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Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries
For genomic selection to be successful, there must be sufficient linkage disequilibrium between the markers and the causal mutations. The objectives of this study were to evaluate the extent of LD in ovine using the Santa Inês breed and to infer the minimum number of markers required to reach reason...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995818/ https://www.ncbi.nlm.nih.gov/pubmed/29892085 http://dx.doi.org/10.1038/s41598-018-27259-7 |
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author | Alvarenga, Amanda Botelho Rovadoscki, Gregori Alberto Petrini, Juliana Coutinho, Luiz Lehmann Morota, Gota Spangler, Matthew L. Pinto, Luís Fernando Batista Carvalho, Gleidson Giordano Pinto Mourão, Gerson Barreto |
author_facet | Alvarenga, Amanda Botelho Rovadoscki, Gregori Alberto Petrini, Juliana Coutinho, Luiz Lehmann Morota, Gota Spangler, Matthew L. Pinto, Luís Fernando Batista Carvalho, Gleidson Giordano Pinto Mourão, Gerson Barreto |
author_sort | Alvarenga, Amanda Botelho |
collection | PubMed |
description | For genomic selection to be successful, there must be sufficient linkage disequilibrium between the markers and the causal mutations. The objectives of this study were to evaluate the extent of LD in ovine using the Santa Inês breed and to infer the minimum number of markers required to reach reasonable prediction accuracy. In total, 38,168 SNPs and 395 samples were used. The mean LD between adjacent marker pairs measured by r(2) and |D′| were 0.166 and 0.617, respectively. LD values between adjacent marker pairs ranged from 0.135 to 0.194 and from 0.568 to 0.650 for r(2) for |D′| across all chromosomes. The average r(2) between all pairwise SNPs on each chromosome was 0.018. SNPs separated by between 0.10 to 0.20 Mb had an estimated average r(2) equal to 0.1033. The identified haplotype blocks consisted of 2 to 21 markers. Moreover, estimates of average coefficients of inbreeding and effective population size were 0.04 and 96, respectively. LD estimated in this study was lower than that reported in other species and was characterized by short haplotype blocks. Our results suggest that the use of a higher density SNP panel is recommended for the implementation of genomic selection in the Santa Inês breed. |
format | Online Article Text |
id | pubmed-5995818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59958182018-06-21 Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries Alvarenga, Amanda Botelho Rovadoscki, Gregori Alberto Petrini, Juliana Coutinho, Luiz Lehmann Morota, Gota Spangler, Matthew L. Pinto, Luís Fernando Batista Carvalho, Gleidson Giordano Pinto Mourão, Gerson Barreto Sci Rep Article For genomic selection to be successful, there must be sufficient linkage disequilibrium between the markers and the causal mutations. The objectives of this study were to evaluate the extent of LD in ovine using the Santa Inês breed and to infer the minimum number of markers required to reach reasonable prediction accuracy. In total, 38,168 SNPs and 395 samples were used. The mean LD between adjacent marker pairs measured by r(2) and |D′| were 0.166 and 0.617, respectively. LD values between adjacent marker pairs ranged from 0.135 to 0.194 and from 0.568 to 0.650 for r(2) for |D′| across all chromosomes. The average r(2) between all pairwise SNPs on each chromosome was 0.018. SNPs separated by between 0.10 to 0.20 Mb had an estimated average r(2) equal to 0.1033. The identified haplotype blocks consisted of 2 to 21 markers. Moreover, estimates of average coefficients of inbreeding and effective population size were 0.04 and 96, respectively. LD estimated in this study was lower than that reported in other species and was characterized by short haplotype blocks. Our results suggest that the use of a higher density SNP panel is recommended for the implementation of genomic selection in the Santa Inês breed. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995818/ /pubmed/29892085 http://dx.doi.org/10.1038/s41598-018-27259-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Alvarenga, Amanda Botelho Rovadoscki, Gregori Alberto Petrini, Juliana Coutinho, Luiz Lehmann Morota, Gota Spangler, Matthew L. Pinto, Luís Fernando Batista Carvalho, Gleidson Giordano Pinto Mourão, Gerson Barreto Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries |
title | Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries |
title_full | Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries |
title_fullStr | Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries |
title_full_unstemmed | Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries |
title_short | Linkage disequilibrium in Brazilian Santa Inês breed, Ovis aries |
title_sort | linkage disequilibrium in brazilian santa inês breed, ovis aries |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995818/ https://www.ncbi.nlm.nih.gov/pubmed/29892085 http://dx.doi.org/10.1038/s41598-018-27259-7 |
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