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We received four Pfizer vaccines, and the one we sequenced is different from any previously analyzed. This may be an earlier version that Pfizer modified later. The vaccine contains a common plasmid used in coronavirus research, which raises questions about its origin. While Pfizer is the likely source, it's possible it leaked from a lab. We found similarities and differences in the components of the vaccines. The contamination hypothesis is unlikely since the plasmids have never been handled in our labs, and formalin fixation prevents spike protein production. Pfizer could have multiple undisclosed plasmids, which would be concerning, especially since we found one in a colon cancer sample that produces spike protein at high levels, indicating it could be replication competent and potentially transmissible. Transmissible cancer is a significant issue.

Every day, just the 1% of the cells of your DNA that gets replicated stretches from here to the sun four times. If you're to line it up end by end, that's very hard to conceptualize. But it should give you a little bit of humility before you go and start monkeying with it with these vaccines that can actually alter your DNA. And that's what I'm gonna show you. Is that the vaccines had a DNA contamination in them that didn't tell you about that could in fact alter your genome. Alright? These people are vibe coding your genome. And this is a major attack surface to the human gene pool because if this thing starts to alter the lifespan of people, it's going to part you with your Bitcoin. You're gonna end up spending money in a fiat system that has no controls, has no liability, and ends up oftentimes inducing mandates to get what it wants done. Many people had have peer have gone and replicated this work. It happened on Twitter. It did not happen very quickly in the peer review system. The peer review system kinda kicked it out. Some of these papers have now been peer reviewed, but it took years for them to come to this conclusion. Now, the FDA, the EMA and the TGA have all admitted that this mistake has happened. How did it happen? There's a big bait and switch. Pfizer actually ran the trial of 22,000 people on the process on the left and after they got to the trial, they then switched to the process on the right and didn't retrial the drug. And in doing so, they left a tremendous amount of excess DNA behind in the product. So all of the vaccine efficiency numbers you've heard in the news are flawed. They're not real because that's not what actually went into the trial. What went to the public was actually something that came out of this process too. It's published now in the BMJ that this fraud happened and no one has yet been prosecuted for it. So what did they leave in there? What they left in there was something we know from the polio scandal. If you're not familiar with the polio scandal, that polio vaccines were also contaminated with something known as SV40 and it created a massive cancer wave. Now the whole virus isn't in these vaccines, but there is a very curious part of this called the SV40 region that Pfizer intentionally removed from the disclosure that they gave to the FDA. So the FDA has admitted that this SV40 material is in there. They did not spell this out to the regulators. The regulators did not find them and they're actually running cover for them saying this DNA is too little consequence to matter, it's too small, and it's not functional. But we know it's functional because Dean et al has published that this piece of DNA drives DNA straight to the nucleus. It gets used in gene therapy vectors.

Pfizer conducted trials using a synthetic PCR process called Process 1, which involved giving 40,000 people a deliberately engineered mRNA sequence for the shots. However, for mass production, a second process was used, tested on only 252 people. This involved using a complementary DNA sequence to make the body produce the spike protein. Essentially, the trials were conducted using a controlled synthetic process, but the majority of the vaccines administered to billions of people used a less tested method. This can be seen as a bait and switch.

The presence of DNA plasmids and undisclosed proteins in the Pfizer COVID-19 vaccine has raised concerns. The DNA plasmids, originating from E. Coli, were not properly removed during manufacturing, resulting in contamination. Additionally, two proteins from the simian virus 40 (SV40) were found in the vaccine, which is associated with certain cancers. SV40 was present in polio vaccines administered to millions of Americans in the past. Injecting these proteins and DNA into the body can potentially lead to mutations and increased risk of cancer. This discovery suggests a higher chance of mutation from the Pfizer COVID-19 vaccine.

Pfizer conducted trials using a synthetic PCR process called Process 1, which involved giving 40,000 people a precise mRNA sequence for the shots. However, for mass production, a second process was used, tested on only 252 people. This involved using a complementary DNA sequence to make the body produce the spike protein. Essentially, the trials were done using a controlled synthetic process, but the majority of the vaccines given to billions of people were made using a less tested method. This can be seen as a bait and switch.

Many are surprised to learn that the vaccines did not undergo traditional clinical trials. Initially, they were manufactured using PCR for 44,000 people, but when scaling up, the process was deemed too costly and was replaced with DNA from E. Coli, which also introduced endotoxins. In pharmaceutical manufacturing, the process is crucial; changing it typically requires new trials. The EMA requested a new trial with 252 patients, but the data was never provided, and it was considered too late since vaccinations had already begun. Thus, the rationale for conducting the trial became irrelevant.

Pfizer conducted trials using a synthetic PCR process called Process 1, which involved giving 40,000 people a deliberately engineered mRNA sequence for the shots. However, for mass production, a second process was used, tested on only 252 people. This involved using a complementary DNA sequence to make the body produce the spike protein. Essentially, the trials were conducted using a controlled synthetic process, but the majority of the vaccines administered to billions of people used a less tested method. This can be seen as a bait and switch.

When COVID-19 vaccines were sequenced, commercial annotation software highlighted functional parts of the plasmids, including antibiotic resistance genes and SV40 components. The speaker claims that Pfizer had to manually remove these annotations before submitting the plasmid map to regulators. According to the speaker, regulators received the DNA sequence, but the sponsor is obligated to annotate every open reading frame and promoter, even if their function is unknown. The speaker alleges that Pfizer intentionally removed annotations, hiding them from the FDA, which the speaker believes is a violation of guidelines. The speaker suggests the reason for hiding SV40 components is due to SV40 virus contamination in polio vaccines and its debated link to cancer. The speaker asserts that while epidemiological data is confounded by vaccine shedding, laboratory studies show SV40 is a potent oncogenic virus. The speaker claims that the vaccines contain some of the more carcinogenic components of that virus, and that these sequences are functional and have consequences.

Kevin McKernan, a genomics expert, discusses the contamination found in mRNA vaccines. He explains that the vaccines on the market differ from those used in clinical trials, with different levels of contamination. The contamination includes plasmid and bacterial DNA, as well as lipopolysaccharides, which can cause adverse reactions. McKernan reveals that certain functional DNA components were intentionally omitted from the plasmid map submitted to regulators. He emphasizes that the vaccines contain a significant amount of contaminating DNA, which is not easily degraded due to its encapsulation in lipid nanoparticles. McKernan's findings have been replicated by various researchers, highlighting the need for further investigation into the potential risks associated with this contamination.

Many labs, including Medicinal Genomics, found DNA contamination in Pfizer and Moderna mRNA vaccines. Regulators like the FDA and EMA admitted to this, but downplayed its significance. The SP 40 sequences omitted by Pfizer are crucial. DNA contamination can cause insertional mutagenesis, as stated in Moderna's patents. Regulatory agencies were deceived and failed to properly address the issue. This poses a serious risk that cannot be ignored.

- The mRNA on plasmids was produced, and after processing, much DNA from plasmids remained; Kevin MacKinnon found that vials were full of plasmid DNA, the whole plasmid and parts of it, and this was published. Authorities claimed it doesn’t matter and that vaccines have saved millions of lives, so why not have some DNA in them. - The DNA in the vaccine vials was packaged in lipid nanoparticles and was shown by colleagues last year (the INMODIA publication) to enter human cells in culture and remain stable in cells for days, as did the mRNA. Despite this, the message given was to poof, never mind, don’t worry, be happy. - A radical change occurred due to a discovery by Kevin MacKinnon three weeks ago: during transcription on the chromosome, byproducts are generated; some mRNA strands do not detach from the DNA where they’re formed, creating hybrids of DNA and RNA that come off together. These hybrids are dangerous. - In cells, an enzyme called RNase H takes care of these sparks and extinguishes them immediately; otherwise they can cause damage to the chromosome, potentially lighting “fires” on the chromosomes. If not extinguished, the fires can cause diverse damage depending on where they occur, potentially leading to illnesses described in medical textbooks, including tumors (neoplastic disease), autoimmune disease, developmental impairment, birth defects, or death. - The speaker asserts these hybrids and their mishandling could lead to a broad range of illnesses, and emphasizes that this situation is not limited to the COVID vaccine but applies to all Moderna RNA vaccines, including new Moderna RNA vaccines entering the market, such as a flu vaccine, and mentions veterinary RNA vaccines as well. - The claim is made that these vaccines will be heavily contaminated with deadly dangerous hybrids, and it is the duty of authorities and controlling authorities to stop proceeding and not turn away; otherwise they will face court for not fulfilling their duties. The speaker has been giving interviews and asserts this narrative is spreading worldwide, framing it as akin to attempted murder and urging physicians to refuse vaccination.

Kevin McKernan, an experienced genomic expert, discusses his findings regarding mRNA vaccines. He discovered that the expression vectors for the vaccines, which are used to produce the spike protein, are still present in the vials. These vectors exceed the guidelines set by the EMA and FDA. McKernan explains the two different processes used in the clinical trials and how residual plasmids from E. coli amplification remain in the vaccines. He specifically highlights the presence of the SV40 promoter in Pfizer vaccines, which was not disclosed to the regulatory agencies. McKernan's team conducted quantitative PCR assays and found high levels of vector DNA in the vials. He emphasizes the importance of understanding the potential risks associated with this contamination and encourages others to replicate his work.

The amount of DNA allowed in vaccines was loosened a thousandfold after liability waivers were granted. These limits assumed naked DNA injection, which degrades quickly. However, mRNA vaccines use lipid nanoparticles (LNPs) that also coat contaminating DNA, invalidating the old limits. Studies show DNA levels in the shots are 10 to 100 times higher than the already obsolete limits. The LNPs deliver this DNA directly into cells, changing its persistence and biological impact. Pfizer used a different, more purified product in its trials than what was injected into billions of people. The initial process included a PCR amplification step to reduce DNA background, but this was dropped for mass production due to cost. This resulted in higher levels of background plasmid DNA and potentially E. coli components like endotoxin in the shots, possibly causing anaphylactic reactions. The presence of plasmids has been confirmed, and this process change, documented in the BMJ, is a major violation of manufacturing standards. The EMA requested a new trial after the process change, but the data was never delivered, rendering the original trial data irrelevant.

In this video, the speakers discuss the omission of the SV40 promoter sequence in the plasmid used in vaccines. They highlight that the plasmid was annotated with various details except for the SV40 region, which is active in a million cells. Health Canada stated that sponsors should identify any biologically functional DNA, such as the SV40 enhancer, during submission. However, Pfizer did not specifically identify the SV40 sequence. The speakers explain that the plasmid map provided by Pfizer did not include annotations for the SV40 region or the F1 origin. They speculate that this omission was intentional and not a simple oversight. The speakers also mention the use of SnapGene software for plasmid annotation.

Pfizer's use of the RiboGreen technique to measure DNA in their vaccines has raised concerns about deceptive practices. The presence of billions of DNA fragments in each dose, some of which are small and more likely to integrate into the genome, is worrying. Preliminary data suggests a correlation between adverse events and contaminated Pfizer vaccines, but more research is needed. The DNA in the vaccines is different from previous contamination and carries a higher risk of integration. The FDA acknowledges the integration risk and the need for lower limits on DNA when copy numbers are high. The DNA is encapsulated in lipid nanoparticles, making it prothrombotic and potentially oncogenic. The presence of endotoxin and the spike protein in the vaccines further complicates the situation. The vaccines have been found in various tissues and can lead to prolonged expression of the spike protein. Insertional mutagenesis and cancer risk are concerns, especially for individuals with weakened immune systems. Regulatory bodies have confirmed the presence of the SV40 sequence in the vaccines, but the clinical implications are still unclear.

"Pfizer vaccine is contaminated with plasma DNA. It's not just mRNA." "This DNA is the DNA vector that was used as the template for the in vitro transcription reaction when they made the mRNA." "I sequenced it in my own lab." "The vials of Pfizer vaccine that were given out here in Colombia, one of my colleagues was in charge of that vaccination program in the College of Pharmacy." "And for reasons that I still don't understand, he kept every single vial." "So he had a whole freezer full of the empty vials." "And I checked these two batches, and I checked them by sequencing." "It's surprising that there's any DNA in there." "This DNA, in my view, it could be causing some of the rare but serious side effects like death from cardiac arrest."

A peer-reviewed paper confirms Pfizer's mRNA vaccine is contaminated with dangerous DNA and SV40 enhancers. During production, bacterial plasmid DNA led to contamination with spike protein genes, antibiotic resistance markers, and SV40 enhancers. Researchers found four to five times more DNA than the safe limit; these DNA fragments could integrate into the human genome due to the SV40 enhancer. Experiments showed the vaccines were toxic to cells, causing pathological changes and spike protein production, potentially spreading body-wide via exosomes. The DNA contamination, tucked into lipid nanoparticles, could lead to unintended gene therapy. The SV40 enhancer, deliberately added but removed from regulatory paperwork, raises questions about Pfizer's intentions. Experts theorize this contamination could be linked to an increase in "turbo cancers," coinciding with Pfizer's acquisition of a cancer drugmaker. An epidemiologist noted the study found DNA from the manufacturing process way over regulatory limits, including the cancer-promoting SV40 promoter enhancer and spike-producing DNA. A separate study found vaccine spike protein expressed in cerebral arteries of stroke patients for up to seventeen months, potentially contributing to autoimmune responses. There are now 11 independent reports that have found, DNA contamination within these shots of up to 60000% above regulatory limits.

Pfizer and Moderna used two processes to create their vaccines. Initially, they used PCR to amplify and create the DNA for clinical trials. However, when they received approval, they needed to produce billions of copies, so they used circular bacterial DNA plasmids. Unfortunately, this led to contamination with junk DNA. Researchers in Ontario, Canada tested 27 mRNA vials from 12 different lots and found billions to hundreds of billions of DNA molecules per dose, exceeding FDA and WHO guidelines by 188 to 509 times. This is a significant amount, far beyond what is considered acceptable.

There is significant DNA contamination found in vaccines, with evidence from multiple researchers in Germany, Japan, and the U.S. Regulatory bodies like the FDA and EMA acknowledge this contamination but downplay its significance, relying on Pfizer's assurances. The clinical trials used cleaner DNA, but the mass-produced vaccines did not undergo the same purification, leading to increased background DNA and endotoxin levels. Regulators received a plasmid map missing crucial annotations, suggesting manipulation. Claims about expired vials and PCR methods used to measure contamination have been challenged, with evidence showing that Moderna's vaccines are cleaner. Regulators are allowing different measurement standards for RNA and DNA, raising concerns about transparency and integrity in the regulatory process.

The Pfizer vaccine contains not only mRNA but also plasma DNA from the vector used in its production. I sequenced samples from two batches of the vaccine in Colombia and found this DNA, which raises concerns about potential health risks. This DNA could integrate into the genomic DNA of cells, leading to permanent changes. Such integration poses theoretical risks, including autoimmune responses and cancer, depending on where the DNA inserts itself in the genome. While these risks may be rare, they warrant investigation to understand their implications better.

Pfizer and Moderna vaccines use two processes. The first process involves using PCR to amplify and create DNA for clinical trials. Once approved, they use circular bacterial DNA plasmid to replicate billions of mRNA DNA sample copies. However, this resulted in contaminated vaccines with junk DNA. A study found DNA fragments in Pfizer and Moderna vaccines in Ontario, Canada. Researchers tested 27 mRNA vials from 12 different lots and discovered billions to 100 billions of DNA molecules per dose, exceeding FDA and WHO guidelines by 188 to 509 times. This is a significant amount, far beyond what is acceptable.

Kevin discovered that the vials used for vaccines are contaminated with bacterial DNA. This is concerning because the modified RNA used in these vaccines creates unusual genetic structures that don't occur naturally. Normally, DNA is in a double helix form, but with modified RNA, there are three strands attached to the DNA. The enzyme used to remove DNA, called DNase, cannot digest these triple-stranded genetic constructs, resulting in DNA contamination in the shots. Pfizer and Moderna should have addressed this issue during the manufacturing process by using different enzymes. This shows that assumptions cannot be made when working with new, unnatural products. The DNA used to manufacture the modified RNA was not properly removed, leading to multiple scary aspects of contamination.

The Pfizer vaccine is contaminated with plasma DNA, not just mRNA. This DNA is the DNA vector used as the template for the in vitro transcription reaction. This was discovered by sequencing vials of Pfizer vaccine from Colombia. It's surprising that there's any DNA in there. The speaker is alarmed about the possible consequences of this, including rare but serious side effects like death from cardiac arrest. Mixing DNA with a lipid complex allows it to enter cells and become a permanent fixture. This is a real hazard for genome modification of long-lived somatic cells, like stem cells, and could cause a sustained autoimmune attack. There is also a very real theoretical risk of future cancer in some people. The risk is not zero and it may be high enough that we ought to figure out if this is happening or not.

Pfizer has been forced to release previously secret documents, including FDA approval packages, due to court orders and successful FOIA requests. These documents reveal that Pfizer tested different versions of their vaccine during preclinical and clinical trials, which goes against FDA guidance. The different versions included modified RNA, unmodified RNA, self-amplifying RNA, and Spike protein alone. Surprisingly, all these versions were tested under the same investigational new drug number, despite FDA guidance stating that multiple versions should have their own individual numbers. Additionally, the toxicity of the mRNA active ingredient in the COVID-19 vaccines was never studied. This raises concerns about the regulatory process and the lack of safety testing.

Kevin discovered that the vials used for vaccines are contaminated with bacterial DNA. This is concerning because the modified RNA used in these vaccines creates unusual genetic structures that don't occur naturally. Normally, DNA is in a double helix form, but with modified RNA, it forms triple strands that can't be easily removed with DNase. This contamination is a result of corners being cut during the manufacturing process. Enzymes that could have eliminated the DNA were not used. This shows that assumptions cannot be made when working with new, unnatural products. The DNA contamination comes from using it to manufacture the modified RNAs.