用AI自动标注脑细胞基因特征,提升未知基因注释准确率。
BRAINCELL-AID: An Agentic AI Created Brain Cell Type Resource for Community Annotation
- 构建多智能体AI系统,融合文献检索与本体标签进行基因集注释。
- 对小鼠基因集前5个预测中77%正确,覆盖5322个脑细胞簇。
- 适合神经科学、单细胞组学研究者用于细胞类型功能分析。
单细胞RNA测序已极大推动了细胞类型及其转录特征的发现,但对功能未明基因的注释仍具挑战。传统方法如基因集富集分析(GSEA)依赖高质量注释,表现不佳。大语言模型虽有潜力,却难以在结构化本体中表达复杂生物学知识。为此,我们提出BRAINCELL-AID,一个整合自由文本描述与本体标签的多智能体AI系统。通过引入检索增强生成(RAG),建立可迭代优化的智能工作流,利用相关PubMed文献减少幻觉并提升可解释性。该方法在小鼠基因集的前5个预测中达到77%的正确率。应用此方法,我们为脑计划细胞普查网络生成的小鼠脑细胞图谱中的5,322个脑细胞簇完成注释,揭示区域特异性基因共表达模式,推断基因组合的功能角色,并识别基底节相关细胞类型的神经学意义描述。该系统为社区驱动的细胞类型注释提供宝贵资源。
原文摘要 · Abstract (English)
Single-cell RNA sequencing has transformed our ability to identify diverse cell types and their transcriptomic signatures. However, annotating these signatures-especially those involving poorly characterized genes-remains a major challenge. Traditional methods, such as Gene Set Enrichment Analysis (GSEA), depend on well-curated annotations and often perform poorly in these contexts. Large Language Models (LLMs) offer a promising alternative but struggle to represent complex biological knowledge within structured ontologies. To address this, we present BRAINCELL-AID (BRAINCELL-AID: https://biodataai.uth.edu/BRAINCELL-AID), a novel multi-agent AI system that integrates free-text descriptions with ontology labels to enable more accurate and robust gene set annotation. By incorporating retrieval-augmented generation (RAG), we developed a robust agentic workflow that refines predictions using relevant PubMed literature, reducing hallucinations and enhancing interpretability. Using this workflow, we achieved correct annotations for 77% of mouse gene sets among their top predictions. Applying this approach, we annotated 5,322 brain cell clusters from the comprehensive mouse brain cell atlas generated by the BRAIN Initiative Cell Census Network, enabling novel insights into brain cell function by identifying region-specific gene co-expression patterns and inferring functional roles of gene ensembles. BRAINCELL-AID also identifies Basal Ganglia-related cell types with neurologically meaningful descriptions. Hence, we create a valuable resource to support community-driven cell type annotation.
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