Abstract
Detection and mutation surveillance of SARS-CoV-2 are crucial for combating the COVID-19 pandemic. Here we describe a lab-based method for multiplex isothermal amplification-based sequencing and real-time analysis of multiple viral genomes. It can simultaneously detect SARS-CoV-2, influenza A, human adenovirus, and human coronavirus and monitor mutations for up to 96 samples in real time. The method proved to be rapid and sensitive (limit of detection: 29 viral RNA copies/μL of extracted nucleic acid) in detecting SARS-CoV-2 in clinical samples. We expect it to offer a promising solution for rapid field-deployable detection and mutational surveillance of pandemic viruses.
Original language | English (US) |
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Title of host publication | Multiplex Biomarker Techniques |
Publisher | Springer US |
Pages | 79-88 |
Number of pages | 10 |
ISBN (Print) | 9781071623947 |
DOIs | |
State | Published - Jul 16 2022 |
Bibliographical note
KAUST Repository Item: Exported on 2022-09-14ASJC Scopus subject areas
- Genetics
- Molecular Biology