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Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era

The horse reference genome from the Thoroughbred mare Twilight has been available for a decade and, together with advances in genomics technologies, has led to unparalleled developments in equine genomics. At the core of this progress is the continuing improvement of the quality, contiguity and comp...

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Autores principales: Raudsepp, T., Finno, C. J., Bellone, R. R., Petersen, J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825885/
https://www.ncbi.nlm.nih.gov/pubmed/31568563
http://dx.doi.org/10.1111/age.12857
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author Raudsepp, T.
Finno, C. J.
Bellone, R. R.
Petersen, J. L.
author_facet Raudsepp, T.
Finno, C. J.
Bellone, R. R.
Petersen, J. L.
author_sort Raudsepp, T.
collection PubMed
description The horse reference genome from the Thoroughbred mare Twilight has been available for a decade and, together with advances in genomics technologies, has led to unparalleled developments in equine genomics. At the core of this progress is the continuing improvement of the quality, contiguity and completeness of the reference genome, and its functional annotation. Recent achievements include the release of the next version of the reference genome (EquCab3.0) and generation of a reference sequence for the Y chromosome. Horse satellite‐free centromeres provide unique models for mammalian centromere research. Despite extremely low genetic diversity of the Y chromosome, it has been possible to trace patrilines of breeds and pedigrees and show that Y variation was lost in the past approximately 2300 years owing to selective breeding. The high‐quality reference genome has led to the development of three different SNP arrays and WGSs of almost 2000 modern individual horses. The collection of WGS of hundreds of ancient horses is unique and not available for any other domestic species. These tools and resources have led to global population studies dissecting the natural history of the species and genetic makeup and ancestry of modern breeds. Most importantly, the available tools and resources, together with the discovery of functional elements, are dissecting molecular causes of a growing number of Mendelian and complex traits. The improved understanding of molecular underpinnings of various traits continues to benefit the health and performance of the horse whereas also serving as a model for complex disease across species.
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spelling pubmed-68258852019-12-20 Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era Raudsepp, T. Finno, C. J. Bellone, R. R. Petersen, J. L. Anim Genet Review Articles The horse reference genome from the Thoroughbred mare Twilight has been available for a decade and, together with advances in genomics technologies, has led to unparalleled developments in equine genomics. At the core of this progress is the continuing improvement of the quality, contiguity and completeness of the reference genome, and its functional annotation. Recent achievements include the release of the next version of the reference genome (EquCab3.0) and generation of a reference sequence for the Y chromosome. Horse satellite‐free centromeres provide unique models for mammalian centromere research. Despite extremely low genetic diversity of the Y chromosome, it has been possible to trace patrilines of breeds and pedigrees and show that Y variation was lost in the past approximately 2300 years owing to selective breeding. The high‐quality reference genome has led to the development of three different SNP arrays and WGSs of almost 2000 modern individual horses. The collection of WGS of hundreds of ancient horses is unique and not available for any other domestic species. These tools and resources have led to global population studies dissecting the natural history of the species and genetic makeup and ancestry of modern breeds. Most importantly, the available tools and resources, together with the discovery of functional elements, are dissecting molecular causes of a growing number of Mendelian and complex traits. The improved understanding of molecular underpinnings of various traits continues to benefit the health and performance of the horse whereas also serving as a model for complex disease across species. John Wiley and Sons Inc. 2019-09-30 2019-12 /pmc/articles/PMC6825885/ /pubmed/31568563 http://dx.doi.org/10.1111/age.12857 Text en © 2019 The Authors. Animal Genetics published by John Wiley & Sons Ltd on behalf of Stichting International Foundation for Animal Genetics This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Raudsepp, T.
Finno, C. J.
Bellone, R. R.
Petersen, J. L.
Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era
title Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era
title_full Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era
title_fullStr Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era
title_full_unstemmed Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era
title_short Ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era
title_sort ten years of the horse reference genome: insights into equine biology, domestication and population dynamics in the post‐genome era
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825885/
https://www.ncbi.nlm.nih.gov/pubmed/31568563
http://dx.doi.org/10.1111/age.12857
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