反褶积
计算机科学
稳健性(进化)
计算生物学
可扩展性
限制
代谢组学
盲反褶积
组学
数据挖掘
蛋白质组学
概化理论
生物学数据
数据类型
生物信息学
系统生物学
稳健统计
生物标志物发现
生物
仿形(计算机编程)
先验与后验
信息基础设施
人工智能
作者
Tianyi Zhao,Renjie Liu,Yuzhi Sun,Bingtian Wang,Liyuan Zhang,Qiuhao Chen,Ruibang Luo,Zhiyuan Yuan,Guohua Wang,Liang Cheng,Yadong Wang
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2026-03-01
卷期号:23 (3): 596-608
被引量:7
标识
DOI:10.1038/s41592-026-03007-y
摘要
Deconvolution algorithms estimate cell-type abundances from tissue-level data, enabling systematic cellular analysis of large cohorts. However, most deconvolution algorithms are specifically designed for single-omics data, thereby limiting their generalizability and scalability for various omics data from different cohorts. Here we present DECODE, a universal deconvolution framework for both cell types and cell states that can be applied to transcriptomic, proteomic and metabolomic data, and that seamlessly integrates diverse multiomics tissue datasets at the cellular level. DECODE fills the gap in metabolomics deconvolution and significantly outperformed state-of-the-art methods on different omics data across donors, disease conditions, healthy states, datasets and measurement platforms. In addition, DECODE exhibits high robustness in scenarios that are closer to real applications so it can accurately deconvolve known cell types even when the reference single-cell data are incomplete. DECODE will serve as a powerful tool for the fully extending multiomics cohort data into cellular level.
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