Zhiguo Hé

Zifan He, Anderson Truong, Yingqi Cao et al.

The rise of deep neural networks (DNNs) has driven an increased demand for computing power and memory. Modern DNNs exhibit high data volume variation (HDV) across tasks, which poses challenges for FPGA acceleration: conventional accelerators rely on fixed execution patterns (dataflow or sequential) that can lead to pipeline stalls or necessitate frequent off-chip memory accesses. To address these challenges, we introduce the Inter-Task Auto-Reconfigurable Accelerator (InTAR), a novel accelerator design methodology for HDV applications on FPGAs. InTAR combines the high computational efficiency of sequential execution with the reduced off-chip memory overhead of dataflow execution. It switches execution patterns automatically with a static schedule determined before circuit design based on resource constraints and problem sizes. Unlike previous reconfigurable accelerators, InTAR encodes reconfiguration schedules during circuit design, allowing model-specific optimizations that allocate only the necessary logic and interconnects. Thus, InTAR achieves a high clock frequency with fewer resources and low reconfiguration time. Furthermore, InTAR supports high-level tools such as HLS for fast design generation. We implement a set of multi-task HDV DNN kernels using InTAR. Compared with dataflow and sequential accelerators, InTAR exhibits $\mathbf{1.8\times}$ and $\mathbf{7.1 \times}$ speedups correspondingly. Moreover, we extend InTAR to GPT-2 medium as a more complex example, which is $\mathbf{3.65 \sim 39.14\times}$ faster and a $\mathbf{1.72 \sim 10.44\times}$ more DSP efficient than SoTA accelerators (Allo and DFX) on FPGAs. Additionally, this design demonstrates $\mathbf{1.66 \sim 7.17\times}$ better power efficiency than GPUs. Code: https://github.com/OswaldHe/InTAR

Teng Wang, Zhangyi Jiang, Zhenqi He et al.

Recent studies show that Large Language Models (LLMs) achieve strong reasoning capabilities through supervised fine-tuning or reinforcement learning. However, a key approach, the Process Reward Model (PRM), suffers from reward hacking, making it unreliable in identifying the best intermediate step. In addition, the cost of annotating reasoning processes for reward modeling is high, making large-scale collection of high-quality data challenging. To address this, we propose a novel reward model approach called the Hierarchical Reward Model (HRM), which evaluates both individual and consecutive reasoning steps at both fine-grained and coarse-grained levels. HRM excels at assessing multi-step reasoning coherence, especially when flawed steps are later corrected through self-reflection. To further reduce the cost of generating training data, we introduce a lightweight and effective data augmentation strategy called Hierarchical Node Compression (HNC), which merges two consecutive reasoning steps into one within the tree structure. By applying HNC to MCTS-generated reasoning trajectories, we enhance the diversity and robustness of HRM training data while introducing controlled noise with minimal computational overhead. Empirical results on the PRM800K dataset show that HRM, together with HNC, provides more stable and reliable evaluations than PRM. Furthermore, cross-domain evaluations on the MATH500 and GSM8K datasets demonstrate HRM's strong generalization and robustness across a variety of reasoning tasks.

Zoe Wanying He, Sean Trott, Meenakshi Khosla

Recent studies show that deep vision-only and language-only models--trained on disjoint modalities--nonetheless project their inputs into a partially aligned representational space. Yet we still lack a clear picture of where in each network this convergence emerges, what visual or linguistic cues support it, whether it captures human preferences in many-to-many image-text scenarios, and how aggregating exemplars of the same concept affects alignment. Here, we systematically investigate these questions. We find that alignment peaks in mid-to-late layers of both model types, reflecting a shift from modality-specific to conceptually shared representations. This alignment is robust to appearance-only changes but collapses when semantics are altered (e.g., object removal or word-order scrambling), highlighting that the shared code is truly semantic. Moving beyond the one-to-one image-caption paradigm, a forced-choice "Pick-a-Pic" task shows that human preferences for image-caption matches are mirrored in the embedding spaces across all vision-language model pairs. This pattern holds bidirectionally when multiple captions correspond to a single image, demonstrating that models capture fine-grained semantic distinctions akin to human judgments. Surprisingly, averaging embeddings across exemplars amplifies alignment rather than blurring detail. Together, our results demonstrate that unimodal networks converge on a shared semantic code that aligns with human judgments and strengthens with exemplar aggregation.

Cheng Jin, Fengtao Zhou, Yunfang Yu et al.

Precision oncology requires accurate molecular insights, yet obtaining these directly from genomics is costly and time-consuming for broad clinical use. Predicting complex molecular features and patient prognosis directly from routine whole-slide images (WSI) remains a major challenge for current deep learning methods. Here we introduce PathLUPI, which uses transcriptomic privileged information during training to extract genome-anchored histological embeddings, enabling effective molecular prediction using only WSIs at inference. Through extensive evaluation across 49 molecular oncology tasks using 11,257 cases among 20 cohorts, PathLUPI demonstrated superior performance compared to conventional methods trained solely on WSIs. Crucially, it achieves AUC $\geq$ 0.80 in 14 of the biomarker prediction and molecular subtyping tasks and C-index $\geq$ 0.70 in survival cohorts of 5 major cancer types. Moreover, PathLUPI embeddings reveal distinct cellular morphological signatures associated with specific genotypes and related biological pathways within WSIs. By effectively encoding molecular context to refine WSI representations, PathLUPI overcomes a key limitation of existing models and offers a novel strategy to bridge molecular insights with routine pathology workflows for wider clinical application.