I think the effort in the testing of the thousands of drugs was to help create the AI model.
This gets to the crux of my skepticism around the big claims around the pace of AI advancement. At a fundamental level the upper limit of AI advancement, in any area, is "the speed of information". For some areas, like pharmaceutical/drug development, the information comes from the real world, human/biological processes (e.g. clinical drug trials), which take time. At the extreme, the outcomes of interest could be long-term (i.e. years or decades). AI surely advances analytically capabilities, but ultimately models can only be developed or refined with new data/information, which unfolds at a rate that may be independent of computational speeds. AI models that are highly predictive and valuable by definition necessitates a feedback loop that is tied back to real-world outcomes/timescales.I'm no expert on AI, but I get this sense that the exponential improvements that many believe will lead to the singularity may in fact reach an inflection point where the curve flattens out becomes linear or asymptotic, as the rate of improvement is governed by the rate of new information in the real world.
Maybe because they don't pay shit, and can be done by the massive amounts of unskilled labor that exist? Really hard to develop a robot cheap enough for the dexterity needed.
But, even then it's a mistake to think this isn't going to be a massive problem. If everything 'expensive' gets automated then that can lead to a huge pool of labor fighting for low paid jobs that can't actually pay for any assets like houses, education, stocks, etc.
> Most jobs are not well-defined / algorithmic and there is no amount of reading that can prepare you for the embodied, dynamic experience of performing those tasks.
Yea, there is, building an embodied robot and feeding it virtual situations based on real situations. As we get closer and closer to AGI the 'general' functioning of the robot is more and more covered and less and less human intervention is needed.
Here we screened ~7,500 molecules for those that inhibited the growth of A. baumannii in vitro. We trained a neural network with this growth inhibition dataset and performed in silico predictions for structurally new molecules with activity against A. baumannii. Through this approach, we discovered abaucin, an antibacterial compound with narrow-spectrum activity against A. baumannii.
https://www.nature.com/articles/s41589-023-01349-8
Not only were both the dataset they created, and the model they trained on it, specific to one organism, the drug they discovered also only works on that one organism ("narrow spectrum activity against A. baumannii"). If they wanted to discover drugs that work on other organisms, like Staphylococcus aureus and Pseudomonas aeruginosa that the BBC article mentions, they'd have to start all over again.
So, not an approach that looks very practical at this time. Maybe in the future, when the sample efficiency and generalisation ability of neural nets has significantly improved it will be useful in practice.
Study:
If we had a model that could predict the next working antibiotic for MRSA that would be amazing. And you'd probably need it multiple times as MRSA keeps evolving new defenses.
Even narrowing down the list of substances to test by 10x it's amazing.
This looks very practical to me.
We can reasonably expect the bacteria to mutate against the new antibiotic if/once it's used. It's one shifty opponent. This may make the model obsolete, but maybe not - there'd cause to try the model. Actually, it would have been preferable to get more than one result at first...
[EDIT: Then again, would they have another candidate list? This model doesn't do toxicology. The second list was created by using existing proven-safe meds. Do they have another couple thousand materials good to go? If not, they won't be able to run a second time. ]