TY - JOUR
T1 - OmniPath
T2 - Integrated knowledgebase for multi-omics analysis
AU - Türei, Dénes
AU - Schaul, Jonathan
AU - Palacio-Escat, Nicolàs
AU - Bohár, Balázs
AU - Bai, Yunfan
AU - Ceccarelli, Francesco
AU - Çevrim, Elif
AU - Daley, Macabe
AU - Darcan, Melih
AU - Dimitrov, Daniel
AU - Doǧan, Tunca
AU - Domingo-Fernández, Daniel
AU - Dugourd, Aurelien
AU - Gábor, Attila
AU - Gul, Lejla
AU - Hall, Benjamin A.
AU - Hoyt, Charles Tapley
AU - Ivanova, Olga
AU - Klein, Michal
AU - Lawrence, Toby
AU - Mañanes, Diego
AU - Módos, Dezső
AU - Müller-Dott, Sophia
AU - Ölbei, Márton
AU - Schmidt, Christina
AU - Şen, Bünyamin
AU - Theis, Fabian J.
AU - Ünlü, Atabey
AU - Ulusoy, Erva
AU - Valdeolivas, Alberto
AU - Korcsmáros, Tamás
AU - Saez-Rodriguez, Julio
N1 - Publisher Copyright:
© 2025 The Author(s).
PY - 2026/1/6
Y1 - 2026/1/6
N2 - 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.
AB - 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.
KW - Knowledge Bases
KW - Software
KW - MicroRNAs/genetics
KW - Databases, Genetic
KW - Genomics/methods
KW - Humans
KW - Protein Processing, Post-Translational
KW - Proteins/metabolism
KW - Internet
KW - Computational Biology/methods
KW - Multiomics
UR - https://www.scopus.com/pages/publications/105027656480
U2 - 10.1093/nar/gkaf1126
DO - 10.1093/nar/gkaf1126
M3 - Article
C2 - 41251164
AN - SCOPUS:105027656480
SN - 0305-1048
VL - 54
SP - D652-D660
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - D1
ER -