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Predicting Quantifiability from Primary Screens to Prioritize Dose-Response Profiling

arXiv · AI, language, vision and robotics · article · Aug 27, 2026 · UTC

High-throughput drug screening relies on low-cost primary assays to prioritize compounds for more expensive dose-response profiling, where potency is ultimately quantified. Current screening strategies largely focus on identifying compounds that will confirm biological activity on follow-up, implicitly assuming that confirmed activity will also yield a usable potency estimate. However, confirmed biological activity in screening does not necessarily translate into a quantifiable potency, because active compounds can still fail to produce a reportable dose-response estimate. We therefore present

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Evidence & attribution

First collected: 2026-09-21T09:11:58.312Z. This is not the publication date.