Dragon Ball Z by Ciro Santilli 40 Updated 2025-07-16
Although this was one of the children cartoons Ciro Santilli liked to watch, watching Dragon Ball Z as an adult feels like watching paint dry, everything takes forever! Apparently padding to sync with the manga: www.quora.com/Why-does-DBZ-drag-on-for-so-long The original Dragon Ball was likely strictly better, as it was much more fun and took itself less seriously. Also in DBZ power level inflation is taken to ridiculous levels. This is why One-Punch Man is good. Out of all evil characters, Frieza is one that made a big impression on Ciro, his graphical design is so good.
This experiment seems to be really hard to do, and so there aren't many super clear demonstration videos with full experimental setup description out there unfortunately.
For single-photon non-double-slit experiments see: single photon production and detection experiments. Those are basically a pre-requisite to this.
photon experiments:
Non-elementary particle:
Video 1.
Single Photon Interference by Veritasium (2013)
Source. Claims to do exactly what we want, but does not describe the setup precisely well enough. Notably, does not justify how he knows that single photons are being produced.
DNA microarray by Ciro Santilli 40 Updated 2025-07-16
Can be seen as a cheap form of DNA sequencing that only test for a few hits. Some major applications:
Metagenomics by Ciro Santilli 40 Updated 2025-07-16
Experiments that involve sequencing bulk DNA found in a sample to determine what species are present, as opposed to sequencing just a single specific specimen. Examples of samples that are often used:
One related application which most people would not consider metagenomics, is that of finding circulating tumor DNA in blood to detect tumors.
RNA-Seq by Ciro Santilli 40 Updated 2025-07-16
Sequencing the DNA tells us what the organism can do. Sequencing the RNA tells us what the organism is actually doing at a given point in time. The problem is not killing the cell while doing that. Is it possible to just take a chunk of the cell to sequence without killing it maybe?
This is an extremely widely used technique as of 2020 and much earlier.
If allows you to amplify "any" sequence of choice (TODO length limitations) between a start and end sequences of interest which you synthesize.
If the sequence of interest is present, it gets amplified exponentially, and you end up with a bunch of DNA at the end.
You can then measure the DNA concentration based on simple light refraction methods to see if there is a lot of DNA or not in the post-processed sample.
One common problem that happens with PCR if you don't design your primers right is: en.wikipedia.org/wiki/Primer_dimer
Sometime it fails: www.reddit.com/r/molecularbiology/comments/1kouomw/when_your_pcr_fails_again_and_you_start/
Nothing humbles you faster than a bandless gel. One minute you’re a scientist, the next you’re just a pipette-wielding wizard casting spells that don’t work. Meanwhile, physicists are out there acting like gravity always behaves. Smash that upvote if your reagents have ever gaslit you.
and a comment:
PCR = Pray, Cry, Repeat
Fog computing by Ciro Santilli 40 Updated 2025-07-16
Our definition of fog computing: a system that uses the computational resources of individuals who volunteer their own devices, in which you give each of the volunteers part of a computational problem that you want to solve.
Folding@home and SETI@home are perfect example of that definition.
E Ink by Ciro Santilli 40 Updated 2025-07-16
Electronic Ink such as that found on Amazon Kindle is the greatest invention ever made by man.
Once E Ink reaches reasonable refresh rates to replace liquid crystal displays, the world will finally be saved.
It would allow Ciro Santilli to spend his entire life in front of a screen rather in the real world without getting tired eyes, and even if it is sunny outside.
Ciro stopped reading non-code non-news a while back though, so the current refresh rates are useless, what a shame.
OMG, this is amazing: getfreewrite.com/

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