbow trout aquaculture industry is to improve fillet yield and fillet quality. Previously, we showed that a 50 K transcribed-SNP chip can be used to detect quantitative trait loci (QTL) associated with fillet yield and fillet firmness. In this study, data from 1568 fish genotyped for the 50 K transcribed-SNP chip and ~ 774 fish phenotyped for fillet yield and fillet firmness were used in a single-step genomic BLUP (ssGBLUP) model to compute the genomic estimated breeding values (GEBV). In addition, pedigree-based best linear unbiased prediction (PBLUP) was used to calculate traditional, family-based estimated breeding values (EBV). Results The genomic predictions outperformed the traditional EBV by 35% for fillet yield and 42% for fillet firmness. The predictive ability for fillet yield and fillet firmness was 0.19–0.20 with PBLUP, and 0.27 with ssGBLUP. Additionally, reducing SNP panel densities indicated that using 500–800 SNPs in genomic predictions still provides predictive abilities higher than PBLUP. Conclusion These results suggest that genomic evaluation is a feasible strategy to identify and select fish with superior genetic merit within rainbow trout families, even with low-density SNP panels.


2020 ◽  
Author(s):  
Rafet Al-Tobasei ◽  
Ali R. Ali ◽  
Andre L. S. Garcia ◽  
Daniela Lourenco ◽  
Tim Leeds ◽  
...  

Abstract Background One of the most important goals for the rainbow trout aquaculture industry is to improve muscle yield and fillet quality. Previously, we showed that a 50K transcribed-SNP chip can be used to detect quantitative trait loci (QTL) associated with muscle yield and fillet firmness. In this study, data from 1,568 fish genotyped for the 50K transcribed-SNP chip and ~774 fish phenotyped for muscle yield and fillet firmness were used in a single-step genomic BLUP (ssGBLUP) model to compute the genomic estimated breeding values (GEBV). In addition, pedigree-based best linear unbiased prediction (PBLUP) was used to calculate traditional, family-based estimated breeding values (EBV). Results The genomic predictions outperformed the traditional EBV by 35% for muscle yield and 42% for fillet firmness. The predictive ability for muscle yield and fillet firmness was 0.19 - 0.20 with PBLUP, and 0.27 with ssGBLUP. Additionally, reducing SNP panel densities indicated that using 500 – 800 SNPs in genomic predictions still provides predictive abilities higher than PBLUP. Conclusion These results suggest that genomic evaluation is a feasible strategy to identify and select fish with superior genetic merit within rainbow trout families, even with low-density SNP panels.


2019 ◽  
Vol 51 (1) ◽  
Author(s):  
Øyvind Nordbø ◽  
Arne B. Gjuvsland ◽  
Leiv Sigbjørn Eikje ◽  
Theo Meuwissen

Abstract Background The main aim of single-step genomic predictions was to facilitate optimal selection in populations consisting of both genotyped and non-genotyped individuals. However, in spite of intensive research, biases still occur, which make it difficult to perform optimal selection across groups of animals. The objective of this study was to investigate whether incomplete genotype datasets with errors could be a potential source of level-bias between genotyped and non-genotyped animals and between animals genotyped on different single nucleotide polymorphism (SNP) panels in single-step genomic predictions. Results Incomplete and erroneous genotypes of young animals caused biases in breeding values between groups of animals. Systematic noise or missing data for less than 1% of the SNPs in the genotype data had substantial effects on the differences in breeding values between genotyped and non-genotyped animals, and between animals genotyped on different chips. The breeding values of young genotyped individuals were biased upward, and the magnitude was up to 0.8 genetic standard deviations, compared with breeding values of non-genotyped individuals. Similarly, the magnitude of a small value added to the diagonal of the genomic relationship matrix affected the level of average breeding values between groups of genotyped and non-genotyped animals. Cross-validation accuracies and regression coefficients were not sensitive to these factors. Conclusions Because, historically, different SNP chips have been used for genotyping different parts of a population, fine-tuning of imputation within and across SNP chips and handling of missing genotypes are crucial for reducing bias. Although all the SNPs used for estimating breeding values are present on the chip used for genotyping young animals, incompleteness and some genotype errors might lead to level-biases in breeding values.


2021 ◽  
Vol 99 (Supplement_3) ◽  
pp. 254-254
Author(s):  
Matias Bermann ◽  
Daniela Lourenco ◽  
Vivian Breen ◽  
Rachel Hawken ◽  
Fernando Brito Lopes ◽  
...  

Abstract The objectives of this study were to model the inclusion of a group of external birds into a local broiler chicken population for the purpose of genomic evaluations and evaluating the behavior of two accuracy estimators under different model specifications. The pedigree was composed by 242,413 birds and genotypes were available for 107,216 birds. A five-trait model that included one growth, two yield, and two efficiency traits was used for the analyses. The strategies to model the introduction of external birds were to include a fixed effect representing the origin of parents and to use UPG or metafounders. Genomic estimated breeding values (GEBV) were obtained with single-step GBLUP (ssGBLUP) using the Algorithm for Proven and Young (APY). Bias, dispersion, and accuracy of GEBV for the validation birds, i.e., from the most recent generation, were computed. The bias and dispersion were estimated with the LR-method, whereas accuracy was estimated by the LR-method and predictive ability. Models with fixed UPG and estimated inbreeding or random UPG resulted in similar GEBV. The inclusion of an extra fixed effect in the model made the GEBV unbiased and reduced the inflation, while models without such an effect were significantly biased. Genomic predictions with metafounders were slightly biased and inflated due to the unbalanced number of observations assigned to each metafounder. When combining local and external populations, the greatest accuracy and smallest bias can be obtained by adding an extra fixed effect to account for the origin of parents plus UPG with estimated inbreeding or random UPG. To estimate the accuracy, the LR-method is more consistent among models, whereas predictive ability greatly depends on the model specification, that is, on the fixed effects included in the model. When changing model specification, the largest variation for the LR-method was 20%, while for predictive ability was 110%.


2018 ◽  
Vol 98 (3) ◽  
pp. 565-575 ◽  
Author(s):  
Mario L. Piccoli ◽  
Luiz F. Brito ◽  
José Braccini ◽  
Fernanda V. Brito ◽  
Fernando F. Cardoso ◽  
...  

The statistical methods used in the genetic evaluations are a key component of the process and can be best compared by using simulated data. The latter is especially true in grazing beef cattle production systems, where the number of proven bulls with highly reliable estimated breeding values is limited to allow for a trustworthy validation of genomic predictions. Therefore, we simulated data for 4980 beef cattle aiming to compare single-step genomic best linear unbiased prediction (ssGBLUP), which simultaneously incorporates pedigree, phenotypic, and genomic data into genomic evaluations, and two-step GBLUP (tsGBLUP) procedures and genomic estimated breeding values (GEBVs) blending methods. The greatest increases in GEBV accuracies compared with the parents’ average estimated breeding values (EBVPA) were 0.364 and 0.341 for ssGBLUP and tsGBLUP, respectively. Direct genomic value and GEBV accuracies when using ssGBLUP and tsGBLUP procedures were similar, except for the GEBV accuracies using Hayes’ blending method in tsGBLUP. There was no significant or slight bias in genomic predictions from ssGBLUP or tsGBLUP (using VanRaden’s blending method), indicating that these predictions are on the same scale compared with the true breeding values. Overall, genetic evaluations including genomic information resulted in gains in accuracy >100% compared with the EBVPA. In addition, there were no significant differences between the selected animals (10% males and 50% females) by using ssGBLUP or tsGBLUP.


2021 ◽  
Vol 99 (4) ◽  
Author(s):  
Matias Bermann ◽  
Daniela Lourenco ◽  
Vivian Breen ◽  
Rachel Hawken ◽  
Fernando Brito Lopes ◽  
...  

Abstract The introduction of animals from a different environment or population is a common practice in commercial livestock populations. In this study, we modeled the inclusion of a group of external birds into a local broiler chicken population for the purpose of genomic evaluations. The pedigree was composed of 242,413 birds and genotypes were available for 107,216 birds. A five-trait model that included one growth, two yield, and two efficiency traits was used for the analyses. The strategies to model the introduction of external birds were to include a fixed effect representing the origin of parents and to use unknown parent groups (UPG) or metafounders (MF). Genomic estimated breeding values (GEBV) were obtained with single-step GBLUP using the Algorithm for Proven and Young. Bias, dispersion, and accuracy of GEBV for the validation birds, that is, from the most recent generation, were computed. The bias and dispersion were estimated with the linear regression (LR) method,whereas accuracy was estimated by the LR method and predictive ability. When fixed UPG were fit without estimated inbreeding, the model did not converge. In contrast, models with fixed UPG and estimated inbreeding or random UPG converged and resulted in similar GEBV. The inclusion of an extra fixed effect in the model made the GEBV unbiased and reduced the inflation. Genomic predictions with MF were slightly biased and inflated due to the unbalanced number of observations assigned to each metafounder. When combining local and external populations, the greatest accuracy can be obtained by adding an extra fixed effect to account for the origin of parents plus UPG with estimated inbreeding or random UPG. To estimate the accuracy, the LR method is more consistent among scenarios, whereas the predictive ability greatly depends on the model specification.


Author(s):  
Gabriel Soares Campos ◽  
Fernando Flores Cardoso ◽  
Claudia Cristina Gulias Gomes ◽  
Robert Domingues ◽  
Luciana Correia de Almeida Regitano ◽  
...  

Abstract Genomic prediction has become the new standard for genetic improvement programs, and currently, there is a desire to implement this technology for the evaluation of Angus cattle in Brazil. Thus, the main objective of this study was to assess the feasibility of evaluating young Brazilian Angus (BA) bulls and heifers for 12 routinely recorded traits using single-step genomic BLUP (ssGBLUP) with and without genotypes from American Angus (AA) sires. The second objective was to obtain estimates of effective population size (Ne) and linkage disequilibrium (LD) in the Brazilian Angus population. The dataset contained phenotypic information for up to 277,661 animals belonging to the Promebo® breeding program, pedigree for 362,900, of which 1,386 were genotyped for 50k, 77k, and 150k SNP panels. After imputation and quality control, 61,666 SNP were available for the analyses. In addition, genotypes from 332 American Angus (AA) sires widely used in Brazil were retrieved from the AA Association database to be used for genomic predictions. Bivariate animal models were used to estimate variance components, traditional EBV, and genomic EBV (GEBV). Validation was carried out with the linear regression method (LR) using young-genotyped animals born between 2013 and 2015 without phenotypes in the reduced dataset and with records in the complete dataset. Validation animals were further split into progeny of BA and AA sires to evaluate if their progenies would benefit by including genotypes from AA sires. The Ne was 254 based on pedigree and 197 based on LD, and the average LD (±SD) and distance between adjacent SNPs across all chromosomes was 0.27 (±0.27) and 40743.68 bp, respectively. Prediction accuracies with ssGBLUP outperformed BLUP for all traits, improving accuracies by, on average, 16% for BA young bulls and heifers. The GEBV prediction accuracies ranged from 0.37 (total maternal for weaning weight and tick count) to 0.54 (yearling precocity) across all traits, and dispersion (LR coefficients) fluctuated between 0.92 and 1.06. Inclusion of genotyped sires from the AA improved GEBV accuracies by 2%, on average, compared to using only the BA reference population. Our study indicated that genomic information could help to improve GEBV accuracies and hence genetic progress in the Brazilian Angus population. The inclusion of genotypes from American Angus sires heavily used in Brazil just marginally increased the GEBV accuracies for selection candidates.


2020 ◽  
Vol 44 (5) ◽  
pp. 994-1002
Author(s):  
Samet Hasan ABACI ◽  
Hasan ÖNDER

This study aims to compare the accuracy of pedigree-based and genomic-based breeding value prediction for different training population sizes. In this study, Bayes (A, B, C, Cpi) and GBLUP methods for genomic selection and BLUP method for pedigree-based selection were used. Genomic and pedigree-based breeding values were estimated for partial milk yield (158 days) of Holstein cows (400 individuals) from a private enterprise in the USA. For this aim, populations were created for indirect breeding value estimates as training (322–360) and test (78–40) populations. In animals genotyped with a 54k SNP, the marker file was encoded as –10, 0, and 10 for AA, AB, and BB marker genotypes, respectively. Bayes and GBLUP methods were performed using GenSel 4.55 software. A total of 50,000 iterations were used, with the first 5000 excluded as the burn-in. Pedigree-based breeding values were estimated by REML using MTDFREML software employing an animal model. Correlations between partial milk yield and estimated breeding values were used to assess the predictive ability for methods. Bayes B method gave the highest accuracy for the indirect estimate of breeding value.


2019 ◽  
Vol 97 (Supplement_2) ◽  
pp. 37-39
Author(s):  
Andrea Plotzki Reis ◽  
Rodrigo Fagundes da Costa ◽  
Fabyano Fonseca e Silva ◽  
Fernando Flores Cardoso ◽  
Matthew L Spangler

Abstract The aim of this study was to investigate selective phenotyping to maintain adequate prediction accuracy. A simulation was conducted, with 10 replicates, using QMSim to mimic the structure and size of a Braford population. A population with 50 generations, 500 animals per generation, was created with phenotyping and genotyping beginning in generation 11. The scenarios investigated were: 1) Randomly phenotype and genotype 10, 25, 50, 75, and 100% of individuals each generation and; 2) Randomly phenotype and genotype 10, 25, 50, 75, and 100% of individuals in every-other generation. Estimated breeding values (EBV) were obtained using single-step GBLUP and accuracy was determined as the correlation between true BV from simulation and those estimated from the blupf90 family of programs. For scenarios where phenotyping and genotyping occurred every generation, EBV accuracies in generation 11 and 50 ranged from 0.32 to 0.32, 0.42 to 0.43, 0.49 to 0.51, 0.53 to 0.56 and 0.57 to 0.59 when 10, 25, 50, 75, and 100% of animals were chosen, respectively. The highest accuracies were 0.40 and 0.50 in generation 38 for scenarios 10 and 25%; 0.56, 0.61 and 0.64 in generation 40 for scenarios 50, 75 and 100%, respectively. When animals were selected every-other generation, EBV accuracy in generation 11 and 50 ranged from 0.24 to 0.26, 0.36 to 0.36, 0.43 to 0.42, 0.48 to 0.44 and 0.53 to 0.48 for 10, 25, 50, 75 and 100% of selected animals, respectively. The highest accuracies were in generation 23 for scenario 10% (0.31), in generation 37 for scenarios 25 (0.43), 50 (0.50) and 75% (0.55) and in generation 39 for 100% (0.59). Although increasing the density of phenotyped and genotyped animals increased prediction accuracy, some gains were marginal. These differences in accuracy must be contemplated in an economic framework to determine the cost-benefit of additional information.


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