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Single-cell and spatial detection of senescent cells using DeepScence.

Yilong Qu1, Beijie Ji2, Runze Dong3

  • 1Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.

Cell Genomics
|October 8, 2025
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Summary

We created DeepScence, a new deep learning method for accurately identifying senescent cells. This tool analyzes single-cell and spatial transcriptomics data, improving upon existing senescence detection methods.

Keywords:
agingcellular senescencemachine learningscRNA-seqsenescence gene setsenescence identificationspatial transcriptomics

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Area of Science:

  • Cellular senescence
  • Transcriptomics
  • Bioinformatics

Background:

  • Accurate identification of senescent cells is crucial for understanding their roles in health and disease.
  • Existing methods for senescent cell detection have limitations in accuracy and scope.
  • Senescence-associated gene expression patterns are key indicators of cellular senescence.

Purpose of the Study:

  • To develop a novel computational method for precise senescent cell identification.
  • To leverage deep neural networks for analyzing transcriptomic data.
  • To create a robust senescence-associated gene set for improved detection.

Main Methods:

  • Development of DeepScence, a deep neural network-based method.
  • Creation of CoreScence, a curated senescence-associated gene set.
  • Application of DeepScence to single-cell and spatial transcriptomics datasets.

Main Results:

  • DeepScence accurately identifies senescent cells in diverse single-cell gene expression datasets (in vitro and in vivo).
  • The method demonstrates high performance on spatial transcriptomics data from various platforms.
  • DeepScence significantly outperforms existing methods for senescent cell identification.

Conclusions:

  • DeepScence provides a powerful and accurate tool for senescent cell identification in transcriptomic studies.
  • The CoreScence gene set enhances the specificity and sensitivity of senescence detection.
  • This method advances the study of cellular senescence in both molecular and spatial contexts.