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1 demonstrated 100% positive agreement for the typing of 179 influenza A viruses and 3 influenza B viru
2 ication was confirmed by multilocus sequence typing of 18 clinical isolates at 18 polymorphic loci.
3                                              Typing of 21 polymorphic markers, evenly spanning the CD
4                           HLA-DRB1-DQA1-DQB1 typing of 2182 individuals was evaluated for this study
5       Molecular techniques were used for HLA typing of 219 white patients with systemic lupus erythem
6 t analyses of these families directed marker typing of 23 additional families.
7                          On the basis of the typing of 24 ancestry-informative biallelic single-nucle
8                                    Molecular typing of 246 Staphylococcus aureus isolates from unsele
9 phylococcal chromosome cassette mec (SCCmec) typing of 261 isolates (including all hVISA isolates) re
10                                              Typing of 277 samples from 260 MSM identified distinct C
11 R exhibited 89% concordance with IS1245-RFLP typing of 28 M. avium subspecies avium strains.
12                  DRB1 and TNF microsatellite typing of 297 Caucasian RA patients (132 men, 165 women)
13 tilocus sequence typing and antigen sequence typing of 3 outer membrane protein (OMP) genes: porA var
14 nverted high-resolution, sequence-based, HLA typing of 310 subjects from an ethnically heterogeneous
15 ormed extensive molecular identification and typing of 42 clinical isolates of M. abscessus, M. massi
16 ne marrow transplantation, we performed CD31 typing of 46 recipients of bone marrow (32 without GVHD
17 ultilocus sequence typing (MLST) results for typing of 49 of the 50 isolates; in addition to the one
18 bsp. equisimilis isolates, and attempted emm typing of 5 Streptococcus canis isolates from a recent p
19 ncy of 0.39 (range 0.13-0.71) based upon PCR typing of 54 feline markers.
20                                The molecular typing of 81 pretreatment Helicobacter pylori isolates a
21  stem cell bank that circumvents prospective typing of a large number of individuals.
22 ent mixture of pathogen subtypes, laboratory typing of a subset of clinical cases can provide inferen
23       We demonstrate the simple, multiplexed typing of a variety of epigenetic cancer biomarker 5mC w
24 ed to open a new venue for the aptamer-based typing of a variety of microorganisms using a rapid, eco
25                             Subsequent blood typing of affected family members confirmed the possessi
26                  Therefore, confirmation and typing of amyloid are essential before initiating treatm
27 c types of systemic amyloidoses, unequivocal typing of amyloid deposits is now essential.
28  amyloidosis, histological demonstration and typing of amyloid deposits is still required for a subst
29                                              Typing of amyloid fibrils, a critical determinant of the
30 ly specific and sensitive novel test for the typing of amyloidosis in routine clinical biopsy specime
31                     Current methods used for typing of amyloidosis such as immunohistochemistry have
32  accelerated the study of fine structure and typing of an important inversion in An. stephensi, putti
33  Ion Torrent PGM with Illumina MiSeq for the typing of antimalarial drug resistance genes.
34                      We report on genomewide typing of approximately 10,000 single-nucleotide polymor
35                                Comparison of typing of B. burgdorferi performed directly on 51 patien
36 scriminatory power of allele-based molecular typing of B. pertussis, we have developed a whole-genome
37  of an aptamer-based impedimetric sensor for typing of bacteria (AIST-B) is presented.
38 n of live bacteria and another 40min for the typing of bacteria strains).
39 or the characterization, identification, and typing of bacterial isolates that has value in epidemiol
40                                To facilitate typing of bacterial isolates, we developed a novel genot
41  electronically portable, allowing molecular typing of bacterial pathogens (or other infectious agent
42 cts and has the important advantage over opa typing of being a more precise method of strain characte
43 e accuracy of the method enables the genetic typing of bi- and triallelic single-nucleotide polymorph
44 , gyrB, and gpi, with that of sequence-based typing of bla(OXA-51-like) genes (SBT-bla(OXA-51-like) g
45                    The accurate and reliable typing of blood groups is essential prior to blood trans
46                            We used molecular typing of Borrelia burgdorferi isolates obtained from pa
47                          Multilocus sequence typing of Borrelia hermsii isolates reveals its divergen
48 cular surveillance of noroviruses, including typing of both polymerase and capsid genes, is important
49 t that using MLST as a first step in routine typing of C. difficile followed by WGS for MLST concorda
50                                       Strain typing of C. difficile isolates from the involved hospit
51                                        Stain typing of C. difficile isolates is documenting the sprea
52 rdized protocol and centralized database for typing of C. difficile pathogens will increase comparabi
53 logies for RAPD typing, ribotyping, and PFGE typing of C. diphtheriae strains were improved to enable
54 apid and discriminatory method for molecular typing of C. rugosa in outbreaks.
55 e of real-time PCR for the genotype-specific typing of C. trachomatis strains that cause sexually tra
56                            cagA genotype and typing of cag pathogenicity island genes were poorly pre
57  and, where available, genetic and antigenic typing of case isolates.
58  and, where available, genetic and antigenic typing of case isolates.
59  universally recognized, further careful sub-typing of cases may provide more precise genomic signals
60                                              Typing of class I and II genes was performed by using DN
61 phoresis (PFGE) using SmaI were compared for typing of Clostridium difficile.
62 110 restriction fragment length polymorphism typing of cultured bacteria was used to compare these is
63 d directly on 51 patient skin specimens with typing of cultures originally isolated from the same tis
64                 The detection and successful typing of dengue virus (DENV) from patients with suspect
65 pid, sensitive, and specific approach to the typing of dengue viruses.
66  A technique for the multiplex detection and typing of DENV serotypes 1 to 4 (DENV-1 to DENV-4) from
67                                   Subsequent typing of DNA samples of individual progeny snails showe
68 udy of transplantation is histocompatibility typing of donors and recipients.
69 ired infection (HAI) BioDetection System for typing of E. coli isolates compared well with the result
70 trachomatis and used it specifically for the typing of either eight genovars from D to K or three gen
71 y of molecular methods for the detection and typing of enteroviral infections.
72  virology and reference laboratories for the typing of enteroviruses, for the study of the epidemiolo
73                                    Molecular typing of ESBL-producing E. coli is useful for surveilla
74 he replacement of traditional serology-based typing of Escherichia coli by WGS is supported by user-f
75 ific bacterial strain identification for the typing of Escherichia coli O157:H7 and other gram-negati
76 ypically characterized, including multilocus typing of five genes and whole-genome sequencing.
77 have not been exploited in the diagnosis and typing of flaviviruses.
78 e feasibility of rapid point-of-analysis DNA typing of forensic casework, of mass disaster samples or
79                                DRB1 and DQB1 typing of founders showed that the three haplotypes cont
80 ituations, uncertainty may be reduced by the typing of further siblings, whose disease status may be
81                        Advances in molecular typing of fusariosis would facilitate the study of its e
82 Furthermore, this method is useful for rapid typing of GAS isolates and culture-negative specimens du
83  were prepared for serological and molecular typing of GBS strains based on the Strep-B-Latex aggluti
84                                        Rapid typing of genetic variation at many regions of the genom
85 matography (GP-dHPLC), for the detection and typing of genital HPV using an automated 96-well plate f
86 rase chain reaction, thereby permitting CD31 typing of genomic DNA from additional normal subjects.
87 miological data were combined with molecular typing of gonococcal isolates by a new methodology based
88                                              Typing of gonococcal strains is a valuable tool for the
89                                              Typing of group A Streptococcus (GAS) is crucial for inf
90  (EQA) studies for molecular and serological typing of group B streptococcus (GBS) strains as part of
91  acid-based test for the rapid detection and typing of herpes simplex virus (HSV) DNA was developed a
92                   The accurate detection and typing of high-risk human papillomavirus (HPV) are criti
93 a where improvements are necessary is in the typing of highly similar samples, such as those samples
94                                     Accurate typing of HLA genes with short-read sequencing data has
95 hing of the donor and recipient was based on typing of HLA-A and -B antigens by serologic methods and
96 ical disease (BHWCD), we performed DNA-based typing of HLA-DPB1, HLA-DQB1, and HLA-DRB1 loci on 55 su
97  and -B antigens by serologic methods and by typing of HLA-DRB1 alleles by molecular methods, and don
98     Included were studies in which molecular typing of HLA-DRB1 alleles was performed and in which th
99                                    Molecular typing of HLA-DRB1 and HLA-DQB1 alleles revealed 335 DRB
100 ith a week-48 visit, blood was available for typing of HLA-DRB1 and HLA-DQB1 in 174 (85%) and success
101                                              Typing of HSV isolates may be useful in persons with rec
102 view the different methods for detection and typing of HSV, including light microscopy, culture, sero
103 y for automated high-throughput simultaneous typing of human erythrocyte antigens (HEAs), platelet an
104 co-workers describe the results of classical typing of human leukocyte antigen (HLA) alleles in 1,404
105                             Molecular strain typing of human prion diseases has focused extensively o
106 noise of single-cell data make accurate cell typing of individual cells difficult.
107 s (ChIMP) method to support multi-label cell typing of individual cells jointly profiled via scRNA-se
108 tween different laboratories involved in the typing of individual species.
109 tion of this technology to the detection and typing of influenza and other viruses.
110                                              Typing of influenza virus strains is an important aspect
111 xchange was confirmed by multilocus sequence typing of isolates and of uncultivated natural consortia
112                                              Typing of isolates around the world shows global spread
113            Multilocus enzyme electrophoresis typing of isolates from 19 case patients identified 5 di
114 In addition to case ascertainment, molecular typing of isolates was performed to characterize the out
115 ical information, sputum cultures, molecular typing of isolates, and immunoassays to measure antibodi
116 oped a system, termed "ATLAS" (amplification typing of L1 active subfamilies), that enables the selec
117                    High resolution molecular typing of large, clinically well-defined cohorts has beg
118 ed typing as the gold standard for DNA-based typing of Legionella pneumophila, the Legionella laborat
119 emonstrate the utility of this technique for typing of Listeria monocytogenes, four outbreaks of epiz
120 reased the discrimination possible in strain typing of M. bovis, with the added benefit of an intuiti
121 nd AFLP provide valuable tools for molecular typing of M. bovis.
122 eful tool as a first-line method for routine typing of M. tuberculosis isolates, especially where Bei
123 lity, stability, and reproducibility of PFGE typing of M. tuberculosis.
124             We have compared high resolution typing of major histocompatibility complex class II loci
125 as become the method of choice for molecular typing of many bacterial and fungal pathogens (and non-p
126                                     Sequence typing of Metarhizium isolates revealed four species, wi
127                     Rapid identification and typing of methicillin (meticillin)-resistant Staphylococ
128  2005 to 31 December 2006), performed SCCmec typing of methicillin-resistant S. aureus (MRSA) isolate
129                     Following microsatellite typing of mice with resistant and susceptible phenotypes
130                                       Strain typing of microbial pathogens has two major aims: (i). t
131 tion of a degenerate P[8] primer resulted in typing of most VP4 strains.
132                                          HLA typing of mothers and sons indicated that HLA compatibil
133 fective, allowing for high-throughput SCCmec typing of MRSA isolates.
134 ysis could be used as a screening method for typing of MRSA strains because of the shorter turnaround
135 ssfully validated it for use for the routine typing of MTBC strains in the research and public health
136                          Multilocus sequence typing of multiple isolates from the same procedure reve
137 aneous detection and identification (genetic typing) of multiple enterotoxin (ent) genes.
138 oratory equipment for the large-scale global typing of Mycobacterium avium subspecies paratuberculosi
139                                              Typing of Mycobacterium avium subspecies paratuberculosi
140      Drug resistance surveillance and strain typing of Mycobacterium leprae are necessary to investig
141                                    Molecular typing of Mycobacterium tuberculosis by using IS6110 sho
142                                    Molecular typing of Mycobacterium tuberculosis can be used to eluc
143 is a tool for the molecular characterization/typing of Mycobacterium tuberculosis complex (MTBC) stra
144 it-variable number tandem repeat (MIRU-VNTR) typing of Mycobacterium tuberculosis complex isolates is
145                                              Typing of Mycobacterium tuberculosis could provide a mor
146 duced the IS6110-PvuII kit for semiautomated typing of Mycobacterium tuberculosis using the RiboPrint
147 TR) analysis (MLVA) method for the molecular typing of Mycoplasma pneumoniae.
148                                    Molecular typing of Neisseria gonorrhoeae and contact tracing prov
149                                    Molecular typing of Neisseria gonorrhoeae strains is an important
150 l-time behavioral analyses, rapid functional typing of neural responses via calcium imaging, optimal
151 dvance for point of care applications, blood typing of newborns, and general blood assays in small mo
152 ates that DNA sequence-based variable region typing of NMSB will be necessary to provide precise info
153  (RT)-PCR assays for the rapid detection and typing of NoV strains belonging to genogroups GI and GII
154                                    Molecular typing of NTHi strains revealed that five of nine patien
155 TS may provide a simple procedure for strain typing of O157 and other bacteria and that further evalu
156 eter cultures, blood cultures, and molecular typing of organisms to determine catheter-related coloni
157 , which have been used effectively in strain typing of other bacteria.
158 tself and have been useful for the molecular typing of other organisms.
159 cal microbiology, and it can be utilized for typing of other pathogenic bacteria species.
160 ollections from different locations, and for typing of other species, was not evaluated and needs fur
161                            Biological strain typing of ovine scrapie isolates by serial passage in co
162 sive, and reliable means for epidemiological typing of P. aeruginosa.
163 variable number of tandem repeat (MIRU-VNTR) typing of pairs of isolates taken by sputum sampling: on
164 2 were type specific and correlated with PCR typing of parasites present at the time of infection.
165 ucleotide microarray was developed for rapid typing of pathogens based on analysis of genomic variati
166                                  Prospective typing of patients and donors in unrelated donor search
167 transfusion is to do prior extensive antigen typing of patients' red cells; however, this is not alwa
168                                      Initial typing of pooled material from each sample identified a
169  modelling approaches along with careful sub-typing of protein families will be a powerful combinatio
170                                     Sequence typing of pspA provides an added level of specificity in
171 d independently validated a workflow for the typing of PTC clinical samples into CLIP2-positive and C
172                                      Genetic typing of rabies viruses allowed us to distinguish trend
173 y on the physical map of the human genome by typing of radiation hybrids or screening YAC libraries.
174                                          MVR typing of rare-length alleles indicates that they are co
175                                    Molecular typing of respiratory specimens from 9 patients revealed
176  I sequences were resolved by sequence-based typing of rhesus, cynomolgus and pig-tailed macaques, ne
177 by multilocus sequence typing (MLST) and ABC typing of rRNA genes and determined their homozygosity o
178                                    Molecular typing of S aureus strains was performed by repetitive-s
179 ed with conventional gel electrophoresis for typing of S. aureus isolates of bovine origin.
180 S-PCR) and virulence gene identification for typing of S. aureus strains.
181 typic typing methods for the epidemiological typing of S. enteritidis.
182             Histo-blood group antigen (HBGA) typing of saliva showed that the norovirus strains infec
183 t the discriminatory ability of MLST for the typing of Salmonella is better than that of serotyping a
184                                Overall, MLVA typing of Salmonella serotype Enteritidis had enhanced r
185  Methods for haplotyping and DNA copy-number typing of single cells are paramount for studying genomi
186 ion for multi-omics lineage mapping and cell typing of single cells.
187 ed method has recently been reported for the typing of single nucleotide polymorphisms using single n
188       We present STHD for probabilistic cell typing of single spots in whole-transcriptome spatial tr
189 eloped the CAMML method for multi-label cell typing of single-cell RNA-sequencing (scRNA-seq) data.
190           The method has been applied to the typing of single-nucleotide polymorphisms in PCR product
191                                    Molecular typing of sputum isolates of nonencapsulated Haemophilus
192 ated the use of IPRP HPLC for the sizing and typing of STR alleles from the HUMTHO1 locus.
193  in A. fumigatus; for example, the molecular typing of strains during infection.
194 ng that PFGE may be unsuitable for long-term typing of strains involved in epidemics.
195                                              Typing of strains revealed cocirculation of multiple mul
196 n addition, the molecular identification and typing of strains were also carried out.
197 culosis and used whole genome sequencing for typing of strains.
198 for whole genome sequencing for phylogenomic typing of strains.
199 s a commonly used method for epidemiological typing of Streptococcus pneumoniae and many other bacter
200                                        HLA-C typing of target cells showed that KIR2DS2 recognition w
201                                              Typing of the 104 carriage isolates demonstrated 21 PFGE
202 ed among the isolates by multilocus sequence typing of the 16S rRNA, flaB, gyrB, and glpQ genes.
203 triction fragment length polymorphism (RFLP) typing of the 16S-23S ribosomal DNA intergenic spacer.
204 ucted next-generation sequencing (NGS)-based typing of the 33 human leukocyte antigen (HLA) genes in
205                                    Molecular typing of the abnormal form of the prion protein (PrP(Sc
206                           Detailed molecular typing of the above alleles has previously not been repo
207                                    Molecular typing of the actinomycete Rhodococcus equi is insuffici
208            A technique was developed for the typing of the aoHGE based on the PCR amplification of th
209 rols showed a clear bimodality, enabling the typing of the cells into larger and smaller than average
210                                          MVR typing of the common alleles a1, a2, a3, and a4 shows th
211           We now present results with direct typing of the CYP3A5 genotype for this group of 180 kidn
212  the present study and are now available for typing of the E. coli O157:H7 lineage.
213 e aim of the present study to assess whether typing of the intergenic spacer region by using restrict
214                                              Typing of the isolates (n = 172) identified all 10 GBS s
215 nes from the microcosms as well phylogenetic typing of the isolates showed that ethenotrophs in the s
216  address this, we performed high-density SNP typing of the MHC in >32,000 individuals with IBD, impli
217 tiplex PCR assay allowed simple and accurate typing of the most prevalent clinical serovars of Salmon
218 uencing of the por gene (POR sequencing) and typing of the opa gene (OPA typing) for the characteriza
219 er than either porB nucleotide sequencing or typing of the opa gene.
220                                      The HLA typing of the patient showed HLA-DQ8, which was previous
221 ologic examination is essential for accurate typing of the polyps to predict malignant potential and
222                                              Typing of the porB variable region (VR) is an epidemiolo
223               On MRSA isolates, we performed typing of the staphylococcal cassette chromosome mec (SC
224                        Isolation and genetic typing of the strain of M. tuberculosis responsible, and
225 ved to enable rapid and convenient molecular typing of the strains.
226 ay of intended transplantation by repeat ABO typing of the thawed unit at our transplantation center.
227 ng out ABO and human leukocyte antigen (HLA) typing of the thawed units before transplantation.
228 nts, in addition to correlating single-locus typing of the TP0548 allele with the T pallidum phylogen
229                                    Molecular typing of the tumor by DNA sequencing supports donor der
230 th GRCh38-based workflows, which enabled the typing of the vast majority of structural variant allele
231 acceptable antigens corresponding to the HLA typing of their previous donor (UA-PD) as a proxy for do
232 LA phenotypes, ascertained by low-resolution typing, of their family members.
233                                              Typing of these agents may complement disease assessment
234                              High-resolution typing of these allelic subsets revealed that HLA-DQB1*0
235 xisting methodologies are inadequate for MHC typing of these key model animals.
236 -throughput alternative to direct laboratory typing of these loci and have enabled important findings
237 e opens the possibility of using array-based typing of these loci for human identification, loss-of-h
238 the proband, mapping of the TNX gene and HLA typing of this family suggest recessive inheritance of T
239                          Continued molecular typing of this organism, particularly during outbreaks,
240 lex disease association studies will require typing of thousands of single-nucleotide polymorphisms (
241 ified16S rRNA genes, and multilocus sequence typing of three housekeeping genes confirmed culture pur
242                                              Typing of TNF microsatellite polymorphisms was carried o
243  advance in this technology that permits the typing of two alleles in a single microtiter well.
244 zygosity at the ELN locus was established by typing of two intragenic polymorphisms, quantitative Sou
245 ion (ISR) sequence analysis to the molecular typing of U.S. PDD-associated Treponema isolates.
246 R assay represents a valuable tool for rapid typing of uncharacterized Shigella isolates and provides
247  a chip-based format, including rapid tissue typing of unrelated volunteer donors.
248 horesis was used for molecular epidemiologic typing of vancomycin-resistant enterococci.
249 ucted a case-series investigation, molecular typing of viral isolates, surveys of rates of vaccinatio

 
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