T细胞受体
模态(人机交互)
代表(政治)
转录组
计算生物学
资源(消歧)
计算机科学
模式
T细胞
生物
人工智能
免疫系统
遗传学
基因
政治学
基因表达
计算机网络
政治
法学
社会科学
社会学
作者
Yicheng Gao,Kejing Dong,Yuli Gao,Xuan Jin,Jingya Yang,Gang Yan,Qi Liu
出处
期刊:Cell genomics
[Elsevier BV]
日期:2024-04-29
卷期号:4 (5): 100553-100553
被引量:13
标识
DOI:10.1016/j.xgen.2024.100553
摘要
Single-cell RNA sequencing (scRNA-seq) and T cell receptor sequencing (TCR-seq) are pivotal for investigating T cell heterogeneity. Integrating these modalities, which is expected to uncover profound insights in immunology that might otherwise go unnoticed with a single modality, faces computational challenges due to the low-resource characteristics of the multimodal data. Herein, we present UniTCR, a novel low-resource-aware multimodal representation learning framework designed for the unified cross-modality integration, enabling comprehensive T cell analysis. By designing a dual-modality contrastive learning module and a single-modality preservation module to effectively embed each modality into a common latent space, UniTCR demonstrates versatility in connecting TCR sequences with T cell transcriptomes across various tasks, including single-modality analysis, modality gap analysis, epitope-TCR binding prediction, and TCR profile cross-modality generation, in a low-resource-aware way. Extensive evaluations conducted on multiple scRNA-seq/TCR-seq paired datasets showed the superior performance of UniTCR, exhibiting the ability of exploring the complexity of immune system.
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