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Posters

Poster Session A - Wednesday 2 September 2026, 16:45-18:30, Museo di Arte Classica, Sapienza University of Rome.

Posters

Biostatistics

A1

ID 0040

GLM-Based Parametric Survival Modeling Under Two-Phase Sampling: A Computational Framework with Application to High-Dimensional Methylation Data

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

ID 0072

Quantum Optimization for Protein-Protein Interaction Network Alignment

ID 0034

Quantum Annealing for De Novo Genome Assembly

ID 0087

Benchmarking LLMs for automated systems biology model replication

ID 3745

Analysis of Prompt Engineering for Drug Toxicity Prediction

ID 0059

Autoresearch Discovery of Interpretable Filter Rules for Antibody Binder Classification

ID 5995

Statistical Model Checking of Uncertain Continuous Time Markov Chain in Systems Biology

ID 5265

A ML-powered Multiscale Computational Platform Based on QSP and PBPK Modeling to Support the Development of mRNA-based Therapies

ID 0029

Computational Framework for the Design of Second-Generation Pharmacochaperones Targeting Allosteric Pockets

ID 0077

Pathway-Mediated Networks for Drug Repurposing in Breast Cancer

ID 0089

Large-scale analysis and clustering of RNA 3D structures

ID 0062

Machine learning approaches for predicting functional lncRNAs and key regulatory interactions in plant gene networks

ID 0023

Computational Prediction of Pathogenic FMR1 Variants in Fragile X Syndrome

ID 0047

VISMA: Vector Integration Site Mutation Analysis

ID 0022

A Network Story: tumor educated platelets transcriptome and Glioblastoma

ID 0033

FLiCoN: Friendship Like differential Coexpression Network for the identification of Tumor-Educated Platelets Driver Genes in Glioma via structural Imbalance

ID 0070

Beyond Differential Expression: Network Centrality measures reveal Tissue-Specific Signatures in Tumor-Educated Platelets

ID 0066

Investigating Immunotherapy Response in Non-Small Cell Lung Cancer Using Machine Learning and Differential Networks

ID 0095

Repeats Enrichment Analysis of sequencing Datasets (READs) reveals unique repair and transcription dynamics of human satellites

ID 0079

Mutational signature in Mycobacterium tuberculosis under pretomanid and nitric oxide exposure

ID 0050

geneslator: a R package for comprehensive gene identifier mapping and annotation

ID 0044

REV-AGE and REV-AGE 2.0: From Systematic Evidence Mapping to AI-Guided Mechanistic Discovery in Aging Research

ID 0035

Toward Accessible and Reproducible Bioinformatics Workflows for Nanopore-Based Virus Surveillance

ID 0086

Learning Read-Level joint genomic and epigenomic status representations from Nanopore sequencing data using Jesica-Fetcher and NTv3-like architecture

ID 0083

Single-Molecule Tissue-of-Origin Profiling for Prenatal and Oncology cfDNA Applications

ID 0030

Integrative analysis of multi-modal single-cell data reveals chromosome alterations underlying critical disease development stages: a proof-of-principle in MDS

ID 0036

Single-cell multi-omics integration for TCR-epitope binding inference in acute myeloid leukemia