Evidence map›Paper›PMID 41398502›Full record

ArticleNature methods2026

MultiCell: geometric learning in multicellular development.

Haiqian Yang, George Roy, Anh Q Nguyen, Dapeng Bi, Tomer Stern, Markus J Buehler, Ming Guo

Abstract read
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In one paragraph

Article in Nature methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Haiqian YangDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA. hqyang@mit.edu.ORCID http://orcid.org/0000-0002-1068-5555
George RoyDepartment of Biologic and Materials Sciences and Prosthodontics, University of Michigan School of Dentistry, Ann Arbor, MI, USA.ORCID http://orcid.org/0009-0009-8862-569X
Anh Q NguyenDepartment of Physics, Northeastern University, Boston, MA, USA.ORCID http://orcid.org/0000-0001-6272-2373
Dapeng BiDepartment of Physics, Northeastern University, Boston, MA, USA.ORCID http://orcid.org/0000-0003-4850-8666
Tomer SternDepartment of Biologic and Materials Sciences and Prosthodontics, University of Michigan School of Dentistry, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-4279-3558
Markus J BuehlerDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Ming GuoDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA. guom@mit.edu.ORCID http://orcid.org/0000-0002-0016-4158

Funding

National Science Foundation (NSF) DMR-2046683National Science Foundation (NSF) PHY-2019745U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) 5R01AR077793U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) 1R01GM140108U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM15049
6 · The paper itself

Abstract

During developmental processes such as embryogenesis, how a group of cells self-organizes into specific structures is a central question in biology. However, it remains a major challenge to understand and predict the behavior of every cell within the living tissue over time during such intricate processes. Here we present MultiCell, a geometric deep learning method that can accurately capture the highly convoluted interactions among cells. We demonstrate that multicellular data can be represented with both granular and foam-like physical pictures through a unified graph data structure, considering both cellular interactions and cell junction networks. Using this method, we achieve interpretable four-dimensional morphological sequence alignment and predict single-cell behaviors before they occur at single-cell resolution during Drosophila embryogenesis. Furthermore, using neural activation map and model ablation studies, we demonstrate that cell geometry and cell junction networks are essential features for predicting cell behaviors during morphogenesis. This method sets the stage for data-driven quantitative studies of dynamic multicellular developmental processes at single-cell precision, offering a proof-of-concept pathway toward a unified morphodynamic atlas.

Indexed as

Deep LearningEmbryonic DevelopmentAnimalsCell CommunicationDrosophilaDrosophila melanogasterEmbryo, NonmammalianMorphogenesisSingle-Cell Analysis

Identifiers

What OpenQuestion holds

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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.