scholarly journals Genomic Analysis Using Bayesian Methods under Different Genotyping Platforms in Korean Duroc Pigs

Animals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 752 ◽  
Author(s):  
Jungjae Lee ◽  
Yongmin Kim ◽  
Eunseok Cho ◽  
Kyuho Cho ◽  
Soojin Sa ◽  
...  
Keyword(s):  
Genomic Prediction ◽  
Genome Wide Association Study ◽  
Genomic Analysis ◽  
Snp Markers ◽  
Snp Genotyping ◽  
Muscle Area ◽  
Bayesian Approaches ◽  
Breeding Values ◽  
Estimated Breeding Values ◽  
Response Variables

Genomic evaluation has been widely applied to several species using commercial single nucleotide polymorphism (SNP) genotyping platforms. This study investigated the informative genomic regions and the efficiency of genomic prediction by using two Bayesian approaches (BayesB and BayesC) under two moderate-density SNP genotyping panels in Korean Duroc pigs. Growth and production records of 1026 individuals were genotyped using two medium-density, SNP genotyping platforms: Illumina60K and GeneSeek80K. These platforms consisted of 61,565 and 68,528 SNP markers, respectively. The deregressed estimated breeding values (DEBVs) derived from estimated breeding values (EBVs) and their reliabilities were taken as response variables. Two Bayesian approaches were implemented to perform the genome-wide association study (GWAS) and genomic prediction. Multiple significant regions for days to 90 kg (DAYS), lean muscle area (LMA), and lean percent (PCL) were detected. The most significant SNP marker, located near the MC4R gene, was detected using GeneSeek80K. Accuracy of genomic predictions was higher using the GeneSeek80K SNP panel for DAYS (Δ2%) and LMA (Δ2–3%) with two response variables, with no gains in accuracy by the Bayesian approaches in four growth and production-related traits. Genomic prediction is best derived from DEBVs including parental information as a response variable between two DEBVs regardless of the genotyping platform and the Bayesian method for genomic prediction accuracy in Korean Duroc pig breeding.

scholarly journals Estimation of Variance Components and Genomic Prediction for Individual Birth Weight Using Three Different Genome-Wide SNP Platforms in Yorkshire Pigs

Animals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2219
Author(s):  
Jungjae Lee ◽  
Sang-Min Lee ◽  
Byeonghwi Lim ◽  
Jun Park ◽  
Kwang-Lim Song ◽  
...  
Keyword(s):  
Birth Weight ◽  
Bayesian Methods ◽  
Genomic Prediction ◽  
Snp Genotyping ◽  
Suitable Model ◽  
Prediction Ability ◽  
Breeding Values ◽  
Yorkshire Pigs ◽  
Estimated Breeding Values ◽  
Estimation Of Variance

This study estimates the individual birth weight (IBW) trait heritability and investigates the genomic prediction efficiency using three types of high-density single nucleotide polymorphism (SNP) genotyping panels in Korean Yorkshire pigs. We use 38,864 IBW phenotypic records to identify a suitable model for statistical genetics, where 698 genotypes match our phenotypic records. During our genomic analysis, the deregressed estimated breeding values (DEBVs) and their reliabilities are used as derived response variables from the estimated breeding values (EBVs). Bayesian methods identify the informative regions and perform the genomic prediction using the IBW trait, in which two common significant window regions (SSC8 27 Mb and SSC15 29 Mb) are identified using the three genotyping platforms. Higher prediction ability is observed using the DEBV-including parent average as a response variable, regardless of the SNP genotyping panels and the Bayesian methods, relative to the DEBV-excluding parent average. Hence, we suggest that fine-mapping studies targeting the identified informative regions in this study are necessary to find the causal mutations to improve the IBW trait’s prediction ability. Furthermore, studying the IBW trait using a genomic prediction model with a larger genomic dataset may improve the genomic prediction accuracy in Korean Yorkshire pigs.

scholarly journals Harnessing Genetic Diversity in the USDA Pea Germplasm Collection Through Genomic Prediction

2021 ◽  
Vol 12 ◽  
Author(s):  
Md. Abdullah Al Bari ◽  
Ping Zheng ◽  
Indalecio Viera ◽  
Hannah Worral ◽  
Stephen Szwiec ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Seed Yield ◽  
Genomic Prediction ◽  
Complex Traits ◽  
Prediction Models ◽  
Germplasm Collection ◽  
Predictive Ability ◽  
Snp Markers ◽  
Breeding Values ◽  
Germplasm Collections

Phenotypic evaluation and efficient utilization of germplasm collections can be time-intensive, laborious, and expensive. However, with the plummeting costs of next-generation sequencing and the addition of genomic selection to the plant breeder’s toolbox, we now can more efficiently tap the genetic diversity within large germplasm collections. In this study, we applied and evaluated genomic prediction’s potential to a set of 482 pea (Pisum sativum L.) accessions—genotyped with 30,600 single nucleotide polymorphic (SNP) markers and phenotyped for seed yield and yield-related components—for enhancing selection of accessions from the USDA Pea Germplasm Collection. Genomic prediction models and several factors affecting predictive ability were evaluated in a series of cross-validation schemes across complex traits. Different genomic prediction models gave similar results, with predictive ability across traits ranging from 0.23 to 0.60, with no model working best across all traits. Increasing the training population size improved the predictive ability of most traits, including seed yield. Predictive abilities increased and reached a plateau with increasing number of markers presumably due to extensive linkage disequilibrium in the pea genome. Accounting for population structure effects did not significantly boost predictive ability, but we observed a slight improvement in seed yield. By applying the best genomic prediction model (e.g., RR-BLUP), we then examined the distribution of genotyped but nonphenotyped accessions and the reliability of genomic estimated breeding values (GEBV). The distribution of GEBV suggested that none of the nonphenotyped accessions were expected to perform outside the range of the phenotyped accessions. Desirable breeding values with higher reliability can be used to identify and screen favorable germplasm accessions. Expanding the training set and incorporating additional orthogonal information (e.g., transcriptomics, metabolomics, physiological traits, etc.) into the genomic prediction framework can enhance prediction accuracy.

scholarly journals Performance of steer progeny of sires differing in genetic potential for fatness and meat yield following postweaning growth at different rates. 2. Carcass traits

2009 ◽  
Vol 49 (6) ◽  
pp. 525 ◽  
Author(s):  
W. A. McKiernan ◽  
J. F. Wilkins ◽  
J. Irwin ◽  
B. Orchard ◽  
S. A. Barwick
Keyword(s):  
Production Systems ◽  
Carcass Traits ◽  
Quality Traits ◽  
Muscle Area ◽  
Eye Muscle ◽  
Meat Yield ◽  
Breeding Values ◽  
Genetic Potential ◽  
Estimated Breeding Values ◽  
Selection Of

The steer progeny of sires genetically diverse for fatness and meat yield were grown at different rates from weaning to feedlot entry and effects on growth, carcass and meat-quality traits were examined. The present paper, the second of a series, reports the effects of genetic and growth treatments on carcass traits. A total of 43 sires, within three ‘carcass class’ categories, defined as high potential for meat yield, marbling or both traits, was used. Where available, estimated breeding values for the carcass traits of retail beef yield (RBY%) and intramuscular fat (IMF%) were used in selection of the sires, which were drawn from Angus, Charolais, Limousin, Black Wagyu and Red Wagyu breeds, to provide a range of carcass sire types across the three carcass classes. Steer progeny of Hereford dams were grown at either conventional (slow: ~0.5 kg/day) or accelerated (fast: ~0.7 kg/day) rates from weaning to feedlot entry weight, with group means of ~400 kg. Accelerated and conventionally grown groups from successive calvings were managed to enter the feedlot at similar mean feedlot entry weights at the same time for the 100-day finish under identical conditions. Faster-backgrounded groups had greater fat levels in the carcass than did slower-backgrounded groups. Dressing percentages and fat colour were unaffected by growth treatment, whereas differences in ossification score and meat colour were explained by age at slaughter. There were significant effects of sire type for virtually all carcass traits measured in the progeny. Differences in hot standard carcass weight showed a clear advantage to European types, with variable outcomes for the Angus and Wagyu progeny. Sire selection by estimated breeding values (within the Angus breed) for yield and/or fat traits resulted in expected differences in the progeny for those traits. There were large differences in both meat yield and fatness among the types of greatest divergence in genetic potential for those traits, with the Black Wagyu and the Angus IMF clearly superior for IMF%, and the European types for RBY%. The Angus IMF progeny performed as well as that of the Black Wagyu for all fatness traits. Differences in RBY% among types were generally reflected by similar differences in eye muscle area. Results here provide guidelines for selecting sire types to target carcass traits for specific markets. The absence of interactions between growth and genetic treatments ensures that consistent responses can be expected across varying management and production systems.

Genomic prediction for carcass traits in Japanese Black cattle using single nucleotide polymorphism markers of different densities

2017 ◽  
Vol 57 (8) ◽  
pp. 1631 ◽  
Author(s):  
Shinichiro Ogawa ◽  
Hirokazu Matsuda ◽  
Yukio Taniguchi ◽  
Toshio Watanabe ◽  
Yuki Kitamura ◽  
...  
Keyword(s):  
Single Nucleotide Polymorphism ◽  
Genomic Prediction ◽  
Carcass Traits ◽  
Snp Markers ◽  
Carcass Weight ◽  
Nucleotide Polymorphism ◽  
Japanese Black Cattle ◽  
Marbling Score ◽  
Single Nucleotide ◽  
Breeding Values

Genomic prediction (GP) of breeding values using single nucleotide polymorphism (SNP) markers can be conducted even when pedigree information is unavailable, providing phenotypes are known and marker data are provided. While use of high-density SNP markers is desirable for accurate GP, lower-density SNPs can perform well in some situations. In the present study, GP was performed for carcass weight and marbling score in Japanese Black cattle using SNP markers of varying densities. The 1791 fattened steers with phenotypic data and 189 having predicted breeding values provided by the official genetic evaluation using pedigree data were treated as the training and validation populations respectively. Genotype data on 565837 autosomal SNPs were available and SNPs were selected to provide different equally spaced SNP subsets of lower densities. Genomic estimated breeding values (GEBVs) were obtained using genomic best linear unbiased prediction incorporating one of two types of genomic relationship matrices (G matrices). The GP accuracy assessed as the correlation between the GEBVs and the corrected records divided by the square root of estimated heritability was around 0.85 for carcass weight and 0.60 for marbling score when using 565837 SNPs. The type of G matrix used gave no substantial difference in the results at a given SNP density for traits examined. Around 80% of the GP accuracy was retained when the SNP density was decreased to 1/1000 of that of all available SNPs. These results indicate that even when a SNP panel of a lower density is used, GP may be beneficial to the pre-selection for the carcass traits in Japanese Black young breeding animals.

scholarly journals Selective genotyping and phenotypic data inclusion strategies of crossbred progeny for combined crossbred and purebred selection in swine breeding

2021 ◽  
Author(s):  
Garrett M See ◽  
Benny E Mote ◽  
Matthew L Spangler
Keyword(s):  
Genetic Gain ◽  
Production Systems ◽  
Snp Markers ◽  
Selective Genotyping ◽  
Phenotypic Data ◽  
Breeding Values ◽  
True Breeding ◽  
Estimated Breeding Values ◽  
Highly Correlated ◽  
Genetic Evaluations

Abstract Inclusion of crossbred (CB) data into traditionally purebred (PB) genetic evaluations has been shown to increase the response in CB performance. Currently it is unrealistic to collect data on all CB animals in swine production systems, thus, a subset of CB animals must be selected to contribute genomic/phenotypic information. The aim of this study was to evaluate selective genotyping strategies in a simulated 3-way swine crossbreeding scheme. The swine crossbreeding scheme was simulated and produced 3-way CB animals for 6 generations with three distinct purebred breeds each with 25 and 175 mating males and females, respectively. F1 crosses (400 mating females) produced 4,000 terminal CB progeny which were subjected to selective genotyping. The genome consisted of 18 chromosomes with 1,800 QTL and 72k SNP markers. Selection was performed using estimated breeding values (EBV) for CB performance. It was assumed that both PB and CB performance was moderately heritable (h2=0.4). Several scenarios altering the genetic correlation between PB and CB performance (rpc=0.1, 0.3, 0.5, 0.7 or 0.9) were considered. CB animals were chosen based on phenotypes to select 200, 400 or 800 CB animals to genotype per generation. Selection strategies included: 1) Random: random selection, 2) Top: highest phenotype, 3) Bottom: lowest phenotype, 4) Extreme: half highest and half lowest phenotypes, and 5) Middle: average phenotype. Each selective genotyping strategy, except for Random, was considered by selecting animals in half-sib (HS) or full-sib (FS) families. The number of PB animals with genotypes and phenotypes each generation was fixed at 1680. Each unique genotyping strategy and rpc scenario was replicated 10 times. Selection of CB animals based on the Extreme strategy resulted in the highest (P<0.05) rates of genetic gain in CB performance (ΔG) when rpc<0.9. For highly correlated traits (rpc=0.9) selective genotyping did not impact (P>0.05) ΔG. No differences (P>0.05) were observed in ΔG between Top, Bottom or Middle when rpc>0.1. Higher correlations between true breeding values (TBV) and EBV were observed using Extreme when rpc<0.9. In general, family sampling method did not impact ΔG or the correlation between TBV and EBV. Overall, the Extreme genotyping strategy produced the greatest genetic gain and the highest correlations between TBV and EBV, suggesting that two tailed sampling of CB animals is the most informative when CB performance is the selection goal.

scholarly journals Investigation of reliability of genomic predictions in the admixed Nordic Red dairy cattle

2012 ◽  
pp. 1-5
Author(s):  
Mahlako L. Makgahlela ◽  
E. A. Mäntysaari ◽  
I. Strandén ◽  
M. Koivula ◽  
U.S. Nielsen ◽  
...  
Keyword(s):  
Dairy Cattle ◽  
Specific Model ◽  
Snp Markers ◽  
Homogeneous Population ◽  
Genomic Breeding ◽  
Breeding Values ◽  
Specific Effects ◽  
Estimated Breeding Values ◽  
Genomic Predictions ◽  
Uniform Population

The success of genomic selection (GS) in small breeds which are likely to have admixed structures has been minimal. This is because accuracy of GS depends on the extent of linkage disequilibrium (LD) between markers and quantitative trait loci (QTL) and LD depends on the genetic structure of the population and marker density. In the current study, we evaluate reliability of genomic predictions in young unproven bulls, when interactions between marker effects and breed of origin are accounted for in the Nordic Red dairy cattle (RDC). The population structure of the RDC is admixed. Data consisted of animal breed proportions calculated from the full pedigree, deregressed proofs (DRP) of published estimated breeding values (EBV) for yield traits and genotypic data for 37,595 SNP markers. Direct genomic breeding values (DGV) were estimated using 2 models, one accounting for breed-specific effects and other assuming uniform population. Validation reliabilities were calculated as the squared correlation between DRP and DGV (r2DRP, DGV), corrected by the mean reliability ofDRP. Using the breed-specific model increased the reliability of DGV by 2% and 3% for milk and protein, respectively, when compared to homogeneous population GBLUP model. The exception was for fat, where there was no gain in reliability. Estimated validation reliabilities were low for milk (0.32) and protein (0.32) and slightly higher (0.42) for fat.

scholarly journals Genomic selection strategies for clonally propagated crops

2020 ◽  
Author(s):  
Christian R. Werner ◽  
R. Chris Gaynor ◽  
Daniel J. Sargent ◽  
Alessandra Lillo ◽  
Gregor Gorjanc ◽  
...  
Keyword(s):  
Genomic Selection ◽  
Genetic Gain ◽  
Genomic Prediction ◽  
Breeding Program ◽  
Selection Methods ◽  
Breeding Programs ◽  
Breeding Values ◽  
Parent Selection ◽  
Estimated Breeding Values ◽  
Selection Of

AbstractFor genomic selection in clonal breeding programs to be effective, crossing parents should be selected based on genomic predicted cross performance unless dominance is negligible. Genomic prediction of cross performance enables a balanced exploitation of the additive and dominance value simultaneously. Here, we compared different strategies for the implementation of genomic selection in clonal plant breeding programs. We used stochastic simulations to evaluate six combinations of three breeding programs and two parent selection methods. The three breeding programs included i) a breeding program that introduced genomic selection in the first clonal testing stage, and ii) two variations of a two-part breeding program with one and three crossing cycles per year, respectively. The two parent selection methods were i) selection of parents based on genomic estimated breeding values, and ii) selection of parents based on genomic predicted cross performance. Selection of parents based on genomic predicted cross performance produced faster genetic gain than selection of parents based on genomic estimated breeding values because it substantially reduced inbreeding when the dominance degree increased. The two-part breeding programs with one and three crossing cycles per year using genomic prediction of cross performance always produced the most genetic gain unless dominance was negligible. We conclude that i) in clonal breeding programs with genomic selection, parents should be selected based on genomic predicted cross performance, and ii) a two-part breeding program with parent selection based on genomic predicted cross performance to rapidly drive population improvement has great potential to improve breeding clonally propagated crops.

scholarly journals Estimation of genetic parameters and accuracy of genomic prediction for production traits in Duroc pigs

2019 ◽  
Vol 64 (No. 4) ◽  
pp. 160-165 ◽  
Author(s):  
Bryan Irvine Lopez ◽  
Vanessa Viterbo ◽  
Choul Won Song ◽  
Kang Seok Seo
Keyword(s):  
Genomic Prediction ◽  
Genetic Parameters ◽  
Average Daily Gain ◽  
Genetic Correlations ◽  
Single Step ◽  
Production Traits ◽  
Muscle Area ◽  
Genomic Breeding ◽  
Breeding Values ◽  
Heritability Estimates

Abstract: Genetic parameters and accuracy of genomic prediction for production traits in a Duroc population were estimated. Data were on 24 828 purebred Duroc pigs born in 2000–2016. After quality control procedures, 30 263 single nucleotide polymorphism markers and 560 animals remained that were used to predict the genomic breeding values of individuals. Accuracies of predicted breeding values for average daily gain (ADG), backfat thickness (BF), loin muscle area (LMA), lean percentage (LP) and age at 90 kg (D90) between pedigree-based and single-step methods were compared. Analyses were carried out with a multivariate animal model to estimate genetic parameters for production traits while univariate analyses were performed to predict the genomic breeding values of individuals. Heritability estimates from pedigree analysis were moderate to high. Heritability estimates and standard error for ADG, BF, LMA, LP and D90 were 0.35 ± 0.01, 0.35 ± 0.11, 0.24 ± 0.04, 0.42 ± 0.11 and 0.37 ± 0.03, respectively. Genetic correlations of ADG with BF and LP were low and negative. Genetic correlations of LMA with ADG, BF, LP and D90 were –0.37, –0.27, 0.48 and 0.31, respectively. High correlations were observed between ADG and D90 (–0.98), and also between BF and LP (–0.93). Accuracies of genomic breeding values for ADG, BF, LMA, LP and D90 were 0.30, 0.33, 0.38, 0.40 and 0.28, respectively. Corresponding accuracies using pedigree-based method were 0.29, 0.32, 0.38, 0.39 and 0.27, respectively. The results showed that the single-step method did not show significant advantage compared to the pedigree-based method.

scholarly journals The impact of QTL allele frequency distribution on the accuracy of genomic prediction

2018 ◽  
Vol 61 (2) ◽  
pp. 207-213 ◽  
Author(s):  
Pourya Davoudi ◽  
Rostam Abdollahi-Arpanahi ◽  
Ardeshir Nejati-Javaremi
Keyword(s):  
Allele Frequency ◽  
Frequency Distribution ◽  
Genomic Prediction ◽  
Prediction Accuracy ◽  
Snp Markers ◽  
Relationship Matrix ◽  
Allele Frequency Distribution ◽  
Breeding Values ◽  
A Genome ◽  
The Impact

Abstract. The accuracy of genomic prediction of quantitative traits based on single nucleotide polymorphism (SNP) markers depends among other factors on the allele frequency distribution of quantitative trait loci (QTL). Therefore, the aim of this study was to investigate different QTL allele frequency distributions and their effect on the accuracy of genomic estimated breeding values (GEBVs) using best linear unbiased genomic prediction (GBLUP) in simulated data. A population of 1000 individuals composed of 500 males and 500 females as well as a genome of 1000 cM consisting of 10 chromosomes and with a mutation rate of 2.5 × 10−5 per locus was simulated. QTL frequencies were derived from five distributions of allele frequency including constant, uniform, U-shaped, L-shaped and minor allele frequency (MAF) less than 0.01 (lowMAF). QTL effects were generated from a standard normal distribution. The number of QTL was assumed to be 500, and the simulation was done in 10 replications. The genomic prediction accuracy in the first-validation generation in constant, and the uniform allele frequency distribution was 0.59 and 0.57, respectively. Results showed that the highest accuracy of GEBVs was obtained with constant and uniform distributions followed by L-shaped, U-shaped and lowMAF QTL allele frequency distribution. The regression of true breeding values on predicted breeding values in the first-validation generation was 0.94, 0.92, 0.88, 0.85 and 0.75 for constant, uniform, L-shaped, U-shaped and lowMAF distributions, respectively. Depite different values of regression coefficients, in all scenarios GEBVs are biased downward. Overall, results showed that when QTL had a lower MAF relative to SNP markers, a low linkage disequilibrium (LD) was observed, which had a negative effect on the accuracy of GEBVs. Hence, the effect of the QTL allele frequency distribution on prediction accuracy can be alleviated through using a genomic relationship weighted by MAF or an LD-adjusted relationship matrix.

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