High-content screening microscopy generates large amounts of live-cell imaging data, yet its potential remains constrained by the inability to determine when and where to image most effectively. Optimally balancing acquisition time, computational capacity, and photobleaching budgets across thousands of dynamically evolving regions of interest remains an open challenge, further complicated by limited field-of-view adjustments and sensor sensitivity. Existing approaches either rely on static sampling or heuristics that neglect the dynamic evolution of biological processes, leading to inefficiencies and missed events. Here, we introduce the restless multi-process multi-armed bandit (RMPMAB), a new decision-theoretic framework in which each experimental region is modeled not as a single process but as an ensemble of Markov chains, thereby capturing the inherent heterogeneity of biological systems such as asynchronous cell cycles and heterogeneous drug responses. Building upon this foundation, we derive closed-form expressions for transient and asymptotic behaviors of aggregated processes, and design scalable Whittle index policies with sub-linear complexity in the number of imaging regions. Through both simulations and a real biological live-cell imaging dataset, we show that our approach achieves substantial improvements in throughput under resource constraints. Notably, our algorithm outperforms Thomson Sampling, Bayesian UCB, epsilon-Greedy, and Round Robin by reducing cumulative regret by more than 37% in simulations and capturing 93% more biologically relevant events in live imaging experiments, underscoring its potential for transformative smart microscopy. Beyond improving experimental efficiency, the RMPMAB framework unifies stochastic decision theory with optimal autonomous microscopy control, offering a principled approach to accelerate discovery across multidisciplinary sciences.
翻译:高内涵筛选显微镜可生成大量活细胞成像数据,但其潜力仍受限于无法确定何时何地进行最有效的成像。在数千个动态演变的感兴趣区域中,如何最优平衡采集时间、计算能力与光漂白预算仍是一个开放挑战,该问题因有限的视场调整能力和传感器灵敏度而进一步复杂化。现有方法要么依赖静态采样,要么采用忽视生物过程动态演变的启发式策略,导致效率低下和事件遗漏。本文提出躁动多进程多臂老虎机(RMPMAB)这一新决策理论框架,其中每个实验区域被建模为马尔可夫链集合而非单一过程,从而捕捉生物系统固有的异质性,例如异步细胞周期和异质性药物响应。基于此框架,我们推导了聚合过程瞬态与渐近行为的闭式表达式,并设计了在成像区域数量上具有次线性复杂度的可扩展Whittle索引策略。通过仿真和真实生物活细胞成像数据集,我们证明该方法在资源约束下实现了通量的显著提升。值得注意的是,我们的算法在仿真中将累积遗憾降低超过37%,在活体成像实验中多捕获93%的生物学相关事件,其表现优于汤普森采样、贝叶斯UCB、ε-贪婪和轮询调度算法,彰显了其在变革性智能显微镜领域的潜力。除提升实验效率外,RMPMAB框架将随机决策理论与最优自主显微镜控制相统一,为加速跨学科科学发现提供了原则性方法。