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STGAT: Graph attention networks for deconvolving spatial transcriptomics data. | LitMetric

STGAT: Graph attention networks for deconvolving spatial transcriptomics data.

Comput Methods Programs Biomed

College of Medicine and Bioinformation Engineering, Northeastern University, Shenyang, 110819, Liaoning, China.

Published: December 2024

AI Article Synopsis

  • Spatially resolved gene expression profiles are important for understanding tissue function, but current methods lack single-cell resolution, which STGAT aims to improve by integrating these profiles with single-cell RNA sequencing data.
  • STGAT uses graph attention networks to create pseudo-spatial transcriptomic data and constructs a combined graph to better analyze the relationships within and between datasets, enhancing accuracy in identifying cell types.
  • Testing on various datasets shows that STGAT outperforms six existing methods, providing more accurate and reliable predictions of cell-type composition.

Article Abstract

Background And Objective: Spatially resolved gene expression profiles are crucial for understanding tissue structure and function. However, the lack of single-cell resolution in these profiles demands their integration with single-cell RNA sequencing data for accurate dataset deconvolution. We propose STGAT, an innovative deconvolution method that leverages graph attention networks to enhance spatial transcriptomic (ST) data analysis.

Methods: STGAT generates pseudo-ST data that more comprehensively represents the cell-type composition within real-ST data by using three different sampling probabilities. A comprehensive combined graph is then constructed to capture the complex relationships both across pseudo- and real-ST data and within each dataset. Moreover, integrating a graph attention network further enables STGAT to dynamically assign the weights to the connections between spots, significantly enhancing the accuracy of cell-type composition predictions.

Results: Extensive comparative experiments on simulated and real-world datasets, demonstrate the superior performance of STGAT for cell-type deconvolution. The method outperforms six established methods and is robust across various biological contexts.

Conclusion: STGAT exhibits more precise results in cell-type composition inference that are more consistent with the known knowledge, suggesting its potential utility in improving the resolution and accuracy of spatial transcriptomics data analysis.

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Source
http://dx.doi.org/10.1016/j.cmpb.2024.108431DOI Listing

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