Evidence map›Paper›PMID 41184554›Full record

ArticleNature methods2026

STORIES: learning cell fate landscapes from spatial transcriptomics using optimal transport.

Geert-Jan Huizing, Jules Samaran, Daniele Capocefalo, Anna Audit, Gabriel Peyré, Laura Cantini

Abstract read
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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Riemannian Metric Learning for Alignment of Spatial Multiomics.bioRxiv : the preprint server for biology · 2025
    Article
  11. Review
  12. Review
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

6 authors.

Geert-Jan Huizing *Institut Pasteur, Université Paris Cité, CNRS UMR 3738, Machine Learning for Integrative Genomics Group, Paris, France.ORCID http://orcid.org/0000-0001-5208-7855
Jules Samaran *Institut Pasteur, Université Paris Cité, CNRS UMR 3738, Machine Learning for Integrative Genomics Group, Paris, France.ORCID http://orcid.org/0000-0001-7317-8190
Daniele CapocefaloInstitut Pasteur, Université Paris Cité, CNRS UMR 3738, Machine Learning for Integrative Genomics Group, Paris, France.
Anna AuditInstitut Pasteur, Université Paris Cité, CNRS UMR 3738, Machine Learning for Integrative Genomics Group, Paris, France.ORCID http://orcid.org/0009-0001-9508-9647
Gabriel PeyréCNRS and DMA de l'Ecole Normale Supérieure, CNRS, Ecole Normale Supérieure, Université PSL, Paris, France.ORCID http://orcid.org/0000-0002-4477-0387
Laura CantiniInstitut Pasteur, Université Paris Cité, CNRS UMR 3738, Machine Learning for Integrative Genomics Group, Paris, France. laura.cantini@pasteur.fr.ORCID http://orcid.org/0000-0001-6360-4440

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-16-CONV-0005EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) ERC StG, MULTIview-CELL, 101115618
6 · The paper itself

Abstract

In dynamic biological processes such as development, spatial transcriptomics is revolutionizing the study of the mechanisms underlying spatial organization within tissues. Inferring cell fate trajectories from spatial transcriptomics profiled at several time points has thus emerged as a critical goal, requiring novel computational methods. Wasserstein gradient flow learning is a promising framework for analyzing sequencing data across time, built around a neural network representing the differentiation potential. However, existing gradient flow learning methods face challenges in analyzing spatially resolved transcriptomic data. Here, we propose STORIES, a method that uses an extension of Optimal Transport to learn a spatially informed potential. We benchmark our approach using three large Stereo-seq spatiotemporal atlases and demonstrate superior spatial coherence compared to existing approaches. Finally, we provide an in-depth analysis of axolotl neural regeneration and mouse gliogenesis, recovering gene trends for known markers such as Nptx1 in neuron regeneration and Aldh1l1 in gliogenesis and additional putative drivers.

Indexed as

Gene Expression ProfilingTranscriptomeAmbystoma mexicanumAnimalsCell DifferentiationComputational BiologyMiceNeurons

Identifiers

PMID41184554
PMCPMC12982121

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.