A1
ID 0040
Posters
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Poster Session A
Wednesday 2 September 2026, 16:45-18:30, Museo di Arte Classica, Sapienza University of Rome
Biostatistics
A2
ID 5486
Functional Shapley Representations for Longitudinal Random Survival Forests using Hierarchical FPCA
A3
ID 8845
Comparative Deep Learning and Statistical Analysis for Spatial Prediction of Lymph Node Metastasis in Gastric Cancer
A4
ID 4182
Spatial host pathogen transcriptomics maps bacterial burden linked urothelial injury and repair in bladder infection
A5
ID 0078
Early Warning of Extremely Rare Events from Pediatric Cardiac Intensive Care Electronic Health Records
A6
ID 0060
QFARM - hierarchical quantitative association rule mining
A7
ID 0024
Modified Gompertz Function in Quantitative Evaluation of Endolysin Lytic Activity in Physiological Fluids
Medical Informatics
A8
ID 0085
AEGLOS V7: Hyperbolic Digital Pathology for Morphology-to-Genomics Prediction in Advanced Non-Small Cell Lung Cancer
A9
ID 3784
A new MRI-based feature for quantifying the Diffuse Low-Grade Glioma brain infiltration and discriminating patterns of patients
A10
ID 6293
On the adoption of Quantum Machine Learning for Privacy-Preserving and Explainable Diabetic Retinopathy Detection and Localisation
A11
ID 0068
FFPE-Open-ST: high-resolution, unbiased spatial transcriptomics profiling of archival samples
A12
ID 0054
Beyond the Diagnosis: Semi-Automated Risk Analysis of Inappropriate Antibiotic Prescribing in Mexico and the Potential for Real-Time Alerts
Bioinformatics
A13
ID 0072
Quantum Optimization for Protein-Protein Interaction Network Alignment
A14
ID 0034
Quantum Annealing for De Novo Genome Assembly
A15
ID 0087
Benchmarking LLMs for automated systems biology model replication
A16
ID 3745
Analysis of Prompt Engineering for Drug Toxicity Prediction
A17
ID 0059
Autoresearch Discovery of Interpretable Filter Rules for Antibody Binder Classification
A18
ID 5995
Statistical Model Checking of Uncertain Continuous Time Markov Chain in Systems Biology
A19
ID 5265
A ML-powered Multiscale Computational Platform Based on QSP and PBPK Modeling to Support the Development of mRNA-based Therapies
A20
ID 0029
Computational Framework for the Design of Second-Generation Pharmacochaperones Targeting Allosteric Pockets
A21
ID 0077
Pathway-Mediated Networks for Drug Repurposing in Breast Cancer
A22
ID 0089
Large-scale analysis and clustering of RNA 3D structures
A23
ID 0062
Machine learning approaches for predicting functional lncRNAs and key regulatory interactions in plant gene networks
A24
ID 0023
Computational Prediction of Pathogenic FMR1 Variants in Fragile X Syndrome
A25
ID 0047
VISMA: Vector Integration Site Mutation Analysis
A26
ID 0022
A Network Story: tumor educated platelets transcriptome and Glioblastoma
A27
ID 0033
FLiCoN: Friendship Like differential Coexpression Network for the identification of Tumor-Educated Platelets Driver Genes in Glioma via structural Imbalance
A28
ID 0070
Beyond Differential Expression: Network Centrality measures reveal Tissue-Specific Signatures in Tumor-Educated Platelets
A29
ID 0066
Investigating Immunotherapy Response in Non-Small Cell Lung Cancer Using Machine Learning and Differential Networks
A30
ID 0095
Repeats Enrichment Analysis of sequencing Datasets (READs) reveals unique repair and transcription dynamics of human satellites
A31
ID 0079
Mutational signature in Mycobacterium tuberculosis under pretomanid and nitric oxide exposure
A32
ID 0050
geneslator: a R package for comprehensive gene identifier mapping and annotation
A33
ID 0044
REV-AGE and REV-AGE 2.0: From Systematic Evidence Mapping to AI-Guided Mechanistic Discovery in Aging Research
A34
ID 0035
Toward Accessible and Reproducible Bioinformatics Workflows for Nanopore-Based Virus Surveillance
A35
ID 0086
Learning Read-Level joint genomic and epigenomic status representations from Nanopore sequencing data using Jesica-Fetcher and NTv3-like architecture
A36
ID 0083
Single-Molecule Tissue-of-Origin Profiling for Prenatal and Oncology cfDNA Applications
A37
ID 0030
Integrative analysis of multi-modal single-cell data reveals chromosome alterations underlying critical disease development stages: a proof-of-principle in MDS
A38
ID 0036
Single-cell multi-omics integration for TCR-epitope binding inference in acute myeloid leukemia
Poster Session B
Thursday 3 September 2026, 10:15-12:30, Museo di Arte Classica, Sapienza University of Rome
Biostatistics
B1
ID 0004
Piecewise Regression Mixture Models with Skewness
B2
ID 2618
Exploring the potential of Bayesian Gaussian Mixture integration for Variational Autoencoders in the generation of synthetic tabular data
B3
ID 0064
Impact of Non-Informative Censoring on the Performance of Propensity Scores Methods for Estimating Absolute Treatment Effects on Survival Outcome; Simulation study
B4
ID 0084
Federated Real World Data, Zero Exchange Framework for Transportability
B5
ID 0025
Exploring the role of marital status in Depression-Free Life Expectancy among older adults
B6
ID 9768
Gimme a rainy week life more: a computational study on the signal-to-noise ratio of epigenetic aging associations
Medical Informatics
B7
ID 0311
ClinAgent: A ReAct-Based Agent for Conversational Access to Clinical Trial Information
B8
ID 7510
Multimodal Learning from Temporally Grounded Narrative Events
B9
ID 9287
An unsupervised clustering analysis of breast cancer data derived from electronic health records enhanced through UMAP dimensionality reduction
B10
ID 0069
Automation of Prescription Analysis in Older Adults: A Big Data Approach in Mexico
B11
ID 9549
Privacy-Preserving Detection of Rare Disease-Associated Cell Subsets via Secure Multi-Party Computation
B12
ID 0041
A unified Medical Informatics black-box framework for integrating environmental sampling and laboratory analytical data at the Luxembourg National Health Laboratory (LNS)
B13
ID 0076
High-Resolution Spatial Transcriptomics Using Open-ST Reveals Alterations across Midbrain Subregions in an Alzheimer's Disease Mouse Model
B14
ID 0090
Proteogenomic insights into complex human diseases
Bioinformatics
B15
ID 0026
TensorPLS: an R package for tensor-aware PLS-based discriminant analysis of longitudinal multi-omics data
B16
ID 7280
NARCOD: Non-Arbitrarily Reproducible Clustering of transcriptOmics Data
B17
ID 0031
Development and Internal Validation of a Multimodal Machine Learning Model Integrating Omics, Clinical and Psychosocial Data for Heart Failure Risk Prediction
B18
ID 0092
Hypothesis-driven integrative transcriptomics reveals distinct Z-disc gene signatures in ischemic and non-ischemic cardiomyopathy
B19
ID 0049
Gene expression models for Alzheimer's Disease vs Mild Cognitive Impairment classification
B20
ID 0043
G4REP: A deep learning framework for the prediction of human RNA G-quadruplex-binding proteins
B21
ID 0045
Closing the Design-Validation Loop for AI-Driven mRNA Therapeutics via Structured Knowledge Accumulation
B22
ID 0082
Liquid biopsy-based multi-omics data integration for triple-negative breast cancer
B23
ID 1805
DQIS: Byzantine Fault Tolerance for Multi-Channel Immune Surveillance - A Quantum-Inspired Quorum-Based Framework Grounded on Melanoma, GBM, and PDAC Single-Cell RNA-Seq Data
B24
ID 0071
Network-Based Comparison of Solid Tissue and Tumor-Educated Platelet Transcriptomes in Glioblastoma
B25
ID 0080
Integration of computational and functional screening reveals novel R-loop-inducing drugs for triple-negative breast cancer treatment
B26
ID 0038
A tumor-agnostic network medicine framework reveals topological rewiring of systemic T-cell immunity in long-surviving cancer patients
B27
ID 0042
From hepatosome to interactome: network-based discovery of UBIAD1 as a lipid-metabolism target in hepatocellular carcinoma
B28
ID 0028
OMICS-query: An AI Agent-Based Chatbot for Bioinformatics Pipelines
B29
ID 0091
MoonLitDB: An LLM-powered database annotating moonlighting proteins from scientific literature
B30
ID 0055
An LLM-RAG System for Interactive Multi-Omic Exploration of 3D Genome Organization and Gene Expression during Mouse Cortical Neurogenesis
B31
ID 0075
Evaluating Genome Language Model Embeddings as Transferable Priors for Metagenomic Binning
B32
ID 0052
MErlin - Methylation-driven Expression & Regulation Linkage in Interacting Nuclear-domains
B33
ID 0058
Torch-eCpG v2: A Scalable and Interpretable Framework for eQTM Mapping and Multi-Omic Network Analysis
B34
ID 0032
Spatial GeoMx NGS profiling to map molecular drivers of pathological response in the tumor microenvironment of pleural mesothelioma patients receiving neoadjuvant chemo-immunotherapy
B35
ID 0067
SOPHYSM: More Steps towards Digital Twins of Solid Tumours
B36
ID 0061
Doski-nf: an integrated computational pipeline for consensus variant calling and comprehensive cancer genomic profiling
B37
ID 0048
Analytical variability across computational workflows in assessing tumor mutational burden and microsatellite instability from NGS data in male breast cancer
B38
ID 0037
Towards Full Bioinformatics Automation at the National Facility for Genomics of Human Technopole
B39
ID 0073