Assembling the perfect bacterial genome using Oxford Nanopore and Illumina sequencing

PLoS Comput Biol. 2023 Mar 2;19(3):e1010905. doi: 10.1371/journal.pcbi.1010905. eCollection 2023 Mar.

Abstract

A perfect bacterial genome assembly is one where the assembled sequence is an exact match for the organism's genome-each replicon sequence is complete and contains no errors. While this has been difficult to achieve in the past, improvements in long-read sequencing, assemblers, and polishers have brought perfect assemblies within reach. Here, we describe our recommended approach for assembling a bacterial genome to perfection using a combination of Oxford Nanopore Technologies long reads and Illumina short reads: Trycycler long-read assembly, Medaka long-read polishing, Polypolish short-read polishing, followed by other short-read polishing tools and manual curation. We also discuss potential pitfalls one might encounter when assembling challenging genomes, and we provide an online tutorial with sample data (github.com/rrwick/perfect-bacterial-genome-tutorial).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Genome, Bacterial / genetics
  • High-Throughput Nucleotide Sequencing
  • Nanopores*
  • Oryzias*
  • Technology

Grants and funding

This work was supported, in whole or in part, by the Bill & Melinda Gates Foundation (KEH, grant number OPP1175797). Under the grant conditions of the Foundation, a Creative Commons Attribution 4.0 Generic License has already been assigned to the Author Accepted Manuscript version that might arise from this submission. This work was also supported by an Australian Government Research Training Program Scholarship (RRW). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.