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> Our serological validation was chiefly limited by use of excess serum specimens from a mostly hospitalized population known to be very recently infected with SARS-CoV-2.

Basically, this test may not be as sensitive (or patients may not seroconvert as often) with mild or asymptomatic cases. To avoid this problem we should run a two-part study, the first part a PCR test of a large random sample, and the second part a follow-up to measure antibodies. Has anyone heard about a study of this kind that may be in progress?



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