So you really don't KNOW who you cast your vote.
1/ I get questions frequently from people who have heard the SOS say that the BMD QR code ballots can be audited to tell who won. I'll explain why he is wrong.
Your BMD ballot vote is stored in the barcode. The text doesn't count. The computer reads only the QR code.

So you really don't KNOW who you cast your vote.
--every voter thoroughly and accurately checks before scanning to be sure that the printed list reflects his choices. (Hard to do, to remember all the contests), AND
--there is a thorough post election audit.
If you pressed the screen for candidate Sam, but the printout & QR code said "Mary," and you didn't check, then your Mary vote was not intended.
Most of us would never notice on our grocery receipt that it was $.45 more and said "organic."

The store's official records are for organic milk because the barcode was miscoded.

But your receipt could be wrong too. The barcode could be for organic milk, but the receipt may say regular milk in the text.
The official record (your vote) was for organic milk! (Which you hate!)
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@franciscodeasis https://t.co/OuQaBRFPu7
Unfortunately the "This work includes the identification of viral sequences in bat samples, and has resulted in the isolation of three bat SARS-related coronaviruses that are now used as reagents to test therapeutics and vaccines." were BEFORE the
chimeric infectious clone grants were there.https://t.co/DAArwFkz6v is in 2017, Rs4231.
https://t.co/UgXygDjYbW is in 2016, RsSHC014 and RsWIV16.
https://t.co/krO69CsJ94 is in 2013, RsWIV1. notice that this is before the beginning of the project
starting in 2016. Also remember that they told about only 3 isolates/live viruses. RsSHC014 is a live infectious clone that is just as alive as those other "Isolates".
P.D. somehow is able to use funds that he have yet recieved yet, and send results and sequences from late 2019 back in time into 2015,2013 and 2016!
https://t.co/4wC7k1Lh54 Ref 3: Why ALL your pangolin samples were PCR negative? to avoid deep sequencing and accidentally reveal Paguma Larvata and Oryctolagus Cuniculus?
Unfortunately the "This work includes the identification of viral sequences in bat samples, and has resulted in the isolation of three bat SARS-related coronaviruses that are now used as reagents to test therapeutics and vaccines." were BEFORE the

chimeric infectious clone grants were there.https://t.co/DAArwFkz6v is in 2017, Rs4231.
https://t.co/UgXygDjYbW is in 2016, RsSHC014 and RsWIV16.
https://t.co/krO69CsJ94 is in 2013, RsWIV1. notice that this is before the beginning of the project
starting in 2016. Also remember that they told about only 3 isolates/live viruses. RsSHC014 is a live infectious clone that is just as alive as those other "Isolates".
P.D. somehow is able to use funds that he have yet recieved yet, and send results and sequences from late 2019 back in time into 2015,2013 and 2016!
https://t.co/4wC7k1Lh54 Ref 3: Why ALL your pangolin samples were PCR negative? to avoid deep sequencing and accidentally reveal Paguma Larvata and Oryctolagus Cuniculus?