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. 2009 Mar 16;551:217–230. doi: 10.1007/978-1-60327-999-4_17

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© Humana Press, a part of Springer Science+Business Media, LLC 2009

This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

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Fig. 3. — Phylogenetic analysis of FMDV genomes from the 2001 outbreak in the United Kingdom. (a) Maximum likelihood phylogenetic tree representing 14 FMDV complete genomes rooted to sequence “1,” constructed using PhyloWIN95 (33), incorporating the HKY model of nucleotide substitution with gamma distributed rate heterogeneity. Bootstrap values from 1,000 replicates are shown. (b) Statistical parsimony representation of the same 14 complete FMDV sequences, constructed using TCS (Version 1.21; 34). Each line represents a nucleotide substitution and each dot a putative ancestor virus.