arXiv subjects

Zihan Pengmei

Publications and source records attributed to Zihan Pengmei.

9 recordsLinked to original sources

arXiv2026

cuGUGA: Operator-Direct Graphical Unitary Group Approach Accelerated with CUDA

We present cuGUGA, an operator-direct graphical unitary group approach (GUGA) configuration interaction (CI) solver in a spin-adapted configuration state function (CSF) basis. Dynamic-programming walk counts provide constant-time CSF ranking/unranking, and pretabulated segment factors enable constant-time evaluation of coupling coefficients. Two-electron contributions are organized through an intermediate-weight formulation that separates sparse generator enumeration from integral contraction and supports both dense and density-fitted/Cholesky backends. We further map the same primitives to GPUs by implementing the irregular DRT traversal and accumulation in custom CUDA kernels while delegating contractions to CUDA libraries. The implementation reproduces reference energies at the 10^{-11} Eh level and matches CPU/GPU sigma-vectors to 10^{-14}. On an RTX 4090, the GPU backend provides up to ~10x speedup over the CPU backend for smaller active spaces and multifold speedups on representative CASCI kernels. Speedup decreases as the active space grows because the workload becomes increasingly dominated by FP64 GEMM, which is not strongly accelerated on consumer GPUs. In addition, the cuGUGA CPU backend generally delivers >2x speedup over PySCF's determinant backend and >4x speedup over PySCF CSF backend.

physics.chem-ph↗

arXiv2025

Hierarchical geometric deep learning enables scalable analysis of molecular dynamics

Molecular dynamics simulations can generate atomically detailed trajectories of complex systems, but analyzing these dynamics can be challenging when systems lack well-established quantitative descriptors (features). Graph neural networks (GNNs) in which messages are passed between nodes that represent atoms that are spatial neighbors promise to obviate manual feature engineering, but the use of GNNs with biomolecular systems of more than a few hundred residues has been limited in the context of analyzing dynamics by both difficulties in capturing the details of long-range interactions with message passing and the memory and runtime requirements associated with large graphs. Here, we show how local information can be aggregated to reduce memory and runtime requirements without sacrificing atomic detail. We demonstrate that this approach opens the door to analyzing simulations of protein-nucleic acid complexes with thousands of residues on single GPUs within minutes. For systems with hundreds of residues, for which there are sufficient data to make quantitative comparisons, we show that the approach improves performance and interpretability.

cs.LG↗

arXiv2025

The Kinetics of Reasoning: How Chain-of-Thought Shapes Learning in Transformers?

Chain-of-thought (CoT) supervision can substantially improve transformer performance, yet the mechanisms by which models learn to follow and benefit from CoT remain poorly understood. We investigate these learning dynamics through the lens of grokking by pretraining transformers on symbolic reasoning tasks with tunable algorithmic complexity and controllable data composition to study their generalization. Models were trained under two settings: (i) producing only final answers, and (ii) emitting explicit CoT traces before answering. Our results show that while CoT generally improves task performance, its benefits depend on task complexity. To quantify these effects, we model the accuracy of the logarithmic training steps with a three-parameter logistic curve, revealing how the learning speed and shape vary with task complexity, data distribution, and the presence of CoT supervision. We also uncover a transient trace unfaithfulness phase: early in training, models often produce correct answers while skipping or contradicting CoT steps, before later aligning their reasoning traces with answers. Empirically, we (1) demonstrate that CoT accelerates generalization but does not overcome tasks with higher algorithmic complexity, such as finding list intersections; (2) introduce a kinetic modeling framework for understanding transformer learning; (3) characterize trace faithfulness as a dynamic property that emerges over training; and (4) show CoT alters internal transformer computation mechanistically.

cs.LG↗

arXiv2024

Using pretrained graph neural networks with token mixers as geometric featurizers for conformational dynamics

Identifying informative low-dimensional features that characterize dynamics in molecular simulations remains a challenge, often requiring extensive manual tuning and system-specific knowledge. Here, we introduce geom2vec, in which pretrained graph neural networks (GNNs) are used as universal geometric featurizers. By pretraining equivariant GNNs on a large dataset of molecular conformations with a self-supervised denoising objective, we obtain transferable structural representations that are useful for learning conformational dynamics without further fine-tuning. We show how the learned GNN representations can capture interpretable relationships between structural units (tokens) by combining them with expressive token mixers. Importantly, decoupling training the GNNs from training for downstream tasks enables analysis of larger molecular graphs (such as small proteins at all-atom resolution) with limited computational resources. In these ways, geom2vec eliminates the need for manual feature selection and increases the robustness of simulation analyses.

cs.LG↗

arXiv2024

Pushing the Limits of All-Atom Geometric Graph Neural Networks: Pre-Training, Scaling and Zero-Shot Transfer

Constructing transferable descriptors for conformation representation of molecular and biological systems finds numerous applications in drug discovery, learning-based molecular dynamics, and protein mechanism analysis. Geometric graph neural networks (Geom-GNNs) with all-atom information have transformed atomistic simulations by serving as a general learnable geometric descriptors for downstream tasks including prediction of interatomic potential and molecular properties. However, common practices involve supervising Geom-GNNs on specific downstream tasks, which suffer from the lack of high-quality data and inaccurate labels leading to poor generalization and performance degradation on out-of-distribution (OOD) scenarios. In this work, we explored the possibility of using pre-trained Geom-GNNs as transferable and highly effective geometric descriptors for improved generalization. To explore their representation power, we studied the scaling behaviors of Geom-GNNs under self-supervised pre-training, supervised and unsupervised learning setups. We find that the expressive power of different architectures can differ on the pre-training task. Interestingly, Geom-GNNs do not follow the power-law scaling on the pre-training task, and universally lack predictable scaling behavior on the supervised tasks with quantum chemical labels important for screening and design of novel molecules. More importantly, we demonstrate how all-atom graph embedding can be organically combined with other neural architectures to enhance the expressive power. Meanwhile, the low-dimensional projection of the latent space shows excellent agreement with conventional geometrical descriptors.

cs.LG↗

arXiv2024

Unifying O(3) Equivariant Neural Networks Design with Tensor-Network Formalism

Many learning tasks, including learning potential energy surfaces from ab initio calculations, involve global spatial symmetries and permutational symmetry between atoms or general particles. Equivariant graph neural networks are a standard approach to such problems, with one of the most successful methods employing tensor products between various tensors that transform under the spatial group. However, as the number of different tensors and the complexity of relationships between them increase, maintaining parsimony and equivariance becomes increasingly challenging. In this paper, we propose using fusion diagrams, a technique widely employed in simulating SU($2$)-symmetric quantum many-body problems, to design new equivariant components for equivariant neural networks. This results in a diagrammatic approach to constructing novel neural network architectures. When applied to particles within a given local neighborhood, the resulting components, which we term "fusion blocks," serve as universal approximators of any continuous equivariant function defined in the neighborhood. We incorporate a fusion block into pre-existing equivariant architectures (Cormorant and MACE), leading to improved performance with fewer parameters on a range of challenging chemical problems. Furthermore, we apply group-equivariant neural networks to study non-adiabatic molecular dynamics of stilbene cis-trans isomerization. Our approach, which combines tensor networks with equivariant neural networks, suggests a potentially fruitful direction for designing more expressive equivariant neural networks.

cs.LG↗

arXiv2024

Technical Report: The Graph Spectral Token -- Enhancing Graph Transformers with Spectral Information

Graph Transformers have emerged as a powerful alternative to Message-Passing Graph Neural Networks (MP-GNNs) to address limitations such as over-squashing of information exchange. However, incorporating graph inductive bias into transformer architectures remains a significant challenge. In this report, we propose the Graph Spectral Token, a novel approach to directly encode graph spectral information, which captures the global structure of the graph, into the transformer architecture. By parameterizing the auxiliary [CLS] token and leaving other tokens representing graph nodes, our method seamlessly integrates spectral information into the learning process. We benchmark the effectiveness of our approach by enhancing two existing graph transformers, GraphTrans and SubFormer. The improved GraphTrans, dubbed GraphTrans-Spec, achieves over 10% improvements on large graph benchmark datasets while maintaining efficiency comparable to MP-GNNs. SubFormer-Spec demonstrates strong performance across various datasets.

cs.LG↗

arXiv2024

Beyond MD17: the reactive xxMD dataset

System specific neural force fields (NFFs) have gained popularity in computational chemistry. One of the most popular datasets as a bencharmk to develop NFFs models is the MD17 dataset and its subsequent extension. These datasets comprise geometries from the equilibrium region of the ground electronic state potential energy surface, sampled from direct adiabatic dynamics. However, many chemical reactions involve significant molecular geometrical deformations, for example, bond breaking. Therefore, MD17 is inadequate to represent a chemical reaction. To address this limitation in MD17, we introduce a new dataset, called Extended Excited-state Molecular Dynamics (xxMD) dataset. The xxMD dataset involves geometries sampled from direct non-adiabatic dynamics, and the energies are computed at both multireference wavefunction theory and density functional theory. We show that the xxMD dataset involves diverse geometries which represent chemical reactions. Assessment of NFF models on xxMD dataset reveals significantly higher predictive errors than those reported for MD17 and its variants. This work underscores the challenges faced in crafting a generalizable NFF model with extrapolation capability.

cs.LG↗

arXiv2023

Transformers are efficient hierarchical chemical graph learners

Transformers, adapted from natural language processing, are emerging as a leading approach for graph representation learning. Contemporary graph transformers often treat nodes or edges as separate tokens. This approach leads to computational challenges for even moderately-sized graphs due to the quadratic scaling of self-attention complexity with token count. In this paper, we introduce SubFormer, a graph transformer that operates on subgraphs that aggregate information by a message-passing mechanism. This approach reduces the number of tokens and enhances learning long-range interactions. We demonstrate SubFormer on benchmarks for predicting molecular properties from chemical structures and show that it is competitive with state-of-the-art graph transformers at a fraction of the computational cost, with training times on the order of minutes on a consumer-grade graphics card. We interpret the attention weights in terms of chemical structures. We show that SubFormer exhibits limited over-smoothing and avoids over-squashing, which is prevalent in traditional graph neural networks.

cs.LG↗