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. 2016 Mar 31;17:272. doi: 10.1186/s12864-016-2597-2

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© Rolfe et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — Graphical representation of the 89 SNP haplotypes discovered across four re-sequenced pathotypes. Pathotype alleles are coded in green or red for the reference (Pb3) or alternate alleles, respectively. Clustering was performed using the default dist fuction of the stats R package