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High throughput nanopore sequencing of SARS-CoV-2 viral genomes from patient samples.

Adrian A PaterMichael S BosmenyAdam A WhiteRourke J SylvainSeth B EddingtonMansi ParasrampuriaKaty N OvingtonPaige E MetzAbadat O YinusaChristopher L BarkauRamadevi ChilamkurthyScott W BenzingerMadison M HebertKeith T Gagnon
Published in: Journal of biological methods (2021)
In late 2019, a novel coronavirus began spreading in Wuhan, China, causing a potentially lethal respiratory viral infection. By early 2020, the novel coronavirus, called SARS-CoV-2, had spread globally, causing the COVID-19 pandemic. The infection and mutation rates of SARS-CoV-2 make it amenable to tracking introduction, spread and evolution by viral genome sequencing. Efforts to develop effective public health policies, therapeutics, or vaccines to treat or prevent COVID-19 are also expected to benefit from tracking mutations of the SARS-CoV-2 virus. Here we describe a set of comprehensive working protocols, from viral RNA extraction to analysis using established visualization tools, for high throughput sequencing of SARS-CoV-2 viral genomes using a MinION instrument. This set of protocols should serve as a reliable "how-to" reference for generating quality SARS-CoV-2 genome sequences with ARTIC primer sets and long-read nanopore sequencing technology. In addition, many of the preparation, quality control, and analysis steps will be generally applicable to other sequencing platforms.
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