Cargando…

Rapid Lineage Assignment of Severe Acute Respiratory Syndrome Coronavirus 2 Cases through Automated Library Preparation, Sequencing, and Bioinformatic Analysis

The coronavirus disease 2019 (COVID-19) pandemic has provided a stage to illustrate that there is considerable value in obtaining rapid, whole-genome–based information about pathogens. This article describes the utility of a commercially available, automated severe acute respiratory syndrome associa...

Descripción completa

Detalles Bibliográficos
Autores principales: Gorzalski, Andrew J., Kerwin, Heather, Verma, Subhash, Hess, David C., Sevinsky, Joel, Libuit, Kevin, Vlasova-St. Louis, Irina, Siao, Danielle, Siao, Lauren, Buñuel, Diego, Van Hooser, Stephanie, Pandori, Mark W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Investigative Pathology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902282/
https://www.ncbi.nlm.nih.gov/pubmed/36754279
http://dx.doi.org/10.1016/j.jmoldx.2023.01.005
Descripción
Sumario:The coronavirus disease 2019 (COVID-19) pandemic has provided a stage to illustrate that there is considerable value in obtaining rapid, whole-genome–based information about pathogens. This article describes the utility of a commercially available, automated severe acute respiratory syndrome associated coronavirus 2 (SARS-CoV-2) library preparation, genome sequencing, and a bioinformatics analysis pipeline to provide rapid, near–real-time SARS-CoV-2 variant description. This study evaluated the turnaround time, accuracy, and other quality-related parameters obtained from commercially available automated sequencing instrumentation, from analysis of continuous clinical samples obtained from January 1, 2021, to October 6, 2021. This analysis included a base-by-base assessment of sequencing accuracy at every position in the SARS-CoV-2 chromosome using two commercially available methods. Mean turnaround time, from the receipt of a specimen for SARS-CoV-2 testing to the availability of the results, with lineage assignment, was <3 days. Accuracy of sequencing by one method was 100%, although certain sites on the genome were found repeatedly to have been sequenced with varying degrees of read error rate.