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A comprehensive survey of dimensionality reduction and clustering methods for single-cell and spatial transcriptomics

Yidi Sun1, Lingling Kong1, Jiayi Huang1

  • 1School of Computer Science and Technology, Hainan University, Haikou 570228, China.

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|June 11, 2024
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This review summarizes essential dimensionality reduction and clustering algorithms for single-cell and spatial transcriptomic data analysis. These methods help visualize and group cells, revealing cellular diversity and guiding further research.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Single-cell transcriptomics and spatial transcriptomics are powerful tools for biological research.
  • Analyzing this data requires dimensionality reduction and clustering due to its high-dimensional nature.
  • These techniques are crucial for visualizing data and identifying distinct cell populations.

Purpose of the Study:

  • To systematically review widely recognized algorithms for dimensionality reduction and clustering.
  • To provide insights for developing novel analytical tools for transcriptomic data.
  • To aid researchers in analyzing and interpreting single-cell and spatial transcriptomic datasets.

Main Methods:

  • Review of established algorithms for dimensionality reduction (e.g., PCA, t-SNE, UMAP).
  • Review of established algorithms for clustering (e.g., k-means, hierarchical clustering, graph-based clustering).
  • Focus on applications in single-cell and spatial transcriptomic data analysis.

Main Results:

  • Identification of key algorithms commonly used for transcriptomic data analysis.
  • Demonstration of how dimensionality reduction aids in data visualization and relationship observation.
  • Explanation of how clustering facilitates the identification of cell subpopulations and cellular diversity.

Conclusions:

  • Dimensionality reduction and clustering are indispensable for analyzing high-dimensional transcriptomic data.
  • A systematic summary of algorithms provides valuable guidance for researchers.
  • This review contributes to the advancement of computational tools in transcriptomics.