Evidence map›Paper›PMID 42527448›Full record

Articlenpj biomedical innovations2026

Rethinking pathology image analysis through shuffling.

Zeyu Liu, Tianyi Zhang, Brian K Chen, Youdan Feng, Shangqing Lyu, Yanli Lei, Nan Ying, Yunlu Feng, Yu Zhao, Peng Zhang and 7 more

Abstract read
In one paragraph

Article in npj biomedical innovations, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Zeyu Liu *School of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Tianyi Zhang *Department of Electrical and Computer Engineering, National University of Singapore, Singapore, Singapore.
Brian K Chen *Bioinformatics Institute (BII), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Youdan FengSchool of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Shangqing LyuPuzzleLogic Pte Ltd, Singapore, Singapore.
Yanli LeiSchool of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Nan YingSchool of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Yunlu FengDepartment of Gastroenterology, Peking Union Medical College Hospital, Beijing, China.
Yu ZhaoDepartment of Pathology, Peking Union Medical College Hospital, Beijing, China.
Peng ZhangSchool of Computer and Information Technology, Shanxi University, Taiyuan, China.
Fan SongSchool of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Chenbin MaSchool of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Yufang HeSchool of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Kenji KawaguchiSchool of Computing, National University of Singapore, Singapore, Singapore.
Hwee Kuan LeeBioinformatics Institute (BII), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore. leehk@bii.a-star.edu.sg.
Yueming JinDepartment of Electrical and Computer Engineering, National University of Singapore, Singapore, Singapore. ymjin@nus.edu.sg.
Guanglei ZhangSchool of Biological Science and Medical Engineering, Beihang University, Beijing, China. guangleizhang@buaa.edu.cn.

Funding

Beijing Natural Science Foundation 7242269National Key Research and Development Program of China 2023YFF0715400National Natural Science Foundation of China 62271023National Natural Science Foundation of China 62506220Natural Science Foundation of Shanxi Province 202403021222024
6 · The paper itself

Abstract

Pathological examination is the current gold standard in cancer diagnosis, yet artificial intelligence (AI) methods still struggle to capture the multi-scale heterogeneity of tumor morphology across patients, tissues, and magnifications. Here, we introduce the PAthoentity Shuffle Strategy (PASS), a principled framework that explicitly models pathoentities, the critical biological structures such as cells, glands, and tissues, and their hierarchical relationships. By controlled shuffling of pathoentities within and across samples, PASS enriches the relational structure available to neural networks, encouraging them to learn both local homogeneity and global heterogeneity. We provide theoretical analysis showing that PASS achieves error bounds comparable to state-of-the-art methods, supporting shuffling as a generalizable computational principle rather than a heuristic. Extensive evaluation on 10 datasets spanning 8 diseases, 9 organs, and 4 magnification levels demonstrates consistent performance gains, robust generalization, and scalability across diverse pathological contexts. Importantly, PASS further shows translational value in a rapid onsite evaluation (ROSE) scenario in gastroenterology, highlighting its potential for clinical deployment. Overall, this study establishes pathoentity shuffling as an effective principle for pathological image analysis, bridging biological insight and computational design to enhance diagnostic modeling and morphological hierarchy learning.

Identifiers

PMID42527448
PMCPMC13421454

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.