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Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens

The MinION is a portable single-molecule DNA sequencing instrument that was released by Oxford Nanopore Technologies in 2014, producing long sequencing reads by measuring changes in ionic flow when single-stranded DNA molecules translocate through the pores. While MinION long reads have an error rat...

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Autores principales: Deschamps, Stéphane, Mudge, Joann, Cameron, Connor, Ramaraj, Thiruvarangan, Anand, Ajith, Fengler, Kevin, Hayes, Kevin, Llaca, Victor, Jones, Todd J., May, Gregory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923883/
https://www.ncbi.nlm.nih.gov/pubmed/27350167
http://dx.doi.org/10.1038/srep28625
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author Deschamps, Stéphane
Mudge, Joann
Cameron, Connor
Ramaraj, Thiruvarangan
Anand, Ajith
Fengler, Kevin
Hayes, Kevin
Llaca, Victor
Jones, Todd J.
May, Gregory
author_facet Deschamps, Stéphane
Mudge, Joann
Cameron, Connor
Ramaraj, Thiruvarangan
Anand, Ajith
Fengler, Kevin
Hayes, Kevin
Llaca, Victor
Jones, Todd J.
May, Gregory
author_sort Deschamps, Stéphane
collection PubMed
description The MinION is a portable single-molecule DNA sequencing instrument that was released by Oxford Nanopore Technologies in 2014, producing long sequencing reads by measuring changes in ionic flow when single-stranded DNA molecules translocate through the pores. While MinION long reads have an error rate substantially higher than the ones produced by short-read sequencing technologies, they can generate de novo assemblies of microbial genomes, after an initial correction step that includes alignment of Illumina sequencing data or detection of overlaps between Oxford Nanopore reads to improve accuracy. In this study, MinION reads were generated from the multi-chromosome genome of Agrobacterium tumefaciens strain LBA4404. Errors in the consensus two-directional (sense and antisense) “2D” sequences were first characterized by way of comparison with an internal reference assembly. Both Illumina-based correction and self-correction were performed and the resulting corrected reads assembled into high-quality hybrid and non-hybrid assemblies. Corrected read datasets and assemblies were subsequently compared. The results shown here indicate that both hybrid and non-hybrid methods can be used to assemble Oxford Nanopore reads into informative multi-chromosome assemblies, each with slightly different outcomes in terms of contiguity and accuracy.
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spelling pubmed-49238832016-06-28 Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens Deschamps, Stéphane Mudge, Joann Cameron, Connor Ramaraj, Thiruvarangan Anand, Ajith Fengler, Kevin Hayes, Kevin Llaca, Victor Jones, Todd J. May, Gregory Sci Rep Article The MinION is a portable single-molecule DNA sequencing instrument that was released by Oxford Nanopore Technologies in 2014, producing long sequencing reads by measuring changes in ionic flow when single-stranded DNA molecules translocate through the pores. While MinION long reads have an error rate substantially higher than the ones produced by short-read sequencing technologies, they can generate de novo assemblies of microbial genomes, after an initial correction step that includes alignment of Illumina sequencing data or detection of overlaps between Oxford Nanopore reads to improve accuracy. In this study, MinION reads were generated from the multi-chromosome genome of Agrobacterium tumefaciens strain LBA4404. Errors in the consensus two-directional (sense and antisense) “2D” sequences were first characterized by way of comparison with an internal reference assembly. Both Illumina-based correction and self-correction were performed and the resulting corrected reads assembled into high-quality hybrid and non-hybrid assemblies. Corrected read datasets and assemblies were subsequently compared. The results shown here indicate that both hybrid and non-hybrid methods can be used to assemble Oxford Nanopore reads into informative multi-chromosome assemblies, each with slightly different outcomes in terms of contiguity and accuracy. Nature Publishing Group 2016-06-28 /pmc/articles/PMC4923883/ /pubmed/27350167 http://dx.doi.org/10.1038/srep28625 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Deschamps, Stéphane
Mudge, Joann
Cameron, Connor
Ramaraj, Thiruvarangan
Anand, Ajith
Fengler, Kevin
Hayes, Kevin
Llaca, Victor
Jones, Todd J.
May, Gregory
Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens
title Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens
title_full Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens
title_fullStr Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens
title_full_unstemmed Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens
title_short Characterization, correction and de novo assembly of an Oxford Nanopore genomic dataset from Agrobacterium tumefaciens
title_sort characterization, correction and de novo assembly of an oxford nanopore genomic dataset from agrobacterium tumefaciens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923883/
https://www.ncbi.nlm.nih.gov/pubmed/27350167
http://dx.doi.org/10.1038/srep28625
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