The likelihood that the code developed naturally is one in three trillion, according to the researchers who discovered the match. This is another piece of evidence showing that the forced experimentation on human populations for the past two years was planned in advance. Moderna is one of the vaccine makers that was given the green light to bypass traditional safety standards in biologics research, to replicate the highly-profitable spike protein in humans.
Prior to the World Health Organization declaring a “global pandemic,” Moderna had already prepared an mRNA vaccine with instructions for replicating the spike protein in human cells. If this wasn’t suspicious enough, now there is a new trail of evidence that the spike protein was engineered by Moderna several years prior and was technically used as a vector to carry out genetic experiments and vaccine experiments on human populations.
The RNA of SARS-CoV-2 contains approximately 30,000 letters of genetic code. Nineteen letters of that genetic code are owned by Moderna. Twelve of the letters were discovered on the furin cleavage site and seven of the letters were found in the nucleotides nearby the furin cleavage site’s genome. SARS-CoV-2 is the first coronavirus to carry these 12 unique letters. These letters activate the furin enzyme, allowing the spike protein to readily spread to neighboring cells and infect humans.
Also noteworthy, this is the first time a coronavirus was discovered to have a furin cleavage site. The furin cleavage site is the part of the virus that binds to human cells and is activated along the spike protein thanks to its unique genetic code. While it’s true that only a certain number of genetic combinations can be contained in a furin cleavage site, why did a novel coronavirus present a furin cleavage site to begin with, and why were Moderna’s patented nucleotides found so close to the site that enhances transmission and infectivity of cells?
This patented sequence of concern is a snippet of the MSH3 gene, which affects damaged cells and their methods of repair. The researchers who matched the DNA believe the Moderna sequence could have been introduced to the SARS-CoV-2 genome by first infecting human cells that express the MSH3 gene. The invention is named, “Modified polynucleotides for the production of oncology-related proteins and peptides.” Apparently, this invention was a valuable part of coronavirus gain-of-function research.
According to the patent, this specific sequence is a pathway to learn how human cells respond to new cancer treatments. Gain-of-function research could be covertly carried out to create a new class of mRNA vaccines for coronaviruses, influenza, HIV and several other cancers. The development of this genetic sequence and the invention of these bioweapons could have been just a foot in the door to allow a new biotech industry to rise up and exploit human genetics.
The patent number for this sequence is US 9,587,003 B2, and the applicant is Moderna Therapeutics, Inc. The Inventors include 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, and Justin Guild.
Because their invention could not have realistically matched SARS-Cov-2 by chance, every single one of these inventors should be interrogated to uncover the intent and motivations behind their patent. How might it be used in bioweapons and vaccine research to exploit populations? A true investigation into the laboratory origins of SARS-CoV-2 would help unveil the predatory nature of these genetic and vaccine experiments and what this new trans-humanist, biotech industry is planning for the future.