Pseudotime-conditioned diffusion models for imputing time-series single-cell data

Abstract Motivation Probabilistic diffusion-based imputation methods have demonstrated superior performance over many state-of-the-art approaches for imputing single-cell data. However, existing methods typically rely on isotropic Gaussian noise and canonical observation time, limiting their ability to capture structured temporal dependencies and continuous cellular dynamics. In time-series single-cell RNA-seq (scRNA-seq) data, these limitations are exacerbated by the small number of experimentally measured time points and the substantial heterogeneity among cells collected at the same time point, causing observed time labels to poorly reflect true biological progression. Results To address these challenges, we propose the first pseudotime-conditioned diffusion-based imputation framework for time-series scRNA-seq data, consisting of two trajectory-aware models: pseudotime-conditioned conditional score-based diffusion imputation (P-CSDI) and pseudotime-conditioned hybrid-noise CSDI (PH-CSDI). P-CSDI incorporates inferred pseudotime as a conditioning signal to guide the denoising process with biologically meaningful temporal structure, while PH-CSDI further introduces hybrid structured noise to improve frequency-aware temporal modeling. By leveraging pseudotime as a continuous representation of cellular progression, both models enable trajectory-aware and temporally coherent reconstruction of missing gene expression values. P-CSDI and PH-CSDI consistently reduce mean absolute error (MAE) and root mean squared error (RMSE) by approximately 40%–60% compared with state-of-the-art imputation methods across two scRNA-seq datasets under diverse missingness settings. These findings highlight the importance of incorporating biologically informed temporal structure into diffusion-based generative models for accurate imputation of dynamic single-cell transcriptomic data. Availability The computer code and data for the proposed method are available on GitHub: https://github.com/gbishop345/pseudotime-CSDI.

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Publication Details

Journal
Bioinformatics Advances
Published
2026-08-24
DOI
https://doi.org/10.1093/bioadv/vbag248
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

Pseudotime-conditioned diffusion models for imputing time-series single-cell data

Haijun Gong, Min-Ho Ku, Tong Si, Graham Bishop et al.
Bioinformatics Advances
Single-cell and spatial transcriptomics
article

Pseudotime-conditioned diffusion models for imputing time-series single-cell data

Haijun Gong, Min-Ho Ku, Tong Si, Graham Bishop, Daniel Lee
article en

Abstract

Abstract Motivation Probabilistic diffusion-based imputation methods have demonstrated superior performance over many state-of-the-art approaches for imputing single-cell data. However, existing methods typically rely on isotropic Gaussian noise and canonical observation time, limiting their ability to capture structured temporal dependencies and continuous cellular dynamics. In time-series single-cell RNA-seq (scRNA-seq) data, these limitations are exacerbated by the small number of experimentally measured time points and the substantial heterogeneity among cells collected at the same time point, causing observed time labels to poorly reflect true biological progression. Results To address these challenges, we propose the first pseudotime-conditioned diffusion-based imputation framework for time-series scRNA-seq data, consisting of two trajectory-aware models: pseudotime-conditioned conditional score-based diffusion imputation (P-CSDI) and pseudotime-conditioned hybrid-noise CSDI (PH-CSDI). P-CSDI incorporates inferred pseudotime as a conditioning signal to guide the denoising process with biologically meaningful temporal structure, while PH-CSDI further introduces hybrid structured noise to improve frequency-aware temporal modeling. By leveraging pseudotime as a continuous representation of cellular progression, both models enable trajectory-aware and temporally coherent reconstruction of missing gene expression values. P-CSDI and PH-CSDI consistently reduce mean absolute error (MAE) and root mean squared error (RMSE) by approximately 40%–60% compared with state-of-the-art imputation methods across two scRNA-seq datasets under diverse missingness settings. These findings highlight the importance of incorporating biologically informed temporal structure into diffusion-based generative models for accurate imputation of dynamic single-cell transcriptomic data. Availability The computer code and data for the proposed method are available on GitHub: https://github.com/gbishop345/pseudotime-CSDI.

Bioinformatics Advances
Saint Louis University (ES), Saint Louis University (US)
National Institutes of Health
Openalex Percentile: Top 17%
Single-cell and spatial transcriptomics
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