OpenAI 把 o3 模型用到罕见病诊断上，还发了 NEJM AI 论文，很实在的应用。
OpenAI 与波士顿儿童医院合作，使用 o3 Deep Research 工具帮助诊断罕见遗传病。相关成果发表在《NEJM AI》期刊上。该工具通过分析全外显子组测序数据，协助医生识别致病基因变异。研究团队在视频中展示了具体诊断案例。
OpenAI for helping families facing rare genetic diseases. This was done with o3 which is over a year...
OpenAI for helping families facing rare genetic diseases. This was done with o3 which is over a year old, amazing to think what will be possible with today’s models. OpenAI Newsroom @OpenAINewsroom For families facing rare genetic diseases, answers can be hard to find. @HallieJackson spoke live with @_perloj and Dr. Catherine Brownstein about the new NEJM AI paper and our work with Boston Children’s Hospital, where experts used o3 Deep Research to help diagnose rare genetic diseases affecting children. Take a look: Your browser does not support the video tag. 🔗 View on Twitter 🔗 View Quoted Tweet 💬 19 🔄 11 ❤️ 136 👀 12339 📊 26 ⚡