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Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly
Atlantic herring (Clupea harengus) is one of the most abundant fish species in the world. It is an important economical and nutritional resource, as well as a crucial part of the North Atlantic ecosystem. In 2016, a draft herring genome assembly was published. Being a species of such importance, we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881392/ https://www.ncbi.nlm.nih.gov/pubmed/31776409 http://dx.doi.org/10.1038/s41598-019-54151-9 |
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author | í Kongsstovu, Sunnvør Mikalsen, Svein-Ole Homrum, Eydna í Jacobsen, Jan Arge Flicek, Paul Dahl, Hans Atli |
author_facet | í Kongsstovu, Sunnvør Mikalsen, Svein-Ole Homrum, Eydna í Jacobsen, Jan Arge Flicek, Paul Dahl, Hans Atli |
author_sort | í Kongsstovu, Sunnvør |
collection | PubMed |
description | Atlantic herring (Clupea harengus) is one of the most abundant fish species in the world. It is an important economical and nutritional resource, as well as a crucial part of the North Atlantic ecosystem. In 2016, a draft herring genome assembly was published. Being a species of such importance, we sought to independently verify and potentially improve the herring genome assembly. We sequenced the herring genome generating paired-end, mate-pair, linked and long reads. Three assembly versions of the herring genome were generated based on a de novo assembly (A1), which was scaffolded using linked and long reads (A2) and then merged with the previously published assembly (A3). The resulting assemblies were compared using parameters describing the size, fragmentation, correctness, and completeness of the assemblies. Results showed that the A2 assembly was less fragmented, more complete and more correct than A1. A3 showed improvement in fragmentation and correctness compared with A2 and the published assembly but was slightly less complete than the published assembly. Thus, we here confirmed the previously published herring assembly, and made improvements by further scaffolding the assembly and removing low-quality sequences using linked and long reads and merging of assemblies. |
format | Online Article Text |
id | pubmed-6881392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68813922019-12-06 Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly í Kongsstovu, Sunnvør Mikalsen, Svein-Ole Homrum, Eydna í Jacobsen, Jan Arge Flicek, Paul Dahl, Hans Atli Sci Rep Article Atlantic herring (Clupea harengus) is one of the most abundant fish species in the world. It is an important economical and nutritional resource, as well as a crucial part of the North Atlantic ecosystem. In 2016, a draft herring genome assembly was published. Being a species of such importance, we sought to independently verify and potentially improve the herring genome assembly. We sequenced the herring genome generating paired-end, mate-pair, linked and long reads. Three assembly versions of the herring genome were generated based on a de novo assembly (A1), which was scaffolded using linked and long reads (A2) and then merged with the previously published assembly (A3). The resulting assemblies were compared using parameters describing the size, fragmentation, correctness, and completeness of the assemblies. Results showed that the A2 assembly was less fragmented, more complete and more correct than A1. A3 showed improvement in fragmentation and correctness compared with A2 and the published assembly but was slightly less complete than the published assembly. Thus, we here confirmed the previously published herring assembly, and made improvements by further scaffolding the assembly and removing low-quality sequences using linked and long reads and merging of assemblies. Nature Publishing Group UK 2019-11-27 /pmc/articles/PMC6881392/ /pubmed/31776409 http://dx.doi.org/10.1038/s41598-019-54151-9 Text en © The Author(s) 2019 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 í Kongsstovu, Sunnvør Mikalsen, Svein-Ole Homrum, Eydna í Jacobsen, Jan Arge Flicek, Paul Dahl, Hans Atli Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly |
title | Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly |
title_full | Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly |
title_fullStr | Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly |
title_full_unstemmed | Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly |
title_short | Using long and linked reads to improve an Atlantic herring (Clupea harengus) genome assembly |
title_sort | using long and linked reads to improve an atlantic herring (clupea harengus) genome assembly |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881392/ https://www.ncbi.nlm.nih.gov/pubmed/31776409 http://dx.doi.org/10.1038/s41598-019-54151-9 |
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