Abstract:Self-supervised topological deep learning (TDL) represents a nascent but underexplored area with significant potential for modeling higher-order interactions in simplicial complexes and cellular complexes to derive representations of unlabeled graphs. Compared to simplicial complexes, cellular complexes exhibit greater expressive power. However, the advancement in self-supervised learning for cellular TDL is largely hindered by two core challenges: \textit{extrinsic structural constraints} inherent to cellular complexes, and intrinsic semantic redundancy in cellular representations. The first challenge highlights that traditional graph augmentation techniques may compromise the integrity of higher-order cellular interactions, while the second underscores that topological redundancy in cellular complexes potentially diminish task-relevant information. To address these issues, we introduce Cellular Complex Contrastive Learning with Adaptive Trimming (CellCLAT), a twofold framework designed to adhere to the combinatorial constraints of cellular complexes while mitigating informational redundancy. Specifically, we propose a parameter perturbation-based augmentation method that injects controlled noise into cellular interactions without altering the underlying cellular structures, thereby preserving cellular topology during contrastive learning. Additionally, a cellular trimming scheduler is employed to mask gradient contributions from task-irrelevant cells through a bi-level meta-learning approach, effectively removing redundant topological elements while maintaining critical higher-order semantics. We provide theoretical justification and empirical validation to demonstrate that CellCLAT achieves substantial improvements over existing self-supervised graph learning methods, marking a significant attempt in this domain.
Abstract:In endoscopic procedures, autonomous tracking of abnormal regions and following circumferential cutting markers can significantly reduce the cognitive burden on endoscopists. However, conventional model-based pipelines are fragile for each component (e.g., detection, motion planning) requires manual tuning and struggles to incorporate high-level endoscopic intent, leading to poor generalization across diverse scenes. Vision-Language-Action (VLA) models, which integrate visual perception, language grounding, and motion planning within an end-to-end framework, offer a promising alternative by semantically adapting to surgeon prompts without manual recalibration. Despite their potential, applying VLA models to robotic endoscopy presents unique challenges due to the complex and dynamic anatomical environments of the gastrointestinal (GI) tract. To address this, we introduce EndoVLA, designed specifically for continuum robots in GI interventions. Given endoscopic images and surgeon-issued tracking prompts, EndoVLA performs three core tasks: (1) polyp tracking, (2) delineation and following of abnormal mucosal regions, and (3) adherence to circular markers during circumferential cutting. To tackle data scarcity and domain shifts, we propose a dual-phase strategy comprising supervised fine-tuning on our EndoVLA-Motion dataset and reinforcement fine-tuning with task-aware rewards. Our approach significantly improves tracking performance in endoscopy and enables zero-shot generalization in diverse scenes and complex sequential tasks.
Abstract:Robotic tactile sensors, including vision-based and taxel-based sensors, enable agile manipulation and safe human-robot interaction through force sensation. However, variations in structural configurations, measured signals, and material properties create domain gaps that limit the transferability of learned force sensation across different tactile sensors. Here, we introduce GenForce, a general framework for achieving transferable force sensation across both homogeneous and heterogeneous tactile sensors in robotic systems. By unifying tactile signals into marker-based binary tactile images, GenForce enables the transfer of existing force labels to arbitrary target sensors using a marker-to-marker translation technique with a few paired data. This process equips uncalibrated tactile sensors with force prediction capabilities through spatiotemporal force prediction models trained on the transferred data. Extensive experimental results validate GenForce's generalizability, accuracy, and robustness across sensors with diverse marker patterns, structural designs, material properties, and sensing principles. The framework significantly reduces the need for costly and labor-intensive labeled data collection, enabling the rapid deployment of multiple tactile sensors on robotic hands requiring force sensing capabilities.
Abstract:Without loss of generality, existing machine learning techniques may learn spurious correlation dependent on the domain, which exacerbates the generalization of models in out-of-distribution (OOD) scenarios. To address this issue, recent works build a structural causal model (SCM) to describe the causality within data generation process, thereby motivating methods to avoid the learning of spurious correlation by models. However, from the machine learning viewpoint, such a theoretical analysis omits the nuanced difference between the data generation process and representation learning process, resulting in that the causal analysis based on the former cannot well adapt to the latter. To this end, we explore to build a SCM for representation learning process and further conduct a thorough analysis of the mechanisms underlying spurious correlation. We underscore that adjusting erroneous covariates introduces bias, thus necessitating the correct selection of spurious correlation mechanisms based on practical application scenarios. In this regard, we substantiate the correctness of the proposed SCM and further propose to control confounding bias in OOD generalization by introducing a propensity score weighted estimator, which can be integrated into any existing OOD method as a plug-and-play module. The empirical results comprehensively demonstrate the effectiveness of our method on synthetic and large-scale real OOD datasets.