1 individuals, 9 polymorphic positions of TNF
were typed by a high-throughput genotyping method based
2 ates obtained from four nosocomial outbreaks
were typed by Afut1 restriction fragment length polymorp
3 s, bacteria recovered from colonized animals
were typed by arbitrarily primed PCR, and host inflammat
4 Group B streptococci (GBS)
are typed by capsular polysaccharide type.
5 One hundred N. meningitidis samples
were typed by comparing MALDI-TOF MS fingerprints of the
6 udies, only a subset of all genomic variants
are typed by current, high-throughput, SNP-genotyping pl
7 The false-positive E. faecalis strains
were typed by Diversilab Rep-PCR (bioMerieux, Marcy l'Et
8 am research repository in North America have
been typed by DNA sequencing and interpreted in terms of
9 and twenty isolates of Staphylococcus aureus
were typed by DNA sequence analysis of the X region of t
10 s with spinal cord injury (SCI) over 2 years
were typed by genomic fingerprinting by repetitive-eleme
11 Available respiratory specimens
were typed by HAdV type-specific real-time polymerase ch
12 /56 (80.4%) isolates with discrepant results
were typed by mPCR/RLB as belonging to serotype V.
13 ae strains, including 322 NTHI strains, have
been typed by multilocus sequence typing and found to ha
14 ed out with 48 isolates from Thailand, which
were typed by multilocus sequence typing (MLST), and 44
15 A large number of strains (41.3%) could
be typed by only one of the two methods or could not be
16 -EPIYA and vacuolating cytotoxin gene (vacA)
were typed by PCR and the cagA EPIYA typing was confirme
17 All C. difficile strains
were typed by PCR-ribotyping.
18 able by DL and one was an unrelated DL type)
were typed by PFGE.
19 Adenoviral isolates
were typed by polymerase chain reaction and type-specifi
20 Isolates
were typed by polymerase chain reaction ribotyping.
21 C. difficile isolates
were typed by polymerase chain reaction-ribotyping and a
22 selective media to detect VRE, and isolates
were typed by pulsed field gel electrophoresis.
23 ery tenth MSSA isolate and all MRSA isolates
were typed by pulsed-field gel electrophoresis (PFGE), s
24 skeletal system infections, or endocarditis,
were typed by pulsed-field gel electrophoresis (PFGE).
25 Isolates
were typed by pulsed-field gel electrophoresis (PFGE).
26 typically, six to eight colonies per sample)
were typed by pulsed-field gel electrophoresis (PFGE).
27 CAZ-RGN isolates
were typed by pulsed-field gel electrophoresis (PFGE).
28 all BWH patients from whom VRE were isolated
were typed by pulsed-field gel electrophoresis of SmaI d
29 olates recovered from June 1992 to June 1997
were typed by pulsed-field gel electrophoresis, and the
30 e broth microdilution, and selected isolates
were typed by pulsed-field gel electrophoresis, repetiti
31 Isolates
were typed by pulsed-field gel electrophoresis.
32 patients and HIV-negative patients; isolates
were typed by pulsed-field gel electrophoresis.
33 First, they
are typed by rapid, simple, PCR-based assays; second, th
34 First, they
are typed by rapid, simple, polymerase chain reaction (P
35 he total number of isolates when the strains
were typed by REA, AP-PCR, and PP, respectively.
36 Isolates of Enterobacteriaceae
were typed by repetitive extragenic, palindromic PCR and
37 Isolates
were typed by repetitive PCR (rep-PCR) (DiversiLab Syste
38 tridium difficile isolates from 102 patients
were typed by restriction enzyme analysis (REA), arbitra
39 The Brazilian isolates
were typed by restriction-fragment length polymorphism a
40 Isolates
were typed by sequencing.
41 For 3, samples could not
be typed by serology or amplified by polymerase chain re
42 is isolates collected from 2008 through 2010
were typed by single-nucleotide polymorphism (SNP) analy
43 These isolates
were typed by SmaI-macrorestricted pulsed-field gel elec
44 Collagen
was typed by sodium dodecyl sulfate-polyacrylamide gel e
45 M. tuberculosis strains (n = 56)
were typed by spoligotyping with rep-PCR as a high-resol
46 Intestinal metaplasia
was typed by staining with periodic acid-Schiff/alcian b
47 The IRS1 G972R polymorphism
was typed by TaqMan allele discrimination.
48 s mirabilis collected over a 19-month period
were typed by the Dienes test and ribotyping.
49 ha-hemolytic colonies resembling pneumococci
were typed by the Quellung reaction.
50 A second panel of 59 HCC that had
been typed by transcriptomics and classified in G1 to G6
51 amples were sequenced for the HVI region and
were typed by use of a panel of five polymorphic nuclear
52 KIR genes
were typed by using high-resolution amplicon-based next-
53 virus, and Sapelovirus, and positive samples
were typed by VP1 sequencing.
54 virus, and Sapelovirus; PCR-positive samples
were typed by VP1 sequencing.