If you are generally aware, the PCR test is used to amplify small amount of genetic material so as to recognize patterns of DNA by “cycling.” (Also, for RNA virus, the RNA is converted to DNA in order to be detected, it’s just the way the test works) This is how we have been able to recognize the genomes in Egyptian mummies and Wooly Mammoths. It works because if you amplify and cycle enough times to “grow” legitimate DNA fragments, you get something with with a fair amount of specificity. What is becoming more and more apparent is that the PCR test was not designed as a diagnostic tool for infection, and really cannot function as one without having a huge amount of false positives, period.
When it comes to COVID, the presence of viral particles picked up by the PCR technique does not and has not been quantitatively linked to an active “symptomatic” infection. It simply cannot be so, because infection threshold as a result of viral load is different for each patient. It turns out, if you “cycle” over around 25 times, the false positivity of COVID infection starts getting very high.
I and others have explained in blogs how people can be exposed to virus, and mount a simple innate immune response and never know any differently. When you test these people with very low viral loads, who are not sick, you can find the viral RNA code that is used to “diagnose” if you cycle enough times. The last I read, Labcorp cycles at least 40 times to detect viral genome fragments. The PCR test was never intended for diagnosis of infection but as a qualitative test for presence of parts of a virus genome. I know there has been some confusion circulating the net about what the inventor Kary Mullis had said about that. But we walk daily with people who have any number of parts of killer virus or bacterial genomes which one could pick up with a PCR test if one had the specific test for it. Would we claim that that individual was an infected patient? No!
PCR Test Designed For False Positive
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