Evidence map›Paper›PMID 41826375›Full record

ArticleScientific data2026

A Subphase-Labeled Mitotic Dataset for AI-powered Cell Division Analysis.

Zsanett Zsofia Ivan, Dominik Hirling, Istvan Grexa, Jonas Ammeling, Csaba Molnar, Tamas Micsik, Katalin Dobra, Levente Kuthi, Farkas Sukosd, Janos Fillinger and 5 more

Abstract readDataset
In one paragraph

Article in Scientific data, 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

15 authors.

Zsanett Zsofia Ivan *HUN-REN Biological Research Centre, Szeged, Hungary. ivan.zsanett@brc.hu.
Dominik Hirling *HUN-REN Biological Research Centre, Szeged, Hungary.
Istvan GrexaHUN-REN Biological Research Centre, Szeged, Hungary.
Jonas AmmelingTechnische Hochschule Ingolstadt, Ingolstadt, Germany.
Csaba MolnarHUN-REN Biological Research Centre, Szeged, Hungary.
Tamas MicsikKarolinska Institutet, Department of Oncology-Pathology, Solna, Sweden.
Katalin DobraKarolinska Institutet, Department of Oncology-Pathology, Solna, Sweden.
Levente KuthiSingle-Cell Technologies Ltd., Szeged, Hungary.
Farkas SukosdDepartment of Pathology, Péterfy Sándor Street Hospital and Outpatient Clinic, Budapest, Hungary.
Janos Fillinger1st Department of Pulmonology, National Koranyi Institute of Pulmonology, Budapest, Hungary.
Judit Moldvay1st Department of Pulmonology, National Koranyi Institute of Pulmonology, Budapest, Hungary.
Erika TothDepartment of Surgical and Molecular Pathology, Tumor Pathology Center, National Institute of Oncology, Budapest, Hungary.
Marc AubrevilleFlensburg University of Applied Sciences, Flensburg, Germany.
Vivien MiczanHUN-REN Biological Research Centre, Szeged, Hungary.
Peter HorvathHUN-REN Biological Research Centre, Szeged, Hungary. horvath.peter@brc.hu.ORCID http://orcid.org/0000-0002-4492-1798

Funding

Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal (NKFI Office) EKÖP-24-4-SZTE-642Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal (NKFI Office) EKÖP-KDP-24-SZTE-11Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal (NKFI Office) OTKA K-147226Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal (NKFI Office) OTKA PD 147127
6 · The paper itself

Abstract

Mitosis detection represents a critical task in digital pathology, as it plays an important role in the tumor grading and prognosis of patients. Manual determination is a labor-intensive task for practitioners with high interobserver variability, thus, automation is a priority. There has been substantial progress towards creating robust mitosis detection algorithms, primarily driven by the Mitosis Domain Generalization (MIDOG) challenges. Also, there has been growing interest in the molecular characterization of mitosis to achieve a more comprehensive understanding of its underlying mechanisms in a subphase-specific manner. We introduce a new mitotic figure dataset annotated with subphase information based on the MIDOG++ dataset as well as a previously unrepresented tumor domain to enhance the diversity and applicability. We envision a new perspective for domain generalization by improving model performance with subtyping mitosis, complemented with an atypical mitotic class. Our work has implications in two main areas: subtyping information can provide helpful information in mitosis detection, while also providing promising new directions in answering biological questions, such as molecular analysis of subphases.

Indexed as

Artificial IntelligenceCell DivisionMitosisAlgorithmsHumans

Identifiers

PMID41826375
PMCPMC13128913

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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.