Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery

The Open Targets Platform (https://platform.opentargets.org) is a unique, open-source, publicly-available knowledge base providing data and tooling for systematic drug target identification, annotation, and prioritisation. Since our last report, we have expanded the scope of the Platform through a number of significant enhancements and data updates, with the aim to enable our users to formulate more flexible and impactful therapeutic hypotheses. In this context, we have completely revamped our target-disease associations page with more interactive facets and built-in functionalities to empower users with additional control over their experience using the Platform, and added a new Target Prioritisation view. This enables users to prioritise targets based upon clinical precedence, tractability, doability and safety attributes. We have also implemented a direction of effect assessment for eight sources of target-disease association evidence, showing the effect of genetic variation on the function of a target is associated with risk or protection for a trait to inform on potential mechanisms of modulation suitable for disease treatment. These enhancements and the introduction of new back and front-end technologies to support them have increased the impact and usability of our resource within the drug discovery community.

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Publication Details

Journal
Nucleic Acids Research
Published
2024-12-06
DOI
https://doi.org/10.1093/nar/gkae1128
Citations
135
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
48.79

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article

Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery

Ian Dunham, Vivien W. Ho, Daniel Considine, James Hayhurst et al.
135 citations
Nucleic Acids Research
Computational Drug Discovery Methods
48.79
article

Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery

Ian Dunham, Vivien W. Ho, Daniel Considine, James Hayhurst, Miguel Carmona, David G. Hulcoop, Manuel Bernal Llinares, Helena Cornu, Polina Rusina, Poonam Uniyal, Kirill Tsukanov, Graham McNeill, Jeremy Schwartzentruber, Juan María Roldán‐Romero, Ellen M. McDonagh, Annalisa Buniello, Javier Ferrer, Irene López, Maria J. Falaguera, Carlos Cruz-Castillo, Luca Fumis, Maya Ghoussaini, Yakov A. Tsepilov, Ines Smit, Dániel Süveges, David Ochoa, Xiangyu Ge, Ricardo Esteban Martinez Osorio, Chintan Mehta, Ehsan Barkhordari, Tobi Alegbe, Szymon Szyszkowski
article en
135 citations

Abstract

The Open Targets Platform (https://platform.opentargets.org) is a unique, open-source, publicly-available knowledge base providing data and tooling for systematic drug target identification, annotation, and prioritisation. Since our last report, we have expanded the scope of the Platform through a number of significant enhancements and data updates, with the aim to enable our users to formulate more flexible and impactful therapeutic hypotheses. In this context, we have completely revamped our target-disease associations page with more interactive facets and built-in functionalities to empower users with additional control over their experience using the Platform, and added a new Target Prioritisation view. This enables users to prioritise targets based upon clinical precedence, tractability, doability and safety attributes. We have also implemented a direction of effect assessment for eight sources of target-disease association evidence, showing the effect of genetic variation on the function of a target is associated with risk or protection for a trait to inform on potential mechanisms of modulation suitable for disease treatment. These enhancements and the introduction of new back and front-end technologies to support them have increased the impact and usability of our resource within the drug discovery community.

Nucleic Acids ResearchVol. 53(D1)
AstraZeneca (United Kingdom) (GB), European Bioinformatics Institute (GB), Wellcome Sanger Institute (GB), Open Targets (GB)
Wellcome Trust
Good health and well-being
Openalex Percentile: Top 0%
Computational Drug Discovery Methods
48.79
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