So was Wakefield rightfully scrutinized and Drosten given a hall pass?
Many of the concerns raised about Wakefields qPCR are significant. But the one most cited (contamination) by Dr. Bustin was not.
He claimed Wakefield omitted an RT-Step.
Bustin is emulating this in 2020.
Wakefield is also nailed for Lack of an SOP.
Same story in the Drosten review.
The proper way to address DNA or RNA contamination is with DNases and RNases.
RT enzymes are active at RTemp and as the cycler ramps its temperature up to 95C.
#BustinBusted nature.com/articles/s4159…
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Bustin continues to push for limited to No RT step in qPCR.
Precisely what he persecuted Wakefield for…and was paid handsomely for the testimony he has since contradicted.
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This experiment clearly shows the mechanism of action that is at play and why the DNA is still in the vaccines and why the regulators are missing it.
@weldeiry @RetsefL @KUPERWASSERLAB @DrJBhattacharya @RobertKennedyJr @RWMaloneMD @MartyMakary
@JesslovesMJK
@CharlesRixey
@joerogan
It comes back to Sutton et al.
DNaseI cannot process RNA/DNA hybrids.
After you make RNA from DNA it will be hybridized to the DNA.
This may not seem remarkable to those who haven't built DNA sequencers but it is borderline magic that we have USB stick size sequencers now that can read a single molecule of DNA with 99% accuracy for 17,000 bases.
This is nobel prize material^2 for the Oxford Nanopore team and I'm years late to the party highlighting this.
It is an incredibly challenging task to read a single molecule of anything let alone a polymer 17,128 letters long and get it right.
A frame work for a new "Peer to Peer" peer review system using @primal_app and Bitcoin.
1)Turn your PDF into a PNG file
2)Post onto to Nostr via @primal_app
3)shasum -a 256 your PNG file.
4)Open datacarriersize=200B
5)Submit Primal/Nostr link + Sha256 Hash to Bitcoin through OP_RETURN via Mara SlipStream
If you don't want another Scamdemic foisted upon society, we need to decentralize peer review.
I went over this with @efenigson after my @BTCPrague keynote. rumble.com/v6wra1g--harm-…
@luijsterburglab @MaryanneDemasi @jeffreyatucker @TonyNikolic10 @ClareCraigPath @JesslovesMJK @dragonfishy @RWMaloneMD @weldeiry @Humanspective @DrEliDavid @kenjaques You are clueless to the fact that PolyA/T also hits RIGI and Pol3.
The proper control for Process 1 (PCR) vs Process 2 (Dam methylated) is what you have been shown but still can’t Grok.
@luijsterburglab @MaryanneDemasi @jeffreyatucker @TonyNikolic10 @ClareCraigPath @JesslovesMJK @dragonfishy @RWMaloneMD @weldeiry @Humanspective @DrEliDavid @kenjaques Note the asterisk and P values.
Still having a hard time?
@luijsterburglab @MaryanneDemasi @jeffreyatucker @TonyNikolic10 @ClareCraigPath @JesslovesMJK @dragonfishy @RWMaloneMD @weldeiry @Humanspective @DrEliDavid @kenjaques Other papers support this so pack it up.
You lost.
🔥New PrePrint out🔥
Hyper-stimulatory N⁶-methyladenine (m6A) in residual SV40 plasmid DNA in mRNA vaccines.
@RetsefL @weldeiry @RWMaloneMD @RobertKennedyJr @KMilhoanMDPhD
Oxford Nanopore Sequencing reveals Pfizer didnt use a Dam knock out E.coli strain and the resulting plasmid DNA contamination is hyper stimulatory to the cGAS-STING pathway. zenodo.org/records/172724…
Also evident in this data is that their plasmid linearization step is incomplete , thus running the risk of full length replication competent plasmid DNA being left in the vials.