Evidence map›Paper›PMID 36585456›Full record

ArticleNature methods2023

Optimizing multiplexed imaging experimental design through tissue spatial segregation estimation.

Pierre Bost, Daniel Schulz, Stefanie Engler, Clive Wasserfall, Bernd Bodenmiller

Abstract read
In one paragraph

Article in Nature methods, 2023. 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.

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  13. Multiplex protein imaging in tumour biology.Nature reviews. Cancer · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Pierre BostUniversity of Zurich, Department of Quantitative Biomedicine, Zurich, Switzerland.
Daniel SchulzUniversity of Zurich, Department of Quantitative Biomedicine, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-0913-1678
Stefanie EnglerUniversity of Zurich, Department of Quantitative Biomedicine, Zurich, Switzerland.
Clive WasserfallDepartment of Pathology, Immunology, and Laboratory Medicine, Diabetes Institute, University of Florida, Gainesville, FL, USA.
Bernd BodenmillerUniversity of Zurich, Department of Quantitative Biomedicine, Zurich, Switzerland. bernd.bodenmiller@uzh.ch.ORCID http://orcid.org/0000-0002-6325-7861

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in multiplexed imaging methods allow simultaneous detection of dozens of proteins and hundreds of RNAs, enabling deep spatial characterization of both healthy and diseased tissues. Parameters for the design of optimal multiplex imaging studies, especially those estimating how much area has to be imaged to capture all cell phenotype clusters, are lacking. Here, using a spatial transcriptomic atlas of healthy and tumor human tissues, we developed a statistical framework that determines the number and area of fields of view necessary to accurately identify all cell phenotypes that are part of a tissue. Using this strategy on imaging mass cytometry data, we identified a measurement of tissue spatial segregation that enables optimal experimental design. This strategy will enable an improved design of multiplexed imaging studies.

Indexed as

NeoplasmsResearch DesignDiagnostic ImagingHumansRNARNA

Identifiers

PMID36585456
PMCPMC9998266

What OpenQuestion holds

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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.