Date of Award
2012
Document Type
Master Thesis
Degree Name
Masters of Science (Research)
Department
Biological Sciences
First Advisor
Dr. Helen O'Shea
Abstract
Globally rotavirus is one of the most important causes of gastroenteritis in children and affects nearly all children by the age of 5 years. It also infects adults with most severe symptoms in the elderly or immune compromised. The most common strains associated with human rotavirus gastroenteritis are G1-G4 and G9 along with P[8],[6]and [4].All previous studies used only neighbour-joining method in the phylogenetic analysis of rotavirus genes. In this study rotavirus genes VP7 and VP4 for rotavirus strains G1 .G3 ,G9 , P[8] and P[4] were analysed in MEGA4.0 using both neighbour-joining and maximum parsimony. The main difference in the use of both methods was the time taken to run the analysis, the data sets were large and maximum parsimony method took at least double the time to run. Neighbour-joining is a distance based method and maximum parsimony a character based method, tree building in both cases use different algorithms. Based on the results of the analysis there was no major difference in results gained between the two methods.
Recommended Citation
Cotter, Jenny, "Phylogenetic Analysis of Rotavirus Strains Gl, G3 5G9 5P[8] and P[4] using both Neighbour-Joining and Maximum Parsimony" (2012). Theses [online].
Available at: https://sword.cit.ie/allthe/254
Access Level
info:eu-repo/semantics/openAccess
Comments
Project Thesis in partial fulfilment for the degree of Masters In Computational Biology 2012.