<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G Girault</style></author><author><style face="normal" font="default" size="100%">P Wattiau</style></author><author><style face="normal" font="default" size="100%">M Saqib</style></author><author><style face="normal" font="default" size="100%">B Martin</style></author><author><style face="normal" font="default" size="100%">F Vorimore</style></author><author><style face="normal" font="default" size="100%">H Singha</style></author><author><style face="normal" font="default" size="100%">M Engelsma</style></author><author><style face="normal" font="default" size="100%">H J Roest</style></author><author><style face="normal" font="default" size="100%">S Spicic</style></author><author><style face="normal" font="default" size="100%">R Grunow</style></author><author><style face="normal" font="default" size="100%">N Vicari</style></author><author><style face="normal" font="default" size="100%">Sigrid C.J. De Keersmaecker</style></author><author><style face="normal" font="default" size="100%">Nancy Roosens</style></author><author><style face="normal" font="default" size="100%">M Fabbi</style></author><author><style face="normal" font="default" size="100%">B N Tripathi</style></author><author><style face="normal" font="default" size="100%">Zientara, S</style></author><author><style face="normal" font="default" size="100%">N Madani</style></author><author><style face="normal" font="default" size="100%">K Laroucau</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High-resolution melting PCR analysis for rapid genotyping of Burkholderia mallei.</style></title><secondary-title><style face="normal" font="default" size="100%">Infect Genet Evol</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Burkholderia mallei</style></keyword><keyword><style  face="normal" font="default" size="100%">DNA, Bacterial</style></keyword><keyword><style  face="normal" font="default" size="100%">Genotype</style></keyword><keyword><style  face="normal" font="default" size="100%">Phylogeny</style></keyword><keyword><style  face="normal" font="default" size="100%">polymerase chain reaction</style></keyword><keyword><style  face="normal" font="default" size="100%">Polymorphism, Single Nucleotide</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2018 09</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">63</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Burkholderia (B.) mallei is the causative agent of glanders. A previous work conducted on single-nucleotide polymorphisms (SNP) extracted from the whole genome sequences of 45 B. mallei isolates identified 3 lineages for this species. In this study, we designed a high-resolution melting (HRM) method for the screening of 15 phylogenetically informative SNPs within the genome of B. mallei that subtype the species into 3 lineages and 12 branches/sub-branches/groups. The present results demonstrate that SNP-based genotyping represent an interesting approach for the molecular epidemiology analysis of B. mallei.&lt;/p&gt;
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