SUPREME
SUPREME integrates genomic, transcriptomic, proteomic, and other multiomics data using a Graph Convolutional Neural Network to generate patient-specific embeddings for cancer subtype prediction.
Key Features:
- Multiomics Data Integration: Integrates high-dimensional genomic, transcriptomic, proteomic, and other omics layers to capture complementary signals across data modalities.
- Graph Neural Network Utilization: Employs Graph Neural Networks / Graph Convolutional Neural Network to learn node embeddings from node features and graph-structured associations.
- Patient Embedding Generation: Generates patient-specific embeddings from multiple similarity networks derived from multiomics features and integrates these embeddings with raw features for classification.
- Performance Superiority: Demonstrated superior performance in breast cancer subtyping across three datasets, with inferred subtypes showing significant survival differences compared to labels based on a single data type.
- Model-Agnostic Application: Applied to two additional datasets and reported consistent outperformance of nine other approaches.
Scientific Applications:
- Cancer subtype prediction: Produces refined cancer subtype classifications by integrating multiomics data and GNN-derived embeddings.
- Patient stratification: Identifies patient groups with distinct biological profiles that correlate with survival differences.
- Ground truth refinement: Refines existing subtype labels by uncovering characteristics from integrated multiomics signals.
Methodology:
Constructs multiple patient similarity networks from multiomics features, generates patient-specific embeddings from those networks, and learns/integrates node embeddings with raw features using a Graph Convolutional Neural Network.
Topics
Details
- License:
- CC-BY-SA-4.0
- Cost:
- Free of charge
- Tool Type:
- workflow
- Programming Languages:
- Python, R
- Added:
- 6/18/2024
- Last Updated:
- 11/24/2024
Operations
Publications
Kesimoglu ZN, Bozdag S. SUPREME: multiomics data integration using graph convolutional networks. NAR Genomics and Bioinformatics. 2023;5(2). doi:10.1093/nargab/lqad063. PMID:37680392. PMCID:PMC10481254.