ライフサイエンスコーパス: be typed by

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 /56 (80.4%) isolates with discrepant results were typed by mPCR/RLB as belonging to serotype V.

12 ae strains, including 322 NTHI strains, have been typed by multilocus sequence typing and found to ha

13 ed out with 48 isolates from Thailand, which were typed by multilocus sequence typing (MLST), and 44

14 A large number of strains (41.3%) could be typed by only one of the two methods or could not be

15 -EPIYA and vacuolating cytotoxin gene (vacA) were typed by PCR and the cagA EPIYA typing was confirme

16 All C. difficile strains were typed by PCR-ribotyping.

17 able by DL and one was an unrelated DL type) were typed by PFGE.

18 Adenoviral isolates were typed by polymerase chain reaction and type-specifi

19 Isolates were typed by polymerase chain reaction ribotyping.

20 C. difficile isolates were typed by polymerase chain reaction-ribotyping and a

21 selective media to detect VRE, and isolates were typed by pulsed field gel electrophoresis.

22 ery tenth MSSA isolate and all MRSA isolates were typed by pulsed-field gel electrophoresis (PFGE), s

23 Isolates were typed by pulsed-field gel electrophoresis (PFGE).

24 typically, six to eight colonies per sample) were typed by pulsed-field gel electrophoresis (PFGE).

25 CAZ-RGN isolates were typed by pulsed-field gel electrophoresis (PFGE).

26 skeletal system infections, or endocarditis, were typed by pulsed-field gel electrophoresis (PFGE).

27 all BWH patients from whom VRE were isolated were typed by pulsed-field gel electrophoresis of SmaI d

28 olates recovered from June 1992 to June 1997 were typed by pulsed-field gel electrophoresis, and the

29 e broth microdilution, and selected isolates were typed by pulsed-field gel electrophoresis, repetiti

30 Isolates were typed by pulsed-field gel electrophoresis.

31 patients and HIV-negative patients; isolates were typed by pulsed-field gel electrophoresis.

32 First, they are typed by rapid, simple, PCR-based assays; second, th

33 First, they are typed by rapid, simple, polymerase chain reaction (P

34 he total number of isolates when the strains were typed by REA, AP-PCR, and PP, respectively.

35 Isolates of Enterobacteriaceae were typed by repetitive extragenic, palindromic PCR and

36 Isolates were typed by repetitive PCR (rep-PCR) (DiversiLab Syste

37 tridium difficile isolates from 102 patients were typed by restriction enzyme analysis (REA), arbitra

38 The Brazilian isolates were typed by restriction-fragment length polymorphism a

39 Isolates were typed by sequencing.

40 For 3, samples could not be typed by serology or amplified by polymerase chain re

41 is isolates collected from 2008 through 2010 were typed by single-nucleotide polymorphism (SNP) analy

42 These isolates were typed by SmaI-macrorestricted pulsed-field gel elec

43 Collagen was typed by sodium dodecyl sulfate-polyacrylamide gel e

44 M. tuberculosis strains (n = 56) were typed by spoligotyping with rep-PCR as a high-resol

45 Intestinal metaplasia was typed by staining with periodic acid-Schiff/alcian b

46 The IRS1 G972R polymorphism was typed by TaqMan allele discrimination.

47 s mirabilis collected over a 19-month period were typed by the Dienes test and ribotyping.

48 ha-hemolytic colonies resembling pneumococci were typed by the Quellung reaction.

49 A second panel of 59 HCC that had been typed by transcriptomics and classified in G1 to G6

50 amples were sequenced for the HVI region and were typed by use of a panel of five polymorphic nuclear

51 virus, and Sapelovirus, and positive samples were typed by VP1 sequencing.

52 virus, and Sapelovirus; PCR-positive samples were typed by VP1 sequencing.