Single-cell sequencing has advanced our understanding of cellular heterogeneity and disease pathology, offering insights into cellular behavior and immune mechanisms. However, extracting meaningful phenotype-related features is challenging due to noise, batch effects, and irrelevant biological signals. To address this, we introduce Deep scSTAR (DscSTAR), a deep learning-based tool designed to enhance phenotype-associated features. DscSTAR identified HSP+ FKBP4+ T cells in CD8+ T cells, which linked to immune dysfunction and resistance to immune checkpoint blockade in non-small cell lung cancer. It has also enhanced spatial transcriptomics analysis of renal cell carcinoma, revealing interactions between cancer cells, CD8+ T cells, and tumor-associated macrophages that may promote immune suppression and affect outcomes. In hepatocellular carcinoma, it highlighted the role of S100A12+ neutrophils and cancer-associated fibroblasts in forming tumor immune barriers and potentially contributing to immunotherapy resistance. These findings demonstrate DscSTAR's capacity to model and extract phenotype-specific information, advancing our understanding of disease mechanisms and therapy resistance.
Deep scSTAR: leveraging deep learning for the extraction and enhancement of phenotype-associated features from single-cell RNA sequencing and spatial transcriptomics data.
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作者:Gao Lianchong, Liu Yujun, Zou Jiawei, Deng Fulan, Liu Zheqi, Zhang Zhen, Zhao Xinran, Chen Lei, Tong Henry H Y, Ji Yuan, Le Huangying, Zou Xin, Hao Jie
| 期刊: | Briefings in Bioinformatics | 影响因子: | 7.700 |
| 时间: | 2025 | 起止号: | 2025 May 1; 26(3):bbaf160 |
| doi: | 10.1093/bib/bbaf160 | ||
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