Official Biochemical And Statistical Evidence Confirmed Moderna Created The C-19 Virus!

The Daily Mail shared an article showing that Moderna has patented the 19 base letter sequence, coding for the Furin Cleavage site in C-19.

They cited Scientists’ Paper from India, Switzerland, Italy, and the US, where the authors say that the chances of a 19 nucleotide sequence patented by Moderna naturally appearing in C-19 in circumstances where it doesn’t appear anywhere is 1 in 3 trillion.

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However, they failed to make a deduction therefrom. They investigated the RNA sequence for the Furin cleavage site in the C-19 Spike Protein to see it happened in nature.

The researchers picked the Furin Cleavage sequence because it’s the only continuous gene letter sequence in C-19 with more than three nucleotides. Also, the Furin Cleavage Site is crucial to the pathogenicity of C-19. If there’s some man-made gain of function included in the virus, this is where they can find it.

The Amino Acid sequence of the Furin cleavage site is PRRA. Every amino acid is coded by a Codon, having three nucleotides. The different genetic codes between C-19 and RaTG13 are at most one Codon long, one amino acid long, other than the Furin Cleavage Sequence: CCT CGG CGG GCA!

The researchers did a BLAST alignment search through every gene sequence in nature.

These are the results:

Table 1 shows that it does exist in the 5 US patents cited below…

US9149506B2: Modified polynucleotides encoding septin-4 –

Inventor: Tirtha Chakraborty, Antonin de Fougerolles
Current Assignee: ModernaTx Inc 

2012-04-02 Priority to US201261618953P
2013-12-16 Application filed by Moderna Therapeutics Inc
2014-05-22 Publication of US20140141067A1
2015-10-06 Publication of US9149506B2
2015-10-06 Application granted
2020-01-10 First worldwide family litigation filed

US9216205B2: Modified polynucleotides encoding granulysin –

Inventor: Tirtha Chakraborty, Antonin de Fougerolles
Current Assignee: ModernaTx Inc 

2012-04-02 Priority to US201261618873P
2013-12-16 Application filed by Moderna Therapeutics Inc
2014-04-24 Publication of US20140113960A1
2015-12-22 Publication of US9216205B2
2015-12-22 Application granted

US9255129B2: Modified polynucleotides encoding SIAH E3 ubiquitin protein ligase 1 –

Inventor: Tirtha Chakraborty, Antonin de Fougerolles
Current Assignee: ModernaTx Inc 

2012-04-02 Priority to US201261618868P
2013-12-16 Application filed by Moderna Therapeutics Inc
2014-05-22 Publication of US20140141068A1
2016-02-09 Application granted
2016-02-09 Publication of US9255129B2

US9301993B2: Modified polynucleotides encoding apoptosis inducing factor 1 –

Inventor: Tirtha Chakraborty, Antonin de Fougerolles
Current Assignee: ModernaTx Inc 

2012-04-02 Priority to US201261618957P
2013-12-16 Application filed by Moderna Therapeutics Inc
2014-04-17 Publication of US20140107189A1
2016-04-05 Application granted
2016-04-05 Publication of US9301993B2
2020-01-10 First worldwide family litigation filed

US9587003B2: Modified polynucleotides for the production of oncology-related proteins and peptides  – 

Inventor: Stephane Bancel, Tirtha Chakraborty, Antonin de Fougerolles, Sayda M. Elbashir, Matthias John, Atanu Roy, Susan Whoriskey, Kristy M. Wood, Paul Hatala, Jason P. Schrum, Kenechi Ejebe, Jeff Lynn Ellsworth, Justin Guild

Current Assignee: ModernaTx Inc 

2012-04-02 Priority to US201261618868P
2016-02-04 Application filed by ModernaTx Inc
2016-06-02 Publication of US20160152678A1
2017-03-07 Publication of US9587003B2
2017-03-07 Application granted”

Moderna applied for a patent for then 19 nucleotide sequences in 2013, on December 16.
Table2: Shows that the sequence occurs in Covid-19 from nucleotide 23601 to 23619.

Table3: Shows that this gene sequence does not exist in nature (but 14 nucleotide parts of it do).

Moderna applied for a Patent not only in the reverse complement of the 12 nucleotide Furin Cleavage Site in C-19 but on the 19 nucleotide sequence containing it as described previously.

Furthermore, they did not merely apply for a patent on 2016 February 4 with US9587003B2: as reported in the Daily Mail. They actually applied on 2013 December 16 for 4 patents with US9149506B2, US9216205B2, US9255129B2, US9301993B2:as well.

According to the Daily Exposed, Moderna had developed ‘’ the 19 nucleotide gene sequence containing the Furin Cleavage Site which gives Covid19 its infectivity to humans by a patented gain of function research as early as 2013, 6 years before the Wuhan outbreak took place. Not three as reported in the Mail and virally elsewhere…

So now we look at the chances of this occurring naturally. The paper calculates the probability of this particular 19 nucleotide sequence occurring randomly in a 30,000 nucleotide virus as

(30,000-18) x (1/4)19 = 1.09 x 10-7

Which is correct because there are 30,000-18 places to start the sequence, given that it needs a further 18 more letters to complete it. But there are actually 29,904 nucleotides in Wuhan HU1 (alpha). So a more accurate calculation would be

(29,904-18) x (1/4)19 = 1.087 x 10-7

Then they calculate the chances that the 19 nucleotide sequence occurs in the patented library of 24,712 sequences with a mean length of 3300 nucleotides. But that calculation is irrelevant because the sequence did not randomly appear in 5 Moderna Patent applications. The sequence was known to code for a Furin Cleavage Site, which is known to provide a gain of function to Coronaviruses.

It was put there deliberately and patented due to its infecting power in humans, which we shall see, later in the article, results from the normal viral Arginine (R) codon AGA (used in 45% of viral Arginine codons) being replaced by the human Arginine codon CGG (used in 0% of viral Arginine codons) in the furin cleavage site.’’

From that page you can enter the Sequence ID quoted in the paper as 11652 and get to which has the following at Nucleotides 2751-2733 reading backwards…

gccctgatca ccatcatggc ccagatcggc agctacgtgc ccgccgagga ggccaccatc     2760

CTACGTGCCCGCCGAGGAG patented by Moderna is the reverse compliment of CTCCTCGGCGGGCACGTAG, the 19 nucleotide sequence which appears in Covid-19 DNA from nucleotide 23601-23619 (which would therefore be covered by their patent).

Likewise you can search for the sequence in US9149506B2 by going to, whereupon you will find the same thing again

gccctgatca ccatcatggc ccagatcggc agctacgtgc ccgccgagga ggccaccatc     2760

I then searched the gene sequence of Wuhan Hu1 (alpha) at and found

23581 ttatcagact cagactaatt ctcctcggcg ggcacgtagt gtagctagtc aatccatcat from

Which has the 19 nucleotide sequence CTCCTCGGCGGGCACGTAG from 23601-23619 as described in table 3.

I then ran my own non aligned blast search of all patented gene sequences for the reverse compliment directly (or perhaps for a back handed compliment) and got the same results as the researchers

The nucleotides from Codons are triplets, so there are 64 possible triplets of the 4 DNA nucleotides ACGT. But, these triplets do occur—one in 72 million.

100% Biochemic Proof that Covid19 was Man-Made

The Double CGG Codon is used in the Moderna Specific Furin Cleavage site, and it doesn’t occur in nature.

Arginine can be encoded by any of the 6 triplets: AGG, AGA, CGA, CGC, CGG, CGT. In C-19, the furin site has 12 nucleotides, and the RR doublet of the furin site is encoded by CGG-CGG.

‘’ Two Biochemists Prof Antonio R. Romeu and Assistant Prof Enric Ollé analyzed the RR doublet from a large sample of furin cleavage sites of several kinds of viruses. They found that there were no RR doublets encoded by the CGG-CGG codons in any virus in nature. They observed that the AGA triplet was the majority codon involved in these viral RR doublets.’’ The Daily Expose reported.

In genetic recombination, the donor code is passed to the acceptor.

But there isn’t a virus with a Moderna Specific Furin Cleavage Sites that exist to donate a Moderna specific cleavage site to C-19.

We can conclude that the only way that this sequence could get into the C19 is from Moderna; it was the donor, not nature.

’ The Spanish Profs decided to analyze the arginine codon usage in every single protein in Covid-19. I found the following…
AGG (13%)
AGA (45%)
CGA (5%)
CGC (10%)
CGG (3%)
CGT (24%).

So the AGA codon triplet was the majority, and interestingly, CGG was the minority codon for Arginine in the virus.

But it gets worse still.

In the specific case of S protein, of the 42 Arginines (R) it has, 20 are encoded by AGA and only two by CGG. These 2, of course, are the two in the Moderna Specific Furin Cleavage Site.

So the only Arginine in the spike protein that is encoded a la Moderna are in the Furin Cleavage site. The other 40 instances do not use CGG at all.

They then go on to comment that each individual species in nature has its own codon preferences. Obviously, viruses like AGA do not like CGG at all in nature.

But guess which species does use CGG for Arginine more than the other five competing codons – yes, it’s jolly old homo sapiens. Our coding preferences for Arginine are

AGG (20%)
AGA (20%)
CGA (11%)
CGC (19%)
CGG (21%)
CGT (9%).

So the CGG codon in the furin cleavage site WILL have come about through Chimeric (human-animal combination) gain of function research.’’ The study shows.

Could Somebody other than Moderna have made Covid-19 using the Moderna Specific Furin Cleavage Site?

“New documents show that just 18 months before the first Covid-19 cases appeared, researchers had submitted plans to release skin-penetrating nanoparticles and aerosols containing “novel chimeric spike proteins” of bat coronaviruses into cave bats in Yunnan, China. They also planned to create chimeric viruses, genetically enhanced to infect humans more easily, and requested $14million from the Defense Advanced Research Projects Agency (Darpa) to fund the work.

Papers, confirmed as genuine by a former member of the Trump administration, show they were hoping to introduce “human-specific cleavage sites” to bat coronaviruses which would make it easier for the virus to enter human cells.

When Covid-19 was first genetically sequenced, scientists were puzzled about how the virus had evolved such a human-specific adaptation at the cleavage site on the spike protein, which is the reason it is so infectious.” – the Telegraph.

The Furin cleavage site itself is not patentable, having been known since at least 2004

US7223390B2: Insertion of furin protease cleavage sites in membrane proteins and uses thereof
2004-05-07 Application filed by Research Development Foundation
2004-11-11 Publication of US20040224391A1
2007-05-29 Application granted

Moderna could have patented the Moderna Specific encoding of the furin cleavage site, which wasn’t known in nature, not even today.

But, it’s a slab leak from Wuhan and the Chinese cover-up and given the Fauci denials exposed by Sen. Rand Paul, and given the NIH, NIAID cover-ups, and the US intelligence services cover-up, when the three-month-long report into the C-19 origin didn’t do anything.

It is the man that mixes up human and viral Arginine codons, not nature.

Prof Luc Montagnier spent the past years proving that the C-19 was artificially created and contained much of the HIV1 genetic code.

Before he died, he did a total analysis of the concept of C-19 natural development, showing that it had a massive equivalence to HIV.

There was no scientific basis to any of the fact-checking. They are globalist disinformation agencies and sons of Goebbels.

See this:

‘’ Since we have proven beyond a reasonable doubt (beyond a 1 in 72 million doubt statically and with 100% certainly biochemically from the Moderna Specific Furin Cleavage Site) that Moderna made Covid-19. And since Moderna and Fauci have not admitted to having made it and have, in fact, covered up evidence to that effect, it may be the case that they are hiding something else as well.

Because the only two theories now left are the accidental lab leak theory and the deliberate lab leak theory. I mean, the vast majority of political leaks are not accidents. They are deliberate strategies to provide an advantage to the leaker or his paymaster. It is well known in the IT industry that viruses appear when antivirus sales are needed. Why would things be any different with human viruses, now that they can be man-made too? Especially when you consider the massive role of Bill Gates and his foundation and GAVI and GVAP in the global vaccination business.’’

If you want to read more about this analysis, visit this page.

Daily Expose The Telegraph

Addison Wilson

A passionate teacher in English Language and Literature ready to give her best! Developing and implementing diverse curriculums covering a wide range of subjects. With my problem-solving skills, every job will be easily completed, so punctuation is my strength. Highly skilled at motivating students through positive encouragement and reinforcement of concepts via interactive classroom instruction and observation. My working style fits every personality type, so it makes me a great team player. I have completed numerous journalistic projects successfully, so digging for further information is my field. Fighter for freedom of speech! The truth must be revealed!

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