Fort Detrick hantavirus genome manufacturing project operated through HHS/NIAID-linked high-containment biodefense contracts worth up to $387.5 million combined.
Sounds eerily familiar to the construction of the Covid pathogen-fill in the missing sequences and add portions of the human genome to guarantee a positive PCR test!
Ah yes, just like covid - the pseudoscientific "de novo assembly". And I bet we can add to your excellent analysis the fact that none of these genetic strands, nor the full genetic sequence, was ever grown in a petri dish and put into a biological being to see if it made them sick with hantavirus symptoms. This is not science, this is ridiculous. Thanks for your reporting on this ridiculous pseudoscience BS.
Another Fatal Flaw in the Virus Scam: The So-Called 'Cytopathic Effect. In order to ‘isolate’ a virus, virology uses a process that is the exact opposite of isolation. It’s classic Orwellian playbook methodology, in which words are used in a manner that totally contradicts their true meaning, and everyone just nods along like nothing untoward is taking place. https://anthonycolpo.substack.com/p/another-fatal-flaw-in-the-virus-scam
You pointed out how Table S3 showed that one patient's L segment had only about 47% coverage. Table S3 includes 29 patients who all have 3 segments: https://www.nejm.org/doi/suppl/10.1056/NEJMoa2009040/suppl_file/nejmoa2009040_appendix_1.pdf. But there was only a single patient whose segments had low coverage, so all 3 segments of all other patients have 97% or higher coverage.
It's common and expected for small parts from the end of a viral genome to be missing from a de-novo assembled genome (or segment in the case of segmented viruses like hantaviruses). Grok said:
> Contigs from next-generation sequencing often miss the terminal ends of viral genomes due to inherent biases in library preparation and sequencing chemistry. RNA is fragmented, adapters are ligated, and short reads are generated. The extreme 5' and 3' termini of linear RNA molecules, especially those with strong secondary structures like the panhandle-forming ends of hantaviruses, are frequently under-represented or fail to be captured efficiently during reverse transcription and amplification steps. Random priming and enzymatic processes tend to have lower efficiency at the very ends, resulting in sparse or absent read coverage in those regions.
> De novo assembly algorithms then build contigs by finding overlapping reads. When coverage drops sharply or is absent at the ends, the assemblers cannot extend the contigs further, producing incomplete fragments that stop short of the true termini. This is a common technical limitation of short-read sequencing technologies when applied to full viral genomes, particularly segmented negative-sense RNA viruses. Gaps at the ends are therefore expected and routinely filled using sequences from closely related reference strains when the internal coverage is high and the terminals are highly conserved.
In your earlier post about BLAST, none of the hantavirus primers or probes even got an exact match to a human genome, but you only got an exact matches for things like a 19-base subsegment of a 23-base primer. Similarly close matches are likely to occur by chance, as is shown by your high E-values. None of the E-values in your screenshots reached below the significance threshold of 0.05, apart from a single set of matches that had an E-value barely below 0.05.
Even though PCR tolerates some degree of mismatches, it's not clear if any of your matches are even close enough to result in a false positive match. And in order for the primer-and-probe set to return a positive match to a human genome, the two primers have to match nearby regions of the human genome, and the match to the probe has to be located between the matches to the primers.
Dr. Nora Volkow, the great-granddaughter of Leon Trotsky and Director of the National Institute on Drug Abuse (NIDA), has continued her leadership role in addiction science during the Trump administration. She is a recognized expert on brain imaging and has engaged with the administration on health initiatives.
"Thus the Drug Trust, while maintaining the Stalinist Communist Government in Russia, simultaneously maintained a Communist back up regime in the United States, the Trotskyite Movement, in case the Stalinist regime should fall."
Sounds eerily familiar to the construction of the Covid pathogen-fill in the missing sequences and add portions of the human genome to guarantee a positive PCR test!
Ah yes, just like covid - the pseudoscientific "de novo assembly". And I bet we can add to your excellent analysis the fact that none of these genetic strands, nor the full genetic sequence, was ever grown in a petri dish and put into a biological being to see if it made them sick with hantavirus symptoms. This is not science, this is ridiculous. Thanks for your reporting on this ridiculous pseudoscience BS.
Another Fatal Flaw in the Virus Scam: The So-Called 'Cytopathic Effect. In order to ‘isolate’ a virus, virology uses a process that is the exact opposite of isolation. It’s classic Orwellian playbook methodology, in which words are used in a manner that totally contradicts their true meaning, and everyone just nods along like nothing untoward is taking place. https://anthonycolpo.substack.com/p/another-fatal-flaw-in-the-virus-scam
Made in the USA. Shared with the W.H.O., they know what it is. Now the accomplice?
Disease causing viruses have never been proven to exist. https://www.ourgreaterdestiny.ca/p/virus-fraud-disclosed-through-cpe
Playing god with g-o-f and deadly viruses shows total lack of morality or just unfixable stupidity.
Outstanding article - greatly appreciate your revealing this.
Dah dah daaaaaahhhhhh
You pointed out how Table S3 showed that one patient's L segment had only about 47% coverage. Table S3 includes 29 patients who all have 3 segments: https://www.nejm.org/doi/suppl/10.1056/NEJMoa2009040/suppl_file/nejmoa2009040_appendix_1.pdf. But there was only a single patient whose segments had low coverage, so all 3 segments of all other patients have 97% or higher coverage.
It's common and expected for small parts from the end of a viral genome to be missing from a de-novo assembled genome (or segment in the case of segmented viruses like hantaviruses). Grok said:
> Contigs from next-generation sequencing often miss the terminal ends of viral genomes due to inherent biases in library preparation and sequencing chemistry. RNA is fragmented, adapters are ligated, and short reads are generated. The extreme 5' and 3' termini of linear RNA molecules, especially those with strong secondary structures like the panhandle-forming ends of hantaviruses, are frequently under-represented or fail to be captured efficiently during reverse transcription and amplification steps. Random priming and enzymatic processes tend to have lower efficiency at the very ends, resulting in sparse or absent read coverage in those regions.
> De novo assembly algorithms then build contigs by finding overlapping reads. When coverage drops sharply or is absent at the ends, the assemblers cannot extend the contigs further, producing incomplete fragments that stop short of the true termini. This is a common technical limitation of short-read sequencing technologies when applied to full viral genomes, particularly segmented negative-sense RNA viruses. Gaps at the ends are therefore expected and routinely filled using sequences from closely related reference strains when the internal coverage is high and the terminals are highly conserved.
In your earlier post about BLAST, none of the hantavirus primers or probes even got an exact match to a human genome, but you only got an exact matches for things like a 19-base subsegment of a 23-base primer. Similarly close matches are likely to occur by chance, as is shown by your high E-values. None of the E-values in your screenshots reached below the significance threshold of 0.05, apart from a single set of matches that had an E-value barely below 0.05.
Even though PCR tolerates some degree of mismatches, it's not clear if any of your matches are even close enough to result in a false positive match. And in order for the primer-and-probe set to return a positive match to a human genome, the two primers have to match nearby regions of the human genome, and the match to the probe has to be located between the matches to the primers.
Thank you, Jon!
‘potentially weaponizable’ - potentially doing some Olympic class heavy lifting here 🤣
For a disease that is not "isolated"?
Dr. Nora Volkow, the great-granddaughter of Leon Trotsky and Director of the National Institute on Drug Abuse (NIDA), has continued her leadership role in addiction science during the Trump administration. She is a recognized expert on brain imaging and has engaged with the administration on health initiatives.
"Thus the Drug Trust, while maintaining the Stalinist Communist Government in Russia, simultaneously maintained a Communist back up regime in the United States, the Trotskyite Movement, in case the Stalinist regime should fall."
Eustace Mullins
Just like Covid
I listened to Dr. McCullough and this virus that was on the ship comes from rats and rats Poop .
It cannot be passed man-to-man and they’ve had this for many many years there’s nothing to worry about. It’s a bunch of bogus as usual.
He' ll be looking to ad it to his Wellness kit. $$
When you’re less qualified than Dr. McCullough…
Qualified as anything…
But I heard him on Fox TV, the Trotskyite network.