| Literature DB >> 33653700 |
Tao Li1, Hye Kyung Chung1, Papa K Pireku1, Brett F Beitzel2, Mark A Sanborn1, Cynthia Y Tang3,4,5,6, Richard D Hammer7, Detlef Ritter7, Xiu-Feng Wan3,4,5,6,8, Irina Maljkovic Berry1, Jun Hang9.
Abstract
The long-lasting global COVID-19 pandemic demands timely genomic investigation of SARS-CoV-2 viruses. Here, we report a simple and efficient workflow for whole-genome sequencing utilizing one-step reverse transcription-PCR (RT-PCR) amplification on a microfluidic platform, followed by MiSeq amplicon sequencing. The method uses Fluidigm integrated fluidic circuit (IFC) and instruments to amplify 48 samples with 39 pairs of primers, including 35 custom-designed primer pairs and four additional primer pairs from the ARTIC network protocol v3. Application of this method on RNA samples from both viral isolates and clinical specimens demonstrates robustness and efficiency in obtaining the full genome sequence of SARS-CoV-2. This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply.Entities:
Keywords: COVID-19; SARS-CoV-2; acute respiratory illness; emerging infectious viral disease; genomes; next-generation sequencing; pandemic
Year: 2021 PMID: 33653700 DOI: 10.1128/JCM.02784-20
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948