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Global multiple protein-protein interaction network alignment by combining pairwise network alignments

BACKGROUND: A wealth of protein interaction data has become available in recent years, creating an urgent need for powerful analysis techniques. In this context, the problem of finding biologically meaningful correspondences between different protein-protein interaction networks (PPIN) is of particu...

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Autores principales: Dohrmann, Jakob, Puchin, Juris, Singh, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597059/
https://www.ncbi.nlm.nih.gov/pubmed/26423128
http://dx.doi.org/10.1186/1471-2105-16-S13-S11
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author Dohrmann, Jakob
Puchin, Juris
Singh, Rahul
author_facet Dohrmann, Jakob
Puchin, Juris
Singh, Rahul
author_sort Dohrmann, Jakob
collection PubMed
description BACKGROUND: A wealth of protein interaction data has become available in recent years, creating an urgent need for powerful analysis techniques. In this context, the problem of finding biologically meaningful correspondences between different protein-protein interaction networks (PPIN) is of particular interest. The PPIN of a species can be compared with that of other species through the process of PPIN alignment. Such an alignment can provide insight into basic problems like species evolution and network component function determination, as well as translational problems such as target identification and elucidation of mechanisms of disease spread. Furthermore, multiple PPINs can be aligned simultaneously, expanding the analytical implications of the result. While there are several pairwise network alignment algorithms, few methods are capable of multiple network alignment. RESULTS: We propose SMAL, a MNA algorithm based on the philosophy of scaffold-based alignment. SMAL is capable of converting results from any global pairwise alignment algorithms into a MNA in linear time. Using this method, we have built multiple network alignments based on combining pairwise alignments from a number of publicly available (pairwise) network aligners. We tested SMAL using PPINs of eight species derived from the IntAct repository and employed a number of measures to evaluate performance. Additionally, as part of our experimental investigations, we compared the effectiveness of SMAL while aligning up to eight input PPINs, and examined the effect of scaffold network choice on the alignments. CONCLUSIONS: A key advantage of SMAL lies in its ability to create MNAs through the use of pairwise network aligners for which native MNA implementations do not exist. Experiments indicate that the performance of SMAL was comparable to that of the native MNA implementation of established methods such as IsoRankN and SMETANA. However, in terms of computational time, SMAL was significantly faster. SMAL was also able to retain many important characteristics of the native pairwise alignments, such as the number of aligned nodes and edges, as well as the functional and homologene similarity of aligned nodes. The speed, flexibility and the ability to retain prior correspondences as new networks are aligned, makes SMAL a compelling choice for alignment of multiple large networks.
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spelling pubmed-45970592015-10-08 Global multiple protein-protein interaction network alignment by combining pairwise network alignments Dohrmann, Jakob Puchin, Juris Singh, Rahul BMC Bioinformatics Proceedings BACKGROUND: A wealth of protein interaction data has become available in recent years, creating an urgent need for powerful analysis techniques. In this context, the problem of finding biologically meaningful correspondences between different protein-protein interaction networks (PPIN) is of particular interest. The PPIN of a species can be compared with that of other species through the process of PPIN alignment. Such an alignment can provide insight into basic problems like species evolution and network component function determination, as well as translational problems such as target identification and elucidation of mechanisms of disease spread. Furthermore, multiple PPINs can be aligned simultaneously, expanding the analytical implications of the result. While there are several pairwise network alignment algorithms, few methods are capable of multiple network alignment. RESULTS: We propose SMAL, a MNA algorithm based on the philosophy of scaffold-based alignment. SMAL is capable of converting results from any global pairwise alignment algorithms into a MNA in linear time. Using this method, we have built multiple network alignments based on combining pairwise alignments from a number of publicly available (pairwise) network aligners. We tested SMAL using PPINs of eight species derived from the IntAct repository and employed a number of measures to evaluate performance. Additionally, as part of our experimental investigations, we compared the effectiveness of SMAL while aligning up to eight input PPINs, and examined the effect of scaffold network choice on the alignments. CONCLUSIONS: A key advantage of SMAL lies in its ability to create MNAs through the use of pairwise network aligners for which native MNA implementations do not exist. Experiments indicate that the performance of SMAL was comparable to that of the native MNA implementation of established methods such as IsoRankN and SMETANA. However, in terms of computational time, SMAL was significantly faster. SMAL was also able to retain many important characteristics of the native pairwise alignments, such as the number of aligned nodes and edges, as well as the functional and homologene similarity of aligned nodes. The speed, flexibility and the ability to retain prior correspondences as new networks are aligned, makes SMAL a compelling choice for alignment of multiple large networks. BioMed Central 2015-09-25 /pmc/articles/PMC4597059/ /pubmed/26423128 http://dx.doi.org/10.1186/1471-2105-16-S13-S11 Text en Copyright © 2015 Dohrmann et al. 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 use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 Proceedings
Dohrmann, Jakob
Puchin, Juris
Singh, Rahul
Global multiple protein-protein interaction network alignment by combining pairwise network alignments
title Global multiple protein-protein interaction network alignment by combining pairwise network alignments
title_full Global multiple protein-protein interaction network alignment by combining pairwise network alignments
title_fullStr Global multiple protein-protein interaction network alignment by combining pairwise network alignments
title_full_unstemmed Global multiple protein-protein interaction network alignment by combining pairwise network alignments
title_short Global multiple protein-protein interaction network alignment by combining pairwise network alignments
title_sort global multiple protein-protein interaction network alignment by combining pairwise network alignments
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597059/
https://www.ncbi.nlm.nih.gov/pubmed/26423128
http://dx.doi.org/10.1186/1471-2105-16-S13-S11
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