DeMoP, a language-model-guided mixture-of-experts framework that serializes structured patient profiles as natural-language sequences and learns adaptive prognostic representations from clinical variables, copy-number alterations, and gene descriptions, provides a unified approach to heterogeneous biomedical data integration, cross-cohort outcome prediction, and model interpretation.
Abstract
Integrating heterogeneous clinical and molecular data for cancer prognosis remains challenging because their dimensionality, semantics and distributions differ across patients and cohorts. Here we present DeMoP, a language-model-guided mixture-of-experts framework that serializes structured patient profiles as natural-language sequences and learns adaptive prognostic representations from clinical variables, copy-number alterations, and gene descriptions. DeMoP combines a fine-tuned DeBERTa-v3-large encoder, attention-based token pooling, and a residual mixture-of-experts prediction head. In held-out tests from two independent pan-cancer cohorts, GENIE (63,090 patients) and TCGA (4,123 patients), DeMoP outperformed the conventional machine-learning and deep-learning baselines evaluated, achieving AUROCs of 0.939 and 0.805 and class-1 F1 scores of 0.72 in both cohorts. A GENIE-trained model transferred directly to TCGA with an overall class-1 F1 score of 0.62. Gene-level ablations recovered established cancer-associated genes and highlighted less-studied candidates. DeMoP provides a unified approach to heterogeneous biomedical data integration, cross-cohort outcome prediction, and model interpretation.
Language models for cancer clinical reports carry two blind spots. They read each report in isolation, ignoring how a patient’s disease changes across visits, and they are evaluated only on cancer types present in their training data. We present the Hierarchical Temporal Transformer (HTT), a two-level architecture that...
The oFM is introduced, a foundation model developed on a real-world oncology cohort of 1.67 million cancer patients that integrates clinical trajectories with DNA, RNA, and H&E pathology and achieves a three-fold higher pooled and scale-normalized treatment-benefit AUTOC than baseline features.
E. Vorontsov, Yi-Kan Wang, A. Bozkurt et al.· 0 citations
Results demonstrate that BFPSM outperforms state-of-the-art methods at the sequence level, highlighting its utility for clinical and functional variant prioritization.
Hai-Zhou-Rong Chen, Si-Yuan Yang, Chen Ye et al.· Computational biology and ch...· 0 citations
Large language models are used as synthetic clinical experts to supervise a variational-autoencoder-based approach that learns low-dimensional latent summaries of visit-level observations to make clinical knowledge available to representation learning and improve clinical faithfulness for longitudinal rare-disease data...
Clemens Schächter, A. Pechmann, Janbernd Kirschner et al.· 0 citations
Cooperative Modular Representation Learning (CMRL), an uncertainty-gated multimodal framework that dynamically regulates inter-modality information flow based on sample-level epistemic uncertainty estimated via Evidential Deep Learning (EDL), is presented.
Sundus M. Jasim, Nabil Hezil, A. Bouridane et al.· bioRxiv· 0 citations
Cancer continues to be a significant worldwide health concern, mostly resulting from modifications in genetic material at the molecular level. The research introduces a hybrid system that integrates raw gene-level multi-omics features with pathway-derived hypergraph embeddings to prioritize glioblastoma genes. The prop...
Nowsheena, Shaima Qureshi· Computational biology and ch...· 0 citations
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