GENOME ANNOUNCEMENT
The isolate was kept in brain heart infusion broth containing 25% glycerol at −80°C following the isolation procedure. For sequencing, genomic DNA was extracted from overnight cultures grown at 37°C on tryptic soy agar using the Qiagen DNeasy blood and tissue DNA purification kit (Qiagen, Inc., Toronto, Ontario, Canada) and quantified using Qubit 3.0 (Life Technologies, Inc., Burlington, Ontario, Canada). The sequencing library was constructed using the Nextera XT DNA library preparation kit (Illumina, Inc., San Diego, CA, USA), and the library quality was analyzed using BioAnalyzer (Agilent Technologies, Santa Clara, CA, USA). The library was sequenced with the MiSeq platform (Illumina, Inc.) using the version 3 sequencing kit. A total of 1,491,678 paired-end reads (300 bp) were generated.
Adapter sequences and low-quality bases were trimmed (bbduk), and overlapping pairs were merged (bbmerge) using the BBtools software suite (http://jgi.doe.gov/data-and-tools/bbtools/). Preprocessed reads were assembled using SPAdes version 3.10.1 (4) and polished with Pilon version 1.22 (5). The assembly resulted in 79 contigs (>200 bp), with an average of 65-fold genome coverage. Contigs were ordered with Mauve version 2015-02-13 (http://darlinglab.org/mauve/mauve.html) using
Accession number(s).
This whole-genome shotgun project has been deposited in DDBJ/ENA/GenBank under the accession no. NKYI00000000. The version described in this paper is the first version, NKYI01000000.
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Abstract
ABSTRACT
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