ライフサイエンスコーパス: PCR assay

1 ICU admission were tested using a multiplex PCR assay.

2 g a previously validated EV-D68-specific rRT-PCR assay.

3 , a dual-target total nucleic acid real-time PCR assay.

4 th 1484 (12%) of these cases confirmed on RT-PCR assay.

5 rcial stool antigen assays, and a commercial PCR assay.

6 h those demonstrated by the duplex real-time PCR assay.

7 ty and technical time may be possible with a PCR assay.

8 as measured by an ultrasensitive single-copy PCR assay.

9 A fraction was quantified by quantitative RT-PCR assay.

10 and tested for SARS-CoV-2 using a real-time PCR assay.

11 la invasion antigen, IpaH3, into a multiplex PCR assay.

12 NAs (miRNA), termed S-Poly(T) Plus real-time PCR assay.

13 edding and VL using a real-time quantitative PCR assay.

14 and 65 (47%) were positive by the real-time PCR assay.

15 genes were assayed by quantitative real-time PCR assay.

16 amples and obtain consistent results with RT-PCR assay.

17 positive visits were measured by a real-time PCR assay.

18 A-Seq were corroborated through real-time RT-PCR assay.

19 ies, showing comparable results to real-time PCR assay.

20 the gold standard of tear collection for RT-PCR assay.

21 to reduced inhibition with the one-step ddRT-PCR assay.

22 ults alone, and both also tested positive by PCR assay.

23 t were corroborated by culture or a clinical PCR assay.

24 nosinic-polycytidylic acid using a sensitive PCR assay.

25 as 7.5 h compared to 40.3 h for the standard PCR assay.

26 ts between established LAMP and conventional PCR assays.

27 the reliance on more expensive and laborious PCR assays.

28 en, the Netherlands) and published multiplex PCR assays.

29 ith mRNA detection based principally upon RT-PCR assays.

30 ssion in single samples using repetitive qRT-PCR assays.

31 as revealed by chromatin immunoprecipitation-PCR assays.

32 NA was isolated and used as template for the PCR assays.

33 e G and P genotyped using nested VP4 and VP7 PCR assays.

34 transcription factors was analyzed by using PCR assays.

35 ound to be more sensitive than the real-time PCR assays.

36 f acanthamoebae with four separate real-time PCR assays.

37 n compared to species-specific SARS-CoV-2 RT-PCR assays.

38 We compared the results obtained with ELISA/PCR assays.

39 vity and specificity compared to centralized PCR assays.

40 L, making it an attractive alternative to RT-PCR assays.

41 pared to 10 to 10(4) copies per reaction for PCR assays.

42 including HRV, using quantitative real-time PCR assays.

43 itative real-time polymerase chain reaction (PCR) assay.

44 triplex real-time polymerase chain reaction (PCR) assay.

45 croscopy and by a polymerase chain reaction (PCR) assay.

46 -transcriptase-polymerase-chain-reaction (RT-PCR) assay.

47 in West Africa by polymerase-chain-reaction (PCR) assay.

48 transcription-polymerase chain reaction (RT-PCR) assay.

49 transcriptase-polymerase-chain-reaction (rRT-PCR) assay.

50 -transcriptase-polymerase-chain-reaction (RT-PCR) assay.

51 and mycobacterial polymerase chain reaction (PCR) assays.

52 donors whose samples tested positive on the PCR assay 2 to 7 months after the implicated donation.

53 by culture and negative for norovirus by RT-PCR assay; 4 specimens were positive for rotavirus by en

54 Using multiple real-time PCR assays across the genome combined with near-full-gen

55 cted from cultured isolates and biopsies for PCR assay after which samples were investigated using st

56 nsitive nested reverse transcription-PCR (RT-PCR) assay allowing the rapid detection of TiLV in fish

57 ea lion populations and results suggest that PCR assays alone may grossly underestimate ZcAV exposure

58 The real-time PCR assay also identified two samples with mixed P. falc

59 ted with both ELISAs and the three real-time PCR assays although mustard was not indicated on the foo

60 The new 23S-5S IGS nested PCR assay amplified all 11Rickettsiaspp., but the assays

61 The RT-PCR assay amplifies a segment of the VP1 gene, with an a

62 step real-time reverse transcription PCR (RT-PCR) assays; an accurate sample-to-answer RT-PCR test wo

63 ng using another commercially available HAdV PCR assay and a molecular typing assay for species ident

64 uenza infection was confirmed by means of RT-PCR assay and culture of nasopharyngeal swabs obtained f

65 total of 905 patients tested by real-time RT-PCR assay and next-generation sequencing RT-PCR, 419 (46

66 as demonstrated by using WHV strain-specific PCR assays and (i) finding WHVNY relaxed circular DNA in

67 Using quantitative PCR assays and a fluorescence miRNA sensor, we show that

68 pective samples were resolved with alternate PCR assays and bidirectional sequencing of amplicons.

69 na in situ hybridisation (ISH), quantitative PCR assays and biomarkers of productive and transforming

70 mized set of oligonucleotide primers for qRT-PCR assays and cloned cDNA plasmids corresponding to the

71 re and broad-range and E. rostratum-specific PCR assays and confirmed the presence of fungal DNA in 2

72 StaphSR) and negative for MRSA by all three PCR assays and culture.

73 ime points was confirmed by variant-specific PCR assays and sequence analysis of single-colony cloned

74 -transcription polymerase chain reaction (RT-PCR) assay and a clinical reference standard established

75 , 41 (29%) were positive by the conventional PCR assay, and 65 (47%) were positive by the real-time P

76 for Orientia tsutsugamushi, three different PCR assays, and an IgM IFA.

77 ession was analyzed by using RNA-sequencing, PCR assays, and immunostaining in patients with EoE; cyt

78 es by comparison to the individual real-time PCR assays, and the TAC exhibited an overall 88% (278/31

79 ole in CODD and confirming that the specific PCR assays are an effective differential diagnostic tool

80 Molecular techniques, including PCR assays, are the preferred diagnostic methods and hav

81 B/RIF Ultra (Xpert Ultra), a fully automated PCR assay, as the initial tuberculous meningitis (TBM) d

82 The detection limit of the qRT-PCR assay at 95% probability was 0.28 FFU/ml as determin

83 as unknowns using 10 different quantitative PCR assays at 5 different laboratories.

84 Laboratory-developed PCR assays at the University of Alabama at Birmingham an

85 yme-linked immunosorbent assay (ELISA) and a PCR assay based on amplification of the pan-Aspergillus

86 ental conditions and identified by molecular PCR assay based on the ITS-5.8S rDNA.

87 Finally, a novel multiplex PCR assay, based on random amplified polymorphic DNA (RA

88 A dual-probe real time PCR assay, based on the simultaneous detection of two Ta

89 ignal produced from probe-based RT-RPA or RT-PCR assays can be monitored using LEDs and a smartphone

90 C, Salt Lake City, UT), a highly multiplexed PCR assay, can identify 24 etiologic agents of sepsis (8

91 he 24 human chromosomes that allow for rapid PCR assays capable of capturing the genomic landscape of

92 We compared an FDA-cleared rapid (<20 min) PCR assay (Cobas Liat; Roche Diagnostics) to our routine

93 tica and E. dispar), our tetraplex real-time PCR assay demonstrated levels of sensitivity and specifi

94 fic real-time reverse transcriptase PCR (rRT-PCR) assay described by F.

95 The beacon-based PCR assay designed in the present study is highly specif

96 was assessed with a multiamplicon, real-time PCR assay designed to analyze locations that are regular

97 otypes IA, IB, and IIIA and a singleplex rRT-PCR assay designed to detect all HAV genotypes infecting

98 The RT-PCR assay detected a virus in 59 samples (78%).

99 ng the 201 specimens tested, the CDC Flu A/B PCR assay detected Flu A/B virus in 107 samples (Flu A v

100 qRT-PCR assay detected higher miR-214 expression in the plas

101 Our PCR assays detected DNAs of various infectious agents in

102 In addition, the RT-RPA and RT-PCR assays do not cross-react with dengue and chikunguny

103 Surprisingly, a PCR assay failed to detect SFV infection in any of these

104 mposite reference method (CRM; two validated PCR assays followed by bidirectional sequencing of ampli

105 isolates was used in both PCR and real-time PCR assays followed by electrophoresis or melting temper

106 obtained by the reference method (alternate PCR assays, followed by bidirectional sequencing).

107 erium abscessus group, a multiplex real-time PCR assay for clarithromycin resistance showed 95% (38/4

108 A multiplex nested PCR assay for detection of F. tularensis, B. anthracis,

109 report the development of a robust real-time PCR assay for determining GBS serotypes.

110 y (Luminex, Austin, TX) is a fully automated PCR assay for direct detection of GAS in throat swab spe

111 vailable genomic sequence data to evaluate a PCR assay for distinguishing Campylobacter species.

112 nducible Cas9 (ciCas9) and a droplet digital PCR assay for double-strand breaks (DSB-ddPCR) to invest

113 City, QC, Canada) is an automated real-time PCR assay for GAS detection from throat swab specimens w

114 Through use of a quantitative PCR assay for HHpgV-1, infection was also detected in 17

115 ice junction, we developed a quantitative RT-PCR assay for K-Ras4A and K-Ras4B message capable of mea

116 ssay was more appropriate than the real-time PCR assay for monitoring the response to treatment.

117 re, we describe a SYBR green-based real-time PCR assay for Plasmodium species identification from who

118 sed-tube Linear-After-The-Exponential (LATE)-PCR assay for pyrazinamide susceptibility in Mycobacteri

119 and extensively validated a novel multiplex PCR assay for ST1193 and its characteristic fimH64 (type

120 t and evaluation of a novel TaqMan real-time PCR assay for the detection and identification of Ricket

121 rformance of a simple, inexpensive real-time PCR assay for the detection of 13 carcinogenic HPV types

122 Previously, we developed a real-time PCR assay for the detection of C. auris from surveillanc

123 lopment and validation of a TaqMan real-time PCR assay for the detection of E. rostratum in body flui

124 the present study was to develop a real-time PCR assay for the identification and quantification of f

125 The paper presents a TaqMan real-time PCR assay for the quantitative determination of roe deer

126 of an in-house developed C. auris real-time PCR assay for the rapid screening of patient and environ

127 Real-time PCR assays for beta-globin and Universal 16S rRNA gene t

128 We developed novel quantitative PCR assays for cell-associated (CA) HIV-1 DNA and RNA, t

129 oV-2 and Hologic Panther Fusion real-time RT-PCR assays for detection of viral RNA in stool specimens

130 and tested by clinically validated real-time PCR assays for Ehrlichia spp., Anaplasma phagocytophilum

131 dized approaches (Fusarium disease severity, PCR assays for Fusarium spp. identification and mycotoxi

132 the case of a DNA standard used in real-time PCR assays for human erythropoietin gene, cDNA or transc

133 ted at baseline and at 6 months by real-time PCR assays for MG detection in urine samples, oro-pharyn

134 ensitive in vitro diagnostic (IVD) real-time PCR assays for respiratory viruses, including an assay f

135 e of the RP panel in comparison to real-time PCR assays for the detection of respiratory pathogens.

136 Blood samples were screened by specific PCR assays for the presence of methanogens.

137 T. pallidum PCR assays for the tpp47 gene were performed on all TMA-

138 by a multiplexed polymerase chain reaction (PCR) assay for 22 bacterial, viral, and protozoan gastro

139 a HAdV-specific laboratory-developed PCR (LD-PCR) assay for confirmation.

140 multiplex real-time quantitative RT-PCR (qRT-PCR) assay for DENV-1, -3, and -4 detection but 10-fold

141 ed a real-time reverse transcriptase PCR (RT-PCR) assay for the detection of human enterovirus D68 (E

142 time, reverse transcription-PCR (triplex rRT-PCR) assay for the identification and discrimination of

143 ltiplex real-time polymerase-chain reaction (PCR) assays for 26 respiratory bacteria and viruses.

144 ies and real-time polymerase-chain-reaction (PCR) assays for B. microti DNA on blood-donation samples

145 -transcriptase-polymerase-chain-reaction (RT-PCR) assays for ZIKV in blood, cerebrospinal fluid, and

146 ormed using a laboratory-developed real-time PCR assay; for the postimplementation group, CSF samples

147 ute respiratory syndrome coronavirus 2 on RT-PCR assay from a nose or throat swab.

148 tative real-time reverse transcriptase (qRT) PCR assays from the Centers for Disease Control and Prev

149 aph ID/R blood culture panel (BCP) multiplex PCR assay (Great Basin Scientific, Salt Lake City, UT) f

150 The nested PCR assay had an overall sensitivity of 42.5%, a specifi

151 Modern HCV-RNA RT-PCR assays have excellent sensitivity for diagnosis of p

152 Polymerase chain reaction (PCR) assays have greatly improved the sensitivity detect

153 ial SARS-CoV-2 reverse transcription-PCR (RT-PCR) assays have received Emergency Use Authorization fr

154 of the BD Max enteric bacterial panel (EBP) PCR assay in comparison to culture for the detection of

155 (kappa of >/=0.723) with the RT-LAMP and qRT-PCR assays in detecting the dengue viremic samples.

156 lico approaches for designing and validating PCR assays in the clinical microbiology laboratory.

157 the gold-standard polymerase chain reaction (PCR) assay in an operator-blinded study.

158 -transcriptase-polymerase-chain-reaction (RT-PCR) assay in urine or blood in an enhanced arboviral cl

159 Multiplexed PCR assays increase the detection of diarrheal pathogens

160 Multiplexed polymerase chain reaction (PCR) assays increase the detection of diarrheal pathogen

161 qRT-PCR assay indicated that compound 1 and DBL exposure up-

162 s detection in the upper airway by multiplex PCR assay is common in critically ill hematology patient

163 results also demonstrate that the real-time PCR assay is extremely susceptible to contamination and

164 ssibility for some assays, in well-optimized PCR assays it can reduce the number of amplifiable targe

165 Current RT-PCR assays lack sensitive and reliable positive controls

166 The ELITe InGenius PCR assay limit of detection was 0.16 CFU/PCR test or 4.

167 to compare Veritor with the Lyra SARS-CoV-2 PCR assay (Lyra).

168 ffectiveness, and the simplicity of the ARMS-PCR assay make it a suitable tool to monitor HIVDR patte

169 Multiplex PCR assay may prove helpful for the risk stratification

170 ssay results it has been concluded that SDRT-PCR assay might be an efficient tool for the verificatio

171 recombination was evaluated by quantitative PCR assay of genomic DNA from liver and spleen.

172 confirmed by real-time reverse transcription PCR assay of SARS-CoV-2 RNA.

173 test, histological analysis of biopsies, and PCR assay of ureA, ureB, and ureAB genes.

174 proficiency testing surveys for quantitative PCR assays of cytomegalovirus (CMV), Epstein-Barr virus

175 transcriptase-polymerase chain reaction (RT-PCR) assay of nasal and pharyngeal swabs.

176 We conclude that the LATE PCR assay offers both a rapid and accurate prediction of

177 loped and validated a TaqMan-based real-time PCR assay on the BD Max platform targeting ribosomal DNA

178 fficiency of the SAF microlens array, the SP-PCR assay on the LOC platform demonstrated a high sensit

179 y assessed the impact of a direct HSV (dHSV) PCR assay on the time to result reporting and the durati

180 report results of measurements from multiple PCR assays, on four human genomic DNAs treated with four

181 In contrast to conventional quantitative PCR assays or decoy cell counts, quantitative urinary PV

182 We evaluated a genus- and group-specific PCR assay panel using 284 prosthetic knee synovial fluid

183 Henceforth, this DNAzyme-based fiber optic PCR assay provides a universally applicable, real-time s

184 action of RNA, the multiplex quantitative RT-PCR assay provides rapid diagnosis for the differential

185 wed an agreement of 97.4% with the real-time PCR assay regarding 464 pathogens found in the clinical

186 age, real-time reverse transcription-PCR (RT-PCR) assays remain the molecular test of choice for the

187 This new phylogenomics-based PCR assay represents a valuable tool for rapid typing of

188 -house nested PCR and quantitative real-time PCR assays, respectively.

189 Quantitative PCR assays revealed that HNF4A and PTBP1 mRNAs were up-

190 Global expression analysis and real-time PCR assays revealed that RhERF1 and RhERF4 modulate the

191 lyzed using two EV-D68-specific real-time RT-PCR assays, Sanger sequencing and metatranscriptomic nex

192 ChIP-PCR assays show that as autoinducer concentration increa

193 The multiplex RT-PCR assay showed 95% sensitivity and 100% specificity fo

194 , chromatin immunoprecipitation-quantitative PCR assay showed enrichment of p63 on Sun1, Syne3, and P

195 Each emm real-time PCR assay showed high specificity and accurately identif

196 ) to our routine influenza A and B real-time PCR assay (Simplexa Flu A/B & RSV Direct; Focus Diagnost

197 otal) and three in-house developed real-time PCR assays (singleplex assay for white mustard, singlepl

198 In vitro culturing, multiple real-time PCR assays (sodC, ctrA and siaD(B)) and a PorA PCR-seque

199 etection of M. pneumoniae The ELITe InGenius PCR assay successfully detected 31 distinct M. pneumonia

200 We developed a novel reverse transcription-PCR assay targeting HHV-6B U38, which identified U38 mRN

201 th those of a laboratory-developed real-time PCR assay targeting repMp1 for detection of M. pneumonia

202 The method consisted of a real-time PCR assay targeting the gene encoding for the germ agglu

203 that of the Public Health England real-time PCR assay targeting the RdRp gene.

204 ing a mouse anti-Zika virus antibody, and RT-PCR assays targeting the NS5 and envelope genes.

205 ted a laboratory-developed real-time PCR (LD-PCR) assay targeting stx1, stx2, and rfbEO157 with 2,386

206 eport a tetraplex polymerase chain reaction (PCR) assay targeting two different DNA regions in beef (

207 sing quantitative polymerase chain reaction (PCR) assays targeting the 16S ribosomal RNA gene.

208 n using real-time polymerase chain reaction (PCR) assays targeting the opa gene and porA pseudogene.

209 with real-time reverse transcription-PCR (RT-PCR) assays targeting the ZKV envelope and NS2B genes.

210 evaluated the performance of a new real-time PCR assay - targeting SP2020 (putative transcriptional r

211 he development and evaluation of a real-time PCR assay that can be performed directly on crude DNA ex

212 a hydrolysis probe-based tetraplex real-time PCR assay that can simultaneously detect and differentia

213 sequence, we developed a multiplex touchdown PCR assay that in a single reaction can confirm the spec

214 We demonstrate a simple droplet digital PCR assay that quickly quantitates a range of indel muta

215 data to evaluate a duplex real-time PCR (RT-PCR) assay that targets mapA and ceuE for the detection

216 volving real-time polymerase chain reaction (PCR) assays that facilitate direct analysis of a single

217 llele-specific polymerase chain reaction (AS-PCR) assays that we developed for Bruton tyrosine kinase

218 were positive by an alternative real-time RT-PCR assay (the Trombley assay); three (17%) of 18 sample

219 Compared to fungal culture and the previous PCR assays, this real-time PCR assay was more sensitive.

220 We used a ligation-mediated PCR assay to detect single-strand breaks and double-stra

221 Here, we describe a new triplex RT-PCR assay to detect tox and distinguish C. diphtheriae f

222 The CDC developed a multitarget PCR assay to differentiate B. pertussis, B. holmesii, an

223 meric proteins, we used an emulsion-based RT-PCR assay to link and amplify TCR pairs.

224 We evaluated a real-time PCR assay to predict ciprofloxacin susceptibility using

225 ing the concentration obtained with the deer PCR assay to that obtained with a reference system which

226 Additionally, we compared the qRT-PCR assay to the gold standard direct fluorescent-antibo

227 The ability of PfLDH- or PfIDEh-based immuno-PCR assays to detect <1 parasite/microL suggests that im

228 ed 783 subjects with RDT-/PCR+ results using PCR assays to detect and confirm deletions of the pfhrp2

229 We used quantitative PCR assays to determine if presence or concentrations of

230 y-to-perform and interpret PCR and real-time PCR assays to identify C. auris and related species: Can

231 f South Africa were used in duplex real-time PCR assays to simultaneously detect A. marginale and A.

232 loped a sensitive polymerase chain reaction (PCR) assay to quantify the HBV RNA load in a supernatant

233 cing and novel reverse transcription-PCR (RT-PCR) assays to distinguish all RNA species in the KSHV l

234 Previous multiplex PCR assays took hours to days from order time to result.

235 irus (EBV) load testing in four quantitative PCR assays, treating digital PCR as a reference assay.

236 rrelated well with those of the real-time RT-PCR assays used as benchmarks.

237 utomated sample-to-result real-time C. auris PCR assay using the BD Max open system.

238 Quantitative RT-PCR assays using apical tissues showed that GA biosynthe

239 herefore, integrated DNA barcodes, Real-Time PCR assays using TaqMan probes and UHPLC-HR-MS system pr

240 species-specific polymerase chain reaction (PCR) assay using conserved regions of mitochondrial DNA

241 , sensitive, specific molecular-beacon-based PCR assay, using primers against pfoB gene of Trichomona

242 with those of laboratory-developed real-time PCR assays, using a variety of previously collected clin

243 The emergence of real-time PCR assays utilizing allele-specific molecular detection

244 ether, all data indicated that this hexaplex PCR assay was a simple, fast, sensitive, specific, and c

245 The ARMS-PCR assay was able to detect M184V, T215Y/F, K103N, and

246 In addition, the DNAzyme-based FO-PCR assay was able to discriminate between the MCR-1 and

247 In addition, the real-time PCR assay was applied to the analysis of commercially av

248 c species ofRickettsia The nested 23S-5S IGS PCR assay was coupled with reverse line blot hybridizati

249 A PCR assay was designed to amplify size-distinguishable f

250 lification refractory mutation system (ARMS)-PCR assay was developed and used to investigate the most

251 A real-time PCR assay was developed for detection of crab, a crustac

252 A hexaplex-conventional PCR assay was developed for identification of five meat

253 A direct pentaplex PCR assay was developed for the identification of meat f

254 A novel nested PCR assay was developed to detectRickettsiaspp. in ticks

255 utatum in complex olive matrices a real-time PCR assay was developed, using olive drupe and oil sampl

256 The performance and reproducibility of PCR assay was evaluated by composite reference standard

257 The multiplex PCR assay was found to be a specific and sensitive metho

258 and the previous PCR assays, this real-time PCR assay was more sensitive.

259 A cytb specific PCR assay was proposed to identify A-lineage honeybees,

260 luate viral inactivation, and a quantitative PCR assay was used to quantify DNA damage.

261 Furthermore, a multiplex PCR assay was validated for rapid molecular differentiat

262 The novel PCR assay was validated using clinical samples from huma

263 ea, positivity of N. gonorrhoeae DNA on both PCR assays was present at days 7 or 14 in 13% (95% confi

264 A panel of RT-PCR assays was used to detect noninfluenza respiratory v

265 At baseline, a polymerase-chain-reaction (PCR) assay was performed on blood samples obtained from

266 and sequential chromatin immunoprecipitation-PCR assay, we found that ZNF322A could form a complex wi

267 Here, using a very sensitive multiplex RT-PCR assay, we screened 1,645 formalin-fixed paraffin-emb

268 n assays, Rho activation and quantitative RT-PCR assays, we investigated the mechanism by which CS-GR

269 cer protection, sequencing, and quantitative PCR assays, we show here that the bacterial 3'-5' exonuc

270 The LOD and LOQ of the real-time PCR assay were 0.1% and 0.4%, respectively.

271 The results of the PCR assay were compared to the results of the Centers fo

272 icile by the GeneXpert C. difficile/Epi tcdB PCR assay were tested with the rapid membrane C.

273 When the ELISAs and real-time PCR assays were applied to the analysis of 15 commercial

274 Individual digital droplet PCR assays were developed for 121 variants (average 5/pa

275 PCR assays were developed for each clade-specific marker

276 New multiplex PCR assays were developed for mating-type determination

277 R group" (the results of serial serum GM and PCR assays were provided to treating physicians) and "GM

278 amplification (RCA) and droplet digital (dd)PCR assays were used to quantify residual intrahepatic c

279 AS-PCR assays were used to screen patients with and without

280 transcription polymerase chain reaction (RT-PCR) assays were compared together and with the final di

281 the relative diagnostic sensitivity of CDC's PCR assay when using a different PCR master mix.

282 We have designed a novel triplex real-time PCR assay which simultaneously amplifies the MT-ND4 gene

283 nformation of ITS2, we developed a Real-Time PCR assay which successfully identified herbal material

284 ency, an advantage of the IPDA over standard PCR assays which generate false-negative results in such

285 Gold standard is the real-time PCR assays, which can be conducted at highly equipped la

286 lidated the first direct multiplex real-time PCR assay with melt curve analysis for the identificatio

287 we compared a laboratory-developed multiplex PCR assay with primers and probes specific for each grou

288 real-time quantitative reverse transcriptase PCR assay with single-copy sensitivity targeting the int

289 The limit of detection for FilmArray and qRT-PCR assays with inactivated ZEBOV, based on duplicate po

290 of four quantitative Epstein-Bar virus (EBV) PCR assays with the WHO and ABI standards as examples.

291 -transcriptase-polymerase-chain-reaction (RT-PCR) assay with the use of the target sequences of NP an

292 quantified by reverse transcriptase PCR (RT-PCR) assays with single-copy sensitivity.

293 CDC 2019-nCoV reverse transcriptase PCR [RT-PCR] assay with RNA extraction by eMag [bioMerieux] and

294 ntrol and Prevention SARS-CoV-2 real-time RT-PCR assay, with 95% positive predictive agreement and 10

295 and Panther Fusion, and their associated RT-PCR assays, with a collection of 389 nasopharyngeal spec

296 tified in silico for all deployed diagnostic PCR assays, with the exception of the Cepheid GeneXpert

297 en tested by different real-time and digital PCR assays, with various magnitudes of bias compared to

298 -transcriptase-polymerase-chain-reaction (RT-PCR) assay, with consistent findings on electron microsc

299 onventional stool testing with a multiplexed PCR assay, without an increase in testing costs.

300 To help ensure that PCR assays yield consistent results over time and place,