反褶积
计算机科学
分布(数学)
组学
计算生物学
数据挖掘
生物
数学
生物信息学
算法
数学分析
作者
Xinxing Yang,Faming Zhao,Tao Ren,Canping Chen,Katelyn T. Byrne,Alexey V. Danilov,Rosalie C. Sears,Peter S. Nelson,Lisa M. Coussens,Gordon B. Mills,Zheng Xia
出处
期刊:Cell genomics
[Elsevier]
日期:2025-07-16
卷期号:5 (9): 100950-100950
被引量:4
标识
DOI:10.1016/j.xgen.2025.100950
摘要
Cell deconvolution estimates cell type proportions from bulk omics data, enabling insights into tissue microenvironments and disease. However, practical applications are often hindered by batch effects between bulk data and referenced single-cell data, a challenge that is frequently overlooked. To address this discrepancy, we developed OmicsTweezer, a distribution-independent cell deconvolution model. By integrating optimal transport with deep learning, OmicsTweezer aligns simulated and real data in a shared latent space, effectively mitigating data shifts and inter-omics distribution differences. OmicsTweezer is versatile, capable of deconvolving bulk RNA-seq, bulk proteomics, and spatial transcriptomics. Extensive evaluations on simulated and real-world datasets demonstrate its robustness and accuracy. Furthermore, applications in prostate and colon cancer showcase OmicsTweezer's ability to identify biologically meaningful cell types. As a unified deconvolution framework for multi-omics data, OmicsTweezer offers an efficient and powerful tool for studying disease microenvironments.
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