A hybrid assembly was generated from ONT MinION sequence reads and Illumina sequence reads in Unicycler, implemented in Galaxy. The recovered genome was fully assembled to a single, closed replicon. Completeness and contamination estimates were done with CheckM v 1. The number and completeness of rRNA genes were determined with barrnap v. 0.9, and the number of tRNAs were determined with tRNAscan-SE v. 2.0.