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Optimal Network Alignment with Graphlet Degree Vectors
Important biological information is encoded in the topology of biological networks. Comparative analyses of biological networks are proving to be valuable, as they can lead to transfer of knowledge between species and give deeper insights into biological function, disease, and evolution. We introduc...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901631/ https://www.ncbi.nlm.nih.gov/pubmed/20628593 |
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author | Milenković, Tijana Ng, Weng Leong Hayes, Wayne Pržulj, Nataša |
author_facet | Milenković, Tijana Ng, Weng Leong Hayes, Wayne Pržulj, Nataša |
author_sort | Milenković, Tijana |
collection | PubMed |
description | Important biological information is encoded in the topology of biological networks. Comparative analyses of biological networks are proving to be valuable, as they can lead to transfer of knowledge between species and give deeper insights into biological function, disease, and evolution. We introduce a new method that uses the Hungarian algorithm to produce optimal global alignment between two networks using any cost function. We design a cost function based solely on network topology and use it in our network alignment. Our method can be applied to any two networks, not just biological ones, since it is based only on network topology. We use our new method to align protein-protein interaction networks of two eukaryotic species and demonstrate that our alignment exposes large and topologically complex regions of network similarity. At the same time, our alignment is biologically valid, since many of the aligned protein pairs perform the same biological function. From the alignment, we predict function of yet unannotated proteins, many of which we validate in the literature. Also, we apply our method to find topological similarities between metabolic networks of different species and build phylogenetic trees based on our network alignment score. The phylogenetic trees obtained in this way bear a striking resemblance to the ones obtained by sequence alignments. Our method detects topologically similar regions in large networks that are statistically significant. It does this independent of protein sequence or any other information external to network topology. |
format | Text |
id | pubmed-2901631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-29016312010-07-13 Optimal Network Alignment with Graphlet Degree Vectors Milenković, Tijana Ng, Weng Leong Hayes, Wayne Pržulj, Nataša Cancer Inform Original Research Important biological information is encoded in the topology of biological networks. Comparative analyses of biological networks are proving to be valuable, as they can lead to transfer of knowledge between species and give deeper insights into biological function, disease, and evolution. We introduce a new method that uses the Hungarian algorithm to produce optimal global alignment between two networks using any cost function. We design a cost function based solely on network topology and use it in our network alignment. Our method can be applied to any two networks, not just biological ones, since it is based only on network topology. We use our new method to align protein-protein interaction networks of two eukaryotic species and demonstrate that our alignment exposes large and topologically complex regions of network similarity. At the same time, our alignment is biologically valid, since many of the aligned protein pairs perform the same biological function. From the alignment, we predict function of yet unannotated proteins, many of which we validate in the literature. Also, we apply our method to find topological similarities between metabolic networks of different species and build phylogenetic trees based on our network alignment score. The phylogenetic trees obtained in this way bear a striking resemblance to the ones obtained by sequence alignments. Our method detects topologically similar regions in large networks that are statistically significant. It does this independent of protein sequence or any other information external to network topology. Libertas Academica 2010-06-30 /pmc/articles/PMC2901631/ /pubmed/20628593 Text en © 2010 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited. |
spellingShingle | Original Research Milenković, Tijana Ng, Weng Leong Hayes, Wayne Pržulj, Nataša Optimal Network Alignment with Graphlet Degree Vectors |
title | Optimal Network Alignment with Graphlet Degree Vectors |
title_full | Optimal Network Alignment with Graphlet Degree Vectors |
title_fullStr | Optimal Network Alignment with Graphlet Degree Vectors |
title_full_unstemmed | Optimal Network Alignment with Graphlet Degree Vectors |
title_short | Optimal Network Alignment with Graphlet Degree Vectors |
title_sort | optimal network alignment with graphlet degree vectors |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901631/ https://www.ncbi.nlm.nih.gov/pubmed/20628593 |
work_keys_str_mv | AT milenkovictijana optimalnetworkalignmentwithgraphletdegreevectors AT ngwengleong optimalnetworkalignmentwithgraphletdegreevectors AT hayeswayne optimalnetworkalignmentwithgraphletdegreevectors AT przuljnatasa optimalnetworkalignmentwithgraphletdegreevectors |