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LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads
BACKGROUND: Owing to the complexity of the assembly problem, we do not yet have complete genome sequences. The difficulty in assembling reads into finished genomes is exacerbated by sequence repeats and the inability of short reads to capture sufficient genomic information to resolve those problemat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524009/ https://www.ncbi.nlm.nih.gov/pubmed/26244089 http://dx.doi.org/10.1186/s13742-015-0076-3 |
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author | Warren, René L. Yang, Chen Vandervalk, Benjamin P. Behsaz, Bahar Lagman, Albert Jones, Steven J. M. Birol, Inanç |
author_facet | Warren, René L. Yang, Chen Vandervalk, Benjamin P. Behsaz, Bahar Lagman, Albert Jones, Steven J. M. Birol, Inanç |
author_sort | Warren, René L. |
collection | PubMed |
description | BACKGROUND: Owing to the complexity of the assembly problem, we do not yet have complete genome sequences. The difficulty in assembling reads into finished genomes is exacerbated by sequence repeats and the inability of short reads to capture sufficient genomic information to resolve those problematic regions. In this regard, established and emerging long read technologies show great promise, but their current associated higher error rates typically require computational base correction and/or additional bioinformatics pre-processing before they can be of value. RESULTS: We present LINKS, the Long Interval Nucleotide K-mer Scaffolder algorithm, a method that makes use of the sequence properties of nanopore sequence data and other error-containing sequence data, to scaffold high-quality genome assemblies, without the need for read alignment or base correction. Here, we show how the contiguity of an ABySS Escherichia coli K-12 genome assembly can be increased greater than five-fold by the use of beta-released Oxford Nanopore Technologies Ltd. long reads and how LINKS leverages long-range information in Saccharomyces cerevisiae W303 nanopore reads to yield assemblies whose resulting contiguity and correctness are on par with or better than that of competing applications. We also present the re-scaffolding of the colossal white spruce (Picea glauca) draft assembly (PG29, 20 Gbp) and demonstrate how LINKS scales to larger genomes. CONCLUSIONS: This study highlights the present utility of nanopore reads for genome scaffolding in spite of their current limitations, which are expected to diminish as the nanopore sequencing technology advances. We expect LINKS to have broad utility in harnessing the potential of long reads in connecting high-quality sequences of small and large genome assembly drafts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13742-015-0076-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4524009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45240092015-08-05 LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads Warren, René L. Yang, Chen Vandervalk, Benjamin P. Behsaz, Bahar Lagman, Albert Jones, Steven J. M. Birol, Inanç Gigascience Research BACKGROUND: Owing to the complexity of the assembly problem, we do not yet have complete genome sequences. The difficulty in assembling reads into finished genomes is exacerbated by sequence repeats and the inability of short reads to capture sufficient genomic information to resolve those problematic regions. In this regard, established and emerging long read technologies show great promise, but their current associated higher error rates typically require computational base correction and/or additional bioinformatics pre-processing before they can be of value. RESULTS: We present LINKS, the Long Interval Nucleotide K-mer Scaffolder algorithm, a method that makes use of the sequence properties of nanopore sequence data and other error-containing sequence data, to scaffold high-quality genome assemblies, without the need for read alignment or base correction. Here, we show how the contiguity of an ABySS Escherichia coli K-12 genome assembly can be increased greater than five-fold by the use of beta-released Oxford Nanopore Technologies Ltd. long reads and how LINKS leverages long-range information in Saccharomyces cerevisiae W303 nanopore reads to yield assemblies whose resulting contiguity and correctness are on par with or better than that of competing applications. We also present the re-scaffolding of the colossal white spruce (Picea glauca) draft assembly (PG29, 20 Gbp) and demonstrate how LINKS scales to larger genomes. CONCLUSIONS: This study highlights the present utility of nanopore reads for genome scaffolding in spite of their current limitations, which are expected to diminish as the nanopore sequencing technology advances. We expect LINKS to have broad utility in harnessing the potential of long reads in connecting high-quality sequences of small and large genome assembly drafts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13742-015-0076-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-04 /pmc/articles/PMC4524009/ /pubmed/26244089 http://dx.doi.org/10.1186/s13742-015-0076-3 Text en © Warren et al. 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 | Research Warren, René L. Yang, Chen Vandervalk, Benjamin P. Behsaz, Bahar Lagman, Albert Jones, Steven J. M. Birol, Inanç LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads |
title | LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads |
title_full | LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads |
title_fullStr | LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads |
title_full_unstemmed | LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads |
title_short | LINKS: Scalable, alignment-free scaffolding of draft genomes with long reads |
title_sort | links: scalable, alignment-free scaffolding of draft genomes with long reads |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524009/ https://www.ncbi.nlm.nih.gov/pubmed/26244089 http://dx.doi.org/10.1186/s13742-015-0076-3 |
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