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

IF 5.4
Boyang Wu, Yuhang Liu, Yue Cheng, Xiangrong Liu, Quan Zou, Leyi Wei, Lei Xu
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Abstract

Motivation: Accurate 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.

Results: We 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.

单细胞微扰预测的条件扩散框架。
动机:准确预测单细胞对外部刺激的反应对于破译基因调控机制和加速数据驱动的药物发现至关重要。然而,有效地捕捉细胞内在状态和外部刺激之间复杂的非线性映射仍然是一个悬而未决的问题。结果:我们提出了scLDM,一个基于潜在扩散模型的生成框架,用于预测单细胞扰动响应。scLDM首先通过变分自编码器将高维基因表达压缩到紧凑的潜在空间中,然后通过条件扩散过程生成后扰动状态,明确由扰动前的细胞状态、细胞类型和扰动类型指导。对不同生物环境下的六个数据集进行系统评估,包括药理学刺激、病毒感染、蠕虫感染、遗传扰动和多物种免疫反应,结果表明,与最先进的方法相比,scLDM具有更高的预测准确性。此外,该模型具有很强的可解释性,因为学习到的微扰嵌入显示出与已知生物机制的高度功能一致性。总的来说,scLDM提供了一个强大的和生物学上一致的策略,在硅微扰筛选。可用性:代码可在https://github.com/samrogers1233/scLDM上获得,并在Zenodo上存档https://doi.org/10.5281/zenodo.22658164.Supplementary: information:补充数据可在Bioinformatics在线获得。
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