Firefliess and coffeeandcroissants,
I’d read that thread too. Really interesting, I didn’t know about what is being counted.
It basically says that although we are using the s-gene drop out from the PCR as a proxy for the new variant (the new variant uniquely has a deletion at 69/70 which means that sequence can’t be amplified), there are actually random drop outs all the time.
So just because there is an S-Gene drop out, it doesn’t necessarily mean it is the new variant.
We’re also only counting the single drop out as a proxy for the new variant , when in fact, it could also sometimes show as having the other genes drop out too.
However, if the random drop outs are truly random, then I would expect the effect to be the same on all variants.
I don’t know what we’ll do if another variant takes off here, we’re incredibly lucky the “U.K. -discovered variant” just so happens to have this property.
If I were Boris, I’d be spending massive amounts of money to extend our U.K. genomics sequencing capability right now.