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Updated: Jan 20, 2026

Mining Spatial Transcriptomics Datasets using DeepSpaceDB
Published on: September 5, 2025
Adding highly variable genes to spatially variable genes can improve cell type clustering performance in spatial
Yijun Li1, Stefan Stanojevic2, Bing He2
1Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, United States.
Combining highly variable (HV) genes with spatially variable (SV) genes enhances cell type clustering in spatial transcriptomics. This integrated approach improves the analysis of gene expression within tissue samples.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- Spatial transcriptomics enables transcriptome analysis within tissue context.
- Spatially variable (SV) genes exhibit spatial autocorrelation and are used for clustering.
- Highly variable (HV) genes show significant cell-to-cell expression variation and are conventionally used for clustering.
Purpose of the Study:
- To evaluate if incorporating highly variable (HV) genes alongside spatially variable (SV) genes improves cell type clustering in spatial transcriptomics data.
- To compare the performance of HV genes, SV genes, and their combined set for clustering.
Main Methods:
- Tested clustering performance using HV genes, SV genes, and their union (concatenation).
- Utilized over 50 diverse spatial transcriptomics datasets across multiple platforms.
- Employed a range of spatial and non-spatial metrics for evaluation.
Main Results:
- Combining HV genes and SV genes demonstrated improved overall cell-type clustering performance.
- The integrated gene set outperformed individual gene sets in various datasets and metrics.
Conclusions:
- The union of highly variable and spatially variable genes offers a more robust approach for cell type identification in spatial transcriptomics.
- This combined strategy enhances the accuracy and reliability of spatial transcriptomics analyses.
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