Evidence map›Paper›PMID 41863296›Full record

ArticleBioinformatics (Oxford, England)2026

SA2E: spatial-aware auto-encoder for cell type deconvolution of spatial transcriptomics data.

Yaxiong Ma, Zengfa Dou, Yuhong Zha, Xiaoke Ma

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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 authors.

Yaxiong MaSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710071, China.
Zengfa DouSchool of Computer and Information Science, Qinghai Institute of Technology, Xining, Qinghai 810003, China.
Yuhong ZhaSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710071, China.
Xiaoke MaSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710071, China.ORCID 0000-0002-5604-7137

Funding

Joint Funds of the National Natural Science Foundation of China 62272361Joint Funds of the National Natural Science Foundation of China 81760608Joint Funds of the National Natural Science Foundation of China U22A20345Noncommunicable Chronic Diseases-National Science and Technology Major Project 2024ZD0531100Noncommunicable Chronic Diseases-National Science and Technology Major Project 2024ZD0531103
6 · The paper itself

Abstract

motivationSpatial transcriptomics (ST) technologies measure gene expression together with spatial locations, but each spot typically contains a mixture of cell types, posing a challenge for downstream analysis. Cell-type deconvolution aims to infer spot-wise cell-type proportions by integrating single-cell RNA-seq (scRNA-seq) and ST data. Many existing methods construct cell-type signatures from predefined marker genes, which can limit performance when marker information is incomplete or unavailable.

resultsTo address this limitation, we propose a spatial-aware auto-encoder framework (SA2E) for cell-type deconvolution without requiring predefined cell-type biomarkers. SA2E learns latent spot representations using a spatially regularized auto-encoder that preserves the local topology of the spot spatial graph. Based on these representations, SA2E learns cell-type signatures by enforcing them to reconstruct ST expression. In our framework, simulated ST data with known proportions are used for supervised pretraining, while real ST data are optimized using the reconstruction objective. Extensive experiments on simulated and real ST datasets demonstrate that SA2E outperforms state-of-the-art deconvolution baselines. AVAILABILITY AND IMPLEMENTATION: The code of SA2E is available at Github (https://github.com/xkmaxidian/SA2E) and Zenodo (DOI: 10.5281/zenodo.18765467).

Indexed as

Computational BiologyGene Expression ProfilingSpatial TranscriptomicsAlgorithmsAnimalsAutoencoderHumansSingle-Cell Gene Expression Analysis

Identifiers

PMID41863296
PMCPMC13070677

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