Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.05.14.654136

Visual analytics framework for survival analysis and biomarker discovery

Abstract

We introduce a visual analytics methodology for survival analysis, and propose a framework that defines a reusable set of visualization and modeling components to support exploratory and hypothesis-driven biomarker discovery. Survival analysis--essential in biomedicine--evaluates patients survival rates and the onset of medically relevant events, given their clinical and genetic profiles and genetic predispositions. Existing approaches often require programming expertise or rely on inflexible analysis pipelines, limiting their usability among biomedical researchers. The lack of advanced, user-friendly tools hinders problem solving, limits accessibility for biomedical researchers, and restricts interactive data exploration. Our methodology emphasizes functionality-driven design and modularity, akin to combining LEGO bricks to build tailored visual workflows. We (1) define a minimal set of reusable visualization and modeling components that support common survival analysis tasks, (2) implement interactive visualizations for discovering survival cohorts and their characteristic features, and (3) demonstrate integration within an existing visual analytics platform. We implemented the methodology as an open-source add-on to Orange Data Mining and validated it through use cases ranging from Kaplan-Meier estimation to biomarker discovery. The resulting framework illustrates how methodological design can drive intuitive, transparent, and effective survival analysis. Author summaryWhen studying diseases like cancer, it is important to understand how factors such as genes or treatments influence how long patients live after medical intervention. Survival analysis is a well-established statistical and bioinformatics approach for uncovering such insights, but it often requires advanced programming skills, which can be a barrier for many clinicians and life science researchers. To help overcome this, we developed a visual analytics tool that makes the analysis of censored data easier, more interactive, and accessible. Instead of writing code, researchers can use our framework to assemble analysis components into workflows through visual programming. They can explore their data by comparing survival curves, identifying meaningful patient subgroups, and discovering potential biomarkers. The tool is implemented as part of Orange Data Mining, a free and open-source data analytics platform. We tested it on real-world cancer datasets to demonstrate how easily and quickly researchers can prototype powerful data analysis workflows. Our goal is to make survival analysis more accessible, empowering researchers to generate and test hypotheses without needing to program. Our goal is to make survival analysis more accessible, empowering researchers to generate and test hypotheses without programming, and contributing to the broader democratization of data science.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Kokosar, J., Turkay, C., Avsec, L., Stajdohar, M., Zupan, B.. 2025-05-17. Visual analytics framework for survival analysis and biomarker discovery. https://doi.org/10.1101/2025.05.14.654136

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

KEEP EXPLORING

Related preprints

spatialMET: an open and scalable framework for spatial metabolomics analysis

Mass spectrometry imaging (MSI) enables spatially resolved metabolomics in intact tissue sections, but analysis remains challenging at scale. Existing MSI workflows often require users to combine multiple software tools, while others rely on proprietary vendor software that limits interoperability and reproducibility. To address these challenges, we developed spatialMET, an open-source framework that provides an end-to-end workflow for MSI analysis. spatialMET provides a unified platform for preprocessing, spatial domain detection, and visualization. Downstream analyses include differential abundance testing, spatial autocorrelation and gradient analysis, dimensionality reduction, and correlation network analysis. Spatial domain detection uses hcdist, a C-based hierarchical clustering implementation that substantially reduces runtime and memory use relative to existing R-based approaches. spatialMET can be run through an interactive R Shiny application or as a standalone command-line workflow for larger datasets or high-performance computing environments. Applied to mouse small cell lung cancer MALDI-MSI data containing 284,673 pixels, spatialMET identified tumor-associated, stromal, and adjacent lung spatial domains that aligned with matched histology. Differential abundance analysis identified 117 m/z features that differed between tumor and stromal regions, while spatial autocorrelation analyses revealed spatially structured abundance patterns. Applying spatialMET to mouse lung adenocarcinoma data from an entire lung lobe containing 338,477 pixels further demonstrated scalability and captured spatial heterogeneity across tumor and surrounding lung tissue. In summary, spatialMET provides a scalable, open-source framework for end-to-end spatial metabolomics analysis, and it is distributed as a Docker container for reproducible deployment. Source code and installation instructions are available at https://github.com/biodatalab/spatialMET.

bioinformatics↗

Probing the transcriptome response to shivering in skeletal muscle using a multilayered bioinformatics approach

Cold acclimation holds therapeutic potential for improving metabolic health. We previously demonstrated that repeated cold-induced shivering enhances insulin sensitivity in humans. However, the molecular pathways that underlie the skeletal muscle shivering response, and how these relate to beneficial physiological effects, remain poorly understood. In this study, we combined complementary bioinformatics approaches to allow in-depth analysis of the transcriptomic response of human skeletal muscle to repeated shivering. We identified a robust transcriptional signature and show a sex-specific component in the shivering skeletal muscle response, which seemed to diminish following cold adaptation. Our findings provide mechanistic insights into cold-induced muscle adaptations, shed light on potential interesting molecular targets for further investigation, and emphasize the importance of including both sexes in future cold acclimation studies.

bioinformatics↗

An Information Geometry approach to model topological trajectories and Gene Expression Radius from UMAP geometry.

Understanding the relationship between gene expression dynamics and cellular identity remains a central challenge in single cell biology. Here, we introduce a novel computational and mathematical framework that integrates information geometry, fuzzy topology, and UMAP analysis to model gene expression landscapes derived from single cell RNA sequencing data. We formalize gene expression data as a fuzzy topological space, where interactions between expression points are governed by probabilistic distributions inspired by manifold learning approaches such as UMAP. Within this framework, we define an information geometric structure through a Fisher metric induced by these distributions, enabling the computation of geodesic trajectories that capture cellular differentiation processes. A key contribution of this work is the derivation of analytical conditions, expressed as expression radius formulas, that characterize local neighborhoods in gene expression space. These conditions allow for the identification of genes associated with stem cell states and predictions in transitional cell types in future work. Application of the proposed framework to single cell datasets reveals biologically meaningful gene sets enriched in key regulatory pathways and transcription factors, demonstrating the capacity of our approach to uncover latent structure in complex gene expression data. Our results suggest that integrating differential geometry with statistical learning theory offers a powerful paradigm for modeling genotype and phenotype relationships and cellular state transitions, with potential implications for precision medicine and systems biology.

bioinformatics↗