反褶积
计算机科学
蛋白质组学
蛋白质组
数据类型
人工智能
深度学习
计算生物学
模式识别(心理学)
数据挖掘
生物信息学
化学
算法
生物
基因
生物化学
程序设计语言
作者
Fang Wang,Fan Yang,Long-Kai Huang,Wei Li,Jiangning Song,Robin B. Gasser,Ruedi Aebersold,Guohua Wang,Jianhua Yao
标识
DOI:10.1038/s42256-023-00737-y
摘要
Cell type deconvolution is a computational method for the determination/resolution of cell type proportions from bulk sequencing data, and is frequently used for the analysis of divergent cell types in tumour tissue samples. However, deconvolution technology is still in its infancy for the analysis of cell types using proteomic data due to challenges with repeatability/reproducibility, variable reference standards and the lack of single-cell proteomic reference data. Here we develop a deep-learning-based deconvolution method (scpDeconv) specifically designed for proteomic data. scpDeconv uses an autoencoder to leverage the information from bulk proteomic data to improve the quality of single-cell proteomic data, and employs a domain adversarial architecture to bridge the single-cell and bulk data distributions and transfer labels from single-cell data to bulk data. Extensive experiments validate the performance of scpDeconv in the deconvolution of proteomic data produced from various species/sources and different proteomic technologies. This method should find broad applicability to areas including tumour microenvironment interpretation and clinical diagnosis/classification. Deconvolution of cell types in tissue proteomic data is a challenging computational task for the bioinformatics community. A deep-learning method termed scpDeconv is introduced that makes efficient use of single-cell proteomics data to deconvolve cell types and states from bulk proteomics measurements.
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