Genetics and anomalies

Is a Showdown Over the Insanity of Genetic Modification in Public Health Developing in Alberta?

The Outcome of Vaccine-Associated Viral Phenotype Selection Will Overrule the Effect of Vaccine-Associated Human Genome Editing.

mRNA Vaccines Actually are "Gene Therapy", Study Shows

Reckless "Gene Editing" with no Oversight is Very Dangerous

We are currently witnessing a major epidemic caused by the 2019 novel coronavirus (2019-nCoV). The evolution of 2019-nCoV remains elusive. We found 4 insertions in the spike glycoprotein (S) which are unique to the 2019-nCoV and are not present in other coronaviruses. Importantly, amino acid residues in all the 4 inserts have identity or similarity to those in the HIV-1 gp120 or HIV-1 Gag. Interestingly, despite the inserts being discontinuous on the primary amino acid sequence, 3D-modelling of the 2019-nCoV suggests that they converge to constitute the receptor binding site. The finding of 4 unique inserts in the 2019-nCoV, all of which have identity /similarity to amino acid residues in key structural proteins of HIV-1 is unlikely to be fortuitous in nature. This work provides yet unknown insights on 2019-nCoV and sheds light on the evolution and pathogenicity of this virus with important implications for diagnosis of this virus.

The "missing link" was there in Pradhan's paper all along, we just needed to ask the right question: "where are the genome sequences for the Gp-120 inserts"

Evidence has emerged which proves beyond a reasonable doubt that the pharmaceutical giant Moderna, the company that has made billions through the sale of an experimental Covid-19 injection, actuall…

Among numerous point mutation differences between the SARS-CoV-2 and the bat RaTG13 coronavirus, only the 12-nucleotide furin cleavage site (FCS) exceeds 3 nucleotides. A BLAST search revealed that a 19 nucleotide portion of the SARS-CoV-2 genome encompassing the furin cleavage site is a 100% complementary match to a codon-optimized proprietary sequence that is the reverse complement of the human mutS homolog (MSH3). The reverse complement sequence present in SARS-CoV-2 may occur randomly but other possibilities must be considered. Recombination in an intermediate host is an unlikely explanation. Single stranded RNA viruses such as SARS-CoV-2 utilize negative strand RNA templates in infected cells, which might lead through copy choice recombination with a negative sense SARS-CoV-2 RNA to the integration of the MSH3 negative strand, including the FCS, into the viral genome. In any case, the presence of the 19-nucleotide long RNA sequence including the FCS with 100% identity to the reverse complement of the MSH3 mRNA is highly unusual and requires further investigations.

The CDC has come up short again. This time, our attorneys simply asked it for “all documents relied upon” for its claims that the Pfizer and Moderna Covid shots do not affect a person’s genetic makeup.

The international team of researchers identified a tiny snippet of code that is identical to part of a genetic sequence patented by the US vaccine maker three years before the pandemic.

If I understood it, you can too

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. Thus, this study also serves for criminal charges and legal disputes against the Pfizer company for conducting genome experiments on humans.