scholarly journals Uses of genomics in livestock agriculture

2012 ◽  
Vol 52 (3) ◽  
pp. 73 ◽  
Author(s):  
M. E. Goddard

World demand for livestock products is likely to increase in coming decades but the cost of production could escalate faster than the price due to competition for land, water, grain and fertiliser and the effects of climate change and its mitigation. To remain competitive for these resources, livestock agriculture has to dramatically increase in efficiency of production. Genetic gain is one mechanism to achieve increased efficiency and there is the opportunity to utilise the scientific advances in genomics. Three ways in which genomics can be used are in additive genetic improvement, exploitation of non-additive genetic variance and management which exploits genotype by environment interactions to optimise management. Genomic selection is already being widely implemented in dairy cattle and beef cattle and sheep will follow in the future once the accuracy of genomic selection is high enough. The accuracy of equations that predict breeding value from DNA genotypes can be increased by increasing the size of the reference population from which the equations are estimated, increasing the density of markers, using genome sequences instead of markers, using more appropriate statistical procedures and incorporating biological information into the prediction. In the long term, genomic selection combined with reproductive technology that reduces the minimum age at breeding will greatly increase the rate of genetic gain. This will allow long-term increases in biological efficiency and short-term tailoring of livestock to meet the demands of particular markets and opportunities.

Author(s):  
Neeraj Budhlakoti ◽  
Dwijesh Chandra Mishra ◽  
Anil Rai ◽  
K.K. Chaturvedi ◽  
Anu Sharma ◽  
...  

Now a days, Genomic Selection (GS) became a preferable choice for selection of appropriate candidate for animal and plant breeding research. Various studies related to GS has been done recently where it has shown potential benefits and advantages over traditional and conventional plant breeding methods. GS has been successfully implemented in various animal and plant breeding programs. It reduces the total costs by selecting the animals at early stage hence shorten the generation interval. Genomic selection is the future of livestock and plant breeding as it improves the genetic gain by decreasing genetic interval and improving reliability. Although there is a need of further investigation to improve the accuracy of genomic estimated breeding value and manage long-term genetic gain. This article provides a brief review what we have achieved through GS till yet and what is future scope and perspective in the GS research.


2021 ◽  
Author(s):  
Marlee R. Labroo ◽  
Jessica E. Rutkoski

Background: Recurrent selection is a foundational breeding method for quantitative trait improvement. It typically features rapid breeding cycles that can lead to high rates of genetic gain. In recurrent phenotypic selection, generations do not overlap, which means that breeding candidates are evaluated and considered for selection for only one cycle. With recurrent genomic selection, candidates can be evaluated based on genomic estimated breeding values indefinitely, therefore facilitating overlapping generations. Candidates with true high breeding values that were discarded in one cycle due to underestimation of breeding value could be identified and selected in subsequent cycles. The consequences of allowing generations to overlap in recurrent selection are unknown. We assessed whether maintaining overlapping and discrete generations led to differences in genetic gain for phenotypic, genomic truncation, and genomic optimum contribution recurrent selection by simulation of traits with various heritabilities and genetic architectures across fifty breeding cycles. We also assessed differences of overlapping and discrete generations in a conventional breeding scheme with multiple stages and cohorts. Results: With phenotypic selection, overlapping generations led to decreased genetic gain compared to discrete generations due to increased selection error bias. Selected individuals, which were in the upper tail of the distribution of phenotypic values, tended to also have high absolute error relative to their true breeding value compared to the overall population. Without repeated phenotyping, these erroneously outlying individuals were repeatedly selected across cycles, leading to decreased genetic gain. With genomic truncation selection, overlapping and discrete generations performed similarly as updating breeding values precluded repeatedly selecting individuals with inaccurately high estimates of breeding values in subsequent cycles. Overlapping generations did not outperform discrete generations in the presence of a positive genetic trend with genomic truncation selection, as past generations had lower mean genetic values than the current generation of selection candidates. With genomic optimum contribution selection, overlapping and discrete generations performed similarly, but overlapping generations slightly outperformed discrete generations in the long term if the targeted inbreeding rate was extremely low. Conclusions: Maintaining discrete generations in recurrent phenotypic mass selection leads to increased genetic gain, especially at low heritabilities, by preventing selection error bias. With genomic truncation selection and genomic optimum contribution selection, genetic gain does not differ between discrete and overlapping generations assuming non-genetic effects are not present. Overlapping generations may increase genetic gain in the long term with very low targeted rates of inbreeding in genomic optimum contribution selection.


2019 ◽  
Author(s):  
Antoine Allier ◽  
Christina Lehermeier ◽  
Alain Charcosset ◽  
Laurence Moreau ◽  
Simon Teyssèdre

AbstractThe implementation of genomic selection in recurrent breeding programs raised several concerns, especially that a higher inbreeding rate could compromise the long term genetic gain. An optimized mating strategy that maximizes the performance in progeny and maintains diversity for long term genetic gain on current and yet unknown future targets is essential. The optimal cross selection approach aims at identifying the optimal set of crosses maximizing the expected genetic value in the progeny under a constraint on diversity in the progeny. Usually, optimal cross selection does not account for within family selection, i.e. the fact that only a selected fraction of each family serves as candidate parents of the next generation. In this study, we consider within family variance accounting for linkage disequilibrium between quantitative trait loci to predict the expected mean performance and the expected genetic diversity in the selected progeny of a set of crosses. These predictions rely on the method called usefulness criterion parental contribution (UCPC). We compared UCPC based optimal cross selection and optimal cross selection in a long term simulated recurrent genomic selection breeding program considering overlapping generations. UCPC based optimal cross selection proved to be more efficient to convert the genetic diversity into short and long term genetic gains than optimal cross selection. We also showed that using the UCPC based optimal cross selection, the long term genetic gain can be increased with only limited reduction of the short term commercial genetic gain.


2020 ◽  
Vol 33 (3) ◽  
pp. 382-389 ◽  
Author(s):  
Yun-Mi Lee ◽  
Chang-Gwon Dang ◽  
Mohammad Z. Alam ◽  
You-Sam Kim ◽  
Kwang-Hyeon Cho ◽  
...  

Objective: This study was conducted to test the efficiency of genomic selection for milk production traits in a Korean Holstein cattle population.Methods: A total of 506,481 milk production records from 293,855 animals (2,090 heads with single nucleotide polymorphism information) were used to estimate breeding value by single step best linear unbiased prediction.Results: The heritability estimates for milk, fat, and protein yields in the first parity were 0.28, 0.26, and 0.23, respectively. As the parity increased, the heritability decreased for all milk production traits. The estimated generation intervals of sire for the production of bulls (L<sub>SB</sub>) and that for the production of cows (L<sub>SC</sub>) were 7.9 and 8.1 years, respectively, and the estimated generation intervals of dams for the production of bulls (L<sub>DB</sub>) and cows (L<sub>DC</sub>) were 4.9 and 4.2 years, respectively. In the overall data set, the reliability of genomic estimated breeding value (GEBV) increased by 9% on average over that of estimated breeding value (EBV), and increased by 7% in cows with test records, about 4% in bulls with progeny records, and 13% in heifers without test records. The difference in the reliability between GEBV and EBV was especially significant for the data from young bulls, i.e. 17% on average for milk (39% vs 22%), fat (39% vs 22%), and protein (37% vs 22%) yields, respectively. When selected for the milk yield using GEBV, the genetic gain increased about 7.1% over the gain with the EBV in the cows with test records, and by 2.9% in bulls with progeny records, while the genetic gain increased by about 24.2% in heifers without test records and by 35% in young bulls without progeny records.Conclusion: More genetic gains can be expected through the use of GEBV than EBV, and genomic selection was more effective in the selection of young bulls and heifers without test records.


2021 ◽  
Author(s):  
Adam R Festa ◽  
Ross Whetten

Computer simulations of breeding strategies are an essential resource for tree breeders because they allow exploratory analyses into potential long-term impacts on genetic gain and inbreeding consequences without bearing the cost, time, or resource requirements of field experiments. Previous work has modeled the potential long-term implications on inbreeding and genetic gain using random mating and phenotypic selection. Reduction in sequencing costs has enabled the use of DNA marker-based relationship matrices in addition to or in place of pedigree-based allele sharing estimates; this has been shown to provide a significant increase in the accuracy of progeny breeding value prediction. A potential pitfall of genomic selection using genetic relationship matrices is increased coancestry among selections, leading to the accumulation of deleterious alleles and inbreeding depression. We used simulation to compare the relative genetic gain and risk of inbreeding depression within a breeding program similar to loblolly pine, utilizing pedigree-based or marker-based relationships over ten generations. We saw a faster rate of purging deleterious alleles when using a genomic relationship matrix based on markers that track identity-by-descent of segments of the genome. Additionally, we observed an increase in the rate of genetic gain when using a genomic relationship matrix instead of a pedigree-based relationship matrix. While the genetic variance of populations decreased more rapidly when using genomic-based relationship matrices as opposed to pedigree-based, there appeared to be no long-term consequences on the accumulation of deleterious alleles within the simulated breeding strategy.


2018 ◽  
Author(s):  
Stefan McKinnon Edwards ◽  
Jaap B. Buntjer ◽  
Robert Jackson ◽  
Alison R. Bentley ◽  
Jacob Lage ◽  
...  

AbstractGenomic selection offers several routes for increasing genetic gain or efficiency of plant breeding programs. In various species of livestock there is empirical evidence of increased rates of genetic gain from the use of genomic selection to target different aspects of the breeder’s equation. Accurate predictions of genomic breeding value are central to this and the design of training sets is in turn central to achieving sufficient levels of accuracy. In summary, small numbers of close relatives and very large numbers of distant relatives are expected to enable accurate predictions.To quantify the effect of some of the properties of training sets on the accuracy of genomic selection in crops we performed an extensive field-based winter wheat trial. In summary, this trial involved the construction of 44 F2:4 bi- and triparental populations, from which 2992 lines were grown on four field locations and yield was measured. For each line, genotype data were generated for 25,000 segregating single nucleotide polymorphism markers. The overall heritability of yield was estimated to 0.65, and estimates within individual families ranged between 0.10 and 0.85. Within cross genomic prediction accuracies of yield BLUEs were 0.125 – 0.127 using two different cross-validation approaches, and generally increased with training set size. Using related crosses in training and validation sets generally resulted in higher prediction accuracies than using unrelated crosses. The results of this study emphasize the importance of the training set design in relation to the genetic material to which the resulting prediction model is to be applied.


2015 ◽  
Vol 47 (1) ◽  
pp. 19 ◽  
Author(s):  
Huiming Liu ◽  
Theo Meuwissen ◽  
Anders C Sørensen ◽  
Peer Berg

2012 ◽  
Vol 52 (3) ◽  
pp. 180 ◽  
Author(s):  
Jennie Pryce ◽  
Ben Hayes

New genomic technologies can help farmers to (1) achieve higher annual rates of genetic gain through using genomically tested bulls in their herds, (2) select for ‘difficult’ to measure traits, such as feed conversion efficiency, methane emissions and energy balance, (3) select the best heifers to become herd replacements, (4) sell pedigree heifers at a premium, (5) use mating plans to optimise rates of genetic gain while controlling inbreeding, (6) achieve certainty in parentage of individual cows and (7) avoid genetic defects that could arise from mating cows to bulls that are known carriers of genetic diseases that are the result of a single lethal mutation. The first use does not require genotyping females and could approximately double the net income per cow that arises due to genetic improvement, mainly through a reduction in generation interval. On the basis of current rates of genetic gain, the net profit from using genotyped bulls could be worth AU$20/cow per year and is permanent and cumulative. One of the most powerful uses of genomic selection is to select for economically important, yet difficult- or expensive-to-measure traits, such as residual feed intake or energy balance. Provided the accuracy of genomic breeding values is high enough (i.e. correlation between the true and estimated breeding values), these traits lend themselves well to genomic selection. For selecting replacement heifers, if genotyping costs are AU$50/cow, the net profit of genotyping 40 heifers to select the top 20 as replacements (per 100 cows) would be worth approximately AU$41 per cow. However, using parent average estimated breeding-value information is free and can already be used to select replacement heifers. So, genotyping costs would need to be very low to be more profitable than selecting on parent average estimated breeding value. However, extra value from genotyping can also be captured by using other strategies. For example, mating plans that use genomic relationships rather than pedigree relationships to capture inbreeding are superior in terms of reducing progeny inbreeding at a desired level of genetic gain, although pedigree does an adequate job. So, again, the benefits of genotyping are small (<AU$10). Ascertainment of pedigree is an additional use of genotyping and is potentially worth ~AU$30 per cow. Avoidance of genetic diseases and selling of pedigree heifers have a value that should be estimated case-by-case. Because genotyping costs continue to fall, it may become increasingly popular to capture the extra value from genotyping females.


BMC Genomics ◽  
2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Yongjun Li ◽  
Jaroslav Klápště ◽  
Emily Telfer ◽  
Phillip Wilcox ◽  
Natalie Graham ◽  
...  

Abstract Background Non-key traits (NKTs) in radiata pine (Pinus radiata D. Don) refer to traits other than growth, wood density and stiffness, but still of interest to breeders. Branch-cluster frequency, stem straightness, external resin bleeding and internal checking are examples of such traits and are targeted for improvement in radiata pine research programmes. Genomic selection can be conducted before the performance of selection candidates is available so that generation intervals can be reduced. Radiata pine is a species with a long generation interval, which if reduced could significantly increase genetic gain per unit of time. The aim of this study was to evaluate the accuracy and predictive ability of genomic selection and its efficiency over traditional forward selection in radiata pine for the following NKTs: branch-cluster frequency, stem straightness, internal checking, and external resin bleeding. Results Nine hundred and eighty-eight individuals were genotyped using exome capture genotyping by sequencing (GBS) and 67,168 single nucleotide polymorphisms (SNPs) used to develop genomic estimated breeding values (GEBVs) with genomic best linear unbiased prediction (GBLUP). The documented pedigree was corrected using a subset of 704 SNPs. The percentage of trio parentage confirmed was about 49% and about 50% of parents were re-assigned. The accuracy of GEBVs was 0.55–0.75 when using the documented pedigree and 0.61–0.80 when using the SNP-corrected pedigree. A higher percentage of additive genetic variance was explained and a higher predictive ability was observed when using the SNP-corrected pedigree than using the documented pedigree. With the documented pedigree, genomic selection was similar to traditional forward selection when assuming a generation interval of 17 years, but worse than traditional forward selection when assuming a generation interval of 14 years. After the pedigree was corrected, genomic selection led to 37–115% and 13–77% additional genetic gain over traditional forward selection when generation intervals of 17 years and 14 years were assumed, respectively. Conclusion It was concluded that genomic selection with a pedigree corrected by SNP information was an efficient way of improving non-key traits in radiata pine breeding.


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