Accounting for Population Structure and Phenotypes From Relatives in Association Mapping for Farm Animals: A Simulation Study

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Population structure or genetic relatedness should be considered in genome association studies to avoid spurious association. The most used methods for genome-wide association studies (GWAS) account for population structure but are limited to genotyped individuals with phenotypes. Single-step GWAS (ssGWAS) can use phenotypes from non-genotyped relatives; however, its ability to account for population structure has not been explored. Here we investigate the equivalence among ssGWAS, efficient mixed-model association expedited (EMMAX), and genomic best linear unbiased prediction GWAS (GBLUP-GWAS), and how they differ from the single-SNP analysis without correction for population structure (SSA-NoCor). We used simulated, structured populations that mimicked fish, beef cattle, and dairy cattle populations with 1040, 5525, and 1,400 genotyped individuals, respectively. Larger populations were also simulated that had up to 10-fold more genotyped animals. The genomes were composed by 29 chromosomes, each harboring one QTN, and the number of simulated SNPs was 35,000 for the fish and 65,000 for the beef and dairy cattle populations. Males and females were genotyped in the fish and beef cattle populations, whereas only males had genotypes in the dairy population. Phenotypes for a trait with heritability varying from 0.25 to 0.35 were available in both sexes for the fish population, but only for females in the beef and dairy cattle populations. In the latter, phenotypes of daughters were projected into genotyped sires (i.e., deregressed proofs) before applying EMMAX and SSA-NoCor. Although SSA-NoCor had the largest number of true positive SNPs among the four methods, the number of false negatives was two–fivefold that of true positives. GBLUP-GWAS and EMMAX had a similar number of true positives, which was slightly smaller than in ssGWAS, although the difference was not significant. Additionally, no significant differences were observed when deregressed proofs were used as pseudo-phenotypes in EMMAX compared to daughter phenotypes in ssGWAS for the dairy cattle population. Single-step GWAS accounts for population structure and is a straightforward method for association analysis when only a fraction of the population is genotyped and/or when phenotypes are available on non-genotyped relatives.

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  • 10.1093/jas/skaa278.018
10 Can single-step genome-wide association analysis (ssGWAA) account for population structure?
  • Nov 30, 2020
  • Journal of Animal Science
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Several methods are available for genome-wide association analysis, including the classical GWAA (cGWAA) based on fixed, single-SNP regression; efficient mixed-model association expedited (EMMAX) that fits single-SNP regressions together with a relationship matrix to account for population structure; and single-step GWAA (ssGWAA) where all data, including non-genotyped animals, are used. The objectives of this study were to: 1) investigate the ability of ssGWAA to account for population structure and correctly identify quantitative trait nucleotides (QTN); and 2) compare ssGWAA with cGWAA and EMMAX. Three simulated datasets were used, which mimic fish, beef cattle, and dairy cattle populations. The fish population was composed of 2,040 fish, out of which 1,040 were genotyped and had phenotypes for a trait with heritability of 0.25. The beef cattle population had 6,010 animals in the pedigree, but only 1,500 with phenotypes (h2 = 0.35) and genotypes. Lastly, the dairy cattle population had 40,800 pedigreed animals, of which 20,000 females had phenotypes (h2 = 0.32) and 2,400 males were genotyped. All phenotypes, pedigree, and genotypes were used in ssGWAA, whereas only genotypes and phenotypes were used in cGWAA and EMMAX for the fish and beef cattle analyses. For the dairy cattle analysis using the last two methods, deregressed proofs had to be used instead of phenotypes. The ability to correctly identify QTN and the number of statistically significant SNP (P < 0.05/number of SNP) was assessed among methods. In all populations, cGWAA was able to identify some of the strongest QTN but showed a large number of false positives. EMMAX and ssGWAA did not show false associations and correctly identified the top QTN, with more signals observed in ssGWAA. The ssGWAA accounts for population structure and is a proper association method, especially for livestock populations where sparse genotyping is a reality and phenotypes may not be recorded in genotyped animals.

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  • 10.1111/jbg.12874
A systematic review with meta-analysis of heritability estimates for temperament-related traits in beef and dairy cattle populations.
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  • Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie
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Temperament (docility) is a key breeding goal in the cattle industry due to its direct relationship with animal welfare, cattle handler's safety and animal productivity. Over the past six decades, numerous studies have reported heritability estimates for temperament-related traits in cattle populations ranging from low to high values. Therefore, the primary objective of this study was to perform a comprehensive systematic review with meta-analysis to obtain weighted estimates of heritability for temperament-related traits in worldwide cattle populations. After data editing and quality control, 106 studies were included in the systematic review, of which 29.2% and 70.8% reported estimates of heritability for temperament-related traits in dairy and beef cattle populations, respectively. Meta-analyses were performed for 95 heritability estimates using a random model approach. The weighted heritability estimates were as follow: (a) flight score at weaning = 0.23 (95% CI: 0.15-0.32); (b) flight speed at weaning = 0.30 (95% CI: 0.26-0.33); (c) joint analysis of flight speed and flight score at weaning = 0.27 (95% CI: 0.22-0.31); (d) flight speed at yearling = 0.26 (95% CI: 0.21-0.30); (e) joint analysis of flight speed at weaning and yearling = 0.27 (95% CI: 0.24-0.30); (f) movement score = 0.12 (95% CI: 0.08-0.15); (g) crush score at weaning = 0.21 (95% CI: 0.17-0.25); (h) pen score at weaning = 0.27 (95% CI: 0.19-0.34); (i) pen score at yearling = 0.20 (95% CI: 0.17-0.23); (j) joint analysis of pen score at weaning and yearling = 0.22 (95% CI: 0.18-0.26); (k) cow's aggressiveness at calving = 0.10 (95% CI: 0.01-0.19); (l) general temperament = 0.13 (95% CI: 0.06-0.19); (m) milking temperament = 0.16 (95% CI: 0.11-0.21); and (n) joint analysis of general and milking temperament = 0.14 (95% CI: 0.11-0.18). The heterogeneity index ranged from 0% to 77%, and the Q-test was significant (p < 0.05) for four single-trait meta-analyses. In conclusion, temperament is moderately heritable in beef cattle populations, and flight speed at weaning had the highest weighted heritability estimate. Moreover, between-study heterogeneity was low or moderate in beef cattle traits, suggesting reasonable standardization across studies. On the other hand, low-weighted heritability and high between-study heterogeneity were estimated for temperament-related traits in dairy cattle, suggesting that more studies are needed to better understand the genetic inheritance of temperament in dairy cattle populations.

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  • Cite Count Icon 22
  • 10.1111/j.1751-0813.1985.tb14246.x
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  • Cite Count Icon 5
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Inbreeding and genetic diversity loss of four cattle beef breeds in Slovakia
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Received: 2016-02-23  |  Accepted: 2016-04-21  |  Available online: 2016-05-30 dx.doi.org/10.15414/afz.2016.19.02.59-63 The aim of the paper was to evaluate trends in inbreeding and loss of genetic diversity in four beef cattle breeds (Blonde d´Aquitaine-BA, Charolais-CH, Limousine-LI, Simmental-SM). The highest ratio of inbred animals was found in the SM breed (63.6 %) and the lowest in the LI (14.1 %). The highest average inbreeding intensity we found in the SM, the lowest in the BA. The amount of genetic diversity in the reference population accounting for diversity loss due to genetic drift and unequal founder contributions was the highest in the SM (6.2 %), following the BA (3.5 %), LI (1.1 %) and CH (0.9 %). The proportion of genetic diversity lost due to genetic drift was higher in BA, CH, LI than the loss of genetic diversity due to unequal founder contribution. Keywords: beef cattle, pedigree analysis, inbreeding, genetic diversity References Boichard, D., Maignel,L. and Verrier. E. (1997) The value of using probabilities of gene origin to measure genetic variability in a population. Genet. Sel. Evol ., vol.29, no. 5, pp.5-23. doi: http://dx.doi.org/10.1186/1297-9686-29-1-5 Cabalero, A. and Toro, M.A. (2000) Interrelations between effective population size and other tools for management of conserved populations. Genet. Res ., vol. 75, no. 3, pp.331-343. doi: http://dx.doi.org/10.1017/S0016672399004449 Gutiérrez, J.P. and Goyache, F. ( 2005) Note on ENDOG: a computer program for analysis pedigree information. J. Anim.Breed. Genet ., vol.122. pp.172-176. Gutiérrez, J.P., Goyache, F. and Cervantes, F. ( 2009) Endog v 4.6. A computer program for monitoring genetic variability of populations using pedigree information. User guide . Madrid: Universidad Complutense de Madrid. 45 p.. Kadlečík, O. and Pavlík,I. (2012) Genealogical analysis in small populations: The case of four Slovak beef cattle breeds. Slovak J. Anim. Sci., vol. 45, no. 4. pp. 111-117. Kasarda. R. and Kadlečík. O. (2007) An economic impact of inbreeding in the purebred population of Pinzgau cattle in Slovakia on milk production traits. Czech J. Anim. Sci., vol. 52, no. 1, pp. 7-11. Krupa, E., Žáková, E. and Krupová, Z. (2015) Evaluation of inbreeding and genetic variability of five pig breeds in Czech Republic. Asian Australas. J.Anim. Sci.. vol. 28, no. 1, pp. 25-36. doi: http://dx.doi.org/10.5713/ajas.14.0251 Lacy, R.C. (1989) Analysis of founder representation in pedigree: Founder equivalents and founder genome equivalents. Zool.Biol ., vol. 8, no. 2, pp. 111-123. doi: http://dx.doi.org/10.1002/zoo.1430080203 Lacy, R.C. (1995) Classification of genetic terms and their use in the management of captive populations. Zoo. Biol ., vol. 14, no. 6, pp. 565-577. doi: http://dx.doi.org/10.1002/zoo.1430140609 Melka, M.G. et al. (2013) Analyses of genetic diversity in five Canadian dairy breeds using pedigree data. J. Anim. Breed. Genet ., vol. 130, pp. 476–486. doi:http://dx.doi.org/10.1111/jbg.12050 McParland, S. et al. (2007) Inbreeding trends and pedigree analysis of Irish dairy and beef cattle populations. Journal of Animal Science , vol. 85, no. 2, pp.322-331. doi: http://dx.doi.org/10.2527/jas.2006-367 Maignel, L., Boichard, D. and Verrier.E. (1996) Genetic variability of French dairy breeds estimated from pedigree information. Interbul Bulletin , vol. 14, pp.49-54. Meuwissen, T.H.E. and Luo,Z. (1992) Computing in breeding coefficients in large populations. Genet. Sel. Evol., vol. 24. pp. 305-313. doi:http://dx.doi.org/10.1186/1297-9686-24-4-305 Pavlík.I, et al. (2014) Pedigree analysis of Thoroughbred horses in Slovakia. Acta fytotechnica et zootechnica, vol. 17, no. 4, pp. 122-126. doi: http://dx.doi.org/10.15414/afz.2014.17.04.122-126 Stachowic, K. et al. (2011) Schenkel Rates of inbreeding and genetic diversity in Canadian Holstein and Jersey cattle. J. Dairy Sci ., vol. 94, no.  10, pp. 5160–5175. doi: http://dx.doi.org/10.3168/jds.2010-3308 ŠIDLOVÁ, V. et al. (2015) Genomic variability among cattle populations based on runs of homozygosity. Poljoprivreda , vol. 21. no. 1 (Supplement), pp. 44-47. Tang, G. Q. et al. (2013) Inbreeding and genetic Ddversity in three imported swine breeds in China using pedigree data Asian Australas. J. Anim .Sci ., vol.26, no. 6, pp.755-765.  doi: http://dx.doi.org/10.5713/ajas.2012.12645 Trakovická, A. et al.(2015) Impact of SNPs in candidate genes on economically important traits in Pinzgau cattle. Poljoprivreda . vol. 21, no. 1(Supplement), pp. 150-154. doi: http://dx.doi.org/10.18047/poljo.21.1.sup.35

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A Case-Control Genome-Wide Association Study of Dark-Cutting in 2 Beef Cattle Populations
  • Jan 1, 2017
  • Meat and Muscle Biology
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ObjectivesDark-cutting beef carcasses are graded Canada B4 in the Canadian Beef Grading System, resulting in economic loss for beef producers. Dark-cutting beef is caused by depletion of muscle glycogen before slaughtering, which may also be affected by animal genetics. This study aimed to identify possible single nucleotide polymorphisms (SNPs) associated with dark-cutting through a case-control genome-wide association study (GWAS) and explore the biological relevance of these SNPs to the formation of dark cutting beef. Materials and MethodsTwo cattle populations were used in this study, population I had 64 beef cattle, of which 40 were graded Canada B4 (dark-cutters, treated as cases), and population II had 837 beef cattle, of which 30 were graded Canada B4. The 2 populations were genotyped using GeneSeek Genomic Profiler for Beef Cattle-HD (GGP-HD) of 76,783 SNPs and Illumina BovineSNP50v2 BeadChip of 54,609 SNPs, respectively. All SNPs with a call rate lower than 90% or a minor allele frequency (MAF) lower than 5% were removed in quality control. Association analyses were conducted using Plink 1.9 and dark-cutting beef was analyzed as a binary trait (cases versus controls) through a logistic regression model under an additive model. UCSC Genome Browser RefSeq genes harboring (1 Mb window) the top 50 SNPs with lowest raw P values in each population were used for GO (Gene Ontology) analysis through DAVID (Database for Annotation, Visualization and Integrated Discovery). ResultsIn total, 418 SNPs were detected in population I, 383 SNPs in population II and 267 SNPs in the combined data with a less stringent significance level (P < 0.01); 12 SNPs in population I, 30 SNPs in population II and 22 SNPs in the combined data with a significance level (P < 0.001); 2 SNPs in population II and 2 SNPs in the combined data with a relatively stringent significance level (P < 0.0001). These detected SNPs showed suggestive association with dark-cutting beef. GO analysis revealed that genes (717 in total) harboring top-scoring variants (150 SNPs in total) were involved in molecular functions like poly (A) RNA binding, and calcium ion and GTP binding which are related to energy metabolism. ConclusionBased on our association study with a relatively small sample size, no evidence was found for a large genetic effect for beef dark-cutting, the trait may therefore be polygenic. Significant SNPs showed suggestive association with dark-cutting beef. Although the detected SNP associations require validation in a larger dataset, the results suggested the possibility in the future for marker-assisted selection or genomic selection in beef cattle to reduce dark cutting.

  • Research Article
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Correlation Analysis Between Population and Production of Livestock Animal in Indonesia on 2009 - 2018
  • Mar 1, 2020
  • Indonesian Journal of Veterinary Science
  • Roza Azizah + 1 more

Livestock animal product is one of important materials to increase of human body endurance. There is some protein in livestock product to support healthy human. The government is also keep growth of livestock productivity, because the population growth of human can influence consume of some products which comes from animal. The objective of this paper was to know the correlation between population and production of livestock animal. In this research was using secondary data from Indonesia Central Bureau of Statistics 2018. Data are population of beef cattle, laying hens, goat, broiler and production of beef, eggs, lamb, chicken meat in 2009-2018. The method was using descriptive statistics and pearson’s correlation analysis. The results of this research, there are correlation between population and production of goat, laying hens, and broiler (sig. &lt; 0.05), but there is no correlation between population and production of beef cattle (sig. &gt; 0.05). Many factors can influence about productivity of livestock animal. The important factors are feed maintenance management and prevent of diseases management.Keywords : Population of Livestock Animal, Production of Livestock Product, Statistics Descriptive, Correlation Analysis

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Micro Policy Interventions to Increase Income in Beef Cattle Business in Kupang District
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A study has been conducted with the aim to determine the actual behavior of beef cattle farmers' income and formulate micro-policies for beef cattle farmers' income in Kupang district. Sampling in this study was conducted in stages. The first stage was purposive sampling of four sub-districts, the second stage was snow ball sampling of 40 farmers and traders and six government officials using an interview approach. The number of key informants depends on the saturation of information obtained. The software used in this research is Ventana Simulation (Vensim) PLE. The results showed that the actual behavior of calf production and income from beef cattle farmers tended to decrease, each by 20.61% and 3.73% per year, respectively. Therefore, policy interventions are needed: 1) increasing calving rate can increase the population of young beef cattle by 3.35% per year and profits by 3.49% per head per year; 2) adding feed supplementation can increase the population of young beef cattle by an average of 4% per year, fattening males by 2.81% per year, and profits by 4.03% per head per year; 3) increasing stakeholder service intensity can increase the population of young beef cattle by 3.12% per year, fattening male production by 5.04% per year, and average profits by 3.37%.

  • Research Article
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  • 10.1016/j.livsci.2014.06.017
Post-partum anoestrus in tropical beef cattle: A systems approach combining gene expression and genome-wide association results
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Post-partum anoestrus in tropical beef cattle: A systems approach combining gene expression and genome-wide association results

  • Research Article
  • Cite Count Icon 44
  • 10.1016/j.agee.2014.06.002
Methane emission inventories for enteric fermentation and manure management of yak, buffalo and dairy and beef cattle in China from 1988 to 2009
  • Jun 26, 2014
  • Agriculture, Ecosystems &amp; Environment
  • B Xue + 2 more

Methane emission inventories for enteric fermentation and manure management of yak, buffalo and dairy and beef cattle in China from 1988 to 2009

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