Evidence map›Paper›PMID 41895261›Full record

ArticleCell reports methods2026

Persistent homology-based segmentation tool for membrane images.

Haruhisa Oda, Yusuke Imoto

Abstract read
In one paragraph

Article in Cell reports methods, 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

2 authors.

Haruhisa OdaDepartment of Preventive Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. Electronic address: haruhisa-oda0722@g.ecc.u-tokyo.ac.jp.
Yusuke ImotoInstitute for the Advanced Study of Human Biology, Kyoto University, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While advances in machine learning have enabled automated cell segmentation, users often face challenges in parameter tuning until reaching their desired results. To address this issue, we developed PomSeg, a membrane segmentation method based on persistent homology. Since persistent homology captures topological features of input data, PomSeg parameters reflect cell shape information, enabling intuitive and efficient parameter tuning. This adaptivity, together with stability for noise of persistent homology, enables robust application of PomSeg to various image types, including coarse-resolution data. By applying PomSeg to early mouse embryo membrane images and other publicly available datasets, we demonstrated its flexibility, versatility, and robustness, along with agreement with ground truth. Additionally, we showed the potential of PomSeg extension by incorporating a machine learning tool in its process. These features make PomSeg a valuable tool for researchers pursuing control and interpretability in segmentation, as well as indicating wider applications beyond a machine learning alternative.

Indexed as

Cell MembraneImage Processing, Computer-AssistedAlgorithmsAnimalsMachine LearningMiceCP: computational biologyCP: imagingembryo membrane imagepersistent homologysegmentationtopological data analysistracking

Identifiers

PMID41895261
PMCPMC13107053

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.