Evidence map›Paper›PMID 41444760›Full record

ArticleCommunications biology2025

EmbSAM: cell boundary localization and Segment Anything Model for fast images of developing embryos.

Guoye Guan, Cunmin Zhao, Zelin Li, Pei Zhang, Yixuan Chen, Pohao Ye, Ming-Kin Wong, Lu-Yan Chan, Hong Yan, Chao Tang and 1 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Guoye Guan *Department of Systems Biology, Harvard Medical School, Boston, USA. guanguoye@gmail.com.ORCID http://orcid.org/0000-0003-4479-4722
Cunmin Zhao *Department of Biology, Hong Kong Baptist University, Hong Kong, China.
Zelin Li *Department of Electrical Engineering, City University of Hong Kong, Hong Kong, China.ORCID http://orcid.org/0000-0002-0985-8420
Pei ZhangDepartment of Biology, Faculty of Arts and Sciences, Beijing Normal University, Zhuhai, China.ORCID http://orcid.org/0000-0001-8046-0282
Yixuan ChenSchool of Physics, Peking University, Beijing, China.
Pohao YeDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.ORCID http://orcid.org/0000-0002-7828-2592
Ming-Kin WongDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.ORCID http://orcid.org/0000-0002-4088-3819
Lu-Yan ChanDepartment of Biology, Hong Kong Baptist University, Hong Kong, China.
Hong YanDepartment of Electrical Engineering, City University of Hong Kong, Hong Kong, China.ORCID http://orcid.org/0000-0001-9661-3095
Chao TangSchool of Physics, Peking University, Beijing, China.ORCID http://orcid.org/0000-0003-1474-3705
Zhongying ZhaoDepartment of Biology, Hong Kong Baptist University, Hong Kong, China. zyzhao@hkbu.edu.hk.ORCID http://orcid.org/0000-0003-2743-9008

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22477010, 22407016
6 · The paper itself

Abstract

Cellular shape dynamics are critical for understanding cell fate determination and organogenesis during development. However, fluorescence live-cell images of cell membranes frequently suffer from a low signal-to-noise ratio, especially during long-duration imaging with high spatiotemporal resolutions. The low ratio is caused by a tradeoff between embryo viability and phototoxicity and photobleaching of fluorescent markers, which hinders effective cell shape reconstruction, particularly in rapidly developing embryos. Here, we devise an integrative computational framework, EmbSAM, that incorporates a deep-learning-based cell boundary localization algorithm and the Segment Anything Model. EmbSAM enables accurate segmentation of three-dimensional cell membrane images for roundworm Caenorhabditis elegans embryos imaged with exceptional temporal resolution, i.e., every 10 seconds per stack. The resolved cell shapes prior to gastrulation quantitatively characterize a series of cell-division-coupled morphodynamics associated with cell position, cell division phase duration, cell division axis reorientation, cell identity, lineage, fate, among others, which can be accessed locally and online.

Indexed as

Caenorhabditis elegansEmbryonic DevelopmentEmbryo, NonmammalianAlgorithmsAnimalsCell DivisionCell ShapeDeep LearningImaging, Three-Dimensional

Identifiers

PMID41444760
PMCPMC12764838

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.