| Literature DB >> 35186325 |
Annika Flint1, Spencer Reaume2, Jennifer Harlow2, Emily Hoover1, Kelly Weedmark1, Neda Nasheri2.
Abstract
Whole-genome sequence analysis of noroviruses is routinely performed by employing a metagenomic approach. While this methodology has several advantages, such as allowing for the examination of co-infection, it has some limitations, such as the requirement of high viral load to achieve full-length or near full-length genomic sequences. In this study, we used a pre-amplification step to obtain full-length genomic amplicons from 39 Canadian GII isolates, followed by deep sequencing on Illumina and Oxford Nanopore platforms. This approach significantly reduced the required viral titre to obtain full-genome coverage. Herein, we compared the coverage and sequences obtained by both platforms and provided an in-depth genomic analysis of the obtained sequences, including the presence of single-nucleotide variants and recombination events. © Crown copyright 2021.Entities:
Keywords: Illumina MiSeq; Oxford Nanopore; full-length amplicons; norovirus; recombination; single-nucleotide variation
Year: 2021 PMID: 35186325 PMCID: PMC8570145 DOI: 10.1093/ve/veab079
Source DB: PubMed Journal: Virus Evol ISSN: 2057-1577