Many Needles in a Haystack: Active Hit Discovery for Perturbation Experiments

High-throughput gene perturbation experiments can test several genetic interventions in parallel, yet experimental budgets remain limited. A central goal is hit discovery: identifying as many perturbations as possible whose phenotypic effect exceeds a predefined threshold. Pure exploration strategies are statistically inefficient, wasting budget on low-value regions. Bayesian optimization methods offer a principled alternative but target a single global optimum, over-exploiting dominant modes while neglecting other high-value regions. We formalize hit discovery as a sequential experimental design problem and propose Probability-of-Hit, an acquisition function that directly targets threshold exceedance by ranking candidates according to their posterior probability of being a hit. We prove asymptotic optimality of this approach and demonstrate strong empirical performance on both synthetic benchmarks and real biological immunology datasets, including up to 6.4% improvement over baselines on the Schmidt IL-2 dataset.

MixFlow: Mixture-Conditioned Flow Matching for Out-of-Distribution Generalization

Achieving robust generalization under distribution shift remains a central challenge in conditional generative modeling, as existing conditional flow-based methods often struggle to extrapolate beyond the training conditions. We introduce MixFlow, a conditional flow-matching framework for descriptor-controlled generation that directly targets this limitation by jointly learning a descriptor-conditioned base distribution and a descriptor-conditioned flow field via shortest-path flow matching. By modeling the base distribution as a learnable, descriptor-dependent mixture, MixFlow enables smooth interpolation and extrapolation to unseen conditions, leading to substantially improved out-of-distribution generalization. We provide analytical insights into the behavior of the proposed framework and empirically demonstrate its effectiveness across multiple domains, including prediction of responses to unseen perturbations in single-cell transcriptomic data and high-content microscopy-based drug screening tasks. Across these diverse settings, MixFlow consistently outperforms standard conditional flow-matching baselines. Overall, MixFlow offers a simple yet powerful approach for achieving robust, generalizable, and controllable generative modeling across heterogeneous domains.