跳到正文
研踪PaperTrail

YOUR RESEARCH, IN SIGHT

让下一篇重要论文,不再错过。

覆盖计算机全学科,以 AI 为快捷入口。关注方向、作者和关键词,把发现变成持续的研究积累。

部分采集异常
正在读取账号与研究记录…

全站更新概况

+1878新增论文
+1565其中 AI 相关
+113已有论文修订
+100新增 AI 导读

arXiv 最近完成扫描:2026-11-10 12:17 · 全站最近入库:2026-11-10 13:19各信源进度 →

统计口径与数据新鲜度

统计 2026-11-09 13:46 — 2026-11-10 13:46(北京时间) · 点击数字查看对应简报;AI 相关包含在新增论文内。

最近完成检查:2026-11-10 12:17最近发现新增版本:2026-11-10 13:19库内论文最新更新时间:2026-11-09 16:22

每分钟刷新已保存的数据。空检查不代表采集异常;新收录可能包含历史论文。AI 导读按新增版本计数。

20,050 已收录论文17,071 AI 相关5,370 有修订112 HF 社区发现

浏览论文库

时间范围跟随排序:版本更新、本站收录或首次发表。最新收录可能包含历史论文。部分信源异常,查看状态 →

找到 1 篇论文 · 按版本更新时间排序上轮扫描起点 2026-11-10 12:16(北京时间)
新论文 · v1arXiv:2611.09851

常规临床组织病理学中人口统计学信息的全医疗系统范围映射

Health-System-Wide Mapping of Demographic Information in Routine Clinical Histopathology

Shengjia Chen, Ruchika Verma, Kevin Clare, Paula Restrepo, Jannes Jegminat, Eugenia Alleva, Kuan-lin Huang, Aryeh Stock 等 11 位作者

AI 速读 基于摘要

作者利用病理基础模型与多实例学习,在约130万张H&E全切片图像上系统评估性别、年龄组和自报种族信息在25个器官中的可检测程度。

cs.CV · q-bio.QM

查看原文摘要

The extent to which demographic-associated information is detectable across organs and disease states in routine clinical histopathology remains unclear. Here, we analyzed 1.3 million hematoxylin and eosin whole-slide images from 257,322 patients across 25 organs, using pathology foundation-model representations and multiple-instance learning to systematically map information associated with sex, age group, and self-reported race. Across 69 organ-demographic combinations, demographic attributes were broadly recoverable, with pan-organ mean AUROCs of 0.828 for sex, 0.733 for age group, and 0.662 for self-reported race, and substantial variation across organs. Demographic-class balancing produced relatively small changes in performance, while evaluation within diagnosis-text clusters showed modest attenuation. Under training with diagnosis-based grouping, demographic-associated signals remained detectable across multiple organs, including sex in gastric tissue (AUROC 0.865), age group in breast (0.816), and self-reported race in skin (0.728). Literature-guided analysis of these settings generated candidate histomorphological and contextual explanations for further investigation. Together, these findings provide a systematic map of demographic-associated information in routine histopathology, informing investigations of its sources, assessments of potential shortcut learning, and the development of more interpretable computational pathology models.