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Each individual cow was identified by use of a plastic ear tag with its corresponding number.
The CR of each patient was identified by use of the personal identification number.
The isolate was identified by use of a multiplex PCR-based, solid-phase, reverse-hybridization assay (GenoType MTBC, Hain Lifescience GmbH, Nehren, Germany), excluding M. bovis BCG (2 ).
The combination of SPN diagnostic tests in both periods was identified by use of SLPMiner, a data-mining algorithm for finding frequent sequential patterns [ 25, 26] (i.e., time-ordered sequences of diagnostic tests performed for patients).
This gene was identified by use of the tetraspanin HMM profile (PF00335) not only in M. grisea but also in other ascomycetes such as C. globosum, S. nodorum, N. crassa, P. anserina and A. nidulans.
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Signature motif of qnorB was identified by using PROSTIE (http://www.prosite.expasy.org/).org/
Heterogeneous elemental composition of bone was identified by using energy dispersive X-ray spectroscopy (EDS).
Microstructure was identified by using scanning electron microscopy and X-ray diffraction.
FITC was identified by using a 530 band pass filter.
FRC24 was identified by using the API Coryne strip (bioMérieux).
N. meningitidis was identified by using standard biochemical tests (17 ).
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