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Canada Builds Live SARS-CoV-2 Viruses From Computer Code Alone That ‘Can Be Used For Gain-of-Function Research’: Journal ‘Viruses’


A closed pandemic loop of digital design, synthetic GOF viruses, and government-controlled verification.

A new peer-reviewed study published in the journal Viruses says that publicly funded Canadian laboratories digitally designed full-length SARS-CoV-2 genomes, chemically synthesized them using commercial services, and generated live, replication-competent coronaviruses without starting from a natural virus sample.

The paper, titled “Developing Synthetic Full-Length SARS-CoV-2 cDNAs and Reporter Viruses for High-Throughput Antiviral Drug Screening,” documents the alleged creation of infectious Delta and Omicron SARS-CoV-2 viruses from computer-designed genetic sequences alone.

Coming in the wake of the COVID-19 pandemic—which killed millions of people worldwide and was linked by multiple intelligence agencies to laboratory research—the study raises national security concerns about the ability of government-funded institutions to create replication-competent pandemic viruses from digital sequence data alone, using commercial infrastructure with limited public oversight.

In light of these capabilities, the study also raises the possibility that governments could define, simulate, and respond to a biological threat almost entirely within digital and laboratory frameworks—leaving the public reliant on official interpretation rather than independently observable evidence.

Viruses Built from Computer Code Alone

The authors state that they did not rely on physical viral isolates to create the viruses.

Instead, they used commercial DNA synthesis services to generate the entire coronavirus genome:

“We opted to use cDNA chemical synthesis services to generate full-length wild-type and reporter Delta and Omicron clones.”

They further explain:

“DNA synthesis is a viable method to rapidly generate coronavirus cDNAs and recombinant viruses.”

Those synthesized genomes were then said to be used to generate live viruses:

“Clone-derived Delta and Omicron wild-type and reporter viruses were successfully rescued and showed replication kinetics comparable to patient-derived isolates.”

The study claims that the resulting viruses were infectious and capable of sustained replication in cell culture.

The paper emphasizes that the same system can be used to generate new viral variants based solely on sequence data:

“DNA synthesis is a viable and rapid option to generate reverse genetic systems for wild-type and reporter viruses using sequence information alone.”

Acknowledged Gain-of-Function Capability

In the Discussion section, the authors explicitly acknowledge that the methodology they used qualifies as gain-of-function (GOF) capable research:

“It is important to acknowledge that the novel approach described in this study—generating replication-competent viruses from synthetic DNA while introducing heterogeneous gene functions—can be used for ‘gain-of-function’ research.”

Where the Viruses Were Said to Be Created

All work involving purportedly live SARS-CoV-2 was conducted in Canada at a high-containment facility:

“All the experiments involving infectious SARS-CoV-2 viruses were conducted at VIDO-InterVac in an approved Biosafety containment level 3 (BSL3) laboratory.”

VIDO-InterVac is part of the University of Saskatchewan, which is a central institutional hub for the research described in the paper.

Author Affiliations

The authors are affiliated with multiple Canadian institutions, including:

  • University of Saskatchewan (Department of Biochemistry, Microbiology, and Immunology; Vaccine and Infectious Disease Organization),
  • University of Alberta (Department of Cell Biology; Department of Medical Microbiology & Immunology; Li Ka Shing Institute of Virology),
  • Sunnybrook Research Institute (Toronto),
  • University of Toronto (Department of Laboratory Medicine and Pathobiology).

Public Funding Sources

The research was funded entirely through public Canadian funding, according to the paper’s funding disclosure:

“This research was funded by the Canadian Institutes of Health Research (CIHR)-funded Coronavirus Variants Rapid Response Network (CoVaRR-Net)… CIHR Operating COVID-19 Rapid Research Funding Opportunity—Therapeutics… and NSERC.”

Additional operational support came from:

“The Government of Saskatchewan… the Government of Canada through Prairies Economic Development Canada… and the Canada Foundation for Innovation Major Science Initiatives for its CL3 facility.”

What the Paper Establishes

The study documents, in the authors’ words, that:

  • Full-length SARS-CoV-2 genomes were digitally designed
  • Those genomes were chemically synthesized
  • Live, replication-competent coronaviruses were said to be generated from that synthetic DNA
  • The method is acknowledged to be usable for gain-of-function research
  • The work was publicly funded and conducted in Canadian government-supported laboratories

These facts are stated directly in the paper and do not rely on inference, speculation, or external interpretation.

Bottom Line

The new Viruses paper reveals that governments claim to possess the technical ability to define a virus digitally, synthesize it physically, and validate its behavior entirely within controlled laboratory systems—allowing modern pandemic response to operate almost entirely inside digital, synthetic, and laboratory environments.

That convergence raises unresolved questions about national security, transparency, independent verification, and how much trust the public is asked to place in closed scientific and governmental frameworks when responding to future biological threats.

The study aligns with earlier FOIA-released DARPA documents showing that U.S. biodefense systems were already built to synthesize viruses and manufacture mRNA countermeasures from sequence data alone, placing the Canadian work within a broader pre-existing digital pandemic infrastructure.

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WHO VigiAccess Lists 5.8 Million COVID-19 Vaccine Adverse Event Reports


World Health Organization data show system-wide adverse event reports spanning neurological, cardiac, immune, gastrointestinal, and reproductive categories.

The World Health Organization’s VigiAccess pharmacovigilance database currently lists 5,811,685 individual adverse drug reaction (ADR) reports associated with COVID-19 vaccines as an active ingredient.

A Harvard Pilgrim Healthcare/HHS study confirms fewer than 1% of vaccine adverse events are reported, meaning the number could be closer to half a billion.

These reports are submitted by national drug regulators worldwide and categorized by affected body system.

Below is the full numerical breakdown exactly as listed in the database.

Reported Potential Side Effects by System Category

  • General disorders and administration site conditions
    3,435,222 reports (26%)
  • Nervous system disorders
    2,162,680 reports (16%)
  • Gastrointestinal disorders
    969,611 reports (7%)
  • Investigations (laboratory abnormalities, diagnostic findings)
    807,850 reports (6%)
  • Infections and infestations
    660,107 reports (5%)
  • Respiratory, thoracic, and mediastinal disorders
    559,163 reports (4%)
  • Skin and subcutaneous tissue disorders
    643,195 reports (5%)
  • Injury, poisoning, and procedural complications
    373,950 reports (3%)
  • Cardiac disorders
    334,064 reports (3%)
  • Psychiatric disorders
    253,443 reports (2%)
  • Blood and lymphatic system disorders
    240,517 reports (2%)
  • Vascular disorders
    245,846 reports (2%)
  • Reproductive system and breast disorders
    280,795 reports (2%)
  • Musculoskeletal and connective tissue disorders
    1,419,363 reports (11%)
  • Immune system disorders
    123,050 reports (1%)
  • Surgical and medical procedures
    121,374 reports (1%)
  • Metabolism and nutrition disorders
    103,797 reports (1%)
  • Eye disorders
    172,469 reports (1%)
  • Ear and labyrinth disorders
    153,026 reports (1%)

Lower-Frequency Categories Still Numerically Significant

  • Renal and urinary disorders
    47,767 reports
  • Endocrine disorders
    13,403 reports
  • Hepatobiliary disorders
    13,323 reports
  • Pregnancy, puerperium, and perinatal conditions
    14,180 reports
  • Congenital, familial, and genetic disorders
    4,533 reports
  • Neoplasms (benign, malignant, unspecified)
    17,770 reports
  • Product issues
    10,919 reports
  • Social circumstances
    47,909 reports

These figures represent submissions from national health authorities participating in the WHO’s global drug-safety monitoring program.

As of March 2025, 182 health authorities (national pharmacovigilance centers) participate in the WHO Program for International Drug Monitoring.

Each report may include multiple symptoms, meaning totals by category exceed the number of individual reports.

The scale and system-wide distribution of these reports are unprecedented for a single pharmaceutical product class in the VigiBase system.

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Would You Care for a Stroke with That Jab, Sir or Madam?


Here is Part 2 of the must-read examination of clean data revealing very dirty deeds.

Yes, sometimes young people have strokes. Sometimes they get cancer. Mostly they don’t. And when well-established population incidence of something such as ALS or stroke or infertility or cancer or lupus, etc., suddenly shoots up, there is always a cause. It is the work of epidemiology, forensics, pathology and similar to look at the pattern and find the cause so it can be remedied.

If, that is, there is any real desire to fix the problem. When the problem is that there is a concerted effort to cause, not fix, the problem because the problem is seen, by someone at the controls, as the solution to some other problem, well, Houston, we most certainly do have a problem.

Here is Aussie 17’s remarkable Part 2 which was promised:

PharmaFiles by Aussie17

The Jab That Keeps on Giving: Part 2. Stroke drug skyrockets 200%!

Before proceeding with this article, it is strongly recommended reading Part 1 first.

Bioweapons, like the ones disguised as mRNA jabs, for example, are designed to maim and kill. Otherwise, they are not effective. They are designed to cloak their presence and impact in mystery. Otherwise, they are not safe for those who made and deployed them. So, yes, the jabs are safe and effective, in those terms, but most certainly not safe and effective as health measures.

Depopulation of a hardy and resilient species with a lot of members living under widely divergent situations takes a LOT of effort and generates a LOT of money.

A LOT of money.

Sicker populations are easier to control and easier to finish off. Sicker populations do not mount effective resistances, or not for long. Sicker populations are more obedient to orders directing and deflecting them.
And sicker populations generate massive wealth before being disposed of.
Pandemic? Chronic illness? What’s not to love, at least if you are a psychopathic predator, serving at the whim of the central parasite, the UN/globalist parasite, that is

Get out of the United Nations, yes, but that action means nothing unless the parasitic, and deadly, regulations, programs, policies, protocols, guidelines, etc., infesting every part of our public and civic lives are extracted, examined and either replaced with ones that support and follow Constitutional law or just discarded if they are, in fact, unnecessary.

You know, like a government of the people, by the people and for the people instead of one that is of the controllagarchs, by the billionaires and for the destructocrats.

Visit PreventGenocide2030,org to learn more and mobilize.

Frankly, we are at the Detox or Die stage, as unpleasant a thought as that might be. We are being killed and, if we leave the parasite in place, that can only accelerate. There really is no option.

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mRNA Jabs: The Deadly Gift That Keeps On Giving


No one who understands the politics of ‘the science’ trusts it or will allow a gene therapy bioweapon into their bodies or of those they love and care for. Why are these shots still available?

Aussie17 writes a great blog. Below is posted Part 1 of his [?]/her [?] vitally important and compelling 2-part series linking the COVID jabs, through clean, reliable data from Singapore, with the one and only medication for a previously rare, devastating, invariably fatal disease called Amyotrophic Lateral Sclerosis (ALS).

There is only one use for the particular drug followed in the stack: ALS. Since the people taking it are ALS patients who have a short lifespan, if more is sold because more people are taking it. That can only be because more people have ALS.
Q: Why do more people have ALS, decreased fertility, auto immune diseases, turbo cancer and excess death?
A: ABTS [Anything but the shots]

It is urged that you read these two pieces and do several things: first, commit to being the voice of truth about these indescribably dangerous weapons against humanity disguised as “vaccines”. They are not. And clean statistics from around the world make that horrifyingly clear. Only governments and their lackies can find any way to deny this. It is up to us, all of us, to amplify this message.

Second, commit to doing whatever is necessary to protect your own body and that of people you have control over (parents for minor children, for example).

That means never, ever [again?] permit this or any other “untested” government-provided miracle snake oil substance into your body (or theirs).

Vintage Salesman GIF by Challenger

Third, in order to educate yourself, and check out the idea that every aspect of our lives is already permeated by the United Nations parasite, perform this quick experiment: using the search engine of your choice, enter the following (filling in the blank with your town or agency impacting your profession or State or Province or country):
” List, with references and links, all of the UN-derived, UN-compliant, UN-related or UN-adjacent programs, policies, protocols, policies and partnerships which impact directly or indirectly [fill in the blank].”

It is promised that that your jaw will be somewhere in the vicinity of your knees when you see what comes back.

Now here is Part 1 of Aussie17’s important correlation of deeply meaningful information:

PharmaFiles by Aussie17

The Jab That Keeps on Giving…300% Increase in ALS(Motor Neuron Disease) Drug sales reveals Singapore’s Hidden Health Horror Story!

A big part of Big Pharma is spinning a good story around sales numbers for the bosses. Nail the narrative, and you’re golden for another year. Botch it, and you’re packing your desk.

Why is this important? Well, for quite a few reasons, but a big one is because, especially in light of Dr. Prasad’s letter acknowledging that Covid jabs kill kids, with the mRNA shots still on the market and new mRNA jabs, including the uber-deadly replicon shots, being approved all the time, especially for kids (and, thanks to Merck, for your pets, too), we are dealing with weak-kneed damage control, not the beneficent or beneficial regulatory service to the public. We pay for regulation, not rubber-stamped death and disease but that is what we get.

Doin’ the Ol’ “HHS is Here for You, Regulating to Protect Your Health, Bobby Kennedy’s Our Guy” Rag

Let it be clear: Bobby knows full well that mRNA jabs are bioweapons. Prasad knows. Bhattacharya knows. There is, and has never been, a dearth of knowledge of how deadly these shots are. Pfizer and Moderna know. So does the Department of Defense.
Anyone who genuinely cares about ending the REAL pandemic, not the COVID propagandemic nonsense, but the deadly reality of the medical murders and the public health harms and, most of all, the bioweapon jabs, would not play nice, bide his time and be a good politician. He would move heaven and earth to end the deadly scourge of gene editing, death dealing weapons killing and maiming us while they destroy our ability to reproduce humankind.

Or he could pretend to be working on it and not accomplish anything even coming close to protecting the public from the bioweapon.

Hey, Mr. Secretary (and Mr. President), did you get caught with your regulatory pants down? Well, just keep on doing what you have done for nearly a year: pretend you are doing performance art and you really meant to be in that awkward position and indicate how much thought went into getting your rear end exposed.

That’s the science we are supposed to trust, after all. And we had that revelation about autism to trust, too. Now that was some seriously trustworthy science, right?

Then, because the public let you get away with that, you can just keep on doing more of same, right?

But don’t, for God’s sake, waste all the time and money and creativity that has gone into this decades long, untold trillions of dollars’ worth of bioweapon program by interfering with it! No, Siree Bob! Cover your tracks first, lie out of every orifice you and your associates can make any sounds out and keep the bioweapons in the rapid approval pipeline.

Most important of all, of course, cover your own ass if you can manage it, and keep on doing what you’re doing.

Maybe nobody will notice while they are exterminated from the bioweapons on the shelves and in the clinics.

Or maybe we will. And maybe we will eject the deadly UN parasite from every cell in the Body Politic and make some real headway to recovery

Nothing less.

And neither the head of the Executive Branch of the US government nor his appointee over at Health and Human Services has done so. Meanwhile, we suffer and die through an entirely man-made plague.

As it turns out, hiding it in Singapore is quite difficult. Thus, this outstanding two-part revelation.

Who is behind it? The genocidal maniacs who think you and I are disposable at their whim and pleasure. That’s right: the globalist parasites who operate the United Nations for their pleasure and profit, and for our pain and punishment. We, after all, are the carbon they intend to eliminate.

The solution? a good, comprehensive detox to get the UN and its bits and pieces out of our lives, our bodies, our government, our schools, our town halls, our clinics and hospitals, our airports, our banks and everywhere else.

Learn more, a lot more, at PreventGenocide2030.org.

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New ACIP Board Continues to Advise Children Take Untested Vaccines With Possible Human Gene Contamination That Could Integrate Into DNA


Federal advisory committee fails to inform public about the risks, despite new RFK Jr.-aligned members.

The newly reconstituted CDC Advisory Committee on Immunization Practices (ACIP) was supposed to be different.

With several new members aligned with Health and Human Services Secretary Robert F. Kennedy Jr.’s mandate for transparency and health freedom, expectations were high that the panel would finally call out the dangers hidden in vaccine development.

Instead, the new board folded.

TurniACIP’s Hollow Move

On Thursday, ACIP voted merely to push back the MMRV shot recommendation to age 4 because of the increased risk of febrile seizures in toddlers.

But the CDC had already admitted back in 2008 that ProQuad (MMRV) increased the risk of febrile seizures in toddlers 12–23 months old, and by 2009 ACIP was discouraging its use as the first dose at 12–15 months.

CDC had already cited studies showing about 4.3 cases per 10,000 doses—roughly double the risk compared to separate MMR and Varivax shots.

Meaning this latest “new” move by ACIP isn’t reform at all, but a belated rehash of mainstream business-as-usual policy that does nothing to protect children, even with so-called health freedom members now on the panel.

The Real Elephant in the Room: Plasmids

Instead of going further—instead of confronting the core problem—the panel stopped short.

They left in place recommendations for children to continue receiving vaccines that could contain plasmid DNA contamination with human gene segments capable of integrating into the human genome, a fact admitted in patents, FDA inserts, and independent lab findings.

MMRV (ProQuad): Recombinant Human Albumin Risk

ProQuad (MMRV) contains recombinant human albumin (rHA), made with a plasmid carrying the human ALB gene that could integrate into the human genome and dysregulate blood and cardiovascular systems (here).

The shot has never been tested for carcinogenicity, mutagenesis, or fertility impairment.

If recombinant human albumin (rHA) gene segments integrated into the human genome—particularly the ALB gene involved in encoding albumin—this could potentially disrupt the regulation of albumin production and its widespread biological functions.

Albumin plays a critical role in multiple physiological systems, especially in blood and cardiovascular homeostasis.

Potential Systems Dysregulated by ALB Gene Integration

  • Blood and Vascular System: Albumin regulates osmotic pressure in the blood vessels, facilitates transport of hormones, fatty acids, and drugs, and has anticoagulant properties by binding antithrombin and inhibiting platelet aggregation. Disruption could cause blood clotting abnormalities, impaired transport functions, and fluid balance issues.
  • Cardiovascular System: Since albumin affects blood volume and pressure regulation, abnormal expression might lead to dysregulated blood pressure, edema, or vascular inflammation.
  • Immune System and Inflammation: Albumin helps regulate inflammatory responses; its disruption could contribute to immune dysregulation, such as vasculitis or hypersensitivity reactions.

Associated Serious Adverse Events (SAEs)

The malfunction or dysregulation of albumin expression caused by integration could manifest as SAEs involving these systems, potentially including:

  • Edema (fluid retention and swelling)
  • Thrombocytopenia or other blood clotting disorders
  • Vasculitis (blood vessel inflammation)
  • Anaphylaxis or severe allergic reactions
  • Cardiovascular abnormalities like hypertension or vascular inflammation
  • Immune-mediated conditions affecting blood and vascular health

This aligns with reported SAEs listed in the FDA insert for ProQuad (MMRV), including thrombocytopenia, vasculitis, edema, anaphylaxis, and severe allergic reactions.

The underlying hypothesis is that integration of human ALB gene segments from recombinant albumin plasmids into the genome could disrupt this key protein’s regulation, leading to these blood and cardiovascular disorders.

Thus, the biological systems regulated by albumin—primarily blood volume/osmotic balance, coagulation, transport, and vascular integrity—are the most plausible targets for dysregulation if human albumin gene plasmid fragments integrate into the human genome, and these are reflected in the types of SAEs observed.

ACIP’s Failure

The new ACIP, with new health freedom-minded members recently appointed, was supposed to be a firewall.

Instead, they chose to deliberate over the timing of doses—not the DNA contamination, not the lack of long-term studies, not the risk of permanent genomic integration in children.

This is not reform, but surrender dressed up as oversight.

What the public got was a board that kept the program alive, keeping dangerous products in circulation under the federal Vaccines for Children program, and dodging the real questions.

Bottom Line

ACIP Chair Martin Kulldorff tried to frame the febrile seizure debate as a matter of “trust,” urging the public to listen to scientists who debate openly.

But the committee didn’t debate the elephant in the room: plasmids, human gene contamination, and the utter absence of mutagenesis and carcinogenicity testing.

Both the newly appointed “health freedom” members and the long-standing vaccine loyalists on ACIP now face a test of credibility.

The authority they’ve been given carries a duty to move beyond procedural adjustments and confront deeper safety questions head-on.

That requires openness, genuine debate, and a willingness to subject their recommendations to far greater public scrutiny.

The public did not support changes to ACIP membership simply to see more of the same.

Parents and citizens expected new voices to raise real concerns and to demand stronger safety standards for children.

That expectation remains unmet, and the responsibility for addressing it lies squarely with the current panel.

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