arXiv:2608.07713cs.CVcs.LG2026-08

医学图像生成中,分词器与生成器需协同优化,单独固定分词器会误导模型表现。

Tokenizer Generator Coupling in Medical Image Generation

论文配图:Tokenizer Generator Coupling in Medical Image Generation
图 1 · 摘自论文原文
  • 在统一潜在空间下联合测试分词器、生成器和采样器的交互影响
  • 重建质量无法可靠选分词器,新指标可精准区分生成效果(AUC=1.00)
  • 重新调优后生成器性能显著提升,适合医疗图像生成研究者参考

潜伏医学图像生成器通常将分词器视为固定预处理。我们在64x64的ChestMNIST控制实验中,交叉测试了离散分词器、生成器族与采样设置,在共享潜在网格下对比连续潜变量参考单元。结果表明,排名同时依赖分词器、生成器和采样器:最优分词器随生成器变化,基于验证集的采样器选择也改变生成器排名。在三个随机种子下重训练词汇表-1024交互模块,交互效应仍存在(9次配对比较中有6次超过三倍种子标准差),并据此扩展单种子网格范围。仅靠重建PSNR无法可靠筛选分词器;我们引入无需生成器的统计量——邻域条件预测增益,能有效区分分词器家族的下游生成质量(秩-AUC=1.00),而重建PSNR与边际词元熵无法做到。在LFQ-1024上,对D3PM与SE-D3PM(在保留验证集上选择)进行再调优后,其在较低NFE下FID-192从默认值0.44/0.41降至0.09/0.10,且在不同种子间可复现;连续参考未进行等效采样器扫描。报告使用FID-192作为内部排序指标,其与标准FID-2048(Spearman 0.80)及无标签分类器双样本检验(0.78)具一致性。结果通过率-失真-模型能力框架解释,其中模型能力取决于生成器、采样器与推理预算。所有实验均在64x64低分辨率医学风格图像上进行,无条件生成,使用非临床的基于FID的度量,且每项结论均限于此设定。代码:https://github.com/liamchalcroft/medtokenizers 和 https://github.com/liamchalcroft/medlatents。

原文摘要 · Abstract (English)

Latent medical image generators usually treat the tokenizer as fixed preprocessing. We test whether this separation is valid in a controlled ChestMNIST study at 64x64, crossing discrete tokenizers, generator families, and sampler settings under a shared latent grid, with continuous-latent reference cells. In this controlled setting, rankings depend jointly on the tokenizer, generator, and sampler: the best quantizer changes with the generator, and validation-based sampler selection changes the apparent generator ranking. We retrain the vocabulary-1024 interaction block at three seeds and the interaction survives (6 of 9 pairwise quantizer comparisons exceed three seed standard deviations), and we scope the wider single-seed grid accordingly. Reconstruction PSNR alone is not a reliable selection criterion; we instead introduce a generator-free statistic, neighbour-conditional predictive gain, that separates the quantizer families by downstream generation quality (rank-AUC 1.00) where reconstruction PSNR and marginal token entropy do not. On LFQ-1024, retuning D3PM and SE-D3PM (selected on a held-out validation split) moves them from default FID-192 0.44/0.41 to 0.09/0.10 at lower NFE, replicated across seeds; the continuous references were not given an equivalent sampler sweep. We report FID-192 as an internal ranking metric; it ranks consistently with standard FID-2048 (Spearman 0.80) and with a label-free classifier two-sample test (0.78). We interpret these results through a rate-distortion-modelability framing, where modelability is conditional on the generator, sampler, and inference budget. All experiments are at 64x64 on low-resolution medical-style images, unconditional, and evaluated with non-clinical FID-based metrics, and we scope every claim to that setting. Code: https://github.com/liamchalcroft/medtokenizers and https://github.com/liamchalcroft/medlatents.

医学图像分词器协同生成质量评估扩散模型

Thank you to arXiv for use of its open access interoperability. PaperDance 不是 arXiv 官方产品;中文卡片由大模型生成,请以原文为准。