This work tests the reliability of perturbations and their alignment with shared perturbation responses, classifying each perturbation as specific, shared, or unreliable, and applies these quality labels to published benchmarks shows that model comparisons depend on perturbation quality.
Abstract
Predicting single-cell transcriptional responses to perturbations is central to building the virtual cell, yet recent benchmarks show that simple baseline methods often outperform complex models, and model comparisons depend on the evaluation metric. Most studies assume that preprocessed RNA sequencing data are reliable ground truth for both training and evaluation. Here, we test this assumption by measuring the reliability of perturbations and their alignment with shared perturbation responses, classifying each perturbation as specific, shared, or unreliable. Among 7,170 perturbations from 29 datasets, 65% are unreliable, 11% shared, and 24% specific. Applying these quality labels to published benchmarks shows that model comparisons depend on perturbation quality. Training with reliable perturbations alone matches or outperforms full-data performance while using 55% of all training perturbations. Our framework also enables prospective experimental design: for most perturbations, a 28-cell pilot experiment accurately predicts how many cells a full screen needs to be reliable.
Predicting cellular responses to genetic perturbations helps prioritize experiments in single-cell genomics, where exhaustive measurement is infeasible. While computational models increasingly predict these responses, three evaluation deficiencies obscure what their scores demonstrate. First, absolute metrics cannot se...
Si-Kai Huang, Zhi-Wen Yang, Kai Yu et al.· 0 citations
Virtual cell models aim to predict how cells respond to perturbations, yet accurate prediction of post-perturbation gene expression can conceal failures to recover context-specific responses. Here we identify context geometry compression (CGC), in which models preserve cellular identity and shared perturbation effects...
Yong-Qi Huang, Han-Zhi Wang, Chen-Yu Li et al.· bioRxiv· 0 citations
Predicting phenotypic and transcriptional responses to perturbations at single-cell resolution provides a powerful tool for probing biological systems. However, existing methods typically rely on fixed mappings learned during training, making it challenging to calibrate distribution shifts or adapt to novel perturbatio...
Jia-Nan Wei, Jia-Jun Hong, Gui-Kun Chen et al.· 0 citations
PopPert predicts perturbation-induced changes in distribution parameters, eliminating the need for cell-level correspondence and reducing sensitivity to single-cell noise, establishing population-level joint distribution learning as an effective paradigm for predicting transcriptional responses from unpaired single-cel...
Han-Dong Wang, Jiaxin Qi, Hao-Chen Feng et al.· 0 citations
Comprehensive experiments demonstrate CellRFT's applicability across different pretrained models and effectiveness in improving perturbation prediction, reveal that optimizing one biological criterion can help or hinder others, and show that complementary rewards can improve criteria beyond those directly optimized.
The performance and flexibility of State set the stage for scaling the development of AI models of cell state, a machine learning model that predicts perturbation effects while accounting for cellular heterogeneity within and across experiments.
Abhinav K. Adduri, Dhruv Gautam, Beatrice Bevilacqua et al.· Cell· 4 citations
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