反褶积
计算机科学
计算生物学
细胞
标杆管理
效应器
贝叶斯概率
电池类型
贝叶斯定理
人工智能
癌症
肿瘤异质性
细胞存活
卷积(计算机科学)
肺癌
国家(计算机科学)
恶性细胞
盲反褶积
生物
作者
Jurriaan Janssen,Mischa Steketee,Aryamaan Bose,Saskia van Asten,Paul P. Eijk,Frederike Dijk,Arantza Fariña Sarasqueta,Febe van Maldegem,David P. Noske,Idris Bahce,Jan Köster,J J Garcia Vallejo,Richard Schoonhoven,Mark A. van de Wiel,T. Radonic,Bauke Ylstra,Yongsoo Kim
标识
DOI:10.1038/s41467-026-74997-8
摘要
Accurate deconvolution of cell states from bulk tumor RNA-seq is hindered by heterogeneous malignant cells specifically in cancer applications. We present Statescope, a Bayesian framework that incorporates DNA-derived malignant cell purity to overcome this heterogeneity and explicitly models inter-sample variation to accurately identify cell states. Comprehensive benchmarking shows Statescope outperforms existing methods in both cell fraction and state estimation, and is unique in its ability to identify states entirely absent from single-cell references. In real-data applications, Statescope successfully recapitulates established cell states, including multiple states in neutrophils, a cell type often missed by single-cell methods in lung cancer. Critically, in the POPLAR/OAK clinical trials, Statescope identifies a combinatorial signature of effector CD8 + T cells and conventional dendritic cell states that together predict a striking survival benefit from immunotherapy. Collectively, Statescope transforms deconvolution into a versatile discovery platform, enabling deeper biological and clinical insights from widely available bulk multi-omics data.
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