Genomic prediction and genome-wide association studies in beef and dairy cattle.

2014 ◽  
pp. 474-501 ◽  
Author(s):  
D. J. Garrick ◽  
R. Fernando
Animals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 541
Author(s):  
Long Chen ◽  
Jennie E. Pryce ◽  
Ben J. Hayes ◽  
Hans D. Daetwyler

Structural variations (SVs) are large DNA segments of deletions, duplications, copy number variations, inversions and translocations in a re-sequenced genome compared to a reference genome. They have been found to be associated with several complex traits in dairy cattle and could potentially help to improve genomic prediction accuracy of dairy traits. Imputation of SVs was performed in individuals genotyped with single-nucleotide polymorphism (SNP) panels without the expense of sequencing them. In this study, we generated 24,908 high-quality SVs in a total of 478 whole-genome sequenced Holstein and Jersey cattle. We imputed 4489 SVs with R2 > 0.5 into 35,568 Holstein and Jersey dairy cattle with 578,999 SNPs with two pipelines, FImpute and Eagle2.3-Minimac3. Genome-wide association studies for production, fertility and overall type with these 4489 SVs revealed four significant SVs, of which two were highly linked to significant SNP. We also estimated the variance components for SNP and SV models for these traits using genomic best linear unbiased prediction (GBLUP). Furthermore, we assessed the effect on genomic prediction accuracy of adding SVs to GBLUP models. The estimated percentage of genetic variance captured by SVs for production traits was up to 4.57% for milk yield in bulls and 3.53% for protein yield in cows. Finally, no consistent increase in genomic prediction accuracy was observed when including SVs in GBLUP.


Genes ◽  
2019 ◽  
Vol 10 (9) ◽  
pp. 669 ◽  
Author(s):  
Peter S. Kristensen ◽  
Just Jensen ◽  
Jeppe R. Andersen ◽  
Carlos Guzmán ◽  
Jihad Orabi ◽  
...  

Use of genetic markers and genomic prediction might improve genetic gain for quality traits in wheat breeding programs. Here, flour yield and Alveograph quality traits were inspected in 635 F6 winter wheat breeding lines from two breeding cycles. Genome-wide association studies revealed single nucleotide polymorphisms (SNPs) on chromosome 5D significantly associated with flour yield, Alveograph P (dough tenacity), and Alveograph W (dough strength). Additionally, SNPs on chromosome 1D were associated with Alveograph P and W, SNPs on chromosome 1B were associated with Alveograph P, and SNPs on chromosome 4A were associated with Alveograph L (dough extensibility). Predictive abilities based on genomic best linear unbiased prediction (GBLUP) models ranged from 0.50 for flour yield to 0.79 for Alveograph W based on a leave-one-out cross-validation strategy. Predictive abilities were negatively affected by smaller training set sizes, lower genetic relationship between lines in training and validation sets, and by genotype–environment (G×E) interactions. Bayesian Power Lasso models and genomic feature models resulted in similar or slightly improved predictions compared to GBLUP models. SNPs with the largest effects can be used for screening large numbers of lines in early generations in breeding programs to select lines that potentially have good quality traits. In later generations, genomic predictions might be used for a more accurate selection of high quality wheat lines.


2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 31-31
Author(s):  
Li Ma

Abstract Genome-wide association studies (GWAS) has been widely used to map quantitative trait loci (QTL) of complex traits and diseases since 2007. To date, the human GWAS catalog has accumulated 4,410 publications and 172,351 associations, and the animal QTLdb has curated 983 publications and 130,407 QTLs for cattle, largest in livestock species. During the past 13 years of development, GWAS methods has evolved from simple linear regression, using principal components to address sample relatedness, mixed models, to Bayesian full model approaches. These methods have their advantages and limitations, so it is important to choose an appropriate method, especially for studies in livestock where sample size is often limited. Note that the most popular GWAS approach, the mixed model method, originated from animal breeding and genetics research. Leveraging the national cattle genomic database at the Council on Dairy Cattle Breeding (CDCB), we have conducted GWAS analyses of various dairy traits to identify QTLs and SNP markers of importance. Combining with sequence and functional annotation data, we seek to understand the genetic basis of complex traits and to reveal useful knowledge that can be incorporated into more accurate genomic predictions in the future.


2019 ◽  
Author(s):  
M. Pérez-Enciso ◽  
L. C. Ramírez-Ayala ◽  
L.M. Zingaretti

AbstractBackgroundGenomic Prediction (GP) is the procedure whereby molecular information is used to predict complex phenotypes. Although GP can significantly enhance predictive accuracy, it can be expensive and difficult to implement. To help in designing optimum experiments, including genome wide association studies and genomic selection experiments, we have developed SeqBreed, a generic and flexible python3 forward simulator.ResultsSeqBreed accommodates sex and mitochondrion chromosomes as well as autopolyploidy. It can simulate any number of complex phenotypes determined by any number of causal loci. SeqBreed implements several GP methods, including single step GBLUP. We demonstrate its functionality with Drosophila Genome Reference Panel (DGRP) sequence data and with tetraploid potato genotypes.ConclusionsSeqBreed is a flexible and easy to use tool appropriate for optimizing GP or genome wide association studies. It incorporates some of the most popular GP methods and includes several visualization tools. Code is open and can be freely modified. Software, documentation and examples are available at https://github.com/miguelperezenciso/SeqBreed.


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