Note the limit set by VRBPAC.
Note the differentiation of DNA types.
Protooncogenes…
Where does an SV40 promoter with a nuclear localization signal fit?
Is C57BL6 the right model for this?
These lab mice have extended telomeres and are less prone to cancer. @BretWeinstein
I get this comment a lot.
They demand I jump through hoops while handing a hall pass to the manufacturers.
Yet its my friends and family that are faced with the threat of these injections if they want a job or an education.
The demand for peer review is always rooted in a midwits distrust in the average intelligence of their peers.
They are afraid other people will think for themselves and can only trust a clergy class to declare the truth we must all listen to.
Modern peer review doesn't guarantee reproducibility. Science is about the latter not the former.
When you lose sight of this, attack surfaces emerge.
Centralization of peer review by journals funded by Pharma who then demand scientists perform free work? Hows that working out?
It’s been 3 years since Nobel laureate Andrew Fire published the sequence of the monovalent vaccines in GitHub (not peer reviewed). They didn’t put reads public.
Where was the outrage over their lack of peer review?
Lack of raw sequence data?
Lack of qPCR, UV spec, etc?
The only time we see outrage is when a group does it with 9 orthogonal techniques and nails the fact that the vectors are there.
RNA-seq
qPCR
RT-qPCR
UV Spec
Quibit
Agilent TS
RNAse seq
DNase/ RNase qPCR.
Ecoli transformation
Our seq is public. Our primers are public.
The low wattage selective outrage is overt. It has nothing to do with quality and everything to do with ideology.
Where was their outrage over Andrew Fires GitHub release of the vaccine sequence with no raw reads to back up their claims?
pUC around and Pfind out-
The EMA document claims Pfizer linearizes their plasmids with Eam1104i. This is a restriction enzyme that cuts DNA based on the below recognition sequence.
Lets looks through the Deep Sequencing in IGV and see if we can find intact molecules.
Upper left is an obvious place where the Cuts end the molecules we sequence.
Upper right is another group of reads where the cut sites are intact.
Lets zoom in on that so you can see the details.
Sequencing OGs will notice there is more sequencing error near these sites as we near poly As and some sequencing adaptors. What does that mean?