Evidence map›Paper›PMID 39300283›Full record

ArticleNature methods2025

Gene-level alignment of single-cell trajectories.

Dinithi Sumanaweera, Chenqu Suo, Ana-Maria Cujba, Daniele Muraro, Emma Dann, Krzysztof Polanski, Alexander S Steemers, Woochan Lee, Amanda J Oliver, Jong-Eun Park and 3 more

Abstract read
In one paragraph

Article in Nature methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Spatial Logic and Evolutionary Innovation in Human Placentation.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
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  15. Review
  16. Article
  17. Article
  18. Computational modeling of single-cell dynamics data.Briefings in bioinformatics · 2025
    Review
  19. TrAGEDy-trajectory alignment of gene expression dynamics.Bioinformatics (Oxford, England) · 2025
    Article
  20. 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

13 authors.

Dinithi Sumanaweera *Wellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0003-4515-0988
Chenqu Suo *Wellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0002-8813-0875
Ana-Maria CujbaWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.
Daniele MuraroWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.
Emma DannWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0002-7400-7438
Krzysztof PolanskiWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0002-2586-9576
Alexander S SteemersWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0002-7162-7279
Woochan LeeWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.
Amanda J OliverWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.
Jong-Eun ParkWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0002-1687-2423
Kerstin B MeyerWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0001-5906-1498
Bianca DumitrascuDepartment of Statistics, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0001-8328-2354
Sarah A TeichmannWellcome Sanger Institute; Wellcome Genome Campus, Hinxton, Cambridge, UK. sat1003@cam.ac.uk.ORCID http://orcid.org/0000-0002-6294-6366

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 101026506Medical Research Council MC_PC_17230Wellcome TrustWellcome Trust (Wellcome) WT206194
6 · The paper itself

Abstract

Single-cell data analysis can infer dynamic changes in cell populations, for example across time, space or in response to perturbation, thus deriving pseudotime trajectories. Current approaches comparing trajectories often use dynamic programming but are limited by assumptions such as the existence of a definitive match. Here we describe Genes2Genes, a Bayesian information-theoretic dynamic programming framework for aligning single-cell trajectories. It is able to capture sequential matches and mismatches of individual genes between a reference and query trajectory, highlighting distinct clusters of alignment patterns. Across both real world and simulated datasets, it accurately inferred alignments and demonstrated its utility in disease cell-state trajectory analysis. In a proof-of-concept application, Genes2Genes revealed that T cells differentiated in vitro match an immature in vivo state while lacking expression of genes associated with TNF signaling. This demonstrates that precise trajectory alignment can pinpoint divergence from the in vivo system, thus guiding the optimization of in vitro culture conditions.

Indexed as

Computational BiologyGene Expression ProfilingSingle-Cell AnalysisAlgorithmsAnimalsBayes TheoremHumansMiceT-Lymphocytes

Identifiers

PMID39300283
PMCPMC11725504

What Socratic 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 Socratic graph.