Greg Brockman· @gdb · X·· 2026-06-20AI 评分45
AI 导读
Greg Brockman 发推介绍 OpenAI 与波士顿儿童医院合作，利用 o3 Deep Research 辅助诊断儿童罕见遗传病，相关成果发表在 NEJM AI。o3 模型虽已发布超过一年，Brockman 感慨如今模型的能力或将带来更大突破。
正文 · 原文
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.
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:在 X 查看被引用的帖子
来源：Greg Brockman · x.com