scGALA advances graph link prediction-based cell alignment for comprehensive data integration and harmonization

Single-cell technologies have transformed our understanding of cellular heterogeneity through multimodal data acquisition. However, robust cell alignment remains a major challenge for data integration and harmonization, including batch correction, label transfer, and multi-omics integration. Many existing methods constrain alignment based on rigid feature-wise distance metrics, limiting their ability to capture accurate cell correspondence across diverse cell populations and conditions. We introduce scGALA, a graph-based learning framework that redefines cell alignment by combining graph attention networks with a score-driven, task-independent optimization strategy. scGALA constructs enriched graphs of cell-cell relationships by integrating gene expression profiles with auxiliary information, such as spatial coordinates, and iteratively refines alignment via self-supervised graph link prediction, where a deep neural network is trained to identify and reinforce high-confidence correspondences across datasets. In extensive benchmarks, scGALA identifies over 25 percent more high-confidence alignments without compromising accuracy. By improving the core step of cell alignment, scGALA serves as a versatile enhancer for a wide range of single-cell data integration tasks.

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Publication Details

Journal
Nature Communications
Published
2025-11-26
DOI
https://doi.org/10.1038/s41467-025-66644-5
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
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article

scGALA advances graph link prediction-based cell alignment for comprehensive data integration and harmonization

Iain C. Clark, Guo Jiang, Jun Ding, Darcy E. Wagner et al.
Nature Communications
Single-cell and spatial transcriptomics
article

scGALA advances graph link prediction-based cell alignment for comprehensive data integration and harmonization

Iain C. Clark, Guo Jiang, Jun Ding, Darcy E. Wagner, Gregory J. Fonseca, Hui Wang, Kailu Song
article en

Abstract

Single-cell technologies have transformed our understanding of cellular heterogeneity through multimodal data acquisition. However, robust cell alignment remains a major challenge for data integration and harmonization, including batch correction, label transfer, and multi-omics integration. Many existing methods constrain alignment based on rigid feature-wise distance metrics, limiting their ability to capture accurate cell correspondence across diverse cell populations and conditions. We introduce scGALA, a graph-based learning framework that redefines cell alignment by combining graph attention networks with a score-driven, task-independent optimization strategy. scGALA constructs enriched graphs of cell-cell relationships by integrating gene expression profiles with auxiliary information, such as spatial coordinates, and iteratively refines alignment via self-supervised graph link prediction, where a deep neural network is trained to identify and reinforce high-confidence correspondences across datasets. In extensive benchmarks, scGALA identifies over 25 percent more high-confidence alignments without compromising accuracy. By improving the core step of cell alignment, scGALA serves as a versatile enhancer for a wide range of single-cell data integration tasks.

Nature CommunicationsVol. 16(1)
QB3 (US), Brigham and Women's Hospital (US), Harvard University (US), Khalifa University of Science and Technology (AE), Shanghai Jiao Tong University (CN), Lund University (SE), McGill University Health Centre (CA), Mila - Quebec Artificial Intelligence Institute (CA), McGill University (CA)
Openalex Percentile: Top 67%
Single-cell and spatial transcriptomics
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