Evidence map›Paper›PMID 35050714›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2022

SCOT: Single-Cell Multi-Omics Alignment with Optimal Transport.

Pinar Demetci, Rebecca Santorella, Björn Sandstede, William Stafford Noble, Ritambhara Singh

Abstract readEvaluation Study
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing 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

76 citing papers in PubMed.

  1. Article
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  4. Unifying multimodal single-cell data with a mixture-of-expertsbioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Multimodal spatial alignment and morphology mapping with MOSAICField.bioRxiv : the preprint server for biology · 2026
    Article
  13. Dissecting spatial patterning and signaling with directional diffusion in spatial multi-omics.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. bioRxiv : the preprint server for biology · 2026
    Article
  15. Article
  16. Article
  17. Deriving genetic codes for molecular phenotypes from first principles.bioRxiv : the preprint server for biology · 2026
    Article
  18. Article
  19. Computational Analyses and Challenges of Single-cell ATAC-seq.Genomics, proteomics & bioinformatics · 2025
    Review
  20. Article

16 more citing papers are in PubMed but not listed here.

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

5 authors.

Pinar DemetciCenter for Computational Molecular Biology, Brown University, Providence, Rhode Island, USA.ORCID 0000-0002-5644-0326
Rebecca SantorellaDivision of Applied Mathematics, Brown University, Providence, Rhode Island, USA.
Björn SandstedeDivision of Applied Mathematics, Brown University, Providence, Rhode Island, USA.
William Stafford NobleDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA.
Ritambhara SinghCenter for Computational Molecular Biology, Brown University, Providence, Rhode Island, USA.ORCID 0000-0002-7523-160X

Funding

University of Washington Center for Nuclear Organization and FunctionU54DK107979 · NIDDK · UNIVERSITY OF WASHINGTON · PI NOBLE, WILLIAM STAFFORD · 2015 to 2019
$11.8M
UW 4-Dimensional Genomic Organization of Mammalian Embryogenesis CenterUM1HG011586 · NHGRI · UNIVERSITY OF WASHINGTON · PI DISTECHE, CHRISTINE M., NOBLE, WILLIAM STAFFORD · 2020 to 2024
$10.3M
NHGRI NIH HHS UM1 HG011586NIDDK NIH HHS U54 DK107979
6 · The paper itself

Abstract

Recent advances in sequencing technologies have allowed us to capture various aspects of the genome at single-cell resolution. However, with the exception of a few of co-assaying technologies, it is not possible to simultaneously apply different sequencing assays on the same single cell. In this scenario, computational integration of multi-omic measurements is crucial to enable joint analyses. This integration task is particularly challenging due to the lack of sample-wise or feature-wise correspondences. We present single-cell alignment with optimal transport (SCOT), an unsupervised algorithm that uses the Gromov-Wasserstein optimal transport to align single-cell multi-omics data sets. SCOT performs on par with the current state-of-the-art unsupervised alignment methods, is faster, and requires tuning of fewer hyperparameters. More importantly, SCOT uses a self-tuning heuristic to guide hyperparameter selection based on the Gromov-Wasserstein distance. Thus, in the fully unsupervised setting, SCOT aligns single-cell data sets better than the existing methods without requiring any orthogonal correspondence information.

Indexed as

AlgorithmsComputational BiologyComputer SimulationDatabases, GeneticGenomicsHumansModels, StatisticalSequence AlignmentSingle-Cell AnalysisUnsupervised Machine Learningdata integrationmanifold alignmentmulti-omicsoptimal transportsingle-cell genomics

Identifiers

PMID35050714
PMCPMC8812493

What OpenQuestion holds

Textmetadata
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.