Yukun Tian

Yukun Tian, Hao Chen, Yongjian Deng et al.

The event camera has demonstrated significant success across a wide range of areas due to its low time latency and high dynamic range. However, the community faces challenges such as data deficiency and limited diversity, often resulting in over-fitting and inadequate feature learning. Notably, the exploration of data augmentation techniques in the event community remains scarce. This work aims to address this gap by introducing a systematic augmentation scheme named EventAug to enrich spatial-temporal diversity. In particular, we first propose Multi-scale Temporal Integration (MSTI) to diversify the motion speed of objects, then introduce Spatial-salient Event Mask (SSEM) and Temporal-salient Event Mask (TSEM) to enrich object variants. Our EventAug can facilitate models learning with richer motion patterns, object variants and local spatio-temporal relations, thus improving model robustness to varied moving speeds, occlusions, and action disruptions. Experiment results show that our augmentation method consistently yields significant improvements across different tasks and backbones (e.g., a 4.87% accuracy gain on DVS128 Gesture). Our code will be publicly available for this community.

Haofeng Xu, Junwei Su, Yukun Tian et al.

Asynchronous execution is essential for scaling reinforcement learning (RL) to modern large model workloads, including large language models and AI agents, but it can fundamentally alter RL optimization behavior. While prior work on asynchronous RL focuses on training throughput and distributional correction, we show that naively applying asynchrony to policy-gradient updates can induce qualitatively different training dynamics and lead to severe training instability. Through systematic empirical and theoretical analysis, we identify a key signature of this instability: asynchronous training exhibits persistently high cosine similarity between consecutive policy gradients, in contrast to the near-orthogonal updates observed under synchronized training. This stale-aligned gradient effect amplifies correlated updates and increases the risk of overshooting and divergence. Motivated by this observation, we propose GRADIENT ALIGNMENT CONTROL(GAC), a simple dynamics-aware stabilization method that regulates asynchronous RL progress along stale-aligned directions via gradient projection. We establish convergence guarantees under bounded staleness and demonstrate empirically that GAC recovers stable, on-policy training dynamics and matches synchronized baselines even at high staleness.

Yiming Lei, Yukun Tian, Hongming Shan et al.

A number of studies on lung nodule classification lack clinical/biological interpretations of the features extracted by convolutional neural network (CNN). The methods like class activation mapping (CAM) and gradient-based CAM (Grad-CAM) are tailored for interpreting localization and classification tasks while they ignored fine-grained features. Therefore, CAM and Grad-CAM cannot provide optimal interpretation for lung nodule categorization task in low-dose CT images, in that fine-grained pathological clues like discrete and irregular shape and margins of nodules are capable of enhancing sensitivity and specificity of nodule classification with regards to CNN. In this paper, we first develop a soft activation mapping (SAM) to enable fine-grained lung nodule shape \& margin (LNSM) feature analysis with a CNN so that it can access rich discrete features. Secondly, by combining high-level convolutional features with SAM, we further propose a high-level feature enhancement scheme (HESAM) to localize LNSM features. Experiments on the LIDC-IDRI dataset indicate that 1) SAM captures more fine-grained and discrete attention regions than existing methods, 2) HESAM localizes more accurately on LNSM features and obtains the state-of-the-art predictive performance, reducing the false positive rate, and 3) we design and conduct a visually matching experiment which incorporates radiologists study to increase the confidence level of applying our method to clinical diagnosis.