Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

OmniPath

General information

URL: https://omnipathdb.org/
Full name: OmniPath
Description: OmniPath is a database combining diverse molecular knowledge from 168 resources. It covers causal protein-protein, gene regulatory, miRNA, and enzyme-PTM (post-translational modification) interactions, cell-cell communication, protein complexes, and information about the function, localization, structure, and many other aspects of biomolecules. It prioritizes literature curated data, and complements it with predictions and large scale databases.
Year founded: 2016
Last update: 2025
Version:
Accessibility:
Accessible
Country/Region: Germany

Contact information

University/Institution: Heidelberg University Hospital
Address: Im Neuenheimer Feld 130.3 Institute for Computational Biomedicine
City: Heidelberg
Province/State:
Country/Region: Germany
Contact name (PI/Team): Saez-Rodriguez
Contact email (PI/Helpdesk): turei.denes@gmail.com

Publications

41251164
OmniPath: integrated knowledgebase for multi-omics analysis. [PMID: 41251164]
Türei D, Schaul J, Palacio-Escat N, Bohár B, Bai Y, Ceccarelli F, Çevrim E, Daley M, Darcan M, Dimitrov D, Doğan T, Domingo-Fernández D, Dugourd A, Gábor A, Gul L, Hall BA, Hoyt CT, Ivanova O, Klein M, Lawrence T, Mañanes D, Módos D, Müller-Dott S, Ölbei M, Schmidt C, Şen B, Theis FJ, Ünlü A, Ulusoy E, Valdeolivas A, Korcsmáros T, Saez-Rodriguez J.

Analysis and interpretation of omics data largely benefit from the use of prior knowledge. However, this knowledge is fragmented across resources and often is not directly accessible for analytical methods. We developed OmniPath (https://omnipathdb.org/), a database combining diverse molecular knowledge from 168 resources. It covers causal protein-protein, gene regulatory, microRNA, and enzyme-post-translational modification interactions, cell-cell communication, protein complexes, and information about the function, localization, structure, and many other aspects of biomolecules. It prioritizes literature curated data, and complements it with predictions and large scale databases. To enable interactive browsing of this large corpus of knowledge, we developed OmniPath Explorer, which also includes a large language model agent that has direct access to the database. Python and R/Bioconductor client packages and a Cytoscape plugin create easy access to customized prior knowledge for omics analysis environments, such as scverse. OmniPath can be broadly used for the analysis of bulk, single-cell, and spatial multi-omics data, especially for mechanistic and causal modeling.

Nucleic Acids Res. 2025:() | 0 Citations (from Europe PMC, 2025-12-06)
33749993
Integrated intra- and intercellular signaling knowledge for multicellular omics analysis. [PMID: 33749993]
Türei D, Valdeolivas A, Gul L, Palacio-Escat N, Klein M, Ivanova O, Ölbei M, Gábor A, Theis F, Módos D, Korcsmáros T, Saez-Rodriguez J.

Molecular knowledge of biological processes is a cornerstone in omics data analysis. Applied to single-cell data, such analyses provide mechanistic insights into individual cells and their interactions. However, knowledge of intercellular communication is scarce, scattered across resources, and not linked to intracellular processes. To address this gap, we combined over 100 resources covering interactions and roles of proteins in inter- and intracellular signaling, as well as transcriptional and post-transcriptional regulation. We added protein complex information and annotations on function, localization, and role in diseases for each protein. The resource is available for human, and via homology translation for mouse and rat. The data are accessible via OmniPath's web service (https://omnipathdb.org/), a Cytoscape plug-in, and packages in R/Bioconductor and Python, providing access options for computational and experimental scientists. We created workflows with tutorials to facilitate the analysis of cell-cell interactions and affected downstream intracellular signaling processes. OmniPath provides a single access point to knowledge spanning intra- and intercellular processes for data analysis, as we demonstrate in applications studying SARS-CoV-2 infection and ulcerative colitis.

Mol Syst Biol. 2021:17(3) | 226 Citations (from Europe PMC, 2025-12-06)
31886476
Bringing data from curated pathway resources to Cytoscape with OmniPath. [PMID: 31886476]
Ceccarelli F, Turei D, Gabor A, Saez-Rodriguez J.

Summary

Multiple databases provide valuable information about curated pathways and other resources that can be used to build and analyze networks. OmniPath combines 61 (and continuously growing) network resources into a comprehensive collection, with over 120 000 interactions. We present here the OmniPath App, a Cytoscape plugin to flexibly import data from OmniPath via a simple and intuitive interface. Thus, it makes possible to directly access the large body of high-quality knowledge provided by OmniPath within Cytoscape for inspection and further use with other tools.

Availability and implementation

The OmniPath App has been developed for Cytoscape 3 in the Java programing language. The latest source code and the plugin can be found at: https://github.com/saezlab/Omnipath_Cytoscape and http://apps.cytoscape.org/apps/omnipath, respectively.

Supplementary information

Supplementary data are available at Bioinformatics online.

Bioinformatics. 2020:36(8) | 34 Citations (from Europe PMC, 2025-12-06)
27898060
OmniPath: guidelines and gateway for literature-curated signaling pathway resources. [PMID: 27898060]
Türei D, Korcsmáros T, Saez-Rodriguez J.
Nat Methods. 2016:13(12) | 480 Citations (from Europe PMC, 2025-12-06)

Ranking

All databases:
217/6895 (96.867%)
Modification:
12/337 (96.736%)
Structure:
19/967 (98.139%)
Interaction:
35/1194 (97.152%)
Pathway:
17/451 (96.452%)
Literature:
28/577 (95.321%)
217
Total Rank
727
Citations
80.778
z-index

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Record metadata

Created on: 2025-09-09
Curated by:
Denes Turei [2025-12-02]
shaosen zhang [2025-09-09]
Denes Turei [2025-09-09]