Broad utility is demonstrated: identifying context-specific regulators of p53 under ribosomal stress, characterizing dose-dependent drug mechanisms of action, and uncovering cytokine-driven B cell heterogeneity during secondary influenza infection in vivo are demonstrated.
Abstract
Single-cell perturbation dictionaries measure how cells respond to genetic and chemical perturbations, creating the opportunity to assign causal interpretations to observational data. We introduce RNA fingerprinting, a statistical framework that maps transcriptional responses from new experiments onto reference perturbation dictionaries. RNA fingerprinting learns perturbation representations, or "fingerprints," from single-cell data, then probabilistically assigns query cells to one or more candidate perturbations. We benchmark on ground-truth datasets, demonstrating accurate assignments at single-cell resolution, scalability to genome-wide screens, and the ability to resolve combinatorial perturbations. We demonstrate broad utility across diverse biological settings: identifying context-specific regulators of p53 under ribosomal stress, characterizing dose-dependent drug mechanisms of action, and uncovering cytokine-driven B cell heterogeneity during secondary influenza infection in vivo. Together, these results establish RNA fingerprinting as a versatile framework for interpreting single-cell datasets by linking cellular states to their underlying perturbations.
The results show that graph-based signal propagation is a biologically grounded alternative to latent-shift perturbation modeling and can improve the recovery of sparse perturbation-induced transcriptional effects.
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ChromaPert is proposed, a chromatin-informed framework for predicting state-dependent perturbation responses that combines molecular and DNA-informed locus priors with paired control RNA--ATAC features to jointly represent target identity and measured cellular context.
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Tahoe-100M, a giga-scale single-cell perturbation atlas comprising 100 million transcriptomes from 50 diverse cancer cell lines treated with 1,100 drug-dose conditions, advances the ability to model gene regulation, drug response, and network dynamics.
Jesse Zhang, Airol A. Ubas, Valentine Svensson et al.· Cell· 8 citations· ⚡2
Perturbations change both RNA abundance and intracellular organization, but gene-count predictors omit the positions needed to model spatial responses. To address this limitation, we introduce SubcellPert, a benchmark for perturbation-response prediction at single-RNA-molecule resolution. It comprises 14 imaging datase...
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
Single-cell RNA sequencing fundamentally depends on defining cell–cell similarity to resolve distinct cell states. However, conventional dimensional-reduction frameworks such as t-SNE and UMAP inherently rely on Euclidean geometry, a construct ill-suited for high-dimensional, sparse count matrices, and produce cluster...
Henry Han, Tian-Yun Zhang, Lu-Yu Niu et al.· bioRxiv· 0 citations
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