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arXiv 最近完成扫描:等待完成 · 全站最近入库:2026-11-02 00:39各信源进度 →

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新论文 · v1arXiv:2610.39853

KV Cache Quantization for Diffusion Language Models

Yan Tai, Yunan Ding, Guangzhao Li, Siqi Luo, Chaoyang Zhang, Guangtao Zhai, Guodong Guo, Xiaohong Liu

KV cache quantization is well studied for autoregressive language models, where cached prefix states are exact under causal attention and quantization is mainly a cache reconstruction problem. Diffusion language models (dLLMs) break this assumption. Fast dLLM inference reuses KV states across denoising steps, but bidirectional token representations can change as masked tokens are revealed, so the reused cache may already differ from full recomputation before quantization is applied. We study KV cache quantization under this cache-reuse error. We adapt KIVI and KVQuant to Fast-dLLM-style prefix and dual cache reuse, and introduce TRACE and dLLM-KVQ. TRACE reconstructs feasible dLLM reveal trajectories from prompt-answer pairs, providing calibration states that match iterative masked decoding. dLLM-KVQ uses these trajectories to choose per-layer K-cache entries that remain in high precision according to output- and attention-level behavior metrics, while applying standard low-bit value quantization. Across LLaDA and Dream evaluations on GSM8K, HumanEval, MATH, and MBPP, dLLM-KVQ achieves the highest average score among quantized methods across the reported 4-bit and 2-bit prefix/dual cache settings.

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cs.CL
arXiv ↗PDF ↗
版本更新 · v2arXiv:2604.00058

GenoBERT: A Language Model for Accurate Genotype Imputation

Lei Huang, Chuan Qiu, Kuan-Jui Su, Anqi Liu, Yun Gong, Weiqiang Lin, Lindong Jiang, Chen Zhao 等 16 位作者

Genotype imputation enables dense variant coverage for genome-wide association and risk-prediction studies, yet conventional reference-panel methods remain limited by ancestry bias and reduced rare-variant accuracy. We present Genotype Bidirectional Encoder Representations from Transformers (GenoBERT), a transformer-based, reference-free framework that tokenizes phased genotypes and uses a self-attention mechanism to capture both short- and long-range linkage disequilibrium (LD) dependencies. Benchmarking on two independent datasets including the Louisiana Osteoporosis Study (LOS) and the 1000 Genomes Project (1KGP) across ancestry groups and multiple genotype missingness levels (5-50%) shows that GenoBERT achieves the highest overall accuracy compared to four baseline methods (Beagle5.4, SCDA, BiU-Net, and STICI). At practical sparsity levels (up to 25% missing), GenoBERT attains high overall imputation accuracy ($r^2 approx 0.98$) across datasets, and maintains robust performance ($r^2 > 0.90$) even at 50% missingness. Experimental results across different ancestries confirm consistent gains across datasets, with resilience to small sample sizes and weak LD. A 128-SNP (single-nucleotide polymorphism) context window (approximately 100 Kb) is validated through LD-decay analyses as sufficient to capture local correlation structures. By eliminating reference-panel dependence while preserving high accuracy, GenoBERT provides a scalable and robust solution for genotype imputation and a foundation for downstream genomic modeling.

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q-bio.GN · cs.AI · cs.LG
arXiv ↗PDF ↗
新论文 · v1arXiv:2610.35842

MedVTok: A General-Purpose Medical Visual Tokenizer

Chenglong Ma, Yuanfeng Ji, Junzhi Ning, Jiyao Liu, Yujie Wei, Shaohao Rui, Chaoyang Zhang, Wenjie Li 等 21 位作者

Multimodal medical AI requires a common visual interface for encoding heterogeneous imaging evidence for patient condition modeling. However, existing medical visual tokenizers are often tied to a specific dimension and imaging modality, forcing multimodal systems to rely on fragmented and poorly reusable representations. We introduce MedVTok, a general-purpose visual tokenizer that maps 2D images and 3D volumes from diverse imaging modalities into a unified token space. Building such a tokenizer poses two key challenges: preserving anatomical structure across dimensions and capturing clinical semantics across modalities. To this end, MedVTok introduces (i) slice differential regularization, which explicitly models inter-slice anatomical coherence missing in previous per-pixel/per-voxel supervision, and (ii) multi-expert representation alignment, which integrates knowledge from multiple medical expert encoders while retaining modality-specific complementary knowledge. Trained on 28M images and 70K volumes across 9 imaging modalities, MedVTok supports classification, retrieval, segmentation, synthesis, visual question answering, and medical report generation through a single tokenizer. Across 24 benchmarks, MedVTok achieves state-of-the-art performance, demonstrating a scalable token interface that unifies medical image dimension, modality, and task usage.

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eess.IV · cs.CV
arXiv ↗PDF ↗