gwSPADE: gene frequency-weighted reference-free deconvolution in spatial transcriptomics

Most spatial transcriptomics (ST) technologies (e.g. 10× Visium) operate at the multicellular level, where each spatial location often contains a mixture of cells with heterogeneous cell types. Thus, effective deconvolution of cell type compositions is critical for downstream analysis. Although reference-based deconvolution methods have been proposed, they depend on the availability of reference data, which may not always be accessible. Additionally, within a deconvolved cell type, cellular heterogeneity may still exist, requiring further deconvolution to uncover finer structures for a better understanding of this complexity. Here, we present gwSPADE, a gene frequency-weighted reference-free SPAtial DEconvolution method for ST data. gwSPADE requires only the gene count matrix and utilizes appropriate weighting schemes within a topic model to accurately recover cell type transcriptional profiles and their proportions at each spatial location, without relying on external single-cell reference information. In various simulations and real data analyses, gwSPADE demonstrates scalability across various platforms and shows superior performance over existing reference-free deconvolution methods such as STdeconvolve.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-09-23
DOI
https://doi.org/10.1093/nar/gkaf966
Citations
1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.81
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article

gwSPADE: gene frequency-weighted reference-free deconvolution in spatial transcriptomics

Nina G. Steele, Yuehua Cui, Aoqi Xie
1 citations
Nucleic Acids Research
Single-cell and spatial transcriptomics
0.81
article

gwSPADE: gene frequency-weighted reference-free deconvolution in spatial transcriptomics

Nina G. Steele, Yuehua Cui, Aoqi Xie
article en
1 citations

Abstract

Most spatial transcriptomics (ST) technologies (e.g. 10× Visium) operate at the multicellular level, where each spatial location often contains a mixture of cells with heterogeneous cell types. Thus, effective deconvolution of cell type compositions is critical for downstream analysis. Although reference-based deconvolution methods have been proposed, they depend on the availability of reference data, which may not always be accessible. Additionally, within a deconvolved cell type, cellular heterogeneity may still exist, requiring further deconvolution to uncover finer structures for a better understanding of this complexity. Here, we present gwSPADE, a gene frequency-weighted reference-free SPAtial DEconvolution method for ST data. gwSPADE requires only the gene count matrix and utilizes appropriate weighting schemes within a topic model to accurately recover cell type transcriptional profiles and their proportions at each spatial location, without relying on external single-cell reference information. In various simulations and real data analyses, gwSPADE demonstrates scalability across various platforms and shows superior performance over existing reference-free deconvolution methods such as STdeconvolve.

Nucleic Acids ResearchVol. 53(18)
Henry Ford Health System (US), Wayne State University (US), Henry Ford Hospital (US), Michigan State University (US), University of Cincinnati Medical Center (US)
Openalex Percentile: Top 23%
Single-cell and spatial transcriptomics
0.81
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