Evidence map›Paper›PMID 38177382›Full record

ArticleMolecular systems biology2024

Detection of PatIent-Level distances from single cell genomics and pathomics data with Optimal Transport (PILOT).

Mehdi Joodaki, Mina Shaigan, Victor Parra, Roman D Bülow, Christoph Kuppe, David L Hölscher, Mingbo Cheng, James S Nagai, Michaël Goedertier, Nassim Bouteldja and 7 more

Abstract read
In one paragraph

Article in Molecular systems biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Decoding pathology: the role of computational pathology in research and diagnostics.Pflugers Archiv : European journal of physiology · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Visualizing scRNA-Seq Data at Population Scale with GloScope.bioRxiv : the preprint server for biology · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Extending the landscape of omics technologies by pathomics.NPJ systems biology and applications · 2023
    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

17 authors.

Mehdi Joodaki *Institute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University Medical School, Aachen, Germany.
Mina Shaigan *Institute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University Medical School, Aachen, Germany.ORCID http://orcid.org/0000-0003-1719-9944
Victor ParraInstitute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University Medical School, Aachen, Germany.
Roman D BülowInstitute of Pathology, RWTH Aachen University Medical School, Aachen, Germany.ORCID http://orcid.org/0000-0002-8527-7353
Christoph KuppeInstitute of Experimental Medicine and Systems Biology, RWTH Aachen University, Aachen, Germany.ORCID http://orcid.org/0000-0003-4597-9833
David L HölscherInstitute of Pathology, RWTH Aachen University Medical School, Aachen, Germany.ORCID http://orcid.org/0000-0001-8595-0694
Mingbo ChengInstitute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University Medical School, Aachen, Germany.ORCID http://orcid.org/0000-0003-3938-0461
James S NagaiInstitute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University Medical School, Aachen, Germany.ORCID http://orcid.org/0000-0002-7655-7206
Michaël GoedertierInstitute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University Medical School, Aachen, Germany.
Nassim BouteldjaInstitute of Pathology, RWTH Aachen University Medical School, Aachen, Germany.
Vladimir TesarDepartment of Nephrology, 1st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.ORCID http://orcid.org/0000-0001-6982-0689
Jonathan BarrattJohn Walls Renal Unit, University Hospital of Leicester National Health Service Trust, Leicester, UK.
Ian Sd RobertsDepartment of Cellular Pathology, Oxford University Hospitals National Health Services Foundation Trust, Oxford, UK.ORCID http://orcid.org/0000-0002-4885-7957
Rosanna CoppoFondazione Ricerca Molinette, Regina Margherita Children's University Hospital, Torino, Italy.
Rafael KramannInstitute of Experimental Medicine and Systems Biology, RWTH Aachen University, Aachen, Germany.ORCID http://orcid.org/0000-0003-4048-6351
Peter BoorInstitute of Pathology, RWTH Aachen University Medical School, Aachen, Germany. pboor@ukaachen.de.ORCID http://orcid.org/0000-0001-9921-4284
Ivan G CostaInstitute for Computational Genomics, Joint Research Center for Computational Biomedicine, RWTH Aachen University Medical School, Aachen, Germany. ivan.costa@rwth-aachen.de.ORCID http://orcid.org/0000-0003-2890-8697

Funding

Bundesministerium für Bildung und Forschung (BMBF) E:med Consortia FibromapBundesministerium für Bildung und Forschung (BMBF) STOP-FSGS-01GM2202CDeutsche Forschungsgemeinschaft (DFG) DFG-GE2811/3Deutsche Forschungsgemeinschaft (DFG) IDs 322900939,454024652,432698239 445703531Deutsche Forschungsgemeinschaft (DFG) KFO 5011EC | ERC | HORIZON EUROPE European Research Council (ERC) No 101001791
6 · The paper itself

Abstract

Although clinical applications represent the next challenge in single-cell genomics and digital pathology, we still lack computational methods to analyze single-cell or pathomics data to find sample-level trajectories or clusters associated with diseases. This remains challenging as single-cell/pathomics data are multi-scale, i.e., a sample is represented by clusters of cells/structures, and samples cannot be easily compared with each other. Here we propose PatIent Level analysis with Optimal Transport (PILOT). PILOT uses optimal transport to compute the Wasserstein distance between two individual single-cell samples. This allows us to perform unsupervised analysis at the sample level and uncover trajectories or cellular clusters associated with disease progression. We evaluate PILOT and competing approaches in single-cell genomics or pathomics studies involving various human diseases with up to 600 samples/patients and millions of cells or tissue structures. Our results demonstrate that PILOT detects disease-associated samples from large and complex single-cell or pathomics data. Moreover, PILOT provides a statistical approach to find changes in cell populations, gene expression, and tissue structures related to the trajectories or clusters supporting interpretation of predictions.

Indexed as

AlgorithmsGenomicsCluster AnalysisHumansClusteringDisease ProgressionMulti-scale AnalysisOptimal TransportWasserstein Distance

Identifiers

PMID38177382
PMCPMC10883279

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Registered trials

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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.