Luis Wyss

h-index9
2papers

2 Papers

LGSep 30, 2025Code
Refine Drugs, Don't Complete Them: Uniform-Source Discrete Flows for Fragment-Based Drug Discovery

Benno Kaech, Luis Wyss, Karsten Borgwardt et al.

We introduce InVirtuoGen, a discrete flow generative model for fragmented SMILES for de novo and fragment-constrained generation, and target-property/lead optimization of small molecules. The model learns to transform a uniform source over all possible tokens into the data distribution. Unlike masked models, its training loss accounts for predictions on all sequence positions at every denoising step, shifting the generation paradigm from completion to refinement, and decoupling the number of sampling steps from the sequence length. For \textit{de novo} generation, InVirtuoGen achieves a stronger quality-diversity pareto frontier than prior fragment-based models and competitive performance on fragment-constrained tasks. For property and lead optimization, we propose a hybrid scheme that combines a genetic algorithm with a Proximal Property Optimization fine-tuning strategy adapted to discrete flows. Our approach sets a new state-of-the-art on the Practical Molecular Optimization benchmark, measured by top-10 AUC across tasks, and yields higher docking scores in lead optimization than previous baselines. InVirtuoGen thus establishes a versatile generative foundation for drug discovery, from early hit finding to multi-objective lead optimization. We further contribute to open science by releasing pretrained checkpoints and code, making our results fully reproducible\footnote{https://github.com/invirtuolabs/InVirtuoGen_results}.

BMMar 27, 2025
A Comprehensive Benchmark for RNA 3D Structure-Function Modeling

Luis Wyss, Vincent Mallet, Wissam Karroucha et al.

The relationship between RNA structure and function has recently attracted interest within the deep learning community, a trend expected to intensify as nucleic acid structure models advance. Despite this momentum, the lack of standardized, accessible benchmarks for applying deep learning to RNA 3D structures hinders progress. To this end, we introduce a collection of seven benchmarking datasets specifically designed to support RNA structure-function prediction. Built on top of the established Python package rnaglib, our library streamlines data distribution and encoding, provides tools for dataset splitting and evaluation, and offers a comprehensive, user-friendly environment for model comparison. The modular and reproducible design of our datasets encourages community contributions and enables rapid customization. To demonstrate the utility of our benchmarks, we report baseline results for all tasks using a relational graph neural network.