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Benchmarking the MinION: Evaluating long reads for microbial profiling
Nanopore based DNA-sequencing delivers long reads, thereby simplifying the decipherment of bacterial communities. Since its commercial appearance, this technology has been assigned several attributes, such as its error proneness, comparatively low cost, ease-of-use, and, most notably, aforementioned...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083898/ https://www.ncbi.nlm.nih.gov/pubmed/32198413 http://dx.doi.org/10.1038/s41598-020-61989-x |
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author | Leidenfrost, Robert Maximilian Pöther, Dierk-Christoph Jäckel, Udo Wünschiers, Röbbe |
author_facet | Leidenfrost, Robert Maximilian Pöther, Dierk-Christoph Jäckel, Udo Wünschiers, Röbbe |
author_sort | Leidenfrost, Robert Maximilian |
collection | PubMed |
description | Nanopore based DNA-sequencing delivers long reads, thereby simplifying the decipherment of bacterial communities. Since its commercial appearance, this technology has been assigned several attributes, such as its error proneness, comparatively low cost, ease-of-use, and, most notably, aforementioned long reads. The technology as a whole is under continued development. As such, benchmarks are required to conceive, test and improve analysis protocols, including those related to the understanding of the composition of microbial communities. Here we present a dataset composed of twelve different prokaryotic species split into four samples differing by nucleic acid quantification technique to assess the specificity and sensitivity of the MinION nanopore sequencer in a blind study design. Taxonomic classification was performed by standard taxonomic sequence classification tools, namely Kraken, Kraken2 and Centrifuge directly on reads. This allowed taxonomic assignments of up to 99.27% on genus level and 92.78% on species level, enabling true-positive classification of strains down to 25,000 genomes per sample. Full genomic coverage is achieved for strains abundant as low as 250,000 genomes per sample under our experimental settings. In summary, we present an evaluation of nanopore sequence processing analysis with respect to microbial community composition. It provides an open protocol and the data may serve as basis for the development and benchmarking of future data processing pipelines. |
format | Online Article Text |
id | pubmed-7083898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70838982020-03-26 Benchmarking the MinION: Evaluating long reads for microbial profiling Leidenfrost, Robert Maximilian Pöther, Dierk-Christoph Jäckel, Udo Wünschiers, Röbbe Sci Rep Article Nanopore based DNA-sequencing delivers long reads, thereby simplifying the decipherment of bacterial communities. Since its commercial appearance, this technology has been assigned several attributes, such as its error proneness, comparatively low cost, ease-of-use, and, most notably, aforementioned long reads. The technology as a whole is under continued development. As such, benchmarks are required to conceive, test and improve analysis protocols, including those related to the understanding of the composition of microbial communities. Here we present a dataset composed of twelve different prokaryotic species split into four samples differing by nucleic acid quantification technique to assess the specificity and sensitivity of the MinION nanopore sequencer in a blind study design. Taxonomic classification was performed by standard taxonomic sequence classification tools, namely Kraken, Kraken2 and Centrifuge directly on reads. This allowed taxonomic assignments of up to 99.27% on genus level and 92.78% on species level, enabling true-positive classification of strains down to 25,000 genomes per sample. Full genomic coverage is achieved for strains abundant as low as 250,000 genomes per sample under our experimental settings. In summary, we present an evaluation of nanopore sequence processing analysis with respect to microbial community composition. It provides an open protocol and the data may serve as basis for the development and benchmarking of future data processing pipelines. Nature Publishing Group UK 2020-03-20 /pmc/articles/PMC7083898/ /pubmed/32198413 http://dx.doi.org/10.1038/s41598-020-61989-x Text en © The Author(s) 2020 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 Leidenfrost, Robert Maximilian Pöther, Dierk-Christoph Jäckel, Udo Wünschiers, Röbbe Benchmarking the MinION: Evaluating long reads for microbial profiling |
title | Benchmarking the MinION: Evaluating long reads for microbial profiling |
title_full | Benchmarking the MinION: Evaluating long reads for microbial profiling |
title_fullStr | Benchmarking the MinION: Evaluating long reads for microbial profiling |
title_full_unstemmed | Benchmarking the MinION: Evaluating long reads for microbial profiling |
title_short | Benchmarking the MinION: Evaluating long reads for microbial profiling |
title_sort | benchmarking the minion: evaluating long reads for microbial profiling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083898/ https://www.ncbi.nlm.nih.gov/pubmed/32198413 http://dx.doi.org/10.1038/s41598-020-61989-x |
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