The CRISPR CAS9 Technology is a genome-editing technique that has been used by Scientists to alterate the genome in a population. The synthetic alteration of a Wildtype population is called Gene Drive. Thus, an mRNA can be engineered that contains the genetic information for the altered gene, the information for the CAS9 enzyme and a guided RNA (gRNA) that tells the CAS9 enzyme, where to cut and paste the altered gene sequence into the human genome. After the mRNA has been injected into human cells, the information on the mRNA will be translated into a CRISPR CAS9 enzyme complex.
The aim of this study was to analyze the Cominarty mRNA for CRISPR-CAS9 gene-editing technology, which would explain the failure in the SARS CoV-2 virus immunization and the increase in fatal side effects after vaccination.
Fragmented SARS CoV-2 spike protein sequences in the mRNA mask the real intention behind the Cominarty vaccine, which is the manipulation of the human genome at Chromosome 5 and Chromosome 19 as part of a human gene drive experiment. The study found three gRNAs at the plus strand with cleavage sites for the CAS enzyme 9 and 12a. The gRNAs with corresponding gRNA IDs from the BLAST database harbor genes of the human reference genome GRCh38 on Chromosome 5 and Chromosome 19.
The Cominarty vaccine intend to create a desired human race using digital calculations and computer predictions. Such computer-predicted perfect gene sequences have now emerged in the Cominarty mRNA vaccine.
https://zenodo.org/record/6210570
