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MicroPIPE: validating an end-to-end workflow for high-quality complete bacterial genome construction.
Murigneux, Valentine; Roberts, Leah W; Forde, Brian M; Phan, Minh-Duy; Nhu, Nguyen Thi Khanh; Irwin, Adam D; Harris, Patrick N A; Paterson, David L; Schembri, Mark A; Whiley, David M; Beatson, Scott A.
Afiliação
  • Murigneux V; QCIF Facility for Advanced Bioinformatics, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia.
  • Roberts LW; University of Queensland Centre for Clinical Research, Brisbane, Queensland, Australia. leah@ebi.ac.uk.
  • Forde BM; Queensland Children's Hospital, Brisbane, Queensland, Australia. leah@ebi.ac.uk.
  • Phan MD; European Bioinformatics Institute, European Molecular Biology Laboratory (EMBL), Hinxton, Cambridge, UK. leah@ebi.ac.uk.
  • Nhu NTK; University of Queensland Centre for Clinical Research, Brisbane, Queensland, Australia.
  • Irwin AD; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.
  • Harris PNA; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.
  • Paterson DL; University of Queensland Centre for Clinical Research, Brisbane, Queensland, Australia.
  • Schembri MA; Queensland Children's Hospital, Brisbane, Queensland, Australia.
  • Whiley DM; University of Queensland Centre for Clinical Research, Brisbane, Queensland, Australia.
  • Beatson SA; Central Microbiology, Pathology Queensland, Royal Brisbane & Women's Hospital, Brisbane, Queensland, Australia.
BMC Genomics ; 22(1): 474, 2021 Jun 25.
Article em En | MEDLINE | ID: mdl-34172000
ABSTRACT

BACKGROUND:

Oxford Nanopore Technology (ONT) long-read sequencing has become a popular platform for microbial researchers due to the accessibility and affordability of its devices. However, easy and automated construction of high-quality bacterial genomes using nanopore reads remains challenging. Here we aimed to create a reproducible end-to-end bacterial genome assembly pipeline using ONT in combination with Illumina sequencing.

RESULTS:

We evaluated the performance of several popular tools used during genome reconstruction, including base-calling, filtering, assembly, and polishing. We also assessed overall genome accuracy using ONT both natively and with Illumina. All steps were validated using the high-quality complete reference genome for the Escherichia coli sequence type (ST)131 strain EC958. Software chosen at each stage were incorporated into our final pipeline, MicroPIPE. Further validation of MicroPIPE was carried out using 11 additional ST131 E. coli isolates, which demonstrated that complete circularised chromosomes and plasmids could be achieved without manual intervention. Twelve publicly available Gram-negative and Gram-positive bacterial genomes (with available raw ONT data and matched complete genomes) were also assembled using MicroPIPE. We found that revised basecalling and updated assembly of the majority of these genomes resulted in improved accuracy compared to the current publicly available complete genomes.

CONCLUSIONS:

MicroPIPE is built in modules using Singularity container images and the bioinformatics workflow manager Nextflow, allowing changes and adjustments to be made in response to future tool development. Overall, MicroPIPE provides an easy-access, end-to-end solution for attaining high-quality bacterial genomes. MicroPIPE is available at https//github.com/BeatsonLab-MicrobialGenomics/micropipe .
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Bacteriano / Escherichia coli Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Bacteriano / Escherichia coli Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Austrália