Built AirCursor at the
@SarvamAI × @GrowthX_Club hack. It is a computer use agent for mobiles.
Speak in any language. It sees your screen and does real world tasks and is also controllable via bluetooth.
running subagents inside of subagents reminds me of nested virtualization.
i like how cs fundamentals correlates in so many instances around us.
the other day i wanted to create a QEMU emulator inside a container, but realized it lacks /dev/kvm, which is super important in order to achieve fast cpu virtualization.
i mean this is exactly how firecracker launches microvms on aws servers with superlow boot time.
fascinating!
We just crossed ONE THOUSAND BOOKS finished on Bookmarkk 🥳 🥹 💪 📚
Reading literally rewires your brain in a way that makes you smarter.
Congrats to all of our users for achieving this insane milestone with us :)) This is literally all you ❤️🔥
You can cold email nearly anyone, but nearly everyone overlooks how powerful it can be.
Sending one email each week that feels like a stretch can change your life. Will you get turned down? Sure, most of the time. But you only need one to pay off for something amazing to happen.
Take your time, write a thoughtful message, and muster the courage to press Send.
When you meet someone for the first time but it somehow feels like you’ve known them for years 😂
Been talking to @AroraBhavyam since the last year on @X , but this was finally our first time meeting IRL and it felt like we’d already been hanging out forever!
Had so much fun chilling with you guys!
CT really does make you meet some insanely cool people 🫶✨
There is a child with a rare disease who is currently suffering and struggling to manage his symptoms. Rare as this is, you can directly help him.
Today we are launching the "Rare Disease, Real Kid" Hackathon, and there are $50,000 in prizes from @AnthropicAI and @awscloud.
We (@huggingface & @Sagebio) are helping this child open his genome and clinical data to the community, so that we can find what's caused his disease and what currently-approved drugs could help him.
I doubt I need to motivate this much further or explain how rare it is for a family to share their child's genome and clinical data, but if you're not sure, consider this:
Until very recently, it wasn't feasible for patients like this to get treatment because their disease was so rare that the economics could never justify the investment. Now, as we've seen, people with rare diseases are starting to be able to find the answers themselves (with the help of AI tools, cheaper sequencing, etc). This kid is not able to do that for himself and neither are his parents, so we're asking you for help. Both for this kid and to prove that it's possible for everyone else suffering from a rare disease.
More details in 🧵.
https://t.co/hjjagALtMu