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Task-driven knowledge graph filtering improves prioritizing drugs for repurposing

BACKGROUND: Drug repurposing aims at finding new targets for already developed drugs. It becomes more relevant as the cost of discovering new drugs steadily increases. To find new potential targets for a drug, an abundance of methods and existing biomedical knowledge from different domains can be le...

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Autores principales: Ratajczak, Florin, Joblin, Mitchell, Ringsquandl, Martin, Hildebrandt, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894843/
https://www.ncbi.nlm.nih.gov/pubmed/35246025
http://dx.doi.org/10.1186/s12859-022-04608-y
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author Ratajczak, Florin
Joblin, Mitchell
Ringsquandl, Martin
Hildebrandt, Marcel
author_facet Ratajczak, Florin
Joblin, Mitchell
Ringsquandl, Martin
Hildebrandt, Marcel
author_sort Ratajczak, Florin
collection PubMed
description BACKGROUND: Drug repurposing aims at finding new targets for already developed drugs. It becomes more relevant as the cost of discovering new drugs steadily increases. To find new potential targets for a drug, an abundance of methods and existing biomedical knowledge from different domains can be leveraged. Recently, knowledge graphs have emerged in the biomedical domain that integrate information about genes, drugs, diseases and other biological domains. Knowledge graphs can be used to predict new connections between compounds and diseases, leveraging the interconnected biomedical data around them. While real world use cases such as drug repurposing are only interested in one specific relation type, widely used knowledge graph embedding models simultaneously optimize over all relation types in the graph. This can lead the models to underfit the data that is most relevant for the desired relation type. For example, if we want to learn embeddings to predict links between compounds and diseases but almost the entirety of relations in the graph is incident to other pairs of entity types, then the resulting embeddings are likely not optimised to predict links between compounds and diseases. We propose a method that leverages domain knowledge in the form of metapaths and use them to filter two biomedical knowledge graphs (Hetionet and DRKG) for the purpose of improving performance on the prediction task of drug repurposing while simultaneously increasing computational efficiency. RESULTS: We find that our method reduces the number of entities by 60% on Hetionet and 26% on DRKG, while leading to an improvement in prediction performance of up to 40.8% on Hetionet and 14.2% on DRKG, with an average improvement of 20.6% on Hetionet and 8.9% on DRKG. Additionally, prioritization of antiviral compounds for SARS CoV-2 improves after task-driven filtering is applied. CONCLUSION: Knowledge graphs contain facts that are counter productive for specific tasks, in our case drug repurposing. We also demonstrate that these facts can be removed, resulting in an improved performance in that task and a more efficient learning process. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04608-y.
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spelling pubmed-88948432022-03-04 Task-driven knowledge graph filtering improves prioritizing drugs for repurposing Ratajczak, Florin Joblin, Mitchell Ringsquandl, Martin Hildebrandt, Marcel BMC Bioinformatics Research BACKGROUND: Drug repurposing aims at finding new targets for already developed drugs. It becomes more relevant as the cost of discovering new drugs steadily increases. To find new potential targets for a drug, an abundance of methods and existing biomedical knowledge from different domains can be leveraged. Recently, knowledge graphs have emerged in the biomedical domain that integrate information about genes, drugs, diseases and other biological domains. Knowledge graphs can be used to predict new connections between compounds and diseases, leveraging the interconnected biomedical data around them. While real world use cases such as drug repurposing are only interested in one specific relation type, widely used knowledge graph embedding models simultaneously optimize over all relation types in the graph. This can lead the models to underfit the data that is most relevant for the desired relation type. For example, if we want to learn embeddings to predict links between compounds and diseases but almost the entirety of relations in the graph is incident to other pairs of entity types, then the resulting embeddings are likely not optimised to predict links between compounds and diseases. We propose a method that leverages domain knowledge in the form of metapaths and use them to filter two biomedical knowledge graphs (Hetionet and DRKG) for the purpose of improving performance on the prediction task of drug repurposing while simultaneously increasing computational efficiency. RESULTS: We find that our method reduces the number of entities by 60% on Hetionet and 26% on DRKG, while leading to an improvement in prediction performance of up to 40.8% on Hetionet and 14.2% on DRKG, with an average improvement of 20.6% on Hetionet and 8.9% on DRKG. Additionally, prioritization of antiviral compounds for SARS CoV-2 improves after task-driven filtering is applied. CONCLUSION: Knowledge graphs contain facts that are counter productive for specific tasks, in our case drug repurposing. We also demonstrate that these facts can be removed, resulting in an improved performance in that task and a more efficient learning process. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04608-y. BioMed Central 2022-03-04 /pmc/articles/PMC8894843/ /pubmed/35246025 http://dx.doi.org/10.1186/s12859-022-04608-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ratajczak, Florin
Joblin, Mitchell
Ringsquandl, Martin
Hildebrandt, Marcel
Task-driven knowledge graph filtering improves prioritizing drugs for repurposing
title Task-driven knowledge graph filtering improves prioritizing drugs for repurposing
title_full Task-driven knowledge graph filtering improves prioritizing drugs for repurposing
title_fullStr Task-driven knowledge graph filtering improves prioritizing drugs for repurposing
title_full_unstemmed Task-driven knowledge graph filtering improves prioritizing drugs for repurposing
title_short Task-driven knowledge graph filtering improves prioritizing drugs for repurposing
title_sort task-driven knowledge graph filtering improves prioritizing drugs for repurposing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894843/
https://www.ncbi.nlm.nih.gov/pubmed/35246025
http://dx.doi.org/10.1186/s12859-022-04608-y
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