MultiPert: An adversarial alignment and dual attention framework for single-cell multi-omics perturbation prediction

Precise prediction of perturbation responses is essential in systems biology research, as it plays a pivotal role in characterizing cellular identities and elucidating the regulatory mechanisms of biological pathways. Existing perturbation-responses prediction approaches are predominantly confined to single-modality transcriptomic data, limiting their capacity to capture cross-layer molecular effects. Here, we present MultiPert, a deep learning framework specifically designed for predicting perturbation responses in single-cell multi-omics data. MultiPert employs modality-specific encoders with dedicated pretraining, integrates perturbation through a dual-attention mechanism, and achieves cross-modal alignment via adversarial training. Benchmarking on human THP-1 and kidney multi-omics datasets demonstrates that MultiPert reliably predicts both perturbed gene expression and protein abundance profiles, achieving superior accuracy and stability compared to state-of-the-art strategies. MultiPert generalizes to unseen perturbations and uncovers regulatory mechanisms of immune checkpoint molecules based on perturbed proteomic predictions. In addition, enrichment analyses of perturbed transcriptomic predictions reveal immune-related pathways. By providing an integrated and interpretable framework, MultiPert expands the scope of perturbation modeling at the multi-omics level, thereby offering a robust methodological foundation for comprehensive research into pathogenesis and drug discovery.

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Publication Details

Journal
PLoS Computational Biology
Published
2026-03-11
DOI
https://doi.org/10.1371/journal.pcbi.1014054
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

MultiPert: An adversarial alignment and dual attention framework for single-cell multi-omics perturbation prediction

Xinyue Tang, Na Zhao, Jijun Tang, Fei Guo et al.
PLoS Computational Biology
Single-cell and spatial transcriptomics
article

MultiPert: An adversarial alignment and dual attention framework for single-cell multi-omics perturbation prediction

Xinyue Tang, Na Zhao, Jijun Tang, Fei Guo, Cheng Liang, Jiawei Li
article en

Abstract

Precise prediction of perturbation responses is essential in systems biology research, as it plays a pivotal role in characterizing cellular identities and elucidating the regulatory mechanisms of biological pathways. Existing perturbation-responses prediction approaches are predominantly confined to single-modality transcriptomic data, limiting their capacity to capture cross-layer molecular effects. Here, we present MultiPert, a deep learning framework specifically designed for predicting perturbation responses in single-cell multi-omics data. MultiPert employs modality-specific encoders with dedicated pretraining, integrates perturbation through a dual-attention mechanism, and achieves cross-modal alignment via adversarial training. Benchmarking on human THP-1 and kidney multi-omics datasets demonstrates that MultiPert reliably predicts both perturbed gene expression and protein abundance profiles, achieving superior accuracy and stability compared to state-of-the-art strategies. MultiPert generalizes to unseen perturbations and uncovers regulatory mechanisms of immune checkpoint molecules based on perturbed proteomic predictions. In addition, enrichment analyses of perturbed transcriptomic predictions reveal immune-related pathways. By providing an integrated and interpretable framework, MultiPert expands the scope of perturbation modeling at the multi-omics level, thereby offering a robust methodological foundation for comprehensive research into pathogenesis and drug discovery.

PLoS Computational BiologyVol. 22(3)
Central South University (CN), Tianjin University (CN), Shenzhen University (CN), Shandong Normal University (CN), Shenzhen Institutes of Advanced Technology (CN), Shenzhen Technology University (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 25%
Single-cell and spatial transcriptomics
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