Evidence map›Paper›PMID 42498882›Full record

ArticleNature methods2026

Spatialproteomics: an interoperable toolbox for analyzing highly multiplexed fluorescence image data.

Matthias Meyer-Bender, Harald Vöhringer, Christina Schniederjohann, Sarah Koziel, Erin Chung, Ekaterina Popova, Alexander Brobeil, Nicklas Griese, Nora Kolks, Lisa-Maria Held and 5 more

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 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. 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

15 authors.

Matthias Meyer-BenderEuropean Molecular Biology Laboratory (EMBL), Heidelberg, Germany. matthias.meyerbender@embl.de.ORCID http://orcid.org/0000-0002-0448-4546
Harald VöhringerEuropean Molecular Biology Laboratory (EMBL), Heidelberg, Germany.ORCID http://orcid.org/0000-0003-2513-4518
Christina SchniederjohannDepartment of Medicine V, Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0009-0001-2693-8086
Sarah KozielDepartment of Hematology and Oncology, University Hospital Düsseldorf, Düsseldorf, Germany.ORCID http://orcid.org/0009-0003-8002-5127
Erin ChungEuropean Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Ekaterina PopovaDepartment of Hematology and Oncology, University Hospital Düsseldorf, Düsseldorf, Germany.ORCID http://orcid.org/0000-0003-2559-3685
Alexander BrobeilDepartment of Pathology, University of Heidelberg, Heidelberg, Germany.
Nicklas GrieseDepartment of Hematology and Oncology, University Hospital Düsseldorf, Düsseldorf, Germany.ORCID http://orcid.org/0009-0009-9461-4364
Nora KolksDepartment of Hematology and Oncology, University Hospital Düsseldorf, Düsseldorf, Germany.
Lisa-Maria HeldDepartment of Hematology and Oncology, University Hospital Düsseldorf, Düsseldorf, Germany.
Aamir MunirDepartment of Hematology and Oncology, University Hospital Düsseldorf, Düsseldorf, Germany.
Scverse Community
Sascha DietrichEuropean Molecular Biology Laboratory (EMBL), Heidelberg, Germany.ORCID http://orcid.org/0000-0002-0648-1832
Peter-Martin Bruch *Department of Medicine V, Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg, Germany. Peter-Martin.Bruch@med.uni-duesseldorf.de.ORCID http://orcid.org/0000-0002-9992-3109
Wolfgang Huber *European Molecular Biology Laboratory (EMBL), Heidelberg, Germany. wolfgang.huber@embl.org.ORCID http://orcid.org/0000-0002-0474-2218

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 964264
6 · The paper itself

Abstract

Highly multiplexed immunofluorescence imaging visualizes and quantifies protein levels at single-cell resolution in intact tissues at low cost and high scalability. Analysis of these data involves multiple steps with many method and parameter choices that must be adapted to the data and analytical objectives. There is an unmet need for a toolbox that offers flexible end-to-end coverage of the workflow. Here we present 'spatialproteomics', a Python package that addresses these challenges. Spatialproteomics enables the processing and analysis of large imaging data, including steps such as segmentation, image processing and cell-type classification, while synchronizing shared coordinates across data modalities. We demonstrate spatialproteomics on images of reactive lymph nodes and B cell non-Hodgkin lymphomas from 132 patients. We showcase an end-to-end analysis from raw images to statistical characterization of how cell type composition and spatial distribution vary across indolent and aggressive lymphomas. Furthermore, we show how spatialproteomics can process Gigapixel whole-slide images.

Indexed as

Image Processing, Computer-AssistedProteomicsSoftwareHumansLymph NodesLymphoma, B-Cell

Identifiers

PMID42498882
PMCPMC13441886

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.