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Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure
BACKGROUND: Developing suitable methods for the identification of protein complexes remains an active research area. It is important since it allows better understanding of cellular functions as well as malfunctions and it consequently leads to producing more effective cures for diseases. In this co...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230023/ https://www.ncbi.nlm.nih.gov/pubmed/24944073 http://dx.doi.org/10.1186/1471-2105-15-204 |
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author | Hanna, Eileen Marie Zaki, Nazar |
author_facet | Hanna, Eileen Marie Zaki, Nazar |
author_sort | Hanna, Eileen Marie |
collection | PubMed |
description | BACKGROUND: Developing suitable methods for the identification of protein complexes remains an active research area. It is important since it allows better understanding of cellular functions as well as malfunctions and it consequently leads to producing more effective cures for diseases. In this context, various computational approaches were introduced to complement high-throughput experimental methods which typically involve large datasets, are expensive in terms of time and cost, and are usually subject to spurious interactions. RESULTS: In this paper, we propose ProRank+, a method which detects protein complexes in protein interaction networks. The presented approach is mainly based on a ranking algorithm which sorts proteins according to their importance in the interaction network, and a merging procedure which refines the detected complexes in terms of their protein members. ProRank + was compared to several state-of-the-art approaches in order to show its effectiveness. It was able to detect more protein complexes with higher quality scores. CONCLUSIONS: The experimental results achieved by ProRank + show its ability to detect protein complexes in protein interaction networks. Eventually, the method could potentially identify previously-undiscovered protein complexes. The datasets and source codes are freely available for academic purposes at http://faculty.uaeu.ac.ae/nzaki/Research.htm. |
format | Online Article Text |
id | pubmed-4230023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42300232014-11-14 Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure Hanna, Eileen Marie Zaki, Nazar BMC Bioinformatics Research Article BACKGROUND: Developing suitable methods for the identification of protein complexes remains an active research area. It is important since it allows better understanding of cellular functions as well as malfunctions and it consequently leads to producing more effective cures for diseases. In this context, various computational approaches were introduced to complement high-throughput experimental methods which typically involve large datasets, are expensive in terms of time and cost, and are usually subject to spurious interactions. RESULTS: In this paper, we propose ProRank+, a method which detects protein complexes in protein interaction networks. The presented approach is mainly based on a ranking algorithm which sorts proteins according to their importance in the interaction network, and a merging procedure which refines the detected complexes in terms of their protein members. ProRank + was compared to several state-of-the-art approaches in order to show its effectiveness. It was able to detect more protein complexes with higher quality scores. CONCLUSIONS: The experimental results achieved by ProRank + show its ability to detect protein complexes in protein interaction networks. Eventually, the method could potentially identify previously-undiscovered protein complexes. The datasets and source codes are freely available for academic purposes at http://faculty.uaeu.ac.ae/nzaki/Research.htm. BioMed Central 2014-06-19 /pmc/articles/PMC4230023/ /pubmed/24944073 http://dx.doi.org/10.1186/1471-2105-15-204 Text en Copyright © 2014 Hanna and Zaki; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Research Article Hanna, Eileen Marie Zaki, Nazar Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure |
title | Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure |
title_full | Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure |
title_fullStr | Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure |
title_full_unstemmed | Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure |
title_short | Detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure |
title_sort | detecting protein complexes in protein interaction networks using a ranking algorithm with a refined merging procedure |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230023/ https://www.ncbi.nlm.nih.gov/pubmed/24944073 http://dx.doi.org/10.1186/1471-2105-15-204 |
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