π€ AI Summary
This study addresses the challenges in multi-omics cancer subtype classification arising from heterogeneous data quality and noise across modalities. Conventional graph-based methods often fail to reliably model patient similarity due to the tight coupling of modality weighting and classification objectives. To overcome this, the authors propose CMGL, a two-stage framework that first estimates sample-wise, modality-specific confidence scores using evidential deep learning and then leverages these frozen confidence scores to guide cross-omics fusion and graph construction, thereby decoupling reliability assessment from graph learning. Notably, CMGL introduces sample-level modality confidence as an independent prior, effectively mitigating the adverse influence of low-quality modalities on graph topology and message passing. Evaluated on four single-cancer tasks, CMGL achieves an average accuracy improvement of 4.03% over the strongest baseline, successfully recapitulates the PAM50 breast cancer subtypes, and demonstrates zero-shot transferability to kidney cancer with significant prognostic stratification.
π Abstract
Motivation: Multi-omics integration can improve cancer subtyping, but modality informativeness and noise vary across cancer types and patients. Existing graph-based methods optimize modality weights jointly with the classification objective and therefore lack independent reliability estimates, so low-quality omics distort patient similarity graphs and amplify noise through message passing.
Results: We propose CMGL, a two-stage framework that estimates per-sample modality reliability through evidential deep learning and uses the frozen confidence scores to guide cross-omics fusion and graph construction. On four MLOmics cancer-subtype tasks and the 32-class pan-cancer task, CMGL consistently improves over the strongest baseline, surpassing it by 4.03% in average accuracy on the four single-cancer tasks. Its representations recover the PAM50 intrinsic subtypes of breast invasive carcinoma (BRCA), and the BRCA-trained model transfers without fine-tuning to kidney renal clear cell carcinoma (KIRC), stratifying patients into prognostically distinct groups.