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Urda-Garcia, B.

Publications and source records attributed to Urda-Garcia, B..

2 recordsLinked to original sources

EBEx: an Ensemble-Based Explainable Framework for Gene Calling in Heterogeneous Diseases

Complex and clinically heterogeneous diseases pose significant challenges for gene prioritisation and patient stratification, as relevant genes often show weak or context-specific signals and transcriptomic datasets are limited in size. These limitations hinder the discovery of robust molecular signatures using traditional case-control approaches and motivate computational pipelines capable of capturing molecular diversity. Here, we present an explainable ensemble-based AI pipeline to prioritise disease-relevant genes from transcriptomic data, using Chronic Obstructive Pulmonary Disease (COPD) as a use case. To retain biologically relevant interactors obscured by molecular heterogeneity, the framework integrates data-driven signals with curated COPD-related gene sets, further expanded through network-based prioritisation and supported by molecular interactions. Gene relevance is evaluated via aggregated explainability scores across multiple classifier configurations to ensure robust candidate selection. The final set comprised < 8% of evaluated genes, [~] 62% arising from network-based expansion, substantially reducing dimensionality while preserving biological heterogeneity. Beyond case-control classification, the approach identified candidate genes and molecular subgroups associated with specific clinical features, capturing patient-level heterogeneity. The prioritised genes recapitulated key disease-related processes, including immune responses and extracellular matrix degradation, and highlighted additional associations like the enrichment of the IL-4 and IL-13 signalling pathway, which is of clinical interest given ongoing biologic developments targeting these axes. Our pipeline outperformed existing methods in discriminating COPD from controls, and the final gene list was validated in independent cohorts. Implemented as a scalable and reusable R package, this framework facilitates the study of molecular heterogeneity in complex diseases like COPD, supporting advances in diagnosis and precision medicine. Availability and implementationEBEx code and tutorials can be found in: https://iposelag.github.io/EBEx/

bioinformatics↗

Exploring the Boundaries of Medulloblastoma Subgroups with Synthetic Data Generation

Medulloblastoma is a childhood brain tumor traditionally classified into four molecular subgroups. Recent evidence suggests that Groups 3 and 4 represent a biological continuum rather than distinct entities, a paradigm shift with significant implications for understanding disease biology and treatment strategies. Nevertheless, assessing this hypothesis is challenging mainly due to data scarcity. In this study, we analyze the largest available transcriptomics dataset to provide compelling evidence for the existence of an intermediate subgroup between Groups 3 and 4, characterized by distinct molecular features. To overcome limitations posed by data scarcity, we employ synthetic data generation using a Variational Autoencoder and apply explainability techniques to identify key relationships between gene expression and disease subgroups. Furthermore, by incorporating Machine Learning Fairness approaches, we demonstrate that overlooking this intermediate subgroup can result in treatment disparities. Our findings are further supported by both existing and newly proposed studies using diverse datasets and methodologies, including graphbased analyses and multi-scale simulations, underscoring the robustness and reproducibility of our results. This study demonstrates the potential of synthetic data generation to refine rare disease subtyping and advance our understanding of the underlying biological mechanisms. Keywords: Medulloblastoma, pediatric cancer, representation learning, autoencoder, synthetic data

bioinformatics↗