{"title":"STGAT:用于解卷积空间转录组学数据的图注意网络。","authors":"","doi":"10.1016/j.cmpb.2024.108431","DOIUrl":null,"url":null,"abstract":"<div><h3>Background and Objective:</h3><div>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.</div></div><div><h3>Methods:</h3><div>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.</div></div><div><h3>Results:</h3><div>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.</div></div><div><h3>Conclusion:</h3><div>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.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":null,"pages":null},"PeriodicalIF":4.9000,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"STGAT: Graph attention networks for deconvolving spatial transcriptomics data\",\"authors\":\"\",\"doi\":\"10.1016/j.cmpb.2024.108431\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background and Objective:</h3><div>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.</div></div><div><h3>Methods:</h3><div>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.</div></div><div><h3>Results:</h3><div>Extensive comparative experiments on simulated and real-world datasets, demonstrate the superior performance of STGAT for cell-type deconvolution. 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引用次数: 0
摘要
背景和目的:空间分辨率的基因表达谱对于了解组织结构和功能至关重要。然而,由于这些图谱缺乏单细胞分辨率,因此需要将其与单细胞 RNA 测序数据整合,以实现准确的数据集解卷。我们提出的 STGAT 是一种创新的解卷积方法,它利用图注意网络来加强空间转录组(ST)数据分析:STGAT 通过使用三种不同的采样概率生成伪 ST 数据,从而更全面地反映真实 ST 数据中的细胞类型组成。方法:STGAT 利用三种不同的采样概率生成伪 ST 数据,更全面地反映真实 ST 数据中的细胞类型组成,然后构建综合的组合图,捕捉伪 ST 数据和真实 ST 数据之间以及每个数据集内部的复杂关系。此外,通过整合图注意网络,STGAT 还能动态分配点之间连接的权重,从而显著提高细胞类型组成预测的准确性:结果:在模拟和真实世界数据集上进行的广泛对比实验证明,STGAT 在细胞类型解卷积方面具有卓越的性能。结果:在模拟和真实世界数据集上进行的大量对比实验证明了 STGAT 在细胞类型解卷积方面的优越性能,该方法优于六种成熟的方法,并且在各种生物环境下都很稳定:STGAT在细胞类型组成推断方面表现出更精确的结果,与已知知识更加一致,这表明它在提高空间转录组学数据分析的分辨率和准确性方面具有潜在的实用性。
STGAT: Graph attention networks for deconvolving spatial transcriptomics data
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.
期刊介绍:
To encourage the development of formal computing methods, and their application in biomedical research and medical practice, by illustration of fundamental principles in biomedical informatics research; to stimulate basic research into application software design; to report the state of research of biomedical information processing projects; to report new computer methodologies applied in biomedical areas; the eventual distribution of demonstrable software to avoid duplication of effort; to provide a forum for discussion and improvement of existing software; to optimize contact between national organizations and regional user groups by promoting an international exchange of information on formal methods, standards and software in biomedicine.
Computer Methods and Programs in Biomedicine covers computing methodology and software systems derived from computing science for implementation in all aspects of biomedical research and medical practice. It is designed to serve: biochemists; biologists; geneticists; immunologists; neuroscientists; pharmacologists; toxicologists; clinicians; epidemiologists; psychiatrists; psychologists; cardiologists; chemists; (radio)physicists; computer scientists; programmers and systems analysts; biomedical, clinical, electrical and other engineers; teachers of medical informatics and users of educational software.