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Using optical mapping data for the improvement of vertebrate genome assemblies

Optical mapping is a technology that gathers long-range information on genome sequences similar to ordered restriction digest maps. Because it is not subject to cloning, amplification, hybridisation or sequencing bias, it is ideally suited to the improvement of fragmented genome assemblies that can...

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Detalles Bibliográficos
Autores principales: Howe, Kerstin, Wood, Jonathan MD
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364110/
https://www.ncbi.nlm.nih.gov/pubmed/25789164
http://dx.doi.org/10.1186/s13742-015-0052-y
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author Howe, Kerstin
Wood, Jonathan MD
author_facet Howe, Kerstin
Wood, Jonathan MD
author_sort Howe, Kerstin
collection PubMed
description Optical mapping is a technology that gathers long-range information on genome sequences similar to ordered restriction digest maps. Because it is not subject to cloning, amplification, hybridisation or sequencing bias, it is ideally suited to the improvement of fragmented genome assemblies that can no longer be improved by classical methods. In addition, its low cost and rapid turnaround make it equally useful during the scaffolding process of de novo assembly from high throughput sequencing reads. We describe how optical mapping has been used in practice to produce high quality vertebrate genome assemblies. In particular, we detail the efforts undertaken by the Genome Reference Consortium (GRC), which maintains the reference genomes for human, mouse, zebrafish and chicken, and uses different optical mapping platforms for genome curation.
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spelling pubmed-43641102015-03-19 Using optical mapping data for the improvement of vertebrate genome assemblies Howe, Kerstin Wood, Jonathan MD Gigascience Review Optical mapping is a technology that gathers long-range information on genome sequences similar to ordered restriction digest maps. Because it is not subject to cloning, amplification, hybridisation or sequencing bias, it is ideally suited to the improvement of fragmented genome assemblies that can no longer be improved by classical methods. In addition, its low cost and rapid turnaround make it equally useful during the scaffolding process of de novo assembly from high throughput sequencing reads. We describe how optical mapping has been used in practice to produce high quality vertebrate genome assemblies. In particular, we detail the efforts undertaken by the Genome Reference Consortium (GRC), which maintains the reference genomes for human, mouse, zebrafish and chicken, and uses different optical mapping platforms for genome curation. BioMed Central 2015-03-18 /pmc/articles/PMC4364110/ /pubmed/25789164 http://dx.doi.org/10.1186/s13742-015-0052-y Text en © Howe and Wood; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Review
Howe, Kerstin
Wood, Jonathan MD
Using optical mapping data for the improvement of vertebrate genome assemblies
title Using optical mapping data for the improvement of vertebrate genome assemblies
title_full Using optical mapping data for the improvement of vertebrate genome assemblies
title_fullStr Using optical mapping data for the improvement of vertebrate genome assemblies
title_full_unstemmed Using optical mapping data for the improvement of vertebrate genome assemblies
title_short Using optical mapping data for the improvement of vertebrate genome assemblies
title_sort using optical mapping data for the improvement of vertebrate genome assemblies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364110/
https://www.ncbi.nlm.nih.gov/pubmed/25789164
http://dx.doi.org/10.1186/s13742-015-0052-y
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