MDICC: novel method for multi-omics data integration and cancer subtype identification

被引:27
|
作者
Yang, Ying [1 ]
Tian, Sha [1 ]
Qiu, Yushan [1 ]
Zhao, Pu [2 ]
Zou, Quan [3 ]
机构
[1] Shenzhen Univ, Coll Math & Stat, Shenzhen 518000, Peoples R China
[2] Northwestern Univ, Coll Life & Hlth Sci, Shenyang 110169, Peoples R China
[3] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610056, Peoples R China
基金
中国国家自然科学基金;
关键词
multi-omics data integration; cancer subtype identification; network fusion; affinity matrix; LATENT VARIABLE MODEL; BREAST; CLASSIFICATION; PREDICTION; LANDSCAPE; GENOME;
D O I
10.1093/bib/bbac132
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Each type of cancer usually has several subtypes with distinct clinical implications, and therefore the discovery of cancer subtypes is an important and urgent task in disease diagnosis and therapy. Using single-omics data to predict cancer subtypes is difficult because genomes are dysregulated and complicated by multiple molecular mechanisms, and therefore linking cancer genomes to cancer phenotypes is not an easy task. Using multi-omics data to effectively predict cancer subtypes is an area of much interest; however, integrating multi-omics data is challenging. Here, we propose a novel method of multi-omics data integration for clustering to identify cancer subtypes (MDICC) that integrates new affinity matrix and network fusion methods. Our experimental results show the effectiveness and generalization of the proposed MDICC model in identifying cancer subtypes, and its performance was better than those of currently available state-of-the-art clustering methods. Furthermore, the survival analysis demonstrates that MDICC delivered comparable or even better results than many typical integrative methods.
引用
收藏
页数:13
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