Hugging Face和Sagebio举办的黑客松,用AI技术帮助罕见病患者,奖金丰厚,值得一试。
Hugging Face与Sagebio联合举办“罕见病,真实儿童”黑客松,旨在通过AI和基因组学技术帮助罕见病患者。活动提供5万美元奖金,参与者有机会帮助一位患有罕见病的儿童。活动详情见链接。
Today we are launching the "Rare Disease, Real Kid" Hackathon together with @sagebio in which you ca...
Today we are launching the "Rare Disease, Real Kid" Hackathon together with @sagebio in which you can literally save a life if you’re interested in AI and genome 🧬 (and incidentally win $50,000 in prizes and compute from our great partners @AnthropicAI and @awscloud ) Check out details below 👇 Georgia Channing @cgeorgiaw 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 🧵. …-real-kid-mva-hackathon-2026.hf.space u Your browser does not support the video tag. 🔗 View on Twitter 🔗 View Quoted Tweet 💬 0 🔄 1 ❤️ 8 👀 863 📊 1 ⚡