Target capture sequencing of SARS-CoV-2 genomes using the ONETest Coronaviruses Plus

被引:4
|
作者
Zhan, Shing H. [1 ]
Alamouti, Sepideh M. [1 ]
Daneshpajouh, Habib [1 ]
Kwok, Brian S. [1 ]
Lee, Meng-Hsun [1 ]
Khattra, Jaswinder [1 ]
Houck, Herbert J. [2 ]
Rand, Kenneth H. [2 ]
机构
[1] Fus Genom Corp, Burnaby, BC, Canada
[2] Univ Florida, Coll Med, Dept Pathol Immunol & Lab Med, Gainesville, FL USA
关键词
COVID-19; Genome sequencing; Target hybridization; Respiratory viruses; READ ALIGNMENT;
D O I
10.1016/j.diagmicrobio.2021.115508
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We introduce a target capture next-generation sequencing methodology, the ONETest Coronaviruses Plus, to sequence the SARS-CoV-2 genome and select loci of other respiratory viruses. We applied the ONETest on 70 respiratory samples (collected in Florida, USA between May and July, 2020), in which SARS-CoV-2 had been detected by a PCR assay. For 48 of the samples, we also applied the ARTIC protocol. Of the 70 ONETest libraries, 45 (64%) had a (near-)complete sequence (>29,000 bases and >90% covered by >9 reads). Of the 48 ARTIC libraries, 25 (52%) had a (near-)complete sequence. In 19 out of 25 (76%) samples in which both the ONETest and ARTIC yielded (near-)complete sequences, the lineages assigned were identical. As a target capture approach, the ONETest is less prone to loss of sequence coverage than amplicon approaches, and thus can provide complete genomic information more often to track and monitor SARS-CoV-2 variants. (c) 2021 Fusion Genomics Corporation. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
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页数:6
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