Alessio Ragno

Federico Di Valerio, Michela Proietti, Alessio Ragno et al.

Continual learning constrains models to learn new tasks over time without forgetting what they have already learned. A key challenge in this setting is catastrophic forgetting, where learning new information causes the model to lose its performance on previous tasks. Recently, explainable AI has been proposed as a promising way to better understand and reduce forgetting. In particular, self-explainable models are useful because they generate explanations during prediction, which can help preserve knowledge. However, most existing explainable approaches use post-hoc explanations or require additional memory for each new task, resulting in limited scalability. In this work, we introduce CIP-Net, an exemplar-free self-explainable prototype-based model designed for continual learning. CIP-Net avoids storing past examples and maintains a simple architecture, while still providing useful explanations and strong performance. We demonstrate that CIPNet achieves state-of-the-art performances compared to previous exemplar-free and self-explainable methods in both task- and class-incremental settings, while bearing significantly lower memory-related overhead. This makes it a practical and interpretable solution for continual learning.

Dylan Savoia, Alessio Ragno, Roberto Capobianco

It is well known that Drug Design is often a costly process both in terms of time and economic effort. While good Quantitative Structure-Activity Relationship models (QSAR) can help predicting molecular properties without the need to synthesize them, it is still required to come up with new molecules to be tested. This is mostly done in lack of tools to determine which modifications are more promising or which aspects of a molecule are more influential for the final activity/property. Here we present an automatic process which involves Graph Convolutional Network models and input-attribution methods to generate new molecules. We also explore the problems of over-optimization and applicability, recognizing them as two important aspects in the practical use of such automatic tools.

Alessio Ragno, Dylan Savoia, Roberto Capobianco

Since the introduction of artificial intelligence in medicinal chemistry, the necessity has emerged to analyse how molecular property variation is modulated by either single atoms or chemical groups. In this paper, we propose to train graph-to-graph neural network using semi-supervised learning for attributing structure-property relationships. As initial case studies we apply the method to solubility and molecular acidity while checking its consistency in comparison with known experimental chemical data. As final goal, our approach could represent a valuable tool to deal with problems such as activity cliffs, lead optimization and de-novo drug design.