MOTIVATION: Cancer is a molecular complex and heterogeneous disease. Each type of cancer is usually composed of several subtypes with different treatment responses and clinical outcomes. Therefore, subtyping is a crucial step in cancer diagnosis and therapy. The rapid advances in high-throughput sequencing technologies provide an increasing amount of multi-omics data, which benefits our understanding of cancer genetic architecture, and yet poses new challenges in multi-omics data integration. RESULTS: We propose a graph convolutional network model, called MRGCN for multi-omics data integrative representation. MRGCN simultaneously encodes and reconstructs multiple omics expression and similarity relationships into a shared latent embedding space. In addition, MRGCN adopts an indicator matrix to denote the situation of missing values in partial omics, so that the full and partial multi-omics processing procedures are combined in a unified framework. Experimental results on 11 multi-omics datasets show that cancer subtypes obtained by MRGCN with superior enriched clinical parameters and log-rank test P-values in survival analysis over many typical integrative methods. AVAILABILITY AND IMPLEMENTATION: https://github.com/Polytech-bioinf/MRGCN.git https://figshare.com/articles/software/MRGCN/23058503.

MOTIVATION: Cancer is a heterogeneous group of diseases. Cancer subtyping is a crucial and critical step to diagnosis, prognosis and treatment. Since high-throughput sequencing technologies provide an unprecedented opportunity to rapidly collect multi-omics data for the same individuals, an urgent need in current is how to effectively represent and integrate these multi-omics data to achieve clinically meaningful cancer subtyping. RESULTS: We propose a novel deep learning model, called Deep Structure Integrative Representation (DSIR), for cancer subtypes dentification by integrating representation and clustering multi-omics data. DSIR simultaneously captures the global structures in sparse subspace and local structures in manifold subspace from multi-omics data and constructs a consensus similarity matrix by utilizing deep neural networks. Extensive tests are performed in 12 different cancers on three levels of omics data from The Cancer Genome Atlas. The results demonstrate that DSIR obtains more significant performances than the state-of-the-art integrative methods. AVAILABILITY AND IMPLEMENTATION: https://github.com/Polytech-bioinf/Deep-structure-integrative-representation.git. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.