Evidence map›Paper›PMID 41354776›Full record

ArticleBMC bioinformatics2025

GeDi: simplifying gene set distances for enhanced omics interpretation in R/Bioconductor.

Annekathrin Silvia Nedwed, Arsenij Ustjanzew, Najla Abassi, Leon Dammer, Alicia Schulze, Sara Salome Helbich, Michael Delacher, Konstantin Strauch, Federico Marini

Abstract read
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Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Annekathrin Silvia NedwedInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany. anedwed@uni-mainz.de.
Arsenij UstjanzewInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Najla AbassiInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Leon DammerInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Alicia SchulzeInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Sara Salome HelbichInstitute of Immunology, University Medical Center Mainz, Mainz, Germany.
Michael DelacherInstitute of Immunology, University Medical Center Mainz, Mainz, Germany.
Konstantin StrauchInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Federico MariniInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University, Mainz, Germany. marinif@uni-mainz.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFunctional enrichment analysis is a standard component in many omics data analysis workflows, supported by a variety of methods and algorithms. However, despite their utility and wide application, these methods often return the results as an extensive and redundant list of gene sets, impeding interpretation and hypothesis generation. Moreover, network based information can provide additional biological context through functional interaction data, yet this is often overlooked by existing tools.

resultsWe developed GeDi, an R/Bioconductor package designed to streamline and standardize the interpretation of functional enrichment results. GeDi aggregates gene sets into biologically meaningful clusters using a suite of gene set distance metrics and clustering algorithms, aimed to reduce redundancy and improve clarity. GeDi also enables the integration of protein–protein interaction (PPI) data, through the implementation of a weighted distance metric, providing a richer biological context by capturing functional connectivity between pathways and their components. The package offers visualizations, aggregation, and automated reporting, and is available as both a stand-alone R-package and an interactive Shiny application.

conclusionGeDi facilitates clearer, faster interpretation of enrichment results by combining clustering and network context. Application to a public RNA-seq dataset revealed coherent biological themes, supporting both experimental and computational research. GeDi is freely available in the Bioconductor project under the MIT license ( https://bioconductor.org/packages/GeDi ), and a demo instance is accessible on the Shiny server ( http://shiny.imbei.uni-mainz.de:3838/GeDi ).

Indexed as

Computational BiologyGenomicsSoftwareAlgorithmsClustering AlgorithmsGene Expression ProfilingData interpretationData visualisationFunctional enrichment analysisRNA-sequencingR packageShiny

Identifiers

PMID41354776
PMCPMC12809992

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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.