Dominique Beaini

Siamak Ravanbakhsh

Kirill Neklyudov

Alexander Tong

Sampling efficiently from a target unnormalized probability density remains a core challenge, with relevance across countless high-impact sc… (see more)ientific applications. A promising approach towards this challenge is the design of amortized samplers that borrow key ideas, such as probability path design, from state-of-the-art generative diffusion models. However, all existing diffusion-based samplers remain unable to draw samples from distributions at the scale of even simple molecular systems. In this paper, we propose Progressive Inference-Time Annealing (PITA), a novel framework to learn diffusion-based samplers that combines two complementary interpolation techniques: I.) Annealing of the Boltzmann distribution and II.) Diffusion smoothing. PITA trains a sequence of diffusion models from high to low temperatures by sequentially training each model at progressively higher temperatures, leveraging engineered easy access to samples of the temperature-annealed target density. In the subsequent step, PITA enables simulating the trained diffusion model to procure training samples at a lower temperature for the next diffusion model through inference-time annealing using a novel Feynman-Kac PDE combined with Sequential Monte Carlo. Empirically, PITA enables, for the first time, equilibrium sampling of N-body particle systems, Alanine Dipeptide, and tripeptides in Cartesian coordinates with dramatically lower energy function evaluations. Code available at: https://github.com/taraak/pita

2025-06-19

ArXiv (preprint)

Self-Refining Training for Amortized Density Functional Theory

Majdi Hassan

Cristian Gabellini

Hatem Helal

Kirill Neklyudov

Density Functional Theory (DFT) allows for predicting all the chemical and physical properties of molecular systems from first principles by… (see more) finding an approximate solution to the many-body Schr\"odinger equation. However, the cost of these predictions becomes infeasible when increasing the scale of the energy evaluations, e.g., when calculating the ground-state energy for simulating molecular dynamics. Recent works have demonstrated that, for substantially large datasets of molecular conformations, Deep Learning-based models can predict the outputs of the classical DFT solvers by amortizing the corresponding optimization problems. In this paper, we propose a novel method that reduces the dependency of amortized DFT solvers on large pre-collected datasets by introducing a self-refining training strategy. Namely, we propose an efficient method that simultaneously trains a deep-learning model to predict the DFT outputs and samples molecular conformations that are used as training data for the model. We derive our method as a minimization of the variational upper bound on the KL-divergence measuring the discrepancy between the generated samples and the target Boltzmann distribution defined by the ground state energy. To demonstrate the utility of the proposed scheme, we perform an extensive empirical study comparing it with the models trained on the pre-collected datasets. Finally, we open-source our implementation of the proposed algorithm, optimized with asynchronous training and sampling stages, which enables simultaneous sampling and training. Code is available at https://github.com/majhas/self-refining-dft.

2025-06-02

ArXiv (preprint)

Virtual Cells: Predict, Explain, Discover

Emmanuel Noutahi

Jason Hartford

Prudencio Tossou

Shawn Whitfield

Ali Denton

Cas Wognum

Kristina Ulicna

Jonathan Hsu

Michael Cuccarese

Emmanuel Bengio

Christopher Gibson

Daniel Cohen

Berton Earnshaw

2025-05-20

ArXiv (preprint)

Virtual Cells: Predict, Explain, Discover

Emmanuel Noutahi

Jason Hartford

Prudencio Tossou

Shawn Whitfield

Ali Denton

Cas Wognum

Kristina Ulicna

Michael Craig

Jonathan Hsu

Michael Cuccarese

Emmanuel Bengio

Christopher Gibson

Daniel Cohen

Berton Earnshaw

2025-05-01

arXiv (published)

Scaling Deep Learning Solutions for Transition Path Sampling

Jungyoon Lee

Michael Plainer

Yuanqi Du

Lars Holdijk

Rob Brekelmans

Carla P Gomes

Kirill Neklyudov

Transition path sampling (TPS) is an important method for studying rare events, such as they happen in chemical reactions or protein folding… (see more). These events occur so infrequently that traditional simulations are often impractical, and even recent machine-learning approaches struggle to address this issue for larger systems. In this paper, we propose using modern deep learning techniques to improve the scalability of TPS methods significantly. We highlight the need for better evaluations in the existing literature and start by formulating TPS as a sampling problem over an unnormalized target density and introduce relevant evaluation metrics to assess the effectiveness of TPS solutions from this perspective. To develop a scalable approach, we explore several design choices, including a problem-informed neural network architecture, simulated annealing, the integration of prior knowledge into the sampling process, and attention mechanisms. Finally, we conduct a comprehensive empirical study and compare these design choices with other recently developed deep-learning methods for rare event sampling.

2025-03-05

ICLR.cc/2025/Workshop/GEM (published)

Molphenix: A Multimodal Foundation Model for PhenoMolecular Retrieval

Philip Fradkin

Puria Azadi Moghadam

Karush Suri

Frederik Wenkel

Maciej Sypetkowski

Predicting molecular impact on cellular function is a core challenge in therapeutic design. Phenomic experiments, designed to capture cellu… (see more)lar morphology, utilize microscopy based techniques and demonstrate a high throughput solution for uncovering molecular impact on the cell. In this work, we learn a joint latent space between molecular structures and microscopy phenomic experiments, aligning paired samples with contrastive learning. Specifically, we study the problem of Contrastive PhenoMolecular Retrieval, which consists of zero-shot molecular structure identification conditioned on phenomic experiments. We assess challenges in multi-modal learning of phenomics and molecular modalities such as experimental batch effect, inactive molecule perturbations, and encoding perturbation concentration. We demonstrate improved multi-modal learner retrieval through (1) a uni-modal pre-trained phenomics model, (2) a novel inter sample similarity aware loss, and (3) models conditioned on a representation of molecular concentration. Following this recipe, we propose MolPhenix, a molecular phenomics model. MolPhenix leverages a pre-trained phenomics model to demonstrate significant performance gains across perturbation concentrations, molecular scaffolds, and activity thresholds. In particular, we demonstrate an 8.1

2024-11-02

NeurIPS.cc/2024/Workshop/FM4Science (oral)

Molphenix: A Multimodal Foundation Model for PhenoMolecular Retrieval

Philip Fradkin

Puria Azadi Moghadam

Karush Suri

Frederik Wenkel

Maciej Sypetkowski

Predicting molecular impact on cellular function is a core challenge in therapeutic design. Phenomic experiments, designed to capture cellu… (see more)lar morphology, utilize microscopy based techniques and demonstrate a high throughput solution for uncovering molecular impact on the cell. In this work, we learn a joint latent space between molecular structures and microscopy phenomic experiments, aligning paired samples with contrastive learning. Specifically, we study the problem of Contrastive PhenoMolecular Retrieval, which consists of zero-shot molecular structure identification conditioned on phenomic experiments. We assess challenges in multi-modal learning of phenomics and molecular modalities such as experimental batch effect, inactive molecule perturbations, and encoding perturbation concentration. We demonstrate improved multi-modal learner retrieval through (1) a uni-modal pre-trained phenomics model, (2) a novel inter sample similarity aware loss, and (3) models conditioned on a representation of molecular concentration. Following this recipe, we propose MolPhenix, a molecular phenomics model. MolPhenix leverages a pre-trained phenomics model to demonstrate significant performance gains across perturbation concentrations, molecular scaffolds, and activity thresholds. In particular, we demonstrate an 8.1

2024-10-13

NeurIPS.cc/2024/Workshop/AIDrugX (poster)

ET-Flow: Equivariant Flow-Matching for Molecular Conformer Generation

Majdi Hassan

Nikhil Shenoy

Jungyoon Lee

Hannes Stärk

Stephan Thaler

Predicting low-energy molecular conformations given a molecular graph is an important but challenging task in computational drug discovery.… (see more) Existing state- of-the-art approaches either resort to large scale transformer-based models that diffuse over conformer fields, or use computationally expensive methods to gen- erate initial structures and diffuse over torsion angles. In this work, we introduce Equivariant Transformer Flow (ET-Flow). We showcase that a well-designed flow matching approach with equivariance and harmonic prior alleviates the need for complex internal geometry calculations and large architectures, contrary to the prevailing methods in the field. Our approach results in a straightforward and scalable method that directly operates on all-atom coordinates with minimal assumptions. With the advantages of equivariance and flow matching, ET-Flow significantly increases the precision and physical validity of the generated con- formers, while being a lighter model and faster at inference. Code is available https://github.com/shenoynikhil/ETFlow.

2024-09-25

NeurIPS.cc/2024/Conference (poster)

How Molecules Impact Cells: Unlocking Contrastive PhenoMolecular Retrieval

Philip Fradkin

Puria Azadi Moghadam

Karush Suri

Frederik Wenkel

Ali Bashashati

Maciej Sypetkowski

Predicting molecular impact on cellular function is a core challenge in therapeutic design. Phenomic experiments, designed to capture cellul… (see more)ar morphology, utilize microscopy based techniques and demonstrate a high throughput solution for uncovering molecular impact on the cell. In this work, we learn a joint latent space between molecular structures and microscopy phenomic experiments, aligning paired samples with contrastive learning. Specifically, we study the problem ofContrastive PhenoMolecular Retrieval, which consists of zero-shot molecular structure identification conditioned on phenomic experiments. We assess challenges in multi-modal learning of phenomics and molecular modalities such as experimental batch effect, inactive molecule perturbations, and encoding perturbation concentration. We demonstrate improved multi-modal learner retrieval through (1) a uni-modal pre-trained phenomics model, (2) a novel inter sample similarity aware loss, and (3) models conditioned on a representation of molecular concentration. Following this recipe, we propose MolPhenix, a molecular phenomics model. MolPhenix leverages a pre-trained phenomics model to demonstrate significant performance gains across perturbation concentrations, molecular scaffolds, and activity thresholds. In particular, we demonstrate an 8.1x improvement in zero shot molecular retrieval of active molecules over the previous state-of-the-art, reaching 77.33% in top-1% accuracy. These results open the door for machine learning to be applied in virtual phenomics screening, which can significantly benefit drug discovery applications.

2024-09-25

NeurIPS.cc/2024/Conference (poster)

On the Scalability of GNNs for Molecular Graphs

Maciej Sypetkowski

Frederik Wenkel

Farimah Poursafaei

Nia Dickson

Karush Suri

Philip Fradkin

Scaling deep learning models has been at the heart of recent revolutions in language modelling and image generation. Practitioners have obse… (see more)rved a strong relationship between model size, dataset size, and performance. However, structure-based architectures such as Graph Neural Networks (GNNs) are yet to show the benefits of scale mainly due to the lower efficiency of sparse operations, large data requirements, and lack of clarity about the effectiveness of various architectures. We address this drawback of GNNs by studying their scaling behavior. Specifically, we analyze message-passing networks, graph Transformers, and hybrid architectures on the largest public collection of 2D molecular graphs. For the first time, we observe that GNNs benefit tremendously from the increasing scale of depth, width, number of molecules, number of labels, and the diversity in the pretraining datasets, resulting in a 30.25% improvement when scaling to 1 billion parameters and 28.98% improvement when increasing size of dataset to eightfold. We further demonstrate strong finetuning scaling behavior on 38 tasks, outclassing previous large models. We hope that our work paves the way for an era where foundational GNNs drive pharmaceutical drug discovery.

2024-09-25

NeurIPS.cc/2024/Conference (poster)

How Molecules Impact Cells: Unlocking Contrastive PhenoMolecular Retrieval

Philip Fradkin

Puria Azadi Moghadam

Karush Suri

Frederik Wenkel

Ali Bashashati

Maciej Sypetkowski

Predicting molecular impact on cellular function is a core challenge in therapeutic design. Phenomic experiments, designed to capture cellul… (see more)ar morphology, utilize microscopy based techniques and demonstrate a high throughput solution for uncovering molecular impact on the cell. In this work, we learn a joint latent space between molecular structures and microscopy phenomic experiments, aligning paired samples with contrastive learning. Specifically, we study the problem ofContrastive PhenoMolecular Retrieval, which consists of zero-shot molecular structure identification conditioned on phenomic experiments. We assess challenges in multi-modal learning of phenomics and molecular modalities such as experimental batch effect, inactive molecule perturbations, and encoding perturbation concentration. We demonstrate improved multi-modal learner retrieval through (1) a uni-modal pre-trained phenomics model, (2) a novel inter sample similarity aware loss, and (3) models conditioned on a representation of molecular concentration. Following this recipe, we propose MolPhenix, a molecular phenomics model. MolPhenix leverages a pre-trained phenomics model to demonstrate significant performance gains across perturbation concentrations, molecular scaffolds, and activity thresholds. In particular, we demonstrate an 8.1x improvement in zero shot molecular retrieval of active molecules over the previous state-of-the-art, reaching 77.33% in top-1% accuracy. These results open the door for machine learning to be applied in virtual phenomics screening, which can significantly benefit drug discovery applications.

2024-09-10

ArXiv (preprint)

Graph Positional and Structural Encoder

Renming Liu

Semih Cantürk

Olivier Lapointe-Gagné

Vincent Létourneau

Guy Wolf

Ladislav Rampášek

Positional and structural encodings (PSE) enable better identifiability of nodes within a graph, as in general graphs lack a canonical node … (see more)ordering. This renders PSEs essential tools for empowering modern GNNs, and in particular graph Transformers. However, designing PSEs that work optimally for a variety of graph prediction tasks is a challenging and unsolved problem. Here, we present the graph positional and structural encoder (GPSE), a first-ever attempt to train a graph encoder that captures rich PSE representations for augmenting any GNN. GPSE can effectively learn a common latent representation for multiple PSEs, and is highly transferable. The encoder trained on a particular graph dataset can be used effectively on datasets drawn from significantly different distributions and even modalities. We show that across a wide range of benchmarks, GPSE-enhanced models can significantly improve the performance in certain tasks, while performing on par with those that employ explicitly computed PSEs in other cases. Our results pave the way for the development of large pre-trained models for extracting graph positional and structural information and highlight their potential as a viable alternative to explicitly computed PSEs as well as to existing self-supervised pre-training approaches.

2024-07-08

Proceedings of the 41st International Conference on Machine Learning (published)