Title :
Some comparison on whole-proteome phylogeny of large dsDNA viruses based on dynamical language approach and feature frequency profiles method
Author :
Li-Qian Zhou ; Zu-Guo Yu ; Guo-Sheng Han ; Guang-ming Zhou ; De-sheng Wang
Author_Institution :
Sch. of Comput. & Commun., Hunan Univ. of Technol., Zhuzhou, China
Abstract :
There has been a growing interest in alignment-free methods for phylogenetic analysis using complete genome data. Among them, CVTree method, feature frequency profiles method and dynamical language approach were used to investigate the whole-proteome phylogeny of large dsDNA viruses. Using the data set of large dsDNA viruses from Gao and Qi (BMC Evol. Biol. 2007), the phylogenetic results based on the CVTree method and the dynamical language approach were compared in Yu et al. (BMC Evol. Biol. 2010). In this paper, we first apply dynamical language approach to the data set of large dsDNA viruses from Wu et al. (Proc. Natl. Acad. Sci. USA 2009) and compare our phylogenetic results with those based on the feature frequency profiles method. Then we construct the whole-proteome phylogeny of the larger dataset combining the above two data sets. According to the report of The International Committee on the Taxonomy of Viruses (ICTV), the trees from our analyses are in good agreement to the latest classification of large dsDNA viruses.
Keywords :
DNA; biology computing; evolution (biological); genomics; microorganisms; pattern classification; trees (mathematics); CVTree method; The International Committee on the Taxonomy of Viruses; complete genome data; dynamical language approach; feature frequency profiles method; large dsDNA virus classification; phylogenetic analysis; whole-proteome phylogeny; Bioinformatics; DNA; Educational institutions; Genomics; Phylogeny; Proteins; Viruses (medical); composition vector; dynamical language; large dsDNA virus; phyogeny;
Conference_Titel :
Natural Computation (ICNC), 2012 Eighth International Conference on
Conference_Location :
Chongqing
Print_ISBN :
978-1-4577-2130-4
DOI :
10.1109/ICNC.2012.6234564