I. Pocrnic
University of Georgia
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Featured researches published by I. Pocrnic.
Genetics | 2016
I. Pocrnic; D. A. L. Lourenco; Y. Masuda; A. Legarra; I. Misztal
The genomic relationship matrix (GRM) can be inverted by the algorithm for proven and young (APY) based on recursion on a random subset of animals. While a regular inverse has a cubic cost, the cost of the APY inverse can be close to linear. Theory for the APY assumes that the optimal size of the subset (maximizing accuracy of genomic predictions) is due to a limited dimensionality of the GRM, which is a function of the effective population size (Ne). The objective of this study was to evaluate these assumptions by simulation. Six populations were simulated with approximate effective population size (Ne) from 20 to 200. Each population consisted of 10 nonoverlapping generations, with 25,000 animals per generation and phenotypes available for generations 1–9. The last 3 generations were fully genotyped assuming genome length L = 30. The GRM was constructed for each population and analyzed for distribution of eigenvalues. Genomic estimated breeding values (GEBV) were computed by single-step GBLUP, using either a direct or an APY inverse of GRM. The sizes of the subset in APY were set to the number of the largest eigenvalues explaining x% of variation (EIGx, x = 90, 95, 98, 99) in GRM. Accuracies of GEBV for the last generation with the APY inverse peaked at EIG98 and were slightly lower with EIG95, EIG99, or the direct inverse. Most information in the GRM is contained in ∼NeL largest eigenvalues, with no information beyond 4NeL. Genomic predictions with the APY inverse of the GRM are more accurate than by the regular inverse.
Genetics Selection Evolution | 2016
I. Pocrnic; D. A. L. Lourenco; Y. Masuda; I. Misztal
BackgroundA genomic relationship matrix (GRM) can be inverted efficiently with the Algorithm for Proven and Young (APY) through recursion on a small number of core animals. The number of core animals is theoretically linked to effective population size (Ne). In a simulation study, the optimal number of core animals was equal to the number of largest eigenvalues of GRM that explained 98% of its variation. The purpose of this study was to find the optimal number of core animals and estimate Ne for different species.MethodsDatasets included phenotypes, pedigrees, and genotypes for populations of Holstein, Jersey, and Angus cattle, pigs, and broiler chickens. The number of genotyped animals varied from 15,000 for broiler chickens to 77,000 for Holsteins, and the number of single-nucleotide polymorphisms used for genomic prediction varied from 37,000 to 61,000. Eigenvalue decomposition of the GRM for each population determined numbers of largest eigenvalues corresponding to 90, 95, 98, and 99% of variation.ResultsThe number of eigenvalues corresponding to 90% (98%) of variation was 4527 (14,026) for Holstein, 3325 (11,500) for Jersey, 3654 (10,605) for Angus, 1239 (4103) for pig, and 1655 (4171) for broiler chicken. Each trait in each species was analyzed using the APY inverse of the GRM with randomly selected core animals, and their number was equal to the number of largest eigenvalues. Realized accuracies peaked with the number of core animals corresponding to 98% of variation for Holstein and Jersey and closer to 99% for other breed/species. Ne was estimated based on comparisons of eigenvalue decomposition in a simulation study. Assuming a genome length of 30 Morgan, Ne was equal to 149 for Holsteins, 101 for Jerseys, 113 for Angus, 32 for pigs, and 44 for broilers.ConclusionsEigenvalue profiles of GRM for common species are similar to those in simulation studies although they are affected by number of genotyped animals and genotyping quality. For all investigated species, the APY required less than 15,000 core animals. Realized accuracies were equal or greater with the APY inverse than with regular inversion. Eigenvalue analysis of GRM can provide a realistic estimate of Ne.
Genetics Selection Evolution | 2017
Carolina A. Garcia-Baccino; A. Legarra; Ole F. Christensen; I. Misztal; I. Pocrnic; Zulma G. Vitezica; R.J.C. Cantet
Background Metafounders are pseudo-individuals that encapsulate genetic heterozygosity and relationships within and across base pedigree populations, i.e. ancestral populations. This work addresses the estimation and usefulness of metafounder relationships in single-step genomic best linear unbiased prediction (ssGBLUP).ResultsWe show that ancestral relationship parameters are proportional to standardized covariances of base allelic frequencies across populations, such as
Journal of Dairy Science | 2017
Sreten Andonov; D. A. L. Lourenco; B. O. Fragomeni; Y. Masuda; I. Pocrnic; S. Tsuruta; I. Misztal
Journal of Animal Science | 2017
I. Pocrnic; D. A. L. Lourenco; H. L. Bradford; C. Y. Chen; I. Misztal
F_{\text{st}}
bioRxiv | 2016
Carolina A. Garcia-Baccino; A. Legarra; Ole F. Christensen; I. Misztal; I. Pocrnic; Zulma G. Vitezica; R.J.C. Cantet
Journal of Animal Breeding and Genetics | 2017
H. L. Bradford; I. Pocrnic; B. O. Fragomeni; D. A. L. Lourenco; I. Misztal
Fst fixation indexes. These covariances of base allelic frequencies can be estimated from marker genotypes of related recent individuals and pedigree. Simple methods for their estimation include naïve computation of allele frequencies from marker genotypes or a method of moments that equates average pedigree-based and marker-based relationships. Complex methods include generalized least squares (best linear unbiased estimator (BLUE)) or maximum likelihood based on pedigree relationships. To our knowledge, methods to infer
Journal of Animal Science | 2017
H. L. Bradford; I. Pocrnic; B. O. Fragomeni; D. A. L. Lourenco; I. Misztal
Journal of Animal Science | 2016
D. A. L. Lourenco; S. Tsuruta; B. D. Fragomeni; Y. Masuda; I. Pocrnic; I. Aguilar; J. K. Bertrand; D. W. Moser; I. Misztal
F_{\text{st}}
Proceedings of the World Congress on Genetics Applied to Livestock Production | 2018
I. Pocrnic; Daniela Al Lourenco; Y. Masuda; A. Legarra; I. Misztal