Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.01.06.631471

Deep Learning for Biomarker Discovery in Cancer Genomes

Abstract

BackgroundAccurate determination of genomic biomarkers from tumor sequencing is fundamental to precision oncology, informing disease classification and treatment decisions. In practice, biomarker inference relies on computational pipelines that often compress high-dimensional mutation data into predefined summaries such as mutational signatures or composite genomic features. While robust and widely adopted, these representations may not fully capture the complexity of cancer genomes. Deep learning (DL) offers an end-to-end alternative by learning features directly from raw genomic data. However, clinical translation remains challenging due to limited empirical validation of new DL models and a lack of systematic comparisons with established machine learning (ML) baselines, particularly when transitioning from information-rich genome or exome data to real-world targeted sequencing profiles. Here, we compare state-of-the-art DL architectures with classical ML models across variant-level, copy-number (CNV), and multimodal inputs, using microsatellite instability (MSI) and homologous recombination deficiency (HRD) prediction as oncologically relevant tasks. We aim to derive practical guidance on modelling strategies across different data modalities and clinical sequencing contexts. MethodsFor MSI and HRD prediction, we trained multiple DL models, including supervised and self-supervised encoders, alongside feature-based ML approaches using tumor mutation data, copy-number alterations, and their multimodal combinations. Analyses were conducted on 5,647 patients in The Cancer Genome Atlas (TCGA), the Clinical Proteomic Tumor Analysis Consortium (CPTAC), and two targeted sequencing panel cohorts. Model performance was evaluated on both whole-exome and panel-based datasets, and explainability analysis were performed for both DL and ML models. ResultsFor MSI, DL demonstrated stronger generalization than ML on external validation data (F1 0.97 vs 0.76) and maintained comparatively high performance under pseudo-panels conditions, whereas ML performance dropped. In a real-world targeted panel cohort, DL again showed more robust generalization than ML, with performance partly affected by cross-assay variability. For HRD, incorporation of CNV data was the primary determinant of predictive performance. Once CNVs were included, DL and ML achieved similar accuracy on external datasets (F1 0.61 vs 0.58). In panel-based settings, DL retained an advantage over ML (F1 0.78 vs 0.62). Model interpretation analyses indicated that both DL and ML relied on mutation and chromosomal patterns consistent with established MSI and HRD biology. ConclusionOverall, predictive performance depended strongly on data availability and clinical sequencing context. When information-rich inputs were available, both DL and classical ML achieved robust biomarker prediction, with DL generally matching or exceeding ML performance. The most pronounced advantages of DL emerged in cross-assay evaluations and data-sparse settings, where generalization was more reliable. Notably, the best-performing DL models were lightweight and interpretable, supporting practical deployment. In clinical genomics workflows, such models may complement established pipelines by leveraging patient sequencing data to provide additional evidence for treatment-relevant biomarker assessment.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Unger, M., Loeffler, C. M. L., Zigutyte, L., Sainath, S., Lenz, T., Vibert, J., Mock, A., Froehling, S., Graham, T. A., Carrero, Z. I., Kather, J. N.. 2025-01-07. Deep Learning for Biomarker Discovery in Cancer Genomes. https://doi.org/10.1101/2025.01.06.631471

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Comparative functional genomics reveals distributed SERPINE1 like characteristics among Drosophila serpins

Serpins (serine protease inhibitors) regulate proteolytic activity through a suicide-substrate inhibitory mechanism, whereby the serpin covalently traps and inactivates their target protease. Serpins are broadly conserved across eukaryotes, but the evolutionary and functional relationships between human SERPINE1, and Drosophila Serpins in incompletely defined. To identify candidate Drosophila functional analogs of SERPINE1/PAI-1, a multi-omics framework was applied to thoroughly compare the serpins across species. The multi-level analysis integrated orthology prediction, protein sequence and structural characterization, phylogenetic reconstruction, bulk tissue transcriptomics, single-cell transcriptomics, and aging-associated expression analysis. Candidate serpins (Spn42Da, Spn42Db, Spn42Dc, Spn42Dd, Spn28B, and Spn28F) were evaluated using DIOPT, AlphaFold/ChimeraX structural comparisons, reactive center loop analyses, phylogenetic distances, GTEx, Human Protein Atlas, FlyAtlas2, Fly Cell Atlas, and Aging Fly Cell Atlas datasets. Comparative analyses demonstrated full-length sequence and reactive center loop (RCL) divergence despite preservation of the canonical serpin fold. Tissue, cell-type, and age-associated expression analysis revealed distinct candidate-specific patterns. Spn42Dd comparisons uncovered similarities to human SERPINE1 in sequence/structural and broad expression but did not represent the strongest overall cross-species expression correlations. Spn42Da and Spn42Db received the highest cross species integrated support. Quality check of the ranking confirmed that Spn42Da and Spn42Db were stable top candidates across orthology, sequence alignment, and expression domains. The multi-domain analysis was unable to identify a single definitive Drosophila serpin as the closest counterpart to human SERPINE1, indicating that cross-species similarity is distributed across multiple candidate serpins. This study therefore provides a quantitative method for prioritizing potential evolutionary and functional analogs across highly divergent species.

bioinformatics↗

CellChat Hotspot: A Targeted Approach to Cell Cell Communication Analysis With Spatial transcriptomics Validation.

Abstract. In recent years, single cell RNA sequencing (scRNA seq) has enabled the investigation of intercellular communication through Cell Cell Communication (CCC) tools such as CellChat. Despite their potential, these approaches remain challenging to interpret, particularly when global analyses generate complex interaction networks that may include biologically irrelevant signals. To address this limitation, we developed a framework termed CellChat Hotspot, designed to improve the biological interpretability of inferred communication networks. This approach integrates gene set enrichment analysis with a context driven filtering strategy, selecting both genes and cells based on their functional relevance prior to communication inference. Applied to stage II colon cancer data, CellChat Hotspot enabled the identification of condition-specific interaction patterns associated with recurrence. Non recurrent patients showed enrichment of immune related processes, whereas recurrent cases were characterized by pathways associated with invasion and metastasis. Notably, a loss of interaction in the HSPG pathway between CALB1+ and stromal cells was observed in recurrent patients, suggesting a potential disruption of cell matrix adhesion mechanisms. To verify the reliability of this finding, we applied the framework to spatial transcriptomics data, which confirmed the presence of the HSPG2 DAG1 interaction in non-recurrent tumors and its near absence in recurrent ones. Overall, this framework provides a biologically guided strategy for studying intercellular communication in complex systems such as the tumor microenvironment.

bioinformatics↗

DiffTernary: a Diffusion Model for Molecular Glue Ternary Complex Docking

Molecular glues (MGs) modulate protein function by inducing or stabilizing protein interactions. However, accurately modeling MG ternary complexes remains challenging. Here, we present DiffTernary, a diffusion-based docking method for the joint prediction of relative protein arrangement and MG binding pose. We introduce Ternary-PDB, a dataset of 76,702 experimentally determined ternary complexes curated from the Protein Data Bank using structural filters and a release cutoff aligned with AlphaFold 3 (AF3). When trained on this dataset, DiffTernary achieved acceptable protein-protein interaction (PPI) predictions (DockQ > 0.23) for 50.0% of MGBench complexes with a single prediction, compared with 51.1% for AF3. In comparisons with AF3, OpenFold3, ESMFold2, Protenix-v1 and Protenix-v2, DiffTernary ranked second with a best-of-25 PPI prediction success rate of 78.4%, behind ESMFold2 (90.9%) and ahead of AF3 (72.7%). A separate DiffTernary model trained on TernaryDB achieved a mean DockQ of 0.306 on the 94 complexes in the TernaryDB MGD test set with a single prediction, compared with 0.228 for DeepTernary. Confidence-based selection among 40 samples yielded acceptable PPI predictions for 41.5% of complexes, compared with 30.9% for DeepTernary. An E2Former variant increased training and sampling throughput 6.90-fold and 4.37-fold, respectively, under the evaluated configurations. Together, DiffTernary and Ternary-PDB provide an efficient docking approach for MG complex prediction and a valuable structural resource for MG discovery and design.

bioinformatics↗