A rapid, cost-effective tailed amplicon method for sequencing SARS-CoV-2

被引:58
|
作者
Gohl, Daryl M. [1 ,2 ]
Garbe, John [1 ]
Grady, Patrick [1 ]
Daniel, Jerry [1 ]
Watson, Ray H. B. [1 ]
Auch, Benjamin [1 ]
Nelson, Andrew [3 ]
Yohe, Sophia [3 ]
Beckman, Kenneth B. [1 ]
机构
[1] Univ Minnesota, Genom Ctr, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Lab Med & Pathol, Div Mol Pathol & Genom, Minneapolis, MN 55455 USA
关键词
COVID-19; SARS-CoV-2; Genome sequencing; Viral surveillance;
D O I
10.1186/s12864-020-07283-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BackgroundThe global COVID-19 pandemic has led to an urgent need for scalable methods for clinical diagnostics and viral tracking. Next generation sequencing technologies have enabled large-scale genomic surveillance of SARS-CoV-2 as thousands of isolates are being sequenced around the world and deposited in public data repositories. A number of methods using both short- and long-read technologies are currently being applied for SARS-CoV-2 sequencing, including amplicon approaches, metagenomic methods, and sequence capture or enrichment methods. Given the small genome size, the ability to sequence SARS-CoV-2 at scale is limited by the cost and labor associated with making sequencing libraries.ResultsHere we describe a low-cost, streamlined, all amplicon-based method for sequencing SARS-CoV-2, which bypasses costly and time-consuming library preparation steps. We benchmark this tailed amplicon method against both the ARTIC amplicon protocol and sequence capture approaches and show that an optimized tailed amplicon approach achieves comparable amplicon balance, coverage metrics, and variant calls to the ARTIC v3 approach.ConclusionsThe tailed amplicon method we describe represents a cost-effective and highly scalable method for SARS-CoV-2 sequencing.
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页数:10
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