The abstract is read at the publisher; the summary is JClub's.
Tahoe-100M profiles 100 million single-cell transcriptomes across 50 cancer cell lines under 1,100 drug-dose conditions, enabling low-batch, multiplexed mapping of drug-induced molecular phenotypes.
- Why it matters: Drug response is heterogeneous and mechanistically complex, and existing data often lacks single-cell, multi-perturbation coverage to quantify phenotypes and fate shifts reliably.
- What they did: Using the Mosaic platform, genetically distinct cell models are multiplexed into balanced “cell villages,” followed by parallel single-cell profiling and systematic phenotype quantification.
- The result: The atlas defines drug-induced expression programs, classifies mechanisms of action, detects off-target and adaptive stress responses linked to resistance, and supports public training of AI predictive models.
The findingWhy it mattersWhat they didThe result
AI summary of the abstract · may contain errors · not medical advice · read the paper.