points by hungryhobbit 2 days ago | 0 comments
I don't follow how "we can see tiny stuff" = "it is possible to build closed system"?
Seeing tiny stuff doesn't magically give you enough info for Claude to reason with the system predictably (the way it can with source code).
[–] bijowo1676 2 days ago
the transition is in-silico => in-vitro => in-vivo
AI already can do in-silico simulation
add microscopes and tiny precision actuators, and we can build closed feedback loop in-vitro system
once we have in-vitro, it will be easier to go in-vivo
[–] randomImmigrant 2 days ago
Why would number 2, which we’ve been able to do for decades, possible affect number 3 on your list?
[–] bijowo1676 1 day ago
currently we rely on meatbags to do 2 and 3, we have not fully built in-vitro done by Claude Code
[–] randomImmigrant 1 day ago
Untrue. And you also don’t have robitics that can do all kinds of cell bio/tissue bio experiments that require the affordances and skills humans hands have but no robot to date does. Seriously, have you been in a lab and seen the kinds of experiments that get done?
[–] bijowo1676 1 day ago
can today's labs prompt Claude Code to do 1488 experiments in-vitro continiously over 48 hrs ?
[–] randomImmigrant 1 day ago
Are you under the assumption “in vitro experiment” is a small set of skills?
[–] sumanthvepa 2 days ago
[–] randomImmigrant 2 days ago
There’s no well-labeled dataset for all this because we don’t know everything we are looking at.
Take a neuron. You can stain it so you can tell apart an axon and a dendrite. But if you don’t it’s very possible to miss or mislabel the axon, because unlike the textbook neuron, the axon isn’t always obviously oriented in a way that promotes ID.
And that’s just one example. With more complex samples, you also have a lot of edges which AI models don’t segment very well.
[–] menaerus 2 days ago
So, I'd say it's a pretty similar process, and yet we have the AI models now almost completely integrated into the SWE domain remediating significant parts of its complexity.
[–] dekhn 1 day ago
[–] menaerus 1 day ago
[–] dekhn 1 day ago
At peak, we had 1-3 million xeon cores running our tasks (protein folding, protein design, drug docking), 24/7. This was before GPUs were really a thing. Each mini-task was basically a rosetta or gromacs or autodock binary running on local inputs and writing local outputs for ~1 hour using ~1GB RAM and no network. Input and output was via colossus, or distributed through a global torrent network (literally all 1-3 million cores formed a single data transfer group, with data passed between clusters at low probability).
I built most of the code of the system (which depended on Google infra) including the scheduler and the machine worker, and also ran the system as on-call "SRE" for 3 years. During that time, we nearly almost didn't take down the Google global network, and had small latency impacts on many services. Managing to run the system for so long without antagonizing ads or search or youtube was a major challenge.
I would say the complexity of the system I built (considering everything down to the OS) was roughly the level of a few human cells in a plate, in terms of interacting components and the complexity of their interactions.
Here are some of the publications that came from running exacycle (we provided strong evidence that using more compute improves outcomes in molecular simulations)
https://pubmed.ncbi.nlm.nih.gov/24345941/ https://pubmed.ncbi.nlm.nih.gov/24265211/
[–] menaerus 1 day ago
Anyway, my point was not in that I would equate software complexity with the complexity found in biology but that I see the same trend and similar type of challenges that can be found in both fields and therefore I see both fields amenable to the AI advancements whereas many people from the thread do not, and I disagree with that.
[–] throwaway132448 1 day ago
[–] menaerus 1 day ago
[–] bijowo1676 1 day ago
[–] meindnoch 1 day ago
https://xkcd.com/1831/
[–] menaerus 1 day ago
[–] randomImmigrant 1 day ago
[–] mrtesthah 2 days ago