Search bioRxiv⌕ Search

Biology subjects

Vasileiou, V.

Publications and source records attributed to Vasileiou, V..

2 recordsLinked to original sources

lncAPNet enables the deciphering of lncRNA and mRNA connections in patient transcriptomic data

MotivationLong non-coding RNAs (lncRNAs) regulate gene expression through chromatin remodeling, transcriptional control, and post-transcriptional modulation, influencing physiological cell homeostasis but also disease onset. Yet most transcriptomic and network-based studies rely on descriptive linear co-expression analyses, missing nonlinear and mechanistic insights. Emerging ML/DL methods offer promise but remain limited by data sparsity, noise, insufficient biological priors, and poor interpretability, constraining systems-level lncRNA-mRNA motif discovery. ResultsIn this manuscript, we introduce lncAPNet, an extended version of APNet workflow, which integrates graph-based nonlinear inference of lncRNA-mRNA interactions using NetBID2s activity logic within an lncRNA-focused SJARACNe co-expression network, coupled with PASNet, a biologically informed sparse deep learning model. This framework enables explainable identification of lncRNA drivers in two different cancer type case studies, Chronic Lymphocytic Leukemia (CLL) and Prostate Adenocarcinoma (PRAD), uncovering lncRNA drivers that illuminate lncRNA-mediated programs in cancer progression. Availability and implementationlncAPNets R scripts, Python scripts, and methodologies are available at github repository: https://github.com/BiodataAnalysisGroup/lncAPNet

bioinformatics↗

APNet, an explainable sparse deep learning model to discover differentially active drivers of severe COVID-19

MotivationComputational analyses of plasma proteomics provide translational insights into complex diseases such as COVID-19 by revealing molecules, cellular phenotypes, and signaling patterns that contribute to unfavorable clinical outcomes. Current in silico approaches dovetail differential expression, biostatistics, and machine learning, but often overlook nonlinear proteomic dynamics, like post-translational modifications, and provide limited biological interpretability beyond feature ranking. ResultsWe introduce APNet, a novel computational pipeline that combines differential activity analysis based on SJARACNe co-expression networks with PASNet, a biologically-informed sparse deep learning model to perform explainable predictions for COVID-19 severity. The APNet driver-pathway network ingests co-expression and classification weights to aid result interpretation and hypothesis generation. APNet outperforms alternative models in patient classification across three COVID-19 proteomic datasets, identifying predictive drivers and pathways, including some confirmed in single-cell omics and highlighting under-explored biomarker circuitries in COVID-19. Availability and ImplementationAPNets R, Python scripts and Cytoscape methodologies are available at https://github.com/BiodataAnalysisGroup/APNet Contactggeorav@certh.gr Supplementary informationSupplementary information can be accessed in Zenodo (10.5281/zenodo.10438830).

systems biology↗