Shikai Guo

Shouyu Yin, Zhao Tian, Junjie Chen et al.

Code generation, which aims to automatically generate source code from given programming requirements, has the potential to substantially improve software development efficiency. With the rapid advancement of large language models (LLMs), LLM-based code generation has attracted widespread attention from both academia and industry. However, as programming requirements become increasingly complex, existing LLMs still exhibit notable performance limitations. To address this challenge, recent studies have proposed training-based curriculum reinforcement learning (CRL) strategies to improve LLM code generation performance. Despite their effectiveness, existing CRL approaches suffer from several limitations, including misaligned requirement difficulty perception, the absence of requirement difficulty optimization, and suboptimal curriculum sampling strategies. In CRL-based code generation, programming requirements serve as the sole input to the model, making their quality and difficulty critical to training effectiveness. Motivated by insights from software requirements engineering, we propose RECRL, a novel requirement-aware curriculum reinforcement learning framework for enhancing LLM-based code generation. RECRL automatically perceives model-specific requirement difficulty, optimizes challenging requirements to improve training data utilization, and employs an adaptive curriculum sampling strategy to construct training batches with smoothly varying difficulty. Extensive experiments on five state-of-the-art LLMs across five widely-used code generation benchmarks by comparing with five state-of-the-art baselines, demonstrate the significant effectiveness of RECRL. For example, RECRL achieves an average Pass@1 improvement of 1.23%-5.62% over all state-of-the-art baselines.

Xin An, Ruijie Li, Qiao Ning et al.

Non-coding RNAs (ncRNAs) play pivotal roles in gene expression regulation and the pathogenesis of various diseases. Accurate classification of ncRNAs is essential for functional annotation and disease diagnosis. To address existing limitations in feature extraction depth and multimodal fusion, we propose HGMamba-ncRNA, a HyperGraphMamba-based multichannel adaptive model, which integrates sequence, secondary structure, and optionally available expression features of ncRNAs to enhance classification performance. Specifically, the sequence of ncRNA is modeled using a parallel Multi-scale Convolution and LSTM architecture (MKC-L) to capture both local patterns and long-range dependencies of nucleotides. The structure modality employs a multi-scale graph transformer (MSGraphTransformer) to represent the multi-level topological characteristics of ncRNA secondary structures. The expression modality utilizes a Chebyshev Polynomial-based Kolmogorov-Arnold Network (CPKAN) to effectively model and interpret high-dimensional expression profiles. Finally, by incorporating virtual nodes to facilitate efficient and comprehensive multimodal interaction, HyperGraphMamba is proposed to adaptively align and integrate multichannel heterogeneous modality features. Experiments conducted on three public datasets demonstrate that HGMamba-ncRNA consistently outperforms state-of-the-art methods in terms of accuracy and other metrics. Extensive empirical studies further confirm the model's robustness, effectiveness, and strong transferability, offering a novel and reliable strategy for complex ncRNA functional classification. Code and datasets are available at https://anonymous.4open.science/r/HGMamba-ncRNA-94D0.

Weihao Sun, Shikai Guo, Siwen Wang et al.

The automation of logic circuit design enhances chip performance, energy efficiency, and reliability, and is widely applied in the field of Electronic Design Automation (EDA).And-Inverter Graphs (AIGs) efficiently represent, optimize, and verify the functional characteristics of digital circuits, enhancing the efficiency of EDA development.Due to the complex structure and large scale of nodes in real-world AIGs, accurate modeling is challenging, leading to existing work lacking the ability to jointly model functional and structural characteristics, as well as insufficient dynamic information propagation capability.To address the aforementioned challenges, we propose AIGer.Specifically, AIGer consists of two components: 1) Node logic feature initialization embedding component and 2) AIGs feature learning network component.The node logic feature initialization embedding component projects logic nodes, such as AND and NOT, into independent semantic spaces, to enable effective node embedding for subsequent processing.Building upon this, the AIGs feature learning network component employs a heterogeneous graph convolutional network, designing dynamic relationship weight matrices and differentiated information aggregation approaches to better represent the original structure and information of AIGs.The combination of these two components enhances AIGer's ability to jointly model functional and structural characteristics and improves its message passing capability. Experimental results indicate that AIGer outperforms the current best models in the Signal Probability Prediction (SSP) task, improving MAE and MSE by 18.95\% and 44.44\%, respectively. In the Truth Table Distance Prediction (TTDP) task, AIGer achieves improvements of 33.57\% and 14.79\% in MAE and MSE, respectively, compared to the best-performing models.

Xin An, Ruijie Li, Qiao Ning et al.

In the study of drug function and precision medicine, identifying new drug-microbe associations is crucial. However, current methods isolate association and similarity analysis of drug and microbe, lacking effective inter-view optimization and coordinated multi-view feature fusion. In our study, a multi-view Divergence-Convergence Feature Augmentation framework for Drug-related Microbes Prediction (DCFA_DMP) is proposed, to better learn and integrate association information and similarity information. In the divergence phase, DCFA_DMP strengthens the complementarity and diversity between heterogeneous information and similarity information by performing Adversarial Learning method between the association network view and different similarity views, optimizing the feature space. In the convergence phase, a novel Bidirectional Synergistic Attention Mechanism is proposed to deeply synergize the complementary features between different views, achieving a deep fusion of the feature space. Moreover, Transformer graph learning is alternately applied on the drug-microbe heterogeneous graph, enabling each drug or microbe node to focus on the most relevant nodes. Numerous experiments demonstrate DCFA_DMP's significant performance in predicting drug-microbe associations. It also proves effectiveness in predicting associations for new drugs and microbes in cold start experiments, further confirming its stability and reliability in predicting potential drug-microbe associations.

Ruijie Li, Xiang Zhao, Qiao Ning et al.

In tennis tournaments, momentum, a critical yet elusive phenomenon, reflects the dynamic shifts in performance of athletes that can decisively influence match outcomes. Despite its significance, momentum in terms of effective modeling and multi-granularity analysis across points, games, sets, and matches in tennis tournaments remains underexplored. In this study, we define a novel Momentum Score (MS) metric to quantify a player's momentum level in multi-granularity tennis tournaments, and design HydraNet, a momentum-driven state-space duality-based framework, to model MS by integrating thirty-two heterogeneous dimensions of athletes performance in serve, return, psychology and fatigue. HydraNet integrates a Hydra module, which builds upon a state-space duality (SSD) framework, capturing explicit momentum with a sliding-window mechanism and implicit momentum through cross-game state propagation. It also introduces a novel Versus Learning method to better enhance the adversarial nature of momentum between the two athletes at a macro level, along with a Collaborative-Adversarial Attention Mechanism (CAAM) for capturing and integrating intra-player and inter-player dynamic momentum at a micro level. Additionally, we construct a million-level tennis cross-tournament dataset spanning from 2012-2023 Wimbledon and 2013-2023 US Open, and validate the multi-granularity modeling capability of HydraNet for the MS metric on this dataset. Extensive experimental evaluations demonstrate that the MS metric constructed by the HydraNet framework provides actionable insights into how momentum impacts outcomes at different granularities, establishing a new foundation for momentum modeling and sports analysis. To the best of our knowledge, this is the first work to explore and effectively model momentum across multiple granularities in professional tennis tournaments.

Xiang Zhao, Ruijie Li, Qiao Ning et al.

The identification of drug-target interactions (DTI) is critical for drug discovery and repositioning, as it reveals potential therapeutic uses of existing drugs, accelerating development and reducing costs. However, most existing models focus only on direct similarity in homogeneous graphs, failing to exploit the rich similarity in heterogeneous graphs. To address this gap, inspired by real-world social interaction behaviors, we propose SOC-DGL, which comprises two specialized modules: the Affinity-Driven Graph Learning (ADGL) module, learning global similarity through an affinity-enhanced drug-target graph, and the Equilibrium-Driven Graph Learning (EDGL) module, capturing higher-order similarity by amplifying the influence of even-hop neighbors using an even-polynomial graph filter based on balance theory. This dual approach enables SOC-DGL to effectively capture similarity information across multiple interaction scales within affinity and association matrices. To address the issue of imbalance in DTI datasets, we propose an adjustable imbalance loss function that adjusts the weight of negative samples by the parameter. Extensive experiments on four benchmark datasets demonstrate that SOC-DGL consistently outperforms existing state-of-the-art methods across both balanced and imbalanced scenarios. Moreover, SOC-DGL successfully predicts the top 9 drugs known to bind ABL1, and further analyzed the 10th drug, which has not been experimentally confirmed to interact with ABL1, providing supporting evidence for its potential binding.