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Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle
BACKGROUND: Inbreeding coefficients can be estimated either from pedigree data or from genomic data, and with genomic data, they are either global or local (when the linkage map is used). Recently, we developed a new hidden Markov model (HMM) that estimates probabilities of homozygosity-by-descent (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741860/ https://www.ncbi.nlm.nih.gov/pubmed/29273000 http://dx.doi.org/10.1186/s12711-017-0370-x |
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author | Solé, Marina Gori, Ann-Stephan Faux, Pierre Bertrand, Amandine Farnir, Frédéric Gautier, Mathieu Druet, Tom |
author_facet | Solé, Marina Gori, Ann-Stephan Faux, Pierre Bertrand, Amandine Farnir, Frédéric Gautier, Mathieu Druet, Tom |
author_sort | Solé, Marina |
collection | PubMed |
description | BACKGROUND: Inbreeding coefficients can be estimated either from pedigree data or from genomic data, and with genomic data, they are either global or local (when the linkage map is used). Recently, we developed a new hidden Markov model (HMM) that estimates probabilities of homozygosity-by-descent (HBD) at each marker position and automatically partitions autozygosity in multiple age-related classes (based on the length of HBD segments). Our objectives were to: (1) characterize inbreeding with our model in an intensively selected population such as the Belgian Blue Beef (BBB) cattle breed; (2) compare the properties of the model at different marker densities; and (3) compare our model with other methods. RESULTS: When using 600 K single nucleotide polymorphisms (SNPs), the inbreeding coefficient (probability of sampling an HBD locus in an individual) was on average 0.303 (ranging from 0.258 to 0.375). HBD-classes associated to historical ancestors (with small segments ≤ 200 kb) accounted for 21.6% of the genome length (71.4% of the total length of the genome in HBD segments), whereas classes associated to more recent ancestors accounted for only 22.6% of the total length of the genome in HBD segments. However, these recent classes presented more individual variation than more ancient classes. Although inbreeding coefficients obtained with low SNP densities (7 and 32 K) were much lower (0.060 and 0.093), they were highly correlated with those obtained at higher density (r = 0.934 and 0.975, respectively), indicating that they captured most of the individual variation. At higher SNP density, smaller HBD segments are identified and, thus, more past generations can be explored. We observed very high correlations between our estimates and those based on homozygosity (r = 0.95) or on runs-of-homozygosity (r = 0.95). As expected, pedigree-based estimates were mainly correlated with recent HBD-classes (r = 0.56). CONCLUSIONS: Although we observed high levels of autozygosity associated with small HBD segments in BBB cattle, recent inbreeding accounted for most of the individual variation. Recent autozygosity can be captured efficiently with low-density SNP arrays and relatively simple models (e.g., two HBD classes). The HMM framework provides local HBD probabilities that are still useful at lower SNP densities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12711-017-0370-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5741860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57418602018-01-03 Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle Solé, Marina Gori, Ann-Stephan Faux, Pierre Bertrand, Amandine Farnir, Frédéric Gautier, Mathieu Druet, Tom Genet Sel Evol Research Article BACKGROUND: Inbreeding coefficients can be estimated either from pedigree data or from genomic data, and with genomic data, they are either global or local (when the linkage map is used). Recently, we developed a new hidden Markov model (HMM) that estimates probabilities of homozygosity-by-descent (HBD) at each marker position and automatically partitions autozygosity in multiple age-related classes (based on the length of HBD segments). Our objectives were to: (1) characterize inbreeding with our model in an intensively selected population such as the Belgian Blue Beef (BBB) cattle breed; (2) compare the properties of the model at different marker densities; and (3) compare our model with other methods. RESULTS: When using 600 K single nucleotide polymorphisms (SNPs), the inbreeding coefficient (probability of sampling an HBD locus in an individual) was on average 0.303 (ranging from 0.258 to 0.375). HBD-classes associated to historical ancestors (with small segments ≤ 200 kb) accounted for 21.6% of the genome length (71.4% of the total length of the genome in HBD segments), whereas classes associated to more recent ancestors accounted for only 22.6% of the total length of the genome in HBD segments. However, these recent classes presented more individual variation than more ancient classes. Although inbreeding coefficients obtained with low SNP densities (7 and 32 K) were much lower (0.060 and 0.093), they were highly correlated with those obtained at higher density (r = 0.934 and 0.975, respectively), indicating that they captured most of the individual variation. At higher SNP density, smaller HBD segments are identified and, thus, more past generations can be explored. We observed very high correlations between our estimates and those based on homozygosity (r = 0.95) or on runs-of-homozygosity (r = 0.95). As expected, pedigree-based estimates were mainly correlated with recent HBD-classes (r = 0.56). CONCLUSIONS: Although we observed high levels of autozygosity associated with small HBD segments in BBB cattle, recent inbreeding accounted for most of the individual variation. Recent autozygosity can be captured efficiently with low-density SNP arrays and relatively simple models (e.g., two HBD classes). The HMM framework provides local HBD probabilities that are still useful at lower SNP densities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12711-017-0370-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-22 /pmc/articles/PMC5741860/ /pubmed/29273000 http://dx.doi.org/10.1186/s12711-017-0370-x Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Article Solé, Marina Gori, Ann-Stephan Faux, Pierre Bertrand, Amandine Farnir, Frédéric Gautier, Mathieu Druet, Tom Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle |
title | Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle |
title_full | Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle |
title_fullStr | Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle |
title_full_unstemmed | Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle |
title_short | Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle |
title_sort | age-based partitioning of individual genomic inbreeding levels in belgian blue cattle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741860/ https://www.ncbi.nlm.nih.gov/pubmed/29273000 http://dx.doi.org/10.1186/s12711-017-0370-x |
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