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Frequently Asked Questions about Laboratory Testing and COVID-19

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www.cdc.gov

FDA has authorized EUAs for both viral and antibody tests for COVID-19. Viral (nucleic acid and antigen) tests are used to diagnose the presence of SARS-CoV-2 infections.

In contrast, antibody tests can detect IgG, IgA, and IgM antibodies from an immune response to SARS-CoV-2. Whenever possible, laboratories should rely on viral tests to diagnose the presence of SARS-CoV-2 infections.

However, a negative result from viral testing does not rule out COVID-19. Most of the PCR-based tests that use two or more targets are likely to have high specificity (few false positives).

However, there is some variation in the stated sensitivity of the different assays, and sensitivity is highly dependent on the stage of the disease.

Read more on cdc.gov
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