
ABSTRACT PCR primers targeting loci in the current Burkholderia cepacia complex multilocus sequence typing scheme were redesigned to (i) more reliably amplify these loci from B . cepacia complex species, (ii) amplify these same loci from additional Burkholderia species, and (iii) enable the use of a single primer set per locus for both amplification and DNA sequencing.
DNA, Bacterial, Burkholderia, Cluster Analysis, Sequence Analysis, DNA, QH426, DNA Fingerprinting, Phylogeny, Bacterial Typing Techniques, DNA Primers
DNA, Bacterial, Burkholderia, Cluster Analysis, Sequence Analysis, DNA, QH426, DNA Fingerprinting, Phylogeny, Bacterial Typing Techniques, DNA Primers
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