Few-shot learning (FSL) aims to recognize novel concepts from only a few labeled support samples. Recent studies enhance support features by incorporating additional semantic information (e.g., class descriptions) or designing complex semantic fusion modules. However, these methods still suffer from hallucinating semantics that contradict the visual evidence due to the lack of grounding in actual instances, resulting in noisy guidance and costly corrections. To address these issues, we propose a novel framework, bridging Vision and Text with LLMs for Few-Shot Learning (VT-FSL), which constructs precise cross-modal prompts conditioned on Large Language Models (LLMs) and support images, seamlessly integrating them through a geometry-aware alignment mechanism. It mainly consists of Cross-modal Iterative Prompting (CIP) and Cross-modal Geometric Alignment (CGA).

Language and vision-language models have shown impressive performance across a wide range of tasks, but their internal mechanisms remain only partly understood. In this work, we study how individual attention heads in text-generative models specialize in specific semantic or visual attributes. Building on an established interpretability method, we reinterpret the practice of probing intermediate activations with the final decoding layer through the lens of signal processing. This lets us analyze multiple samples in a principled way and rank attention heads based on their relevance to target concepts. Our results show consistent patterns of specialization at the head level across both unimodal and multimodal transformers. Remarkably, we find that editing as few as 1% of the heads, selected using our method, can reliably suppress or enhance targeted concepts in the model output.

Deep neural networks operating on non-Euclidean geometries have recently demonstrated impressive performance across various machine-learning applications. Several studies have extended the attention mechanism to different manifolds. However, most existing non-Euclidean attention models are tailored to specific geometries, limiting their applicability. On the other hand, recent studies show that several matrix manifolds, such as Symmetric Positive Definite (SPD), Symmetric Positive Semi-Definite (SPSD), and Grassmannian manifolds, admit gyrovector structures, which extend vector addition and scalar product into manifolds. Leveraging these properties, we propose a Gyro Attention (GyroAtt) framework over general gyrovector spaces, applicable to various matrix geometries.

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Deep neural networks with short residual connections have demonstrated remarkable success across domains, but increasing depth often introduces computational redundancy without corresponding improvements in representation quality. We introduce Auto-Compressing Networks (ACNs), an architectural variant where additive long feedforward connections from each layer to the output replace traditional short residual connections. By analyzing the distinct dynamics induced by this modification, we reveal a unique property we coin as --the ability of a network to organically compress information during training with gradient descent, through architectural design alone. Through auto-compression, information is dynamically pushed into early layers during training, enhancing their representational quality and revealing potential redundancy in deeper ones. We theoretically show that this property emerges from layer-wise training patterns found only in ACNs, where layers are dynamically utilized during training based on task requirements. We also find that ACNs exhibit enhanced noise robustness compared to residual networks, superior performance in low-data settings, improved transfer learning capabilities, and mitigate catastrophic forgetting suggesting that they learn representations that generalize better despite using fewer parameters. Our results demonstrate up to 18\% reduction in catastrophic forgetting and 30-80\% architectural compression while maintaining accuracy across vision transformers, MLP-mixers, and BERT architectures. These findings establish ACNs as a practical approach to developing efficient neural architectures that automatically adapt their computational footprint to task complexity, while learning robust representations suitable for noisy real-world tasks and continual learning scenarios.

Decoding visual stimuli from neural population activity is crucial for understanding the brain and for applications in brain-machine interfaces. However, such biological data is often scarce, particularly in primates or humans, where high-throughput recording techniques, such as two-photon imaging, remain challenging or impossible to apply. This, in turn, poses a challenge for deep learning decoding techniques. To overcome this, we introduce MEIcoder, a biologically informed decoding method that leverages neuron-specific most exciting inputs (MEIs), a structural similarity index measure loss, and adversarial training. MEIcoder achieves state-of-the-art performance in reconstructing visual stimuli from single-cell activity in primary visual cortex (V1), especially excelling on small datasets with fewer recorded neurons. Using ablation studies, we demonstrate that MEIs are the main drivers of the performance, and in scaling experiments, we show that MEIcoder can reconstruct high-fidelity natural-looking images from as few as 1,000-2,500 neurons and less than 1,000 training data points. We also propose a unified benchmark with over 160,000 samples to foster future research. Our results demonstrate the feasibility of reliable decoding in early visual system and provide practical insights for neuroscience and neuroengineering applications.

We present in this paper a novel post-training quantization (PTQ) method, dubbed AccuQuant, for diffusion models. We show analytically and empirically that quantization errors for diffusion models are accumulated over denoising steps in a sampling process. To alleviate the error accumulation problem, AccuQuant minimizes the discrepancies between outputs of a full-precision diffusion model and its quantized version within a couple of denoising steps. That is, it simulates multiple denoising steps of a diffusion sampling process explicitly for quantization, accounting the accumulated errors over multiple denoising steps, which is in contrast to previous approaches to imitating a training process of diffusion models, namely, minimizing the discrepancies independently for each step. We also present an efficient implementation technique for AccuQuant, together with a novel objective, which reduces a memory complexity significantly from $\mathcal{O}(n)$ to $\mathcal{O}(1)$, where $n$ is the number of denoising steps. We demonstrate the efficacy and efficiency of AccuQuant across various tasks and diffusion models on standard benchmarks.

Dynamic functional brain networks (DFBNs) are powerful tools in neuroscience research. Recent studies reveal that DFBNs contain heterogeneous neural nodes with more extensive connections and more drastic temporal changes, which play pivotal roles in coordinating the reorganization of the brain. Moreover, the spatio-temporal patterns of these nodes are modulated by the brain's historical states. However, existing methods not only ignore the spatio-temporal heterogeneity of neural nodes, but also fail to effectively encode the temporal propagation mechanism of heterogeneous activities. These limitations hinder the deep exploration of spatio-temporal relationships within DFBNs, preventing the capture of abnormal neural heterogeneity caused by brain diseases.

The rapid extension of context windows in large vision-language models has given rise to long-context vision-language models (LCVLMs), which are capable of handling hundreds of images with interleaved text tokens in a single forward pass. In this work, we introduce MMLongBench, the first benchmark covering a diverse set of long-context vision-language tasks, to evaluate LCVLMs effectively and thoroughly. MMLongBench is composed of 13,331 examples spanning five different categories of downstream tasks, such as Visual RAG and Many-Shot ICL. It also provides broad coverage of image types, including various natural and synthetic images. To assess the robustness of the models to different input lengths, all examples are delivered at five standardized input lengths (8K-128K tokens) via a cross-modal tokenization scheme that combines vision patches and text tokens. Through a thorough benchmarking of 46 closed-source and open-source LCVLMs, we provide a comprehensive analysis of the current models' vision-language long-context ability. Our results show that: i) performance on a single task is a weak proxy for overall long-context capability; ii) both closed-source and open-source models face challenges in long-context vision-language tasks, indicating substantial room for future improvement; iii) models with stronger reasoning ability tend to exhibit better long-context performance. By offering wide task coverage, various image types, and rigorous length control, MMLongBench provides the missing foundation for diagnosing and advancing the next generation of LCVLMs.

Transformers have revolutionized nucleotide sequence analysis, yet capturing long range dependencies remains challenging. Recent studies show that autoregressive transformers often exhibit Markovian behavior by relying on fixed-length context windows for next-token prediction. However, standard self-attention mechanisms are computationally inefficient for long sequences due to their quadratic complexity and do not explicitly enforce global transition consistency. We introduce CARMANIA (Context-Aware Regularization with Markovian Integration for Attention-Based Nucleotide Analysis), a self-supervised pretraining framework that augments next-token (NT) prediction with a transition-matrix (TM) loss. The TM loss aligns predicted token transitions with empirically derived n-gram statistics from each input sequence, encouraging the model to capture higher-order dependencies beyond local context. This integration enables CARMANIA to learn organism-specific sequence structures that reflect both evolutionary constraints and functional organization. We evaluate CARMANIA across diverse genomic tasks, including regulatory element prediction, functional gene classification, taxonomic inference, antimicrobial resistance detection, and biosynthetic gene cluster classification. CARMANIA outperforms the previous best long-context model by at least 7\%, matches state-of-the-art on shorter sequences (exceeding prior results on 20/40 tasks while running $\sim$2.5$\times$