Deciphering Cell Cycle Dynamics and Cell States in Single-cell RNA-seq data with SPAE

Rapid advances in single-cell RNA sequencing (scRNA-seq) technology have enabled the investigation of gene expression changes at the single-cell level, particularly for elucidating the heterogeneity among cells and complex biological processes. This technique reveals subtle molecular differences within individual cells, thereby offering a unique viewpoint for the investigation of cell cycle progression, cellular differentiation, and disease pathogenesis. However, accurately identifying and analyzing cell cycle dynamics in scRNA-seq data remains challenging due to the complexity of the data and the subtle differences between cell states. To address this challenge, we developed the integrated Sinusoidal and Piecewise AutoEncoder (SPAE), an autoencoder-based piecewise linear model, for characterizing the cell cycle dynamics and cell states in scRNA-seq data. Compared with existing methods, SPAE demonstrates substantially improved accuracy and robustness in cell cycle characterization. Additionally, SPAE can accurately predict cancer cell cycle transitions and effectively facilitate the removal of cell cycle effects from gene expression data. SPAE is available for non-commercial use at https://github.com/YaJahn/SPAE .

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-03-08
DOI
https://doi.org/10.64898/2026.03.05.709782
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

Deciphering Cell Cycle Dynamics and Cell States in Single-cell RNA-seq data with SPAE

Jiahao Yi, X. Zhou, Yuan-nong Ye, Jiajia Liu et al.
bioRxiv (Cold Spring Harbor Laboratory)
Single-cell and spatial transcriptomics
article

Deciphering Cell Cycle Dynamics and Cell States in Single-cell RNA-seq data with SPAE

Jiahao Yi, X. Zhou, Yuan-nong Ye, Jiajia Liu, Peng Guo
article en

Abstract

Rapid advances in single-cell RNA sequencing (scRNA-seq) technology have enabled the investigation of gene expression changes at the single-cell level, particularly for elucidating the heterogeneity among cells and complex biological processes. This technique reveals subtle molecular differences within individual cells, thereby offering a unique viewpoint for the investigation of cell cycle progression, cellular differentiation, and disease pathogenesis. However, accurately identifying and analyzing cell cycle dynamics in scRNA-seq data remains challenging due to the complexity of the data and the subtle differences between cell states. To address this challenge, we developed the integrated Sinusoidal and Piecewise AutoEncoder (SPAE), an autoencoder-based piecewise linear model, for characterizing the cell cycle dynamics and cell states in scRNA-seq data. Compared with existing methods, SPAE demonstrates substantially improved accuracy and robustness in cell cycle characterization. Additionally, SPAE can accurately predict cancer cell cycle transitions and effectively facilitate the removal of cell cycle effects from gene expression data. SPAE is available for non-commercial use at https://github.com/YaJahn/SPAE .

bioRxiv (Cold Spring Harbor Laboratory)
Guiyang Medical University (CN), Affiliated Hospital of Guizhou Medical University (CN), The University of Texas Health Science Center (US), The University of Texas Health Science Center at Houston (US)
National Science Foundation, National Natural Science Foundation of China, National Institutes of Health
Openalex Percentile: Top 29%
Single-cell and spatial transcriptomics
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Deciphering Cell Cycle Dynamics and Cell States in Single-cell RNA-seq data with SPAE — Jiahao Yi, X. Zhou, et al. · bioRxiv (Cold Spring Harbor Laboratory) (2026) | TGRS Research Map | TGRS