I can assure you, the number of patients whose samples are genetically sequenced is tiny, contrasted against the number whose samples are simply run through the standard PCR.
So there is no way to know that the Delta variant now accounts for the majority of COVID cases in the US. And using the standard PCR, there is no way to know ANY specific patient has the Delta. It’s all fiction. We have this from the American Lung Association: “Regular COVID-19 tests do not detect which variant is involved in a patient’s case—that information does not change the approach to care or therapy. The variant identification requires genomic sequencing, a process separate from regular virus tests and one that not all labs are able to do or do not do on a routine basis for patient care but are done more for public health monitoring.”
Let me break down how this game works. To be excessively generous, let’s say that 3 out of every 1000 positive PCR tests in America are sent to high-level labs, where genetic sequencing is done.
A certain percentage of THOSE sequencing tests come up positive for the Delta Variant. Based on these results, MODELS are constructed. Now we’re REALLY into fake science. The models estimate what percentage of ALL positive PCR tests are really positive for Delta. I’m sorry to break this newsflash, but modelers are notorious charlatans. Their dense calculations are as far from science as a Model-T Ford is from a spaceship." There is more so read on. Bombshell: PCR tests can’t identify Delta Variant; it’s all fiction « Jon Rappoport's Blog (nomorefakenews.com)
CDC/FDA smoking gun of smoking guns.
They confess: they had no virus when they concocted the test for the virus; they “contrived” a model by pretending to find what they wanted to find; it’s called a self-fulfilling prophecy. This is the con and the crime that drove millions of lives, and economies, into ruin. The CDC has issued a document that bulges with devastating admissions. The release is titled, “07/21/2021: Lab Alert: Changes to CDC RT-PCR for SARS-CoV-2 Testing.” It begins explosively: “After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives.” Many people believe this means the CDC is giving up on the PCR test as a means of “detecting the virus.” The CDC isn’t saying that at all. They’re saying the PCR technology will continue to be used, but they’re replacing what the test is looking FOR with a better “reference sample.” A better marker. A better target. A better piece of RNA supposedly derived from SARS-CoV-2. CDC/FDA are confessing there has been a PROBLEM with the PCR test which has been used to detect the virus, starting in February of 2020—right up to this minute. In other words, the millions and millions of “COVID cases” based on the PCR test in use are all suspect. Actually, that statement is too generous. Every test result of every PCR test should be thrown out." [...]
Translation: We, at the CDC, did not have a specimen of the
SARS-CoV-2 virus when we concocted the PCR test for SARS-CoV-2. Yes,
it’s unbelievable, right? And that’s the test we’ve been using all
along. So we CONTRIVED samples of the virus. We fabricated. We lied. We
made up [invented] synthetic gene sequences and we SAID these sequences
HAD TO BE close to the sequence of SARS-CoV-2, without having the
faintest idea of what we were doing, because, again, we didn’t have an
actual specimen of the virus. We had no proof THERE WAS something called
SARS-CoV-2. This
amazing FDA document goes to say the Agency has granted emergency
approval to 59 different PCR tests since the beginning of the (fake)
pandemic. 59. And, “…it is not feasible to precisely compare the
performance of various tests that used contrived specimens because each
test validated performance using samples derived from different gene
specific, synthetic, or genomic nucleic acid sources.” There is more so
read on. CDC/FDA smoking gun of smoking guns « Jon Rappoport's Blog (nomorefakenews.com)
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