Evidence map›Paper›PMID 38940138›Full record

ArticleBioinformatics (Oxford, England)2024

GraphCompass: spatial metrics for differential analyses of cell organization across conditions.

Mayar Ali, Merel Kuijs, Soroor Hediyeh-Zadeh, Tim Treis, Karin Hrovatin, Giovanni Palla, Anna C Schaar, Fabian J Theis

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Topology across scales on heterogeneous cell data.PLoS computational biology · 2025
    Article
  7. Article
  8. Article
  9. Article
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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

8 authors.

Mayar AliInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.ORCID 0000-0002-0398-5699
Merel KuijsInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.ORCID 0000-0003-4193-1138
Soroor Hediyeh-ZadehInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.ORCID 0000-0001-7513-6779
Tim TreisInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.ORCID 0000-0002-9686-4799
Karin HrovatinInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.ORCID 0000-0003-3319-9645
Giovanni PallaInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.ORCID 0000-0002-8004-4462
Anna C SchaarInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.
Fabian J TheisInstitute of Computational Biology, Helmholtz Munich, Neuherberg, 85764, Germany.ORCID 0000-0002-2419-1943

Funding

ERC DeepCell-101054957European UnionHelmholtz AssociationHelmholtz Association's Initiative and Networking Fund through CausalCellDynamicsJoachim Herz Stiftung via Add-on Fellowships for Interdisciplinary Life ScienceMunich School for Data Science
6 · The paper itself

Abstract

summarySpatial omics technologies are increasingly leveraged to characterize how disease disrupts tissue organization and cellular niches. While multiple methods to analyze spatial variation within a sample have been published, statistical and computational approaches to compare cell spatial organization across samples or conditions are mostly lacking. We present GraphCompass, a comprehensive set of omics-adapted graph analysis methods to quantitatively evaluate and compare the spatial arrangement of cells in samples representing diverse biological conditions. GraphCompass builds upon the Squidpy spatial omics toolbox and encompasses various statistical approaches to perform cross-condition analyses at the level of individual cell types, niches, and samples. Additionally, GraphCompass provides custom visualization functions that enable effective communication of results. We demonstrate how GraphCompass can be used to address key biological questions, such as how cellular organization and tissue architecture differ across various disease states and which spatial patterns correlate with a given pathological condition. GraphCompass can be applied to various popular omics techniques, including, but not limited to, spatial proteomics (e.g. MIBI-TOF), spot-based transcriptomics (e.g. 10× Genomics Visium), and single-cell resolved transcriptomics (e.g. Stereo-seq). In this work, we showcase the capabilities of GraphCompass through its application to three different studies that may also serve as benchmark datasets for further method development. With its easy-to-use implementation, extensive documentation, and comprehensive tutorials, GraphCompass is accessible to biologists with varying levels of computational expertise. By facilitating comparative analyses of cell spatial organization, GraphCompass promises to be a valuable asset in advancing our understanding of tissue function in health and disease. .

Indexed as

SoftwareAnimalsComputational BiologyGenomicsHumansProteomicsSingle-Cell AnalysisTranscriptome

Identifiers

PMID38940138
PMCPMC11256915

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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.