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Detecting Network Communities: An Application to Phylogenetic Analysis
Author(s) -
Roberto F. S. Andrade,
Ivan Carmo Rocha-Neto,
Leonardo Bacelar Lima Santos,
Charles Novaes de Santana,
Marcelo V.C. Diniz,
Thierry Petit Lobão,
Aristóteles GoésNeto,
Suani T. R. Pinho,
Charbel Niño El-Hani
Publication year - 2011
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1001131
Subject(s) - genbank , phylogenetic tree , distance matrices in phylogeny , similarity (geometry) , computer science , consistency (knowledge bases) , network analysis , set (abstract data type) , data mining , biological data , phylum , bayesian network , biological network , artificial intelligence , computational biology , biology , bioinformatics , gene , genetics , physics , quantum mechanics , image (mathematics) , programming language
This paper proposes a new method to identify communities in generally weighted complex networks and apply it to phylogenetic analysis. In this case, weights correspond to the similarity indexes among protein sequences, which can be used for network construction so that the network structure can be analyzed to recover phylogenetically useful information from its properties. The analyses discussed here are mainly based on the modular character of protein similarity networks, explored through the Newman-Girvan algorithm, with the help of the neighborhood matrix. The most relevant networks are found when the network topology changes abruptly revealing distinct modules related to the sets of organisms to which the proteins belong. Sound biological information can be retrieved by the computational routines used in the network approach, without using biological assumptions other than those incorporated by BLAST. Usually, all the main bacterial phyla and, in some cases, also some bacterial classes corresponded totally (100%) or to a great extent (>70%) to the modules. We checked for internal consistency in the obtained results, and we scored close to 84% of matches for community pertinence when comparisons between the results were performed. To illustrate how to use the network-based method, we employed data for enzymes involved in the chitin metabolic pathway that are present in more than 100 organisms from an original data set containing 1,695 organisms, downloaded from GenBank on May 19, 2007. A preliminary comparison between the outcomes of the network-based method and the results of methods based on Bayesian, distance, likelihood, and parsimony criteria suggests that the former is as reliable as these commonly used methods. We conclude that the network-based method can be used as a powerful tool for retrieving modularity information from weighted networks, which is useful for phylogenetic analysis.

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