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Dimensionality of genomic information and performance of the Algorithm for Proven and Young for different livestock species
A 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 (N ). In a simulation study, the optimal number of core a...
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Published in: | Genetics selection evolution (Paris) 2016-10, Vol.48 (1), p.82-82, Article 82 |
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description | A 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 (N
). 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 N
for different species.
Datasets 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.
The 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. N
was estimated based on comparisons of eigenvalue decomposition in a simulation study. Assuming a genome length of 30 Morgan, N
was equal to 149 for Holsteins, 101 for Jerseys, 113 for Angus, 32 for pigs, and 44 for broilers.
Eigenvalue 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 N
. |
doi_str_mv | 10.1186/s12711-016-0261-6 |
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). 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 N
for different species.
Datasets 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.
The 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. N
was estimated based on comparisons of eigenvalue decomposition in a simulation study. Assuming a genome length of 30 Morgan, N
was equal to 149 for Holsteins, 101 for Jerseys, 113 for Angus, 32 for pigs, and 44 for broilers.
Eigenvalue 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 N
.</description><identifier>ISSN: 1297-9686</identifier><identifier>ISSN: 0999-193X</identifier><identifier>EISSN: 1297-9686</identifier><identifier>DOI: 10.1186/s12711-016-0261-6</identifier><identifier>PMID: 27799053</identifier><language>eng</language><publisher>France: BioMed Central Ltd</publisher><subject>Algorithms ; Analysis ; Animals ; Beef cattle ; Breeding ; Cattle ; Cattle - genetics ; Chickens ; Chickens - genetics ; Computer Simulation ; Datasets ; Decomposition ; Eigenvalues ; Genetic algorithms ; Genetic aspects ; Genome ; Genomics ; Genotype ; Genotypes ; Genotyping ; Health aspects ; Hogs ; Life Sciences ; Livestock ; Livestock - genetics ; Models, Genetic ; Nucleotides ; Phenotype ; Phenotypes ; Polymorphism, Single Nucleotide ; Population ; Population Density ; Population number ; Poultry ; Simulation ; Single nucleotide polymorphisms ; Single-nucleotide polymorphism ; Species ; Swine - genetics ; Variation ; Weaning</subject><ispartof>Genetics selection evolution (Paris), 2016-10, Vol.48 (1), p.82-82, Article 82</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>2016. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>The Author(s) 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c730t-a1cf62dfae8f57e818067f47b505928215c13edecdcb5f9b9c835b17450adabc3</citedby><cites>FETCH-LOGICAL-c730t-a1cf62dfae8f57e818067f47b505928215c13edecdcb5f9b9c835b17450adabc3</cites><orcidid>0000-0001-5246-7428</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088690/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2575270505?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27799053$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01390765$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Pocrnic, Ivan</creatorcontrib><creatorcontrib>Lourenco, Daniela A L</creatorcontrib><creatorcontrib>Masuda, Yutaka</creatorcontrib><creatorcontrib>Misztal, Ignacy</creatorcontrib><title>Dimensionality of genomic information and performance of the Algorithm for Proven and Young for different livestock species</title><title>Genetics selection evolution (Paris)</title><addtitle>Genet Sel Evol</addtitle><description>A 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 (N
). 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 N
for different species.
Datasets 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.
The 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. N
was estimated based on comparisons of eigenvalue decomposition in a simulation study. Assuming a genome length of 30 Morgan, N
was equal to 149 for Holsteins, 101 for Jerseys, 113 for Angus, 32 for pigs, and 44 for broilers.
Eigenvalue 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 N
.</description><subject>Algorithms</subject><subject>Analysis</subject><subject>Animals</subject><subject>Beef cattle</subject><subject>Breeding</subject><subject>Cattle</subject><subject>Cattle - genetics</subject><subject>Chickens</subject><subject>Chickens - genetics</subject><subject>Computer Simulation</subject><subject>Datasets</subject><subject>Decomposition</subject><subject>Eigenvalues</subject><subject>Genetic algorithms</subject><subject>Genetic aspects</subject><subject>Genome</subject><subject>Genomics</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Genotyping</subject><subject>Health aspects</subject><subject>Hogs</subject><subject>Life Sciences</subject><subject>Livestock</subject><subject>Livestock - genetics</subject><subject>Models, Genetic</subject><subject>Nucleotides</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Population</subject><subject>Population Density</subject><subject>Population number</subject><subject>Poultry</subject><subject>Simulation</subject><subject>Single nucleotide polymorphisms</subject><subject>Single-nucleotide polymorphism</subject><subject>Species</subject><subject>Swine - 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genetics</topic><topic>Chickens</topic><topic>Chickens - genetics</topic><topic>Computer Simulation</topic><topic>Datasets</topic><topic>Decomposition</topic><topic>Eigenvalues</topic><topic>Genetic algorithms</topic><topic>Genetic aspects</topic><topic>Genome</topic><topic>Genomics</topic><topic>Genotype</topic><topic>Genotypes</topic><topic>Genotyping</topic><topic>Health aspects</topic><topic>Hogs</topic><topic>Life Sciences</topic><topic>Livestock</topic><topic>Livestock - genetics</topic><topic>Models, Genetic</topic><topic>Nucleotides</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Population</topic><topic>Population Density</topic><topic>Population number</topic><topic>Poultry</topic><topic>Simulation</topic><topic>Single nucleotide polymorphisms</topic><topic>Single-nucleotide polymorphism</topic><topic>Species</topic><topic>Swine - genetics</topic><topic>Variation</topic><topic>Weaning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pocrnic, Ivan</creatorcontrib><creatorcontrib>Lourenco, Daniela A L</creatorcontrib><creatorcontrib>Masuda, Yutaka</creatorcontrib><creatorcontrib>Misztal, Ignacy</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Science in Context</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetics selection evolution (Paris)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pocrnic, Ivan</au><au>Lourenco, Daniela A L</au><au>Masuda, Yutaka</au><au>Misztal, Ignacy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dimensionality of genomic information and performance of the Algorithm for Proven and Young for different livestock species</atitle><jtitle>Genetics selection evolution (Paris)</jtitle><addtitle>Genet Sel Evol</addtitle><date>2016-10-31</date><risdate>2016</risdate><volume>48</volume><issue>1</issue><spage>82</spage><epage>82</epage><pages>82-82</pages><artnum>82</artnum><issn>1297-9686</issn><issn>0999-193X</issn><eissn>1297-9686</eissn><abstract>A 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 (N
). 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 N
for different species.
Datasets 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.
The 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. N
was estimated based on comparisons of eigenvalue decomposition in a simulation study. Assuming a genome length of 30 Morgan, N
was equal to 149 for Holsteins, 101 for Jerseys, 113 for Angus, 32 for pigs, and 44 for broilers.
Eigenvalue 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 N
.</abstract><cop>France</cop><pub>BioMed Central Ltd</pub><pmid>27799053</pmid><doi>10.1186/s12711-016-0261-6</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-5246-7428</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Analysis Animals Beef cattle Breeding Cattle Cattle - genetics Chickens Chickens - genetics Computer Simulation Datasets Decomposition Eigenvalues Genetic algorithms Genetic aspects Genome Genomics Genotype Genotypes Genotyping Health aspects Hogs Life Sciences Livestock Livestock - genetics Models, Genetic Nucleotides Phenotype Phenotypes Polymorphism, Single Nucleotide Population Population Density Population number Poultry Simulation Single nucleotide polymorphisms Single-nucleotide polymorphism Species Swine - genetics Variation Weaning |
title | Dimensionality of genomic information and performance of the Algorithm for Proven and Young for different livestock species |
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