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.

PMID: 37680392
Funding: - National Institutes of Health: R35GM133657