Pushing the Limits of Inverse Lithography with Generative Reinforcement Learning

Inverse lithography (ILT) is critical for modern semiconductor manufacturing but suffers from highly non-convex objectives that often trap optimization in poor local minima. Generative AI has been explored to warm-start ILT, yet most approaches train deterministic image-to-image translators to mimic sub-optimal datasets, providing limited guidance for escaping non-convex traps during refinement. We reformulate mask synthesis as conditional sampling: a generator learns a distribution over masks conditioned on the design and proposes multiple candidates. The generator is first pretrained with WGAN plus a reconstruction loss, then fine-tuned using Group Relative Policy Optimization (GRPO) with an ILT-guided imitation loss. At inference, we sample a small batch of masks, run fast batched ILT refinement, evaluate lithography metrics (e.g., EPE, process window), and select the best candidate. On \texttt{LithoBench} dataset, the proposed hybrid framework reduces EPE violations under a 3\,nm tolerance and roughly doubles throughput versus a strong numerical ILT baseline, while improving final mask quality. We also present over 20\% EPE improvement on \texttt{ICCAD13} contest cases with 3$\times$ speedup over the SOTA numerical ILT solver. By learning to propose ILT-friendly initializations, our approach mitigates non-convexity and advances beyond what traditional solvers or GenAI can achieve.

A Hypertoroidal Covering for Perfect Color Equivariance

When the color distribution of input images changes at inference, the performance of conventional neural network architectures drops considerably. A few researchers have begun to incorporate prior knowledge of color geometry in neural network design. These color equivariant architectures have modeled hue variation with 2D rotations, and saturation and luminance transformations as 1D translations. While this approach improves neural network robustness to color variations in a number of contexts, we find that approximating saturation and luminance (interval valued quantities) as 1D translations introduces appreciable artifacts. In this paper, we introduce a color equivariant architecture that is truly equivariant. Instead of approximating the interval with the real line, we lift values on the interval to values on the circle (a double-cover) and build equivariant representations there. Our approach resolves the approximation artifacts of previous methods, improves interpretability and generalizability, and achieves better predictive performance than conventional and equivariant baselines on tasks such as fine-grained classification and medical imaging tasks. Going beyond the context of color, we show that our proposed lifting can also extend to geometric transformations such as scale.

Harmonic Beltrami Signature Network: a Shape Prior Module in Deep Learning Framework

This paper presents the Harmonic Beltrami Signature Network (HBSN), a novel deep learning architecture for computing the Harmonic Beltrami Signature (HBS) from binary-like images. HBS is a shape representation that provides a one-to-one correspondence with 2D simply connected shapes, with invariance to translation, scaling, and rotation. By exploiting the function approximation capacity of neural networks, HBSN enables efficient extraction and utilization of shape prior information. The proposed network architecture incorporates a pre-Spatial Transformer Network (pre-STN) for shape normalization, a UNet-based backbone for HBS prediction, and a post-STN for angle regularization. Experiments show that HBSN accurately computes HBS representations, even for complex shapes. Furthermore, we demonstrate how HBSN can be directly incorporated into existing deep learning segmentation models, improving their performance through the use of shape priors. The results confirm the utility of HBSN as a general-purpose module for embedding geometric shape information into computer vision pipelines.

Diffusion Probe: Generated Image Result Prediction Using CNN Probes

Text-to-image (T2I) diffusion models lack an efficient mechanism for early quality assessment, leading to costly trial-and-error in multi-generation scenarios such as prompt iteration, agent-based generation, and flow-grpo. We reveal a strong correlation between early diffusion cross-attention distributions and final image quality. Based on this finding, we introduce Diffusion Probe, a framework that leverages internal cross-attention maps as predictive signals. We design a lightweight predictor that maps statistical properties of early-stage cross-attention extracted from initial denoising steps to the final image's overall quality. This enables accurate forecasting of image quality across diverse evaluation metrics long before full synthesis is complete. We validate Diffusion Probe across a wide range of settings. On multiple T2I models, across early denoising windows, resolutions, and quality metrics, it achieves strong correlation (PCC > 0.7) and high classification performance (AUC-ROC > 0.9). Its reliability translates into practical gains. By enabling early quality-aware decisions in workflows such as prompt optimization, seed selection, and accelerated RL training, the probe supports more targeted sampling and avoids computation on low-potential generations. This reduces computational overhead while improving final output quality.Diffusion Probe is model-agnostic, efficient, and broadly applicable, offering a practical solution for improving T2I generation efficiency through early quality prediction.

Geometrically Constrained Outlier Synthesis

Deep neural networks for image classification often exhibit overconfidence on out-of-distribution (OOD) samples. To address this, we introduce Geometrically Constrained Outlier Synthesis (GCOS), a training-time regularization framework aimed at improving OOD robustness during inference. GCOS addresses a limitation of prior synthesis methods by generating virtual outliers in the hidden feature space that respect the learned manifold structure of in-distribution (ID) data. The synthesis proceeds in two stages: (i) a dominant-variance subspace extracted from the training features identifies geometrically informed, off-manifold directions; (ii) a conformally-inspired shell, defined by the empirical quantiles of a nonconformity score from a calibration set, adaptively controls the synthesis magnitude to produce boundary samples. The shell ensures that generated outliers are neither trivially detectable nor indistinguishable from in-distribution data, facilitating smoother learning of robust features. This is combined with a contrastive regularization objective that promotes separability of ID and OOD samples in a chosen score space, such as Mahalanobis or energy-based. Experiments demonstrate that GCOS outperforms state-of-the-art methods using standard energy-based inference on near-OOD benchmarks, defined as tasks where outliers share the same semantic domain as in-distribution data. As an exploratory extension, the framework naturally transitions to conformal OOD inference, which translates uncertainty scores into statistically valid p-values and enables thresholds with formal error guarantees, providing a pathway toward more predictable and reliable OOD detection.

Tell2Adapt: A Unified Framework for Source Free Unsupervised Domain Adaptation via Vision Foundation Model

Source Free Unsupervised Domain Adaptation (SFUDA) is critical for deploying deep learning models across diverse clinical settings. However, existing methods are typically designed for low-gap, specific domain shifts and cannot generalize into a unified, multi-modalities, and multi-target framework, which presents a major barrier to real-world application. To overcome this issue, we introduce Tell2Adapt, a novel SFUDA framework that harnesses the vast, generalizable knowledge of the Vision Foundation Model (VFM). Our approach ensures high-fidelity VFM prompts through Context-Aware Prompts Regularization (CAPR), which robustly translates varied text prompts into canonical instructions. This enables the generation of high-quality pseudo-labels for efficiently adapting the lightweight student model to target domain. To guarantee clinical reliability, the framework incorporates Visual Plausibility Refinement (VPR), which leverages the VFM's anatomical knowledge to re-ground the adapted model's predictions in target image's low-level visual features, effectively removing noise and false positives. We conduct one of the most extensive SFUDA evaluations to date, validating our framework across 10 domain adaptation directions and 22 anatomical targets, including brain, cardiac, polyp, and abdominal targets. Our results demonstrate that Tell2Adapt consistently outperforms existing approaches, achieving SOTA for a unified SFUDA framework in medical image segmentation. Code are avaliable at https://github.com/derekshiii/Tell2Adapt.

WildSVG: Towards Reliable SVG Generation Under Real-Word Conditions

We introduce the task of SVG extraction, which consists in translating specific visual inputs from an image into scalable vector graphics. Existing multimodal models achieve strong results when generating SVGs from clean renderings or textual descriptions, but they fall short in real-world scenarios where natural images introduce noise, clutter, and domain shifts. A central challenge in this direction is the lack of suitable benchmarks. To address this need, we introduce the WildSVG Benchmark, formed by two complementary datasets: Natural WildSVG, built from real images containing company logos paired with their SVG annotations, and Synthetic WildSVG, which blends complex SVG renderings into real scenes to simulate difficult conditions. Together, these resources provide the first foundation for systematic benchmarking SVG extraction. We benchmark state-of-the-art multimodal models and find that current approaches perform well below what is needed for reliable SVG extraction in real scenarios. Nonetheless, iterative refinement methods point to a promising path forward, and model capabilities are steadily improving

Provable Subspace Identification of Nonlinear Multi-view CCA

We investigate the identifiability of nonlinear Canonical Correlation Analysis (CCA) in a multi-view setup, where each view is generated by an unknown nonlinear map applied to a linear mixture of shared latents and view-private noise. Rather than attempting exact unmixing, a problem proven to be ill-posed, we instead reframe multi-view CCA as a basis-invariant subspace identification problem. We prove that, under suitable latent priors and spectral separation conditions, multi-view CCA recovers the pairwise correlated signal subspaces up to view-wise orthogonal ambiguity. For $N \geq 3$ views, the objective provably isolates the jointly correlated subspaces shared across all views while eliminating view-private variations. We further establish finite-sample consistency guarantees by translating the concentration of empirical cross-covariances into explicit subspace error bounds via spectral perturbation theory. Experiments on synthetic and rendered image datasets validate our theoretical findings and confirm the necessity of the assumed conditions.

Scalable Multilingual Multimodal Machine Translation with Speech-Text Fusion

Multimodal Large Language Models (MLLMs) have achieved notable success in enhancing translation performance by integrating multimodal information. However, existing research primarily focuses on image-guided methods, whose applicability is constrained by the scarcity of multilingual image-text pairs. The speech modality overcomes this limitation due to its natural alignment with text and the abundance of existing speech datasets, which enable scalable language coverage. In this paper, we propose a Speech-guided Machine Translation (SMT) framework that integrates speech and text as fused inputs into an MLLM to improve translation quality. To mitigate reliance on low-resource data, we introduce a Self-Evolution Mechanism. The core components of this framework include a text-to-speech model, responsible for generating synthetic speech, and an MLLM capable of classifying synthetic speech samples and iteratively optimizing itself using positive samples. Experimental results demonstrate that our framework surpasses all existing methods on the Multi30K multimodal machine translation benchmark, achieving new state-of-the-art results. Furthermore, on general machine translation datasets, particularly the FLORES-200, it achieves average state-of-the-art performance in 108 translation directions. Ablation studies on CoVoST-2 confirms that differences between synthetic and authentic speech have negligible impact on translation quality. The code and models are released at https://github.com/yxduir/LLM-SRT.

BRIGHT: A Collaborative Generalist-Specialist Foundation Model for Breast Pathology

Generalist pathology foundation models (PFMs), pretrained on large-scale multi-organ datasets, have demonstrated remarkable predictive capabilities across diverse clinical applications. However, their proficiency on the full spectrum of clinically essential tasks within a specific organ system remains an open question due to the lack of large-scale validation cohorts for a single organ as well as the absence of a tailored training paradigm that can effectively translate broad histomorphological knowledge into the organ-specific expertise required for specialist-level interpretation. In this study, we propose BRIGHT, the first PFM specifically designed for breast pathology, trained on approximately 210 million histopathology tiles from over 51,000 breast whole-slide images derived from a cohort of over 40,000 patients across 19 hospitals. BRIGHT employs a collaborative generalist-specialist framework to capture both universal and organ-specific features. To comprehensively evaluate the performance of PFMs on breast oncology, we curate the largest multi-institutional cohorts to date for downstream task development and evaluation, comprising over 25,000 WSIs across 10 hospitals. The validation cohorts cover the full spectrum of breast pathology across 24 distinct clinical tasks spanning diagnosis, biomarker prediction, treatment response and survival prediction. Extensive experiments demonstrate that BRIGHT outperforms three leading generalist PFMs, achieving state-of-the-art (SOTA) performance in 21 of 24 internal validation tasks and in 5 of 10 external validation tasks with excellent heatmap interpretability. By evaluating on large-scale validation cohorts, this study not only demonstrates BRIGHT's clinical utility in breast oncology but also validates a collaborative generalist-specialist paradigm, providing a scalable template for developing PFMs on a specific organ system.