Here is a basic question: how are the sensitivity and specificity (false negative and false positive rates, IIRC) of these tests determined?
It seems like a learning problem with noisy labels. Does anyone know what they do in practice? Especially chaotic situations like this where there aren't reference tests? Are there reference positive and negative samples?
One concern also referenced for the Stanford study was that, as mentioned in a USC popular writeup on this study linked elsewhere on this post,
> Premier Biotech, the manufacturer of the test that USC and L.A. County are using, tested blood from COVID-19-positive patients with a 90 to 95% accuracy rate.
They must be factoring this into the 2-5% infection rate number somewhere?