Cargando…
Understanding and predicting disease relationships through similarity fusion
MOTIVATION: Combining disease relationships across multiple biological levels could aid our understanding of common processes taking place in disease, potentially indicating opportunities for drug sharing. Here, we propose a similarity fusion approach which accounts for differences in information co...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449746/ https://www.ncbi.nlm.nih.gov/pubmed/30169824 http://dx.doi.org/10.1093/bioinformatics/bty754 |
_version_ | 1783408915557384192 |
---|---|
author | Oerton, Erin Roberts, Ian Lewis, Patrick S H Guilliams, Tim Bender, Andreas |
author_facet | Oerton, Erin Roberts, Ian Lewis, Patrick S H Guilliams, Tim Bender, Andreas |
author_sort | Oerton, Erin |
collection | PubMed |
description | MOTIVATION: Combining disease relationships across multiple biological levels could aid our understanding of common processes taking place in disease, potentially indicating opportunities for drug sharing. Here, we propose a similarity fusion approach which accounts for differences in information content between different data types, allowing combination of each data type in a balanced manner. RESULTS: We apply this method to six different types of biological data (ontological, phenotypic, literature co-occurrence, genetic association, gene expression and drug indication data) for 84 diseases to create a ‘disease map’: a network of diseases connected at one or more biological levels. As well as reconstructing known disease relationships, 15% of links in the disease map are novel links spanning traditional ontological classes, such as between psoriasis and inflammatory bowel disease. 62% of links in the disease map represent drug-sharing relationships, illustrating the relevance of the similarity fusion approach to the identification of potential therapeutic relationships. AVAILABILITY AND IMPLEMENTATION: Freely available under the MIT license at https://github.com/e-oerton/disease-similarity-fusion SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6449746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64497462019-04-09 Understanding and predicting disease relationships through similarity fusion Oerton, Erin Roberts, Ian Lewis, Patrick S H Guilliams, Tim Bender, Andreas Bioinformatics Original Papers MOTIVATION: Combining disease relationships across multiple biological levels could aid our understanding of common processes taking place in disease, potentially indicating opportunities for drug sharing. Here, we propose a similarity fusion approach which accounts for differences in information content between different data types, allowing combination of each data type in a balanced manner. RESULTS: We apply this method to six different types of biological data (ontological, phenotypic, literature co-occurrence, genetic association, gene expression and drug indication data) for 84 diseases to create a ‘disease map’: a network of diseases connected at one or more biological levels. As well as reconstructing known disease relationships, 15% of links in the disease map are novel links spanning traditional ontological classes, such as between psoriasis and inflammatory bowel disease. 62% of links in the disease map represent drug-sharing relationships, illustrating the relevance of the similarity fusion approach to the identification of potential therapeutic relationships. AVAILABILITY AND IMPLEMENTATION: Freely available under the MIT license at https://github.com/e-oerton/disease-similarity-fusion SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-04-01 2018-08-30 /pmc/articles/PMC6449746/ /pubmed/30169824 http://dx.doi.org/10.1093/bioinformatics/bty754 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Oerton, Erin Roberts, Ian Lewis, Patrick S H Guilliams, Tim Bender, Andreas Understanding and predicting disease relationships through similarity fusion |
title | Understanding and predicting disease relationships through similarity fusion |
title_full | Understanding and predicting disease relationships through similarity fusion |
title_fullStr | Understanding and predicting disease relationships through similarity fusion |
title_full_unstemmed | Understanding and predicting disease relationships through similarity fusion |
title_short | Understanding and predicting disease relationships through similarity fusion |
title_sort | understanding and predicting disease relationships through similarity fusion |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449746/ https://www.ncbi.nlm.nih.gov/pubmed/30169824 http://dx.doi.org/10.1093/bioinformatics/bty754 |
work_keys_str_mv | AT oertonerin understandingandpredictingdiseaserelationshipsthroughsimilarityfusion AT robertsian understandingandpredictingdiseaserelationshipsthroughsimilarityfusion AT lewispatricksh understandingandpredictingdiseaserelationshipsthroughsimilarityfusion AT guilliamstim understandingandpredictingdiseaserelationshipsthroughsimilarityfusion AT benderandreas understandingandpredictingdiseaserelationshipsthroughsimilarityfusion |