Kevin McKernan Profile picture
Jul 14, 2021 35 tweets 12 min read Read on X
The Credibility Trap.
When you want things to be true, you are most exposed to getting burned.

Let's examine the David Martin video that is going viral and see if it passes a few sniff tests.
Here is his dossier.
f.hubspotusercontent10.net/hubfs/8079569/…
It makes two claims about collusion with the CDC and Ralph Baric.
1)CDC illegally patented the SARs virus
2)Ralph Baric locked up all research on the synthetic versions of these.

Let us look at the CDC patent. Image
CDC patent was filed in the US in 2003 before Myriad case law. This means Diamond vs Chakrabarty set the legal precedence and natural sequence was patent eligible under 35-US-101. This contradicts David’s claims.
Don’t believe me. You can look this up in the USPTO PAIR system.
Here is how you do it.

portal.uspto.gov/pair/ PublicPair
Plug in patent number 7,220,852
Click the Patent Number search option Image
You’ll get a page that looks like this. Navigate to the Image File Wrapper page to see the prosecution history Image
You’ll see the entire public patent prosecution online. Image
Navigate to the Applicant Remarks/Made in an Amendment link. You will see only 102 rejection. Not 101 rejections like David claims. These 102 rejections were easily traversed once the CDC demonstrated that the prior art used their sequence. Image
There was nothing illegal about this in 2003. I don’t even think it’s Illegal post Myriad as the claim language only claimed an “isolated nucleic acid”. Here is the patent: patentimages.storage.googleapis.com/6b/c3/21/a62eb…
Notice there is only 1 claim. This is common with defensive patents. Notice the language regarding an ‘isolated nucleic acid’. This language was key to the Myriad patents. Image
I’m familiar with this case law as I invented and published a method to navigate the Myriad patents. This was published in Nature Biotech.
nature.com/articles/nbt.2…
researchgate.net/publication/33… Image
The CDC filed in the US which was a 1st to file jurisdiction at the time. But they were beat to pub by Marco Marra in CA which is a 1st to invent juris. The patents were doomed to end up in interference which is why we have not seen the CDC try to enforce these. HKU also filed.
A really good read on this history is include below. law.unimelb.edu.au/__data/assets/…
I worked with Marco on the Human Genome Project. Stand up guy. He also agrees with the sentiments in our Nature paper. Natural sequence should not be patentable …BUT IT WAS! Image
So If Marco was first to invent but CDC beat them to filing, you have patent mess. Particularly when one inventor refuses to believe it is patentable. Image
So David’s claims regarding the CDC illegal patenting of the SARs genome are easily dismantled with public information. No 101 violations and even with Myriad case law, isolated nucleic acids likely fall under the Parke-Davis purification of adrenal/ Learned hand argument.
But this is a smoke grenade. Whether they are legal are not, doesn’t line up with his claims that they created a lock on the research in the field as a result of this.
Any researcher can order the SARs-CoV-2 genomic RNA or DNA from Biobanks like ATCC. Image
Nowhere on their product information or MTA does it mention CDC patents. This is usually where ATCC would remind the customers of additional licenses required for use of the product. No dice. Nothing. Zilch. Product Spec sheet attached.
atcc.org/api/pdf/produc…
Now let’s look at the other CDC patent related to qPCR detection of SARs1…not SARs2.
US Patent 7,776,521.
These are primers specific to SARs1. Image
The largest provider of CDC assays in the world is IDT.
It is customary for patent numbers to be exposed on the label of the products that utilize them.
I challenge anyone to find the CDC patent numbers on the PCR kits being used for C19 detection.
idtdna.com/pages/landing/…
IDT has sold over 62M of these tests. How is the CDC patent creating a lock on C19 investigation? Image
Next up is one of the Baric patents.
U.S. Patent 6,593,111
patentimages.storage.googleapis.com/a6/c6/8c/1d501… Image
This provides no lock on the market as it is easy to get around. Modular genetics also has tools to get around traditional restriction enzymes and ligases. Image
Here is one way around it. Image
I’m familiar with this space as we used tools like this to construct libraries for SOLiD sequencing.
Nick Translation End Repair was a key part of long mate pair libraries in SOLiD. The tool is also applied in synbio. patents.google.com/patent/US20100…
Finally, David makes some confused claims about DNA assembly giving you any virus you dream of. This is just non-sense and even if it were true with short read platforms like Illumina, ONT systems now deliver 30Kb reads and don’t require any DNA assembly.sciencedirect.com/science/articl… Image
I have not interrogated every aspect of his dossier. I have only interrogated sections where I am a subject matter expert. None of those details check out.
This is what many of us call a Credibility trap.
It sounds like a bomb to end the pandemic but it's really a bomb to kill your credibility by citing it. It looks like a classic honey pot. There are plenty of critiques to go around on Baric and the CDC but I try to only stick to ones I think will hold up in court.
I have this flipped. US was 1st to invent. Canada was 1st to File. Damn Twitter/edit function. US is not harmonized with 1st to file law.
@ThreadReader unroll
US is Now harmonized with 1st to file but in 2003 it was 1st to invent.
So patent interferences could occur. No one would engage in this expensive process if CDC was not enforcing these and left them as defensive patents.
This is an important 2013 ruling.
Note what Justice Thomas says about cDNAs.
How do you sequence a 29kb RNA virus without making a cDNA...
In 2003.. you don’t. You make a cDNA.
This is why there is no Ex parte re-exam on the patent and it’s still valid today. Image
A discussion on this topic with @Bretigne

podcasts.apple.com/us/podcast/wha…

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More from @Kevin_McKernan

Dec 11
Have a look at this. Image
Globin depletion will suppress the BNT162b2 signal. It has a known Beta Globin 5' UTR Image
Read 5 tweets
Dec 4
This is a dense read but it will help you to understand why the DNA fluorometer data is lighting up so much on modRNA. This is much more cross-talk than you see with traditional ssRNA.
That is because these are intercalating dyes that bind to minor grooves are only found in double stranded nucleic acids.
The fact that RNaseA is showing such a reduction in signal is because the RNA isnt single stranded.
At least half of it is digestable by a dsRNA specific nuclease known as RNaseIII.
Another portion responds to RNaseH which only digests RNA in RNA:DNA hybrids.
The fraction that responds to RNAseIII should worry you. Your cells have RNaseIII and its the start of the RNA interference pathway.
To make matters worse, Pharma is using an ELISA that is blind to dsRNA <400bp. It cant see this problem. And they know it exists
Read 7 tweets
Dec 3
This is worth a full read.
They really knocked it out of the park on this study.

publichealthpolicyjournal.com/biontech-rna-b…
First…
They measure how long is spike expressed in cells.
7 days out it is higher than day 1. Peaks at day 5. Image
Using 3 different Fluorometry methods they zero in on DNA levels before and after RNaseA treatments.
4-5X over once RNA is removed.
The AccuBlue dyes had the least cross talk. Image
Read 10 tweets
Nov 3
If there is one paper you should read this weekend…

This is it.

It’s not too thick.

journals.asm.org/doi/pdf/10.112…Image
I’ve posted on this before and have a stack about this if you want a TL/DR

They demonstrate research plasmids used to study the vaccine, infect lab staff and their housemates. Image
This triggered a fake casedemic as they all tested positive for Nucleocapsid on COVID tests.

What if this plasmid encoded something more inflammatory like spike?

These are shuttle vectors that can replicate in ecoli and mammalian cells.
They can leave the lab with employees and infect others.
Read 7 tweets
Oct 18
Your response to peoples request for your qPCR protocol is misinformation.
No transparency on your methods but we can already see that you are using only 1 assay in the vector (Kan gene) so you are under estimating the load 100X.

You should know this by now as Speicher et al published this a year ago.Image
@TGAgovau This is misinformation. Dr. David Speicher's latest test used RNaseA. There is no RNA interfering with the fluorometry.
Did you not even read the report?
Life must be good at the TGA when you can be a year behind all the time. Image
@TGAgovau Part of GMP and ISO is having your protocol open for inspection.

Rules for thee but not for me at the TGA.
Read 4 tweets
Oct 14
Is SV40 Large Tumor Antigen required for SV40 origin of replication activity.

No Image
Here we detect Pfizer plasmid DNA in a colon tumor biopsy 1 year after vaccination.

And its not small amounts of DNA. Its so much DNA that it can only be explained by plasmid amplification post vaccination or genome integration and amplification. Image
Variants are found in the SV40 Promoter that do not exist when you sequence the vaccine directly suggestive of replication errors once transfected into mammalian cells. Image
Read 8 tweets

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