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A knowledge graph approach to predict and interpret disease-causing gene interactions

BACKGROUND: Understanding the impact of gene interactions on disease phenotypes is increasingly recognised as a crucial aspect of genetic disease research. This trend is reflected by the growing amount of clinical research on oligogenic diseases, where disease manifestations are influenced by combin...

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Autores principales: Renaux, Alexandre, Terwagne, Chloé, Cochez, Michael, Tiddi, Ilaria, Nowé, Ann, Lenaerts, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463539/
https://www.ncbi.nlm.nih.gov/pubmed/37644440
http://dx.doi.org/10.1186/s12859-023-05451-5
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author Renaux, Alexandre
Terwagne, Chloé
Cochez, Michael
Tiddi, Ilaria
Nowé, Ann
Lenaerts, Tom
author_facet Renaux, Alexandre
Terwagne, Chloé
Cochez, Michael
Tiddi, Ilaria
Nowé, Ann
Lenaerts, Tom
author_sort Renaux, Alexandre
collection PubMed
description BACKGROUND: Understanding the impact of gene interactions on disease phenotypes is increasingly recognised as a crucial aspect of genetic disease research. This trend is reflected by the growing amount of clinical research on oligogenic diseases, where disease manifestations are influenced by combinations of variants on a few specific genes. Although statistical machine-learning methods have been developed to identify relevant genetic variant or gene combinations associated with oligogenic diseases, they rely on abstract features and black-box models, posing challenges to interpretability for medical experts and impeding their ability to comprehend and validate predictions. In this work, we present a novel, interpretable predictive approach based on a knowledge graph that not only provides accurate predictions of disease-causing gene interactions but also offers explanations for these results. RESULTS: We introduce BOCK, a knowledge graph constructed to explore disease-causing genetic interactions, integrating curated information on oligogenic diseases from clinical cases with relevant biomedical networks and ontologies. Using this graph, we developed a novel predictive framework based on heterogenous paths connecting gene pairs. This method trains an interpretable decision set model that not only accurately predicts pathogenic gene interactions, but also unveils the patterns associated with these diseases. A unique aspect of our approach is its ability to offer, along with each positive prediction, explanations in the form of subgraphs, revealing the specific entities and relationships that led to each pathogenic prediction. CONCLUSION: Our method, built with interpretability in mind, leverages heterogenous path information in knowledge graphs to predict pathogenic gene interactions and generate meaningful explanations. This not only broadens our understanding of the molecular mechanisms underlying oligogenic diseases, but also presents a novel application of knowledge graphs in creating more transparent and insightful predictors for genetic research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05451-5.
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spelling pubmed-104635392023-08-30 A knowledge graph approach to predict and interpret disease-causing gene interactions Renaux, Alexandre Terwagne, Chloé Cochez, Michael Tiddi, Ilaria Nowé, Ann Lenaerts, Tom BMC Bioinformatics Research BACKGROUND: Understanding the impact of gene interactions on disease phenotypes is increasingly recognised as a crucial aspect of genetic disease research. This trend is reflected by the growing amount of clinical research on oligogenic diseases, where disease manifestations are influenced by combinations of variants on a few specific genes. Although statistical machine-learning methods have been developed to identify relevant genetic variant or gene combinations associated with oligogenic diseases, they rely on abstract features and black-box models, posing challenges to interpretability for medical experts and impeding their ability to comprehend and validate predictions. In this work, we present a novel, interpretable predictive approach based on a knowledge graph that not only provides accurate predictions of disease-causing gene interactions but also offers explanations for these results. RESULTS: We introduce BOCK, a knowledge graph constructed to explore disease-causing genetic interactions, integrating curated information on oligogenic diseases from clinical cases with relevant biomedical networks and ontologies. Using this graph, we developed a novel predictive framework based on heterogenous paths connecting gene pairs. This method trains an interpretable decision set model that not only accurately predicts pathogenic gene interactions, but also unveils the patterns associated with these diseases. A unique aspect of our approach is its ability to offer, along with each positive prediction, explanations in the form of subgraphs, revealing the specific entities and relationships that led to each pathogenic prediction. CONCLUSION: Our method, built with interpretability in mind, leverages heterogenous path information in knowledge graphs to predict pathogenic gene interactions and generate meaningful explanations. This not only broadens our understanding of the molecular mechanisms underlying oligogenic diseases, but also presents a novel application of knowledge graphs in creating more transparent and insightful predictors for genetic research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05451-5. BioMed Central 2023-08-29 /pmc/articles/PMC10463539/ /pubmed/37644440 http://dx.doi.org/10.1186/s12859-023-05451-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Renaux, Alexandre
Terwagne, Chloé
Cochez, Michael
Tiddi, Ilaria
Nowé, Ann
Lenaerts, Tom
A knowledge graph approach to predict and interpret disease-causing gene interactions
title A knowledge graph approach to predict and interpret disease-causing gene interactions
title_full A knowledge graph approach to predict and interpret disease-causing gene interactions
title_fullStr A knowledge graph approach to predict and interpret disease-causing gene interactions
title_full_unstemmed A knowledge graph approach to predict and interpret disease-causing gene interactions
title_short A knowledge graph approach to predict and interpret disease-causing gene interactions
title_sort knowledge graph approach to predict and interpret disease-causing gene interactions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463539/
https://www.ncbi.nlm.nih.gov/pubmed/37644440
http://dx.doi.org/10.1186/s12859-023-05451-5
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