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Xixian Liu

Doctorat - Université de Montréal
Superviseur⋅e principal⋅e
Jian Tang
Sujets de recherche
Apprentissage multimodal
IA pour la science
Réseaux de neurones en graphes
Traitement du langage naturel
Site web
Google Scholar

Publications

Plausibility Is Not Prediction: Contrastive Evidence for LLM-Based Cellular Perturbation Reasoning
Xinyu Yuan
Xixian Liu
Jianan Zhao
Yashi Zhang
Hongyu Guo
Jian Tang
Perturbation experiments are central to understanding cellular mechanisms, but remain costly and sparse, motivating prediction of gene expre… (voir plus)ssion responses for unobserved conditions. A promising recent direction leverages large language models (LLMs) as"virtual cell"simulators-using stepwise, knowledge-grounded mechanistic reasoning to infer differential expression-pointing toward an interpretable, knowledge-driven paradigm that transcends purely data-driven approaches. However, we find that plausibility is not prediction: despite producing biologically plausible explanations, these methods fail to capture perturbation-specific effects: systematically overestimating differential expression, often underperforming a simple gene-frequency baseline in aggregate evaluations, and collapsing to chance-level performance at the per-gene level. This reveals a reliance on intrinsic gene response tendencies rather than true perturbation reasoning. We trace this failure to how evidence is presented: existing methods evaluate perturbation-gene pairs in isolation, without exposing how related perturbations differ in their effects on the same gene. To address this limitation, we introduce CORE (Contrastive Organization of Relational Evidence), which reframes prediction as a comparison task by organizing evidence into positive and negative outcomes from related perturbations. Using a biomedical knowledge graph for evidence retrieval, CORE improves calibration and substantially boosts perturbation-specific prediction in both LLM-based and non-LLM settings: for example, on drug-perturbation data, CORE-Reasoning improves Qwen3.5-9B aggregate metrics by up to 28.6%, while on generic perturbation data, CORE-Voting raises macro-per-gene AUROC from chance to 0.703 in average across four cell lines. This highlights contrastive evidence organization as essential to reliable LLM-based perturbation reasoning
2026-05-30
arXiv (prépublication)
doi.org
arxiv.org
Learning Structure, Energy, and Dynamics: A Survey of Artificial Intelligence for Protein Dynamics
Haocheng Tang
Liang Shi
Ya-Shi Zhang
Xixian Liu
Jian Tang
Jiarui Lu
Protein dynamics underlie many biological functions, yet remain difficult to characterize due to the high computational cost of molecular dy… (voir plus)namics simulations and the scarcity of dynamic structural data. This survey reviews recent advances in artificial intelligence for protein dynamics from three perspectives: learning from structural ensembles and trajectories, learning from physical energy signals, and learning to accelerate molecular simulations. We summarize representative methods for conformation ensemble generation, trajectory generation, Boltzmann generators, physics-aware adaptation, machine learning potentials, coarse-grained modeling, and collective variable discovery. We further discuss available datasets and key open challenges, such as scalability, thermodynamic consistency, kinetic fidelity, and integration with experimental constraints.
2026-04-27
arXiv (prépublication)
doi.org
arxiv.org
PerturbDiff: Functional Diffusion for Single-Cell Perturbation Modeling
Xinyu Yuan
Xixian Liu
Yashi Zhang
Zuobai Zhang
Hongyu Guo
Jian Tang
Building Virtual Cells that can accurately simulate cellular responses to perturbations is a long-standing goal in systems biology. A fundam… (voir plus)ental challenge is that high-throughput single-cell sequencing is destructive: the same cell cannot be observed both before and after a perturbation. Thus, perturbation prediction requires mapping unpaired control and perturbed populations. Existing models address this by learning maps between distributions, but typically assume a single fixed response distribution when conditioned on observed cellular context (e.g., cell type) and the perturbation type. In reality, responses vary systematically due to unobservable latent factors such as microenvironmental fluctuations and complex batch effects, forming a manifold of possible distributions for the same observed conditions. To account for this variability, we introduce PerturbDiff, which shifts modeling from individual cells to entire distributions. By embedding distributions as points in a Hilbert space, we define a diffusion-based generative process operating directly over probability distributions. This allows PerturbDiff to capture population-level response shifts across hidden factors. Benchmarks on established datasets show that PerturbDiff achieves state-of-the-art performance in single-cell response prediction and generalizes substantially better to unseen perturbations. See our project page (https://katarinayuan.github.io/PerturbDiff-ProjectPage/), where code and data will be made publicly available (https://github.com/DeepGraphLearning/PerturbDiff).
2026-02-22
arXiv (prépublication)
doi.org
openreview.net
GeneZip: Region-Aware Compression for Long Context DNA Modeling
Jianan Zhao
Xixian Liu
Zhihao Zhan
Xinyu Yuan
Hongyu Guo
Jian Tang
Genomic sequences span billions of base pairs (bp), posing a fundamental challenge for genome-scale foundation models. Existing approaches l… (voir plus)argely sidestep this barrier by either scaling relatively small models to long contexts or relying on heavy multi-GPU parallelism. Here we introduce GeneZip, a DNA compression model that leverages a key biological prior: genomic information is highly imbalanced. Coding regions comprise only a small fraction (about 2 percent) yet are information-dense, whereas most non-coding sequence is comparatively information-sparse. GeneZip couples HNet-style dynamic routing with a region-aware compression-ratio objective, enabling adaptive allocation of representation budget across genomic regions. As a result, GeneZip learns region-aware compression and achieves 137.6x compression with only 0.31 perplexity increase. On downstream long-context benchmarks, GeneZip achieves comparable or better performance on contact map prediction, expression quantitative trait loci prediction, and enhancer-target gene prediction. By reducing effective sequence length, GeneZip unlocks simultaneous scaling of context and capacity: compared to the prior state-of-the-art model JanusDNA, it enables training models 82.6x larger at 1M-bp context, supporting a 636M-parameter GeneZip model at 1M-bp context. All experiments in this paper can be trained on a single A100 80GB GPU.
2026-02-18
arXiv (prépublication)
doi.org
openreview.net