GENOME ANNOUNCEMENT
De novo assembly was performed using 55,294 subreads as input with the Hierarchical Genome Assembly Process (HGAP) version 3 (6) implemented in the PacBio SMRT Analysis 2.3.0 package. This step was followed by polishing with Quiver (6) and error correction with Pilon version 1.16 (7), utilizing 793,039 MiSeq paired-end reads. The final consensus assembly generated one contig, containing the complete circular genome of 3,157,380 bp, with a mean G+C content of 45.5% and average coverage of 201.5-fold.
Taxonomic identification using Phyla-AMPHORA (8) showed 99.3% identity to the genus
Genome annotation was performed using NCBI’s Prokaryotic Genome Annotation Pipeline (PGAP) version 4.2 (10). PGAP predicted 3,054 genes, including 2,808 protein-coding genes (PCGs), 21 rRNA subunits (seven clusters of 5S, 16S, and 23S), 80 tRNAs, 4 noncoding RNAs, and 141 pseudogenes. Additionally, subsystems-based functional annotation was performed using Rapid Annotations using Subsystems Technology (RAST) (11–13) and assigned most genes to amino acid and derivative metabolism (316) and cofactor, vitamin, prosthetic group, and pigment (235) subsystems.
Accession number(s).
The complete genome sequence of
b Asian School of the Environment, Nanyang Technological University, Singapore
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Abstract
ABSTRACT
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