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Rapid High-Throughput Whole-Genome Sequencing of SARS-CoV-2 by Using One-Step Reverse Transcription-PCR Amplification with an Integrated Microfluidic System and Next-Generation Sequencing.
Li, Tao; Chung, Hye Kyung; Pireku, Papa K; Beitzel, Brett F; Sanborn, Mark A; Tang, Cynthia Y; Hammer, Richard D; Ritter, Detlef; Wan, Xiu-Feng; Maljkovic Berry, Irina; Hang, Jun.
Affiliation
  • Li T; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Chung HK; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Pireku PK; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Beitzel BF; US Army Medical Research Institute of Infectious Disease Center for Genome Sciences, Fort Detrick, Maryland, USA.
  • Sanborn MA; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Tang CY; MU Center for Influenza and Emerging Infectious Diseases (CIEID), University of Missouri, Columbia, Missouri, USA.
  • Hammer RD; Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, Missouri, USA.
  • Ritter D; Bond Life Sciences Center, University of Missouri, Columbia, Missouri, USA.
  • Wan XF; MU Institute for Data Science and Informatics, University of Missouri, Columbia, Missouri, USA.
  • Maljkovic Berry I; Department of Pathology, School of Medicine, University of Missouri, Columbia, Missouri, USA.
  • Hang J; Department of Pathology, School of Medicine, University of Missouri, Columbia, Missouri, USA.
J Clin Microbiol ; 59(5)2021 04 20.
Article in En | MEDLINE | ID: mdl-33653700
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome, Viral / Microfluidics / High-Throughput Nucleotide Sequencing / Whole Genome Sequencing / SARS-CoV-2 Type of study: Guideline Limits: Humans Language: En Journal: J Clin Microbiol Year: 2021 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome, Viral / Microfluidics / High-Throughput Nucleotide Sequencing / Whole Genome Sequencing / SARS-CoV-2 Type of study: Guideline Limits: Humans Language: En Journal: J Clin Microbiol Year: 2021 Document type: Article Affiliation country: United States