Evidence map›Paper›PMID 42804716›Full record

ArticleBioinformatics (Oxford, England)2026

scLDM: a conditional diffusion framework for single-cell perturbation prediction.

Boyang Wu, Yuhang Liu, Yue Cheng, Xiangrong Liu, Quan Zou, Leyi Wei, Lei Xu

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Boyang WuSchool of Information, Xiamen University, Xiamen, 361005, China.
Yuhang LiuFaculty of Applied Sciences, Macao Polytechnic University, Macao SAR, 999078, China.
Yue ChengSchool of Electronic and Communication Engineering, Shenzhen Polytechnic University, Shenzhen, 518055, China.
Xiangrong LiuSchool of Information, Xiamen University, Xiamen, 361005, China.ORCID 0000-0001-9885-1978
Quan ZouInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, 611731, China.ORCID 0000-0001-6406-1142
Leyi WeiFaculty of Applied Sciences, Macao Polytechnic University, Macao SAR, 999078, China.
Lei XuSchool of Electronic and Communication Engineering, Shenzhen Polytechnic University, Shenzhen, 518055, China.ORCID 0000-0002-6440-6881

Funding

National Natural Science Foundation of China 62131004National Natural Science Foundation of China 62271329National Natural Science Foundation of China 62322112National Natural Science Foundation of China 62422113Shenzhen Polytechnic University Research Fund 6025310047K
6 · The paper itself

Abstract

motivationAccurate prediction of single-cell responses to external stimuli is pivotal for deciphering gene regulatory mechanisms and accelerating data-driven drug discovery. However, effectively capturing the complex, non-linear mapping between intrinsic cell states and external stimuli remains an open problem.

resultsWe propose scLDM, a generative framework based on latent diffusion models for predicting single-cell perturbation responses. scLDM first compresses high-dimensional gene expression into a compact latent space via a variational autoencoder, followed by a conditional diffusion process to generate post-perturbation states, explicitly guided by pre-perturbation cellular state, cell type, and perturbation type. Systematic evaluations on six datasets across diverse biological settings, spanning pharmacological stimulation, viral infection, helminth infection, genetic perturbations, and multi-species immune response contexts, demonstrate that scLDM achieves superior predictive accuracy compared to state-of-the-art methods. Furthermore, the model exhibits strong interpretability, as the learned perturbation embeddings show high functional alignment with known biological mechanisms. Overall, scLDM provides a robust and biologically consistent strategy for in silico perturbation screening. AVAILABILITY: The code is available at https://github.com/samrogers1233/scLDM and archived on Zenodo at https://doi.org/10.5281/zenodo.22658164.

Indexed as

Computational BiologySingle-Cell AnalysisAlgorithmsAnimalsAutoencoderHumansSingle-Cell Gene Expression Analysis

Identifiers

PMID42804716
PMCPMC13661255

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.