Jian Tang

Biographie

Jian Tang est professeur agrégé au département de sciences de la décision de HEC. Il est aussi professeur associé au département informatique et recherche opérationnelle (DIRO) de l'Université de Montréal et un membre académique principal à Mila – Institut québécois d’intelligence artificielle. Il est titulaire d'une chaire de recherche en IA Canada-CIFAR et le fondateur de BioGeometry, une entreprise en démarrage spécialisée dans l'IA générative pour la découverte d'anticorps. Ses principaux domaines de recherche sont les modèles génératifs profonds, l'apprentissage automatique des graphes et leurs applications à la découverte de médicaments. Il est un leader international dans le domaine de l'apprentissage automatique des graphes, et son travail représentatif sur l'apprentissage de la représentation des nœuds, LINE, a été largement reconnu et cité plus de 5 000 fois. Il a également réalisé de nombreux travaux pionniers sur l'IA pour la découverte de médicaments, notamment le premier cadre d'apprentissage automatique à source ouverte pour la découverte de médicaments, TorchDrug et TorchProtein.

Étudiants actuels

Huiyu Cai

Doctorat - UdeM

Doctorat - UdeM

Superviseur⋅e principal⋅e :

Xixian Liu

Doctorat - Université de Montréal

Jiarui Lu

Doctorat - UdeM

Github

Chence Shi

Doctorat - UdeM

Sophie Xhonneux

Doctorat - UdeM

Superviseur⋅e principal⋅e :

Gauthier Gidel

Xinyu Yuan

Doctorat - UdeM

Github

Zhihao Zhan

Doctorat - UdeM

Doctorat - UdeM

Doctorat - HEC

Jianan Zhao

Doctorat - UdeM

Github

Publications

Reaction-conditioned De Novo Enzyme Design with GENzyme

Chenqing Hua

Jiarui Lu

Yang Liu

Odin Zhang

Rex Ying

Wengong Jin

Guy Wolf

Doina Precup

Shuangjia Zheng

The introduction of models like RFDiffusionAA, AlphaFold3, AlphaProteo, and Chai1 has revolutionized protein structure modeling and interact… (voir plus)ion prediction, primarily from a binding perspective, focusing on creating ideal lock-and-key models. However, these methods can fall short for enzyme-substrate interactions, where perfect binding models are rare, and induced fit states are more common. To address this, we shift to a functional perspective for enzyme design, where the enzyme function is defined by the reaction it catalyzes. Here, we introduce \textsc{GENzyme}, a \textit{de novo} enzyme design model that takes a catalytic reaction as input and generates the catalytic pocket, full enzyme structure, and enzyme-substrate binding complex. \textsc{GENzyme} is an end-to-end, three-staged model that integrates (1) a catalytic pocket generation and sequence co-design module, (2) a pocket inpainting and enzyme inverse folding module, and (3) a binding and screening module to optimize and predict enzyme-substrate complexes. The entire design process is driven by the catalytic reaction being targeted. This reaction-first approach allows for more accurate and biologically relevant enzyme design, potentially surpassing structure-based and binding-focused models in creating enzymes capable of catalyzing specific reactions. We provide \textsc{GENzyme} code at https://github.com/WillHua127/GENzyme.

2024-11-09

ArXiv (prépublication)

arxiv.org

GraphText: Graph Reasoning in Text Space

Jianan Zhao

Le Zhuo

Yikang Shen

Meng Qu

Kai Liu

Michael M. Bronstein

2024-10-09

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

Any2Policy: Learning Visuomotor Policy with Any-Modality

Yichen Zhu

Zhicai Ou

Feifei Feng

Humans can communicate and observe media with different modalities, such as texts, sounds, and images. For robots to be more generalizable e… (voir plus)mbodied agents, they should be capable of following instructions and perceiving the world with adaptation to diverse modalities. Current robotic learning methodologies often focus on single-modal task specification and observation, thereby limiting their ability to process rich multi-modal information. Addressing this limitation, we present an end-to-end general-purpose multi-modal system named Any-to-Policy Embodied Agents. This system empowers robots to handle tasks using various modalities, whether in combinations like text-image, audio-image, text-point cloud, or in isolation. Our innovative approach involves training a versatile modality network that adapts to various inputs and connects with policy networks for effective control. Because of the lack of existing multi-modal robotics datasets for evaluation, we assembled a comprehensive real-world dataset encompassing 30 robotic tasks. Each task in this dataset is richly annotated across multiple modalities, providing a robust foundation for assessment. We conducted extensive validation of our proposed unified modality embodied agent using several simulation benchmarks, including Franka Kitchen, Meta-World, and Maniskill2, as well as in our real-world settings. Our experiments showcase the promising capability of building embodied agents that can adapt to diverse multi-modal in a unified framework.

2024-09-24

NeurIPS.cc/2024/Conference (poster)

EDT: An Efficient Diffusion Transformer Framework Inspired by Human-like Sketching

Xinwang Chen

Ning Liu

Yichen Zhu

Feifei Feng

Transformer-based Diffusion Probabilistic Models (DPMs) have shown more potential than CNN-based DPMs, yet their extensive computational req… (voir plus)uirements hinder widespread practical applications. To reduce the computation budget of transformer-based DPMs, this work proposes the Efficient Diffusion Transformer (EDT) framework. This framework includes a lightweight-design diffusion model architecture, and a training-free Attention Modulation Matrix and its alternation arrangement in EDT inspired by human-like sketching. Additionally, we propose a token relation-enhanced masking training strategy tailored explicitly for EDT to augment its token relation learning capability. Our extensive experiments demonstrate the efficacy of EDT. The EDT framework reduces training and inference costs and surpasses existing transformer-based diffusion models in image synthesis performance, thereby achieving a significant overall enhancement. With lower FID, EDT-S, EDT-B, and EDT-XL attained speed-ups of 3.93x, 2.84x, and 1.92x respectively in the training phase, and 2.29x, 2.29x, and 2.22x respectively in inference, compared to the corresponding sizes of MDTv2. Our code is available at https://github.com/xinwangChen/EDT.

2024-09-24

NeurIPS.cc/2024/Conference (poster)

Multi-Scale Representation Learning for Protein Fitness Prediction

Zuobai Zhang

Pascal Notin

Yining Huang

Aurelie Lozano

Vijil Chenthamarakshan

Debora Marks

Payel Das

Designing novel functional proteins crucially depends on accurately modeling their fitness landscape. Given the limited availability of func… (voir plus)tional annotations from wet-lab experiments, previous methods have primarily relied on self-supervised models trained on vast, unlabeled protein sequence or structure datasets. While initial protein representation learning studies solely focused on either sequence or structural features, recent hybrid architectures have sought to merge these modalities to harness their respective strengths. However, these sequence-structure models have so far achieved only incremental improvements when compared to the leading sequence-only approaches, highlighting unresolved challenges effectively leveraging these modalities together. Moreover, the function of certain proteins is highly dependent on the granular aspects of their surface topology, which have been overlooked by prior models. To address these limitations, we introduce the Sequence-Structure-Surface Fitness (S3F) model - a novel multimodal representation learning framework that integrates protein features across several scales. Our approach combines sequence representations from a protein language model with Geometric Vector Perceptron networks encoding protein backbone and detailed surface topology. The proposed method achieves state-of-the-art fitness prediction on the ProteinGym benchmark encompassing 217 substitution deep mutational scanning assays, and provides insights into the determinants of protein function. Our code is at https://github.com/DeepGraphLearning/S3F.

2024-09-24

NeurIPS.cc/2024/Conference (poster)

BioPathNet: Enhancing Link Prediction in Biomedical Knowledge Graphs through Path Representation Learning

Annalisa Marsico

Yue Hu

Svitlana Oleshko

Samuele Firmani

Hui Cheng

Maria Ulmer

Matthias Arnold

Maria Colomé-Tatché

Sophie Xhonneux

Abstract

Understanding complex interactions in biomedical networks is crucial for advancements in biomedic… (voir plus)ine, but traditional link prediction (LP) methods are limited in capturing this complexity. Representation-based learning techniques improve prediction accuracy by mapping nodes to low-dimensional embeddings, yet they often struggle with interpretability and scalability. We present BioPathNet, a novel graph neural network framework based on the Neural Bellman-Ford Network (NBFNet), addressing these limitations through path-based reasoning for LP in biomedical knowledge graphs. Unlike node-embedding frameworks, BioPathNet learns representations between node pairs by considering all relations along paths, enhancing prediction accuracy and interpretability. This allows visualization of influential paths and facilitates biological validation. BioPathNet leverages a background regulatory graph (BRG) for enhanced message passing and uses stringent negative sampling to improve precision. In evaluations across various LP tasks, such as gene function annotation, drug-disease indication, synthetic lethality, and lncRNA-mRNA interaction prediction, BioPathNet consistently outperformed shallow node embedding methods, relational graph neural networks and task-specific state-of-the-art methods, demonstrating robust performance and versatility. Our study predicts novel drug indications for diseases like acute lymphoblastic leukemia (ALL) and Alzheimer’s, validated by medical experts and clinical trials. We also identified new synthetic lethality gene pairs and regulatory interactions involving lncRNAs and target genes, confirmed through literature reviews. BioPathNet's interpretability will enable researchers to trace prediction paths and gain molecular insights, making it a valuable tool for drug discovery, personalized medicine and biology in general.

2024-09-16

Research Square (publié)

Are Heterophily-Specific GNNs and Homophily Metrics Really Effective? Evaluation Pitfalls and New Benchmarks

Sitao Luan

Qincheng Lu

Chenqing Hua

Xinyu Wang

Jiaqi Zhu

Xiao-Wen Chang

Guy Wolf

Over the past decade, Graph Neural Networks (GNNs) have achieved great success on machine learning tasks with relational data. However, rece… (voir plus)nt studies have found that heterophily can cause significant performance degradation of GNNs, especially on node-level tasks. Numerous heterophilic benchmark datasets have been put forward to validate the efficacy of heterophily-specific GNNs and various homophily metrics have been designed to help people recognize these malignant datasets. Nevertheless, there still exist multiple pitfalls that severely hinder the proper evaluation of new models and metrics. In this paper, we point out three most serious pitfalls: 1) a lack of hyperparameter tuning; 2) insufficient model evaluation on the real challenging heterophilic datasets; 3) missing quantitative evaluation benchmark for homophily metrics on synthetic graphs. To overcome these challenges, we first train and fine-tune baseline models on

2024-09-08

ArXiv (prépublication)

arxiv.org

In-Context Learning, Can It Break Safety?

David Dobre

2024-06-27

ICML.cc/2024/Workshop/NextGenAISafety (poster)

Path-based reasoning for biomedical knowledge graphs with BioPathNet

Yue Hu

Svitlana Oleshko

Samuele Firmani

Hui Cheng

Maria Ulmer

Matthias Arnold

Maria Colomé-Tatché

Sophie Xhonneux

Annalisa Marsico

Understanding complex interactions in biomedical networks is crucial for advancements in biomedicine, but traditional link prediction (LP) m… (voir plus)ethods are limited in capturing this complexity. Representation-based learning techniques improve prediction accuracy by mapping nodes to low-dimensional embeddings, yet they often struggle with interpretability and scalability. We present BioPathNet, a novel graph neural network framework based on the Neural Bellman-Ford Network (NBFNet), addressing these limitations through path-based reasoning for LP in biomedical knowledge graphs. Unlike node-embedding frameworks, BioPathNet learns representations between node pairs by considering all relations along paths, enhancing prediction accuracy and interpretability. This allows visualization of influential paths and facilitates biological validation. BioPathNet leverages a background regulatory graph (BRG) for enhanced message passing and uses stringent negative sampling to improve precision. In evaluations across various LP tasks, such as gene function annotation, drug-disease indication, synthetic lethality, and lncRNA-mRNA interaction prediction, BioPathNet consistently outperformed shallow node embedding methods, relational graph neural networks and task-specific state-of-the-art methods, demonstrating robust performance and versatility. Our study predicts novel drug indications for diseases like acute lymphoblastic leukemia (ALL) and Alzheimer’s, validated by medical experts and clinical trials. We also identified new synthetic lethality gene pairs and regulatory interactions involving lncRNAs and target genes, confirmed through literature reviews. BioPathNet’s interpretability will enable researchers to trace prediction paths and gain molecular insights, making it a valuable tool for drug discovery, personalized medicine and biology in general.

2024-06-17

bioRxiv (publié)

Augmenting Evolutionary Models with Structure-based Retrieval

Yining Huang

Zuobai Zhang

Debora Susan Marks

Pascal Notin

2024-06-16

ICML.cc/2024/Workshop/ML4LMS (poster)

NPA: Improving Large-scale Graph Neural Networks with Non-parametric Attention.

Wentao Zhang

Guochen Yan

Yu Shen

Yangyu Tao

Bin CUI

Recent works show great interest in designing Graph Neural Networks (GNNs) that scale to large graphs. While previous work focuses on design… (voir plus)ing advanced sampling techniques for existing GNNs, the design of non-parametric GNNs, an orthogonal direction for scalable performance, has aroused lots of concerns recently. For example, nearly all top solutions in the Open Graph Benchmark leaderboard are non-parametric GNNs. Despite their high predictive performance and scalability, non-parametric GNNs still face two limitations. First, due to the propagation of over-smoothed features, they suffer from severe performance degradation along with the propagation depth. More importantly, they only consider the graph structure and ignore the feature influence during the non-parametric propagation, leading to sub-optimal propagated features. To address these limitations, we present non-parametric attention (NPA), a plug-and-play module that is compatible with non-parametric GNNs, to get scalable and deep GNNs simultaneously. We have deployed NPA in Tencent with the Angel platform, and we further evaluate NPA on both real-world datasets and large-scale industrial datasets. Experimental results on seven homophilic graphs (including the industrial Tencent Video graph) and five heterophilic graphs demonstrate NPA enjoys high performance -- achieves large performance gain over existing non-parametric GNNs, deeper architecture -- improves non-parametric GNNs with large model depth, and high scalability -- can support large-scale graphs with low time costs. Notably, it achieves state-of-the-art performance on the large ogbn-papers100M dataset.

2024-06-08

SIGMOD Conference Companion (publié)

The 1st International Workshop on Graph Foundation Models (GFM).

Haitao Mao

Jianan Zhao

Xiaoxin He

Zhikai Chen

Qian Huang

Michael M. Bronstein

Xavier Bresson

Bryan Hooi

Haiyang Zhang

Xianfeng Tang

Zhikai Chen

Jiliang Tang

Foundation models such as GPT-4 for natural language processing (NLP), Flamingo for computer vision (CV), have set new benchmarks in AI by d… (voir plus)elivering state-of-the-art results across various tasks with minimal task-specific data. Despite their success, the application of these models to the graph domain is challenging due to the relational nature of graph-structured data. To address this gap, we propose the Graph Foundation Model (GFM) Workshop, the first workshop for GFMs, dedicated to exploring the adaptation and development of foundation models specifically designed for graph data. The GFM workshop focuses on two critical questions: (1) How can the underlying capabilities of existing foundation models be effectively applied to graph data? (2) What foundational principles should guide the creation of models tailored to the graph domain? Through a curated set of panel sections, keynote talks, and paper presentations, our workshop intends to catalyze innovative approaches and theoretical frameworks for Graph Foundation Models (GFMs). We target a broad audience, encompassing researchers, practitioners, and students, and aim to lay the groundwork for the next wave of breakthroughs in integrating graph data with foundation models.

2024-05-12

Companion Proceedings of the ACM on Web Conference 2024 (publié)