HistoWAS: A Pathomics Framework for Large-Scale Feature-Wide Association Studies of Tissue Topology and Patient Outcomes

Fuente: arXiv
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Autores principales: Yang, Yuechen, Guo, Junlin, Zhu, Yanfan, Yue, Jialin, Zhu, Junchao, Wang, Yu, Zhao, Shilin, Yang, Haichun, Guo, Xingyi, Tanevski, Jovan, Barisoni, Laura, Rosenberg, Avi Z., Huo, Yuankai
Formato: Preprint
Publicado: 2025
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author Yang, Yuechen
Guo, Junlin
Zhu, Yanfan
Yue, Jialin
Zhu, Junchao
Wang, Yu
Zhao, Shilin
Yang, Haichun
Guo, Xingyi
Tanevski, Jovan
Barisoni, Laura
Rosenberg, Avi Z.
Huo, Yuankai
author_facet Yang, Yuechen
Guo, Junlin
Zhu, Yanfan
Yue, Jialin
Zhu, Junchao
Wang, Yu
Zhao, Shilin
Yang, Haichun
Guo, Xingyi
Tanevski, Jovan
Barisoni, Laura
Rosenberg, Avi Z.
Huo, Yuankai
contents High-throughput "pathomic" analysis of Whole Slide Images (WSIs) offers new opportunities to study tissue characteristics and for biomarker discovery. However, the clinical relevance of the tissue characteristics at the micro- and macro-environment level is limited by the lack of tools that facilitate the measurement of the spatial interaction of individual structure characteristics and their association with clinical parameters. To address these challenges, we introduce HistoWAS (Histology-Wide Association Study), a computational framework designed to link tissue spatial organization to clinical outcomes. Specifically, HistoWAS implements (1) a feature space that augments conventional metrics with 30 topological and spatial features, adapted from Geographic Information Systems (GIS) point pattern analysis, to quantify tissue micro-architecture; and (2) an association study engine, inspired by Phenome-Wide Association Studies (PheWAS), that performs mass univariate regression for each feature with statistical correction. As a proof of concept, we applied HistoWAS to analyze a total of 102 features (72 conventional object-level features and our 30 spatial features) using 385 PAS-stained WSIs from 206 participants in the Kidney Precision Medicine Project (KPMP). The code and data have been released to https://github.com/hrlblab/histoWAS.
format Preprint
id arxiv_https___arxiv_org_abs_2512_19954
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle HistoWAS: A Pathomics Framework for Large-Scale Feature-Wide Association Studies of Tissue Topology and Patient Outcomes
Yang, Yuechen
Guo, Junlin
Zhu, Yanfan
Yue, Jialin
Zhu, Junchao
Wang, Yu
Zhao, Shilin
Yang, Haichun
Guo, Xingyi
Tanevski, Jovan
Barisoni, Laura
Rosenberg, Avi Z.
Huo, Yuankai
Computer Vision and Pattern Recognition
High-throughput "pathomic" analysis of Whole Slide Images (WSIs) offers new opportunities to study tissue characteristics and for biomarker discovery. However, the clinical relevance of the tissue characteristics at the micro- and macro-environment level is limited by the lack of tools that facilitate the measurement of the spatial interaction of individual structure characteristics and their association with clinical parameters. To address these challenges, we introduce HistoWAS (Histology-Wide Association Study), a computational framework designed to link tissue spatial organization to clinical outcomes. Specifically, HistoWAS implements (1) a feature space that augments conventional metrics with 30 topological and spatial features, adapted from Geographic Information Systems (GIS) point pattern analysis, to quantify tissue micro-architecture; and (2) an association study engine, inspired by Phenome-Wide Association Studies (PheWAS), that performs mass univariate regression for each feature with statistical correction. As a proof of concept, we applied HistoWAS to analyze a total of 102 features (72 conventional object-level features and our 30 spatial features) using 385 PAS-stained WSIs from 206 participants in the Kidney Precision Medicine Project (KPMP). The code and data have been released to https://github.com/hrlblab/histoWAS.
title HistoWAS: A Pathomics Framework for Large-Scale Feature-Wide Association Studies of Tissue Topology and Patient Outcomes
topic Computer Vision and Pattern Recognition
url https://arxiv.org/abs/2512.19954