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Among the 34 genotypes identified in our study by multispacer sequence typing, 28 (82%) were associated with disease in humans.
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Genotyping was performed by using multispacer sequence typing for intergenic regions (9 ).
We genotyped C. burnetii positive DNA from the feces and from 6 of the 16 ticks by using multispacer sequence typing as described (5 ).
Multilocus sequencing analysis [ 23] and multispacer sequence typing [ 24] differentiated M. massiliense from M. bolletii.
Genotyping performed by using multispacer sequence typing showed that MST17, a unique genotype of C. burnetii, circulates in Cayenne and is responsible for epidemics of Q fever (5 ).
A total of 12 samples: (cattle, n = 6, sheep, n = 5 and human, n = 1) collected from across Hungary were studied by a 10-loci multispacer sequence typing (MST) and 6-loci multiple-locus variable-number of tandem repeat analysis (MLVA).
Recently, two PCR-based typing methods have come into view: multispacer sequence typing (MST) [ 17] and multi-locus variable-number tandem repeat analysis (MLVA) [ 18, 19].
Genotypes were determined by a 6-loci Multiple Locus Variable number tandem repeat analysis (MLVA) panel and Multispacer Sequence Typing (MST).
We investigated Multispacer Sequence Typing (MST) for M. tuberculosis genotyping.
Multispacer sequence typing (MST) genotyping is based on the sequencing of several intergenic regions selected after complete genome sequence analysis.
Multispacer sequence typing is the first reliable method for typing Coxiella burnetii isolates.
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