Open AccessComparison of long-read sequencing technologies in the hybrid assembly of complex bacterial genomes
Author(s) -
Nicola De Maio,
Liam P. Shaw,
Alasdair T. M. Hubbard,
Sophie George,
N Sanderson,
Jeremy Swann,
Ryan R. Wick,
Manal AbuOun,
Emma Stubberfield,
Sarah Hoosdally,
Derrick Crook,
Peto Tea.,
Anna E. Sheppard,
M S Bailey,
Daniel S. Read,
Anjum Mf,
A. Sarah Walker,
Nicole Stoesser
Publication year - 2019
Publication title -
microbial genomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.476
H-Index - 28
ISSN - 2057-5858
DOI - 10.1099/mgen.0.000294
Subject(s) - sequence assembly , genome , nanopore sequencing , hybrid genome assembly , illumina dye sequencing , computational biology , bacterial genome size , dna sequencing , reference genome , biology , minion , whole genome sequencing , genetics , gene , gene expression , transcriptome
Illumina sequencing allows rapid, cheap and accurate whole genome bacterial analyses, but short reads (<300 bp) do not usually enable complete genome assembly. Long-read sequencing greatly assists with resolving complex bacterial genomes, particularly when combined with short-read Illumina data (hybrid assembly). However, it is not clear how different long-read sequencing methods affect hybrid assembly accuracy. Relative automation of the assembly process is also crucial to facilitating high-throughput complete bacterial genome reconstruction, avoiding multiple bespoke filtering and data manipulation steps. In this study, we compared hybrid assemblies for 20 bacterial isolates, including two reference strains, using Illumina sequencing and long reads from either Oxford Nanopore Technologies (ONT) or SMRT Pacific Biosciences (PacBio) sequencing platforms. We chose isolates from the family Enterobacteriaceae , as these frequently have highly plastic, repetitive genetic structures, and complete genome reconstruction for these species is relevant for a precise understanding of the epidemiology of antimicrobial resistance. We de novo assembled genomes using the hybrid assembler Unicycler and compared different read processing strategies, as well as comparing to long-read-only assembly with Flye followed by short-read polishing with Pilon. Hybrid assembly with either PacBio or ONT reads facilitated high-quality genome reconstruction, and was superior to the long-read assembly and polishing approach evaluated with respect to accuracy and completeness. Combining ONT and Illumina reads fully resolved most genomes without additional manual steps, and at a lower consumables cost per isolate in our setting. Automated hybrid assembly is a powerful tool for complete and accurate bacterial genome assembly.