Cargando…

Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications

The MinION sequencer (Oxford Nanopore Technologies) is a paradigm shifting device allowing rapid, real time long read sequencing of nucleic acids. Yet external benchmarking of this technologies’ capabilities has not been extensively reported, nor has thorough evaluation of its utility for field-base...

Descripción completa

Detalles Bibliográficos
Autores principales: Tyler, Andrea D., Mataseje, Laura, Urfano, Chantel J., Schmidt, Lisa, Antonation, Kym S., Mulvey, Michael R., Corbett, Cindi R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053456/
https://www.ncbi.nlm.nih.gov/pubmed/30026559
http://dx.doi.org/10.1038/s41598-018-29334-5
_version_ 1783340825665601536
author Tyler, Andrea D.
Mataseje, Laura
Urfano, Chantel J.
Schmidt, Lisa
Antonation, Kym S.
Mulvey, Michael R.
Corbett, Cindi R.
author_facet Tyler, Andrea D.
Mataseje, Laura
Urfano, Chantel J.
Schmidt, Lisa
Antonation, Kym S.
Mulvey, Michael R.
Corbett, Cindi R.
author_sort Tyler, Andrea D.
collection PubMed
description The MinION sequencer (Oxford Nanopore Technologies) is a paradigm shifting device allowing rapid, real time long read sequencing of nucleic acids. Yet external benchmarking of this technologies’ capabilities has not been extensively reported, nor has thorough evaluation of its utility for field-based analysis with sub-optimal sample types been described. The aim of this study was to evaluate the capability of the MinION sequencer for bacterial genomic and metagenomic applications, with specific emphasis placed on the quality, yield, and accuracy of generated sequence data. Two independent laboratories at the National Microbiology Laboratory (Public Health Agency of Canada), sequenced a set of microbes in replicate, using the currently available flowcells, sequencing chemistries, and software available at the time of the experiment. Overall sequencing yield and quality improved through the course of this set of experiments. Sequencing alignment accuracy was high reaching 97% for all 2D experiments, though was slightly lower for 1D sequencing (94%). 1D sequencing provided much longer sequences than 2D. Both sequencing chemistries performed equally well in constructing genomic assemblies. There was evidence of barcode cross-over using both the native and PCR barcoding methods. Despite the sub-optimal nature of samples sequenced in the field, sequences attributable to B. anthracis the target organism used in this scenario, could none-the-less be detected. Together, this report showcases the rapid advancement in this technology and its utility in the context of genomic sequencing of microbial isolates of importance to public health.
format Online
Article
Text
id pubmed-6053456
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-60534562018-07-23 Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications Tyler, Andrea D. Mataseje, Laura Urfano, Chantel J. Schmidt, Lisa Antonation, Kym S. Mulvey, Michael R. Corbett, Cindi R. Sci Rep Article The MinION sequencer (Oxford Nanopore Technologies) is a paradigm shifting device allowing rapid, real time long read sequencing of nucleic acids. Yet external benchmarking of this technologies’ capabilities has not been extensively reported, nor has thorough evaluation of its utility for field-based analysis with sub-optimal sample types been described. The aim of this study was to evaluate the capability of the MinION sequencer for bacterial genomic and metagenomic applications, with specific emphasis placed on the quality, yield, and accuracy of generated sequence data. Two independent laboratories at the National Microbiology Laboratory (Public Health Agency of Canada), sequenced a set of microbes in replicate, using the currently available flowcells, sequencing chemistries, and software available at the time of the experiment. Overall sequencing yield and quality improved through the course of this set of experiments. Sequencing alignment accuracy was high reaching 97% for all 2D experiments, though was slightly lower for 1D sequencing (94%). 1D sequencing provided much longer sequences than 2D. Both sequencing chemistries performed equally well in constructing genomic assemblies. There was evidence of barcode cross-over using both the native and PCR barcoding methods. Despite the sub-optimal nature of samples sequenced in the field, sequences attributable to B. anthracis the target organism used in this scenario, could none-the-less be detected. Together, this report showcases the rapid advancement in this technology and its utility in the context of genomic sequencing of microbial isolates of importance to public health. Nature Publishing Group UK 2018-07-19 /pmc/articles/PMC6053456/ /pubmed/30026559 http://dx.doi.org/10.1038/s41598-018-29334-5 Text en © The Author(s) 2018 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
Tyler, Andrea D.
Mataseje, Laura
Urfano, Chantel J.
Schmidt, Lisa
Antonation, Kym S.
Mulvey, Michael R.
Corbett, Cindi R.
Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications
title Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications
title_full Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications
title_fullStr Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications
title_full_unstemmed Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications
title_short Evaluation of Oxford Nanopore’s MinION Sequencing Device for Microbial Whole Genome Sequencing Applications
title_sort evaluation of oxford nanopore’s minion sequencing device for microbial whole genome sequencing applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053456/
https://www.ncbi.nlm.nih.gov/pubmed/30026559
http://dx.doi.org/10.1038/s41598-018-29334-5
work_keys_str_mv AT tylerandread evaluationofoxfordnanoporesminionsequencingdeviceformicrobialwholegenomesequencingapplications
AT matasejelaura evaluationofoxfordnanoporesminionsequencingdeviceformicrobialwholegenomesequencingapplications
AT urfanochantelj evaluationofoxfordnanoporesminionsequencingdeviceformicrobialwholegenomesequencingapplications
AT schmidtlisa evaluationofoxfordnanoporesminionsequencingdeviceformicrobialwholegenomesequencingapplications
AT antonationkyms evaluationofoxfordnanoporesminionsequencingdeviceformicrobialwholegenomesequencingapplications
AT mulveymichaelr evaluationofoxfordnanoporesminionsequencingdeviceformicrobialwholegenomesequencingapplications
AT corbettcindir evaluationofoxfordnanoporesminionsequencingdeviceformicrobialwholegenomesequencingapplications