“…The library was loaded on a SpotON Mk I (R9.4) flow cell and sequenced using MinKNOW version 1.7.14, and raw sequence data (FAST5 format) were base-called using Albacore Sequencing Pipeline version 2.0.2 software. The reads were de novo assembled into two contigs (6,456,544 bp and 173,286 bp) with Canu version 1.5 ( 15 , 16 , 17 ), and the assembled genome was circularized by manually trimming the repeated sequences. Illumina paired-end (2 × 150-bp) reads (266,781,451 reads) were obtained with the MiniSeq system (Illumina, San Diego, CA, USA) and mapped to the assembly using the Burrows-Wheeler aligner ( 15 , 17 , 18 ) for sequence and assembly error correction with Pilon ( 15 , 17 , 19 ).…”