2020
DOI: 10.1128/mra.00960-20
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Complete Genome Sequence of a Canadian Klebsiella michiganensis Strain, Obtained Using Oxford Nanopore Technologies Sequencing

Abstract: Klebsiella michiganensis is a Gram-negative opportunistic pathogen that is associated with many hospital-acquired infections in humans. Here, we report the complete genome sequence of a K. michiganensis strain isolated from a Canadian wastewater treatment facility.

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Cited by 10 publications
(5 citation statements)
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References 10 publications
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“…Nanopore sequencing was performed using a one-dimensional native barcoding gDNA protocol (EXP-NBD104 and SQK-LSK109; Oxford Nanopore Technologies, UK) without shearing followed by sequencing using a FLO-MIN106 (R9.4.1) flow cell on a MinION Mk1C device. Nanopore sequencing base calling was performed using Super Accuracy mode in Guppy v5.0.11, trimming using Porechop v0.2.3 ( 3 ), and filtration using Filtlong v0.2.1 ( 4 ). Assembly of the Nanopore long reads was performed using Flye v2.7 ( 5 ), corrected using Medaka v1.4.4, and polished with Illumina MiSeq reads using a combination of NextPolish v1.4.0, ntEdit v1.3.5, and Polypolish v0.5.0 after trimming/filtering with fastp v0.23.2.…”
Section: Announcementmentioning
confidence: 99%
“…Nanopore sequencing was performed using a one-dimensional native barcoding gDNA protocol (EXP-NBD104 and SQK-LSK109; Oxford Nanopore Technologies, UK) without shearing followed by sequencing using a FLO-MIN106 (R9.4.1) flow cell on a MinION Mk1C device. Nanopore sequencing base calling was performed using Super Accuracy mode in Guppy v5.0.11, trimming using Porechop v0.2.3 ( 3 ), and filtration using Filtlong v0.2.1 ( 4 ). Assembly of the Nanopore long reads was performed using Flye v2.7 ( 5 ), corrected using Medaka v1.4.4, and polished with Illumina MiSeq reads using a combination of NextPolish v1.4.0, ntEdit v1.3.5, and Polypolish v0.5.0 after trimming/filtering with fastp v0.23.2.…”
Section: Announcementmentioning
confidence: 99%
“…Nanopore sequencing library was generated using the 1D Native barcoding gDNA protocol (EXP-NBD104 and SQK-LSK109) (Oxford Nanopore Technologies, UK), and sequenced using a FLO-MIN106 (R9.4.1) flow cell in MinION MK1C. Basecalling was performed using Super Accuracy mode in Guppy v5.0.11, trimming using Porechop v0.2.3 ( 3 ) and filtration using Filtlong v0.2.1 ( 4 ). Long reads assembly was performed using Flye v2.7 ( 5 ), corrected using Medaka v1.4.4 and polished with Illumina MiSeq reads using a combination of NextPolish v1.4.0, ntEdit v1.3.5 and Polypolish v0.5.0 after trimming/filtering with fastp v0.23.2.…”
Section: Announcementmentioning
confidence: 99%
“…FastQC v0.11.9 ( https://www.bioinformatics.babraham.ac.uk/projects/fastqc ) and pycoQC v2.5.2 ( https://github.com/a-slide/pycoQC ) were used to assess read quality for Illumina and Nanopore reads, respectively. Long reads were trimmed and filtered with Porechop v0.2.3 ( 3 ) and Filtlong v0.2.1, respectively ( 4 ), and assembled with Flye v2.7 ( 5 ). The assembly was corrected using Medaka v1.4.4 ( https://github.com/nanoporetech/medaka ) and polished with short reads using a combination of NextPolish v1.4.0 ( 6 ), ntEdit v1.3.5 ( 7 ), and Polypolish v0.5.0 ( 8 ) after trimming/filtering with fastp v0.23.2 ( 9 ).…”
Section: Announcementmentioning
confidence: 99%