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DeCoaD: determining correlations among diseases using protein interaction networks

BACKGROUND: Disease–disease similarities can be investigated from multiple perspectives. Identifying similar diseases based on the underlying biomolecular interactions can be especially useful, because it may shed light on the common causes of the diseases and therefore may provide clues for possibl...

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Autores principales: Hamaneh, Mehdi B, Yu, Yi-Kuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467632/
https://www.ncbi.nlm.nih.gov/pubmed/26047952
http://dx.doi.org/10.1186/s13104-015-1211-z
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author Hamaneh, Mehdi B
Yu, Yi-Kuo
author_facet Hamaneh, Mehdi B
Yu, Yi-Kuo
author_sort Hamaneh, Mehdi B
collection PubMed
description BACKGROUND: Disease–disease similarities can be investigated from multiple perspectives. Identifying similar diseases based on the underlying biomolecular interactions can be especially useful, because it may shed light on the common causes of the diseases and therefore may provide clues for possible treatments. Here we introduce DeCoaD, a web-based program that uses a novel method to assign pair-wise similarity scores, called correlations, to genetic diseases. FINDINGS: DeCoaD uses a random walk to model the flow of information in a network within which nodes are either diseases or proteins and links signify either protein–protein interactions or disease–protein associations. For each protein node, the total number of visits by the random walker is called the weight of that node. Using a disease as both the starting and the terminating points of the random walks, a corresponding vector, whose elements are the weights associated with the proteins, can be constructed. The similarity between two diseases is defined as the cosine of the angle between their associated vectors. For a user-specified disease, DeCoaD outputs a list of similar diseases (with their corresponding correlations), and a graphical representation of the disease families that they belong to. Based on a probabilistic clustering algorithm, DeCoaD also outputs the clusters that the disease of interest is a member of, and the corresponding probabilities. The program also provides an interface to run enrichment analysis for the given disease or for any of the clusters that contains it. CONCLUSIONS: DeCoaD uses a novel algorithm to suggest non-trivial similarities between diseases with known gene associations, and also clusters the diseases based on their similarity scores. DeCoaD is available at http://www.ncbi.nlm.nih.gov/CBBresearch/Yu/mn/DeCoaD/.
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spelling pubmed-44676322015-06-16 DeCoaD: determining correlations among diseases using protein interaction networks Hamaneh, Mehdi B Yu, Yi-Kuo BMC Res Notes Technical Note BACKGROUND: Disease–disease similarities can be investigated from multiple perspectives. Identifying similar diseases based on the underlying biomolecular interactions can be especially useful, because it may shed light on the common causes of the diseases and therefore may provide clues for possible treatments. Here we introduce DeCoaD, a web-based program that uses a novel method to assign pair-wise similarity scores, called correlations, to genetic diseases. FINDINGS: DeCoaD uses a random walk to model the flow of information in a network within which nodes are either diseases or proteins and links signify either protein–protein interactions or disease–protein associations. For each protein node, the total number of visits by the random walker is called the weight of that node. Using a disease as both the starting and the terminating points of the random walks, a corresponding vector, whose elements are the weights associated with the proteins, can be constructed. The similarity between two diseases is defined as the cosine of the angle between their associated vectors. For a user-specified disease, DeCoaD outputs a list of similar diseases (with their corresponding correlations), and a graphical representation of the disease families that they belong to. Based on a probabilistic clustering algorithm, DeCoaD also outputs the clusters that the disease of interest is a member of, and the corresponding probabilities. The program also provides an interface to run enrichment analysis for the given disease or for any of the clusters that contains it. CONCLUSIONS: DeCoaD uses a novel algorithm to suggest non-trivial similarities between diseases with known gene associations, and also clusters the diseases based on their similarity scores. DeCoaD is available at http://www.ncbi.nlm.nih.gov/CBBresearch/Yu/mn/DeCoaD/. BioMed Central 2015-06-06 /pmc/articles/PMC4467632/ /pubmed/26047952 http://dx.doi.org/10.1186/s13104-015-1211-z Text en © Hamaneh and Yu 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Technical Note
Hamaneh, Mehdi B
Yu, Yi-Kuo
DeCoaD: determining correlations among diseases using protein interaction networks
title DeCoaD: determining correlations among diseases using protein interaction networks
title_full DeCoaD: determining correlations among diseases using protein interaction networks
title_fullStr DeCoaD: determining correlations among diseases using protein interaction networks
title_full_unstemmed DeCoaD: determining correlations among diseases using protein interaction networks
title_short DeCoaD: determining correlations among diseases using protein interaction networks
title_sort decoad: determining correlations among diseases using protein interaction networks
topic Technical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467632/
https://www.ncbi.nlm.nih.gov/pubmed/26047952
http://dx.doi.org/10.1186/s13104-015-1211-z
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