Evaluation of the EasyNAT SARS-CoV-2 assay PCR test for the diagnosis of SARS-CoV-2 infection

Author:

Fernández-Sánchez Fernando,Martín-Bautista Elena,Rivas-Ruiz Francisco,Wu Winnie,García-Aranda Marilina

Funder

Innovative Medicines Initiative

European Federation of Pharmaceutical Industries and Associations

Horizon 2020 Framework Programme

European Social Fund Plus

Publisher

Elsevier BV

Reference25 articles.

1. Administration, Fa.D., Xpert® Xpress SARS-CoV-2 Instructions for Use For Use Under an Emergency Use Authorization (EUA) Only. 2022: fda.gov.

2. The rapid antigen detection test for SARS-CoV-2 underestimates the identification of COVID-19 positive cases and compromises the diagnosis of the SARS-CoV-2 (K417N/T, E484K, and N501Y) variants;Barrera-Avalos;Front. Public Health,2022

3. Evaluation of Xpert® MTB/RIF and Ustar EasyNAT™ TB IAD for diagnosis of tuberculous lymphadenitis of children in Tanzania: a prospective descriptive study;Bholla;BMC Infect. Dis.,2016

4. Evaluation of the analytical performance of the 15-minute point-of-care DASH™ SARS-CoV-2 RT-qPCR test;Butzler;Diagn. Microbiol. Infect. Dis.,2023

5. Recommendations for use of antigenic tests in the diagnosis of acute SARS-CoV-2 infection in the second pandemic wave: attitude in different clinical settings;Candel;Rev. Española De. Quimioter.,2020

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