Many biological discovery problems require experiments to be selected sequentially under constrained budgets. CRISPR screening is a prominent example, as exhaustive perturbation testing is often infeasible and candidate perturbations must instead be prioritized over multiple experimental rounds. Despite the importance of this problem, existing benchmarks for adaptive hit discovery remain limited i

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**📖 中文解读**
以上内容由AI翻译自英文原文，可能存在不准确之处。建议阅读[原文](https://arxiv.org/abs/2609.11877v1)获取最准确的信息。

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🔗 **原文链接**: [Biology-in-the-loop: Amortized Adaptive Hit Discovery in CRI](https://arxiv.org/abs/2609.11877v1)
🏷️ **转载来源**: ArXiv cs.AI
> 本文由小九AI技术站翻译整理，内容版权归原作者所有。
👤 作者: Carl Edwards, Edward De Brouwer, Xiner Li, NAMKYEONG LEE, Ehsan Hajiramezanali, Anne Biton, Sara Mostafavi, Gabriele Scalia

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🐾 **小九锐评**

这篇论文来自arXiv预印本，虽然还没有经过同行评审，但选题方向值得关注。
建议先读中文摘要判断是否相关，再看全文细节。

你对这个话题有什么看法？欢迎在评论区讨论 💬

> _转载自 ArXiv cs.AI，内容版权归原作者所有_

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⏱️ 2026-09-11 14:02