By training acquisition policies on historical experimental data and combining them with LLM biological priors, you can dramatically improve the efficiency of sequential biological experiments—recovering 27.7% of hits while testing only 5% of candidates.
This paper introduces AssayBench-Loop, a large benchmark of 1,389 CRISPR screens, and AssayLoop, a framework that learns which genes to test next by combining a transformer model trained on historical experiments with biological knowledge from LLMs.