ライフサイエンスコーパス: DNA analysis

1 r evaluation, including echocardiography and DNA analysis.

2 en generally supported by more sophisticated DNA analysis.

3 r increased sensitivity on DNA arrays or for DNA analysis.

4 escein is a widely used fluorescent probe in DNA analysis.

5 ighly suitable for characterization by sperm DNA analysis.

6 ar polyacrylamide and polyethylene oxide for DNA analysis.

7 or leap in the efficiency of high-throughput DNA analysis.

8 y the nanoparticles may make them useful for DNA analysis.

9 esis (PFGE) and random amplified polymorphic DNA analysis.

10 st lobules or ducts in 9 cases available for DNA analysis.

11 sue DNA analyses were also negative by stool DNA analysis.

12 sequence and by random amplified polymorphic DNA analysis.

13 with FDCM underwent clinical evaluation and DNA analysis.

14 ilm can improve the MALDI-TOF performance in DNA analysis.

15 re examined for O. formigenes by culture and DNA analysis.

16 erase chain reaction (PCR) and Southern blot DNA analysis.

17 ng a 32-gauge needle and underwent cell-free DNA analysis.

18 equences may be observed after mitochondrial DNA analysis.

19 ssfully detected through the maternal plasma DNA analysis.

20 ociation and natural selection to non-coding DNA analysis.

21 distinct phenotypical appearance, as well as DNA analysis.

22 ected, portable device that allows real-time DNA analysis.

23 ing galactosylceramidase (GALC) activity and DNA analysis.

24 e/consensus IGS sequence, as well as genomic DNA analysis.

25 or the authentication of seafood by means of DNA analysis.

26 on include performing cyst wall cytology and DNA analysis.

27 CR/LiPA25 HPV genotyping system was used for DNA analysis.

28 ational frameshift as shown by complementary DNA analysis.

29 tedness using randomly amplified polymorphic DNA analysis.

30 and 304 nasal samples were eligible for HPV DNA analysis.

31 nd screen samples for radiocarbon dating and DNA analysis.

32 nces, which provides another means for rapid DNA analysis.

33 ies that exist in Hawaii using mitochondrial DNA analysis.

34 etection applications such as nanopore-based DNA analysis.

35 6 patients with blood available for germline DNA analysis.

36 testing procedures, either skin biopsies or DNA analysis.

37 ew designs for lab-on-a-chip devices used in DNA analysis.

38 ny legal systems have developed for forensic DNA analysis.

39 supporting stroma comprised, by murine Cot-1 DNA analysis, 30% of the tumor.

40 tudy who provided baseline blood samples for DNA analysis, 374 suffered first myocardial infarction a

41 rated into the microchip for high-throughput DNA analysis, a miniaturized purification process must b

42 ious studies on morphology and mitochondrial DNA analysis, a number of issues regarding the details o

43 Finally, circulating tumor DNA analysis accurately measured subclone abundance and

44 rs offers the promise of rapid, miniaturized DNA analysis across various biotechnological application

45 Here we developed parallel RNA and DNA analysis after deep sequencing (PRDD-seq), which com

46 By 16S ribosomal DNA analysis, all six permafrost isolates were identifie

47 suggested by morphological and mitochondrial DNA analysis alone.

48 Our ancient DNA analysis also revealed that a Viking expedition incl

49 mitochondrial pathology by histochemical and DNA analysis and a poor response to immunosuppressive th

50 another optimal skeletal element for ancient DNA analysis and add to a growing toolkit of sampling me

51 Participants provided blood for DNA analysis and cancer family history, and cancer treat

52 ection limits for other applications such as DNA analysis and clinical diagnostics.

53 discuss 'Type II' REases, the kind used for DNA analysis and cloning.

54 each visit, a cervical cell specimen for HPV DNA analysis and cytology and a fasting blood sample to

55 network analysis, single fibre mitochondrial DNA analysis and deep re-sequencing of mitochondrial DNA

56 omic taxonomic identification, mitochondrial DNA analysis and direct radiocarbon dating of human rema

57 6-diamidino-2-phenylindole for simultaneous DNA analysis and immunophenotyping.

58 with those of randomly amplified polymorphic DNA analysis and internally transcribed spacer region se

59 , as defined by random-amplified polymorphic DNA analysis and pulsed-field gel electrophoresis.

60 Current identification methods, such as DNA analysis and radiocarbon dating, are costly and dest

61 This work reviews cutting-edge methods for DNA analysis and recommends avenues to improve biosecuri

62 A comparison of the B19 DNA analysis and the results of TAB indicated a statisti

63 tic cell death at 72 h that was supported by DNA analysis and TUNEL staining.

64 Study provided baseline blood specimens for DNA analysis and were followed prospectively for a mean

65 bivariate proliferating nuclear cell antigen/DNA analysis) and activation (percent lymphocytes expres

66 and granulocyte lineages to donor origin by DNA analysis, and (4) increased ADA activity and metabol

67 l vs external (inside vs outside the capsid) DNA analysis, and contaminated samples.

68 cations in biophysics, clinical diagnostics, DNA analysis, and drug discovery.

69 rcomas (UPS), longitudinal circulating tumor DNA analysis, and evolutionary biology computational pip

70 ctrophoresis, randomly amplified polymorphic DNA analysis, and phage typing as epidemiological tools.

71 ssed using laser capture microdissection and DNA analysis, and revealed no significant intratumor het

72 vidence for senescence; normal karyotype and DNA analysis; and expression of vimentin, CD90 (thy1.1),

73 Two mitochondrial DNA analysis approaches were explored to detect the pres

74 ations of these submicrometer structures for DNA analysis are discussed.

75 n disorders, as well as in the technology of DNA analysis, are rapidly changing the landscape of mole

76 d explore how advances in circulating tumour DNA analysis, artificial intelligence and multi-omics mi

77 ular subtypes of RS and highlights cell-free DNA analysis as a potential tool for early diagnosis and

78 s study, young patients identified by direct DNA analysis as carriers of a RET mutation characteristi

79 pecific variants was used for ctDNA and cHPV DNA analysis at baseline, cycle 3 day 1 (C3D1, post-CRT)

80 ensitivity of 85% to detect SCNAs defined by DNA analysis, at high specificity (~95%).

81 ion has the potential to impact the forensic DNA analysis backlog of sexual assault cases by circumve

82 highlight the potential of high-performance DNA analysis based on miniaturized all-electronic settin

83 tly verified by random amplified polymorphic DNA analysis-based genotyping and by restriction enzyme

84 sequencing required for genome-wide ancient DNA analysis by a median of around 250-fold, allowing us

85 ted vaginal swab specimens were sent for HPV DNA analysis by L1 consensus polymerase chain reaction f

86 itives improve sensitivity and resolution of DNA analysis by MALDI.

87 DNA analysis by matrix-assisted laser desorption/ionizat

88 Quantitative trait locus mapping and genomic DNA analysis by microarray hybridization were used to id

89 es in these diseases have largely focused on DNA analysis by next-generation sequencing techniques, i

90 ere collected, at 4-month intervals, for HPV-DNA analysis by polymerase chain reaction.

91 DNA analysis by this method identified two major cluster

92 e of European ancestry and were targeted for DNA analysis by use of probands with a heavy-smoking phe

93 Body fluids can easily be identified, and DNA analysis can be used to link a stain found at a crim

94 Circulating tumour DNA analysis can be used to track tumour burden and anal

95 m) surface improves the MALDI performance in DNA analysis compared to the commonly used metal surface

96 was performed in order to analyze realistic DNA analysis conditions within microdevices.

97 Subsequent DNA analysis confirmed 5 of the additionally identified

98 DNA analysis confirmed that nuclear DNA was identical to

99 ther characterization through morphology and DNA analysis confirmed these candidates as Lasiodiplodia

100 sors including aptasensors, immunoassays and DNA analysis, cytosensor, molecularly imprinted sensors,

101 The diagnostic reliability of circulating DNA analysis depends on the fractional concentration of

102 logy for the construction of high-throughput DNA analysis devices.

103 Off-target DNA analysis did not detect off-target editing in treate

104 All patients who were sampled for DNA analysis due to molecularly unconfirmed retinal dyst

105 In recent years, honey has become subject of DNA analysis due to potential risks evoked by microorgan

106 DNA analysis excluded mutations in the transforming grow

107 DNA analysis failed to detect mutations in the genes enc

108 nasal potential difference measurement, and DNA analysis for additional mutations.

109 On-site DNA analysis for diagnostic or forensic purposes is much

110 ion and emphasize the importance of parental DNA analysis for establishing an etiologic relation betw

111 lood-lymphocyte karyotype and the results of DNA analysis for fragile-X syndrome and of other routine

112 med by polymerase chain reaction (PCR)-based DNA analysis for polymorphic short tandem tetrameric rep

113 ical sensitivity, and underwent both nuclear DNA analysis for SOD2 variants and mitochondrial haplogr

114 cing innovations from fields such as ancient DNA analysis, forensics can deliver long-awaited answers

115 Cheek swab samples were obtained for DNA analysis from 116 case/parent trios.

116 Skin swab samples were obtained for DNA analysis from 4 sites around the abscess site (herea

117 s that are more than a million years old.(2) DNA analysis from hair is a well-established approach(3)

118 report an optimised pipeline for faecal host DNA analysis from the point-of-collection to droplet dig

119 A) that we developed for this assay, genomic DNA analysis from thirteen relapsed patients revealed th

120 1) or by combining the trypsinogen test with DNA analysis (from July 1991 through June 1994).

121 Multiple target DNA analysis gave over 86% detection of total TRFs predi

122 be predominantly maternal, and mitochondrial DNA analysis has become a standard taxonomic tool.

123 Although DNA analysis has been carried out successfully in both c

124 Environmental DNA analysis has emerged as a key component of biodivers

125 Whilst DNA analysis has helped to combat this type of fraud som

126 As DNA analysis has revolutionized forensic criminology, we

127 During the past 10 years, DNA analysis has revolutionized the determination of ide

128 advances in the sensitivity and accuracy of DNA analysis have allowed for genotyping of cfDNA for so

129 Advances in DNA analysis have substantially affected clinical practi

130 oach for non-invasive, direct, and efficient DNA analysis, herein, we present a promising strategy fo

131 Thus, our ancient DNA analysis identifies DNA from neurotoxigenic C. tetan

132 Nuclear DNA analysis identifies the presumed maker or wearer of

133 We performed DNA analysis in 44 of these patients to search for a gen

134 DNA analysis in 47 cases (68%) revealed a significant as

135 t and simplified magnetic bead actuation for DNA analysis in a continuous flow platform with minimal

136 This study utilises circulating tumour DNA analysis in a large clinical trial to demonstrate th

137 liable instruments may facilitate the use of DNA analysis in applications such as rapid medical diagn

138 ctional genomics, proteomics, and regulatory DNA analysis in essentially any transformed human cell t

139 Here, we demonstrate direct DNA analysis in paper-based devices, uniquely enabled by

140 s 1 and 2, which will help limit unnecessary DNA analysis in the diagnosis and management of this gen

141 diagnosis was undertaken by chorionic villus DNA analysis in two unrelated families with the inherite

142 ll 25 Cryptosporidium isolates submitted for DNA analysis, including 3 from the ill foodhandler, were

143 ement efficient sample-handling practices in DNA analysis, including DNA fragment sizing flow cytomet

144 Genomic DNA analysis indicates that the 17-amino-acid insert is

145 ration or, conversely, for low cost portable DNA analysis instruments in point-of-care medical diagno

146 However, the prevailing methods for DNA analysis involve a series of tedious and complicated

147 Current experience suggests that DNA analysis is a better test for diagnosis as compared

148 DNA analysis is a fast and economic tool to identify pla

149 DNA analysis is essential for diagnosis and monitoring o

150 DNA analysis is making a valuable contribution to the un

151 This shows that DNA analysis is necessary to exclude emerin mutations in

152 Thus, circulating tumor DNA analysis is perhaps one of the most practical and pr

153 s microplate and scanner for high-throughput DNA analysis is presented.

154 In China, circulating tumor DNA analysis is widely used and numerous assays are avai

155 ogenomics, also known as genome-wide ancient DNA analysis, is transforming our understanding of the h

156 The standard protocols for DNA analysis largely involve polymerase chain reaction (

157 bone marker assessment (ICTP) and microbial DNA analysis (levels and proportions of 40 bacterial spe

158 evaluated for cell survival, cell number by DNA analysis, matrix production by particle exclusion as

159 g molecular techniques such as 16S ribosomal DNA analysis may lead to interventions that shift the va

160 nostic modalities based on muscle biopsy and DNA analysis mean that diagnoses within the heterogeneou

161 In the present work, a barcode-DNA analysis method is described for the detection of pl

162 (ENFSI) and the Scientific Working Group on DNA Analysis Methods (SWGDAM) using 500 samples.

163 ing data from the Technical Working Group on DNA Analysis Methods (TWGDAM)-sponsored "Large Fragment

164 below the sensitivity limitations of routine DNA analysis methods.

165 ers in tissues, based upon quantitative flaB DNA analysis, nor did treatment affect RNA levels of sev

166 DNA analysis of a human pituitary tumor, breast carcinom

167 was shown by immunofluorescence staining and DNA analysis of biopsied tissue.

168 DNA analysis of C57BL/6 mice from common commercial vend

169 microarray sensors was developed to perform DNA analysis of complex biological sample solutions.

170 Gilbert et al. presented DNA analysis of coprolites recovered from an Oregon cave

171 ng decontamination procedures during ancient DNA analysis of dental calculus to reduce contaminant DN

172 We examine this problem through ancient DNA analysis of early 16(th) century cattle bone from Se

173 DNA analysis of eight periodontal bacteria was performed

174 reports results obtained from microsatellite DNA analysis of genetic structure for populations of the

175 related disease was confirmed by comparative DNA analysis of genomic sequences from the donor liver,

176 50 years; this was later challenged based on DNA analysis of historical herbarium specimens.

177 Ancient DNA analysis of human oral microbial communities within

178 DNA analysis of members of the extended family revealed

179 was assessed by random amplified polymorphic DNA analysis of multiple H. pylori clones from each pati

180 B and T cells, similar results were seen on DNA analysis of muscle, but these mice also demonstrated

181 ators with the immediate capacity to perform DNA analysis of normal and diseased genomes in a global

182 Forensic DNA analysis of samples obtained from sexual assault evi

183 Forensic DNA analysis of sexual assault evidence requires separat

184 DNA analysis of single blastomeres indicating whether em

185 use collagen mass fingerprinting and ancient DNA analysis of some of the first stratified and directl

186 d extinct taxa, we have conducted an ancient DNA analysis of subfossil species.

187 Checkerboard hybridization DNA analysis of subgingival plaque from ligated sextants

188 Single-molecule DNA analysis of testicular germ cells isolated by laser

189 Primate DNA analysis of the same loci revealed one human haploty

190 tact p16 and 10 lacked its protein and mRNA; DNA analysis of these 10 cell lines showed 2 homozygous

191 DNA analysis of these cell lines, whose genome is clonal

192 The RFLP markers were tested by gel blot DNA analysis of wheat group 1 nullisomic-tetrasomic line

193 cular alterations, use of circulating tumour DNA, analysis of the gut microbiome, as well as the role

194 have developed a highly sensitive method for DNA analysis on 3D gel element microarrays, a technique

195 42), in situ detection of DNA fragments, and DNA analysis on agarose gels indicated that apoptosis wa

196 rated by DNA fragmentation and quantified by DNA analysis on FACS, yet the majority of the cells died

197 Circulating tumor DNA analysis, once sensitive and broad enough, will acce

198 Conclusions and Relevance: Circulating tumor DNA analysis, once sensitive and broad enough, will acce

199 genotyping, and random amplified polymorphic DNA analysis, over 50% of papG-positive fecal E. coli co

200 On the basis of DNA analysis, overall prevalence of anal HPV infection w

201 ts Stratified by RAS Status from Circulating DNA Analysis) phase 2 randomized clinical trial.

202 Phylogenetic rRNA-encoding DNA analysis places many of the hyperthermophilic Archae

203 Compared with tissue-based tumour DNA analysis, plasma ctDNA is more convenient to test, m

204 d to improve the sensitivity of microfluidic DNA analysis platforms.

205 uit for the delivery of a step change in the DNA analysis process: A fully integrated instrument for

206 While DNA analysis provides individualization, it lacks inform

207 Cloning and DNA analysis revealed 30 DNA sequences and included eigh

208 DNA analysis revealed a heterozygous CAA-->TAA mutation

209 DNA analysis revealed a homozygous 15-base pair (bp) in-

210 The patient's DNA analysis revealed a homozygous nucleotide exchange c

211 Sperm DNA analysis revealed a second class of mutation occurri

212 Genomic DNA analysis revealed a T-->G mutation at the splice don

213 Genomic DNA analysis revealed eight epidemiologically distinct g

214 Whole heart genomic DNA analysis revealed iterative oxidative cytosine modif

215 DNA analysis revealed mutations in DPM2, 1 of the subuni

216 Genomic DNA analysis revealed substantial methylation of the Ubi

217 Microscopic investigation and 16S ribosomal DNA analysis revealed that a previously overlooked bacte

218 Both immunohistochemical and genomic DNA analysis revealed that in vivo, sorted CD8 alpha+ DC

219 Genomic DNA analysis revealed that the apple PGIP probably belon

220 DNA analysis revealed that the OHSt patients have 1 of 2

221 tion to primary bile acids, was confirmed by DNA analysis revealing a missense mutation (S52P) in the

222 Double Stranded Genomic Linkers for Improved DNA Analysis (RIGID-DNA).

223 Radiocarbon dating and DNA analysis show that the rib is associated with the ot

224 Plasmid DNA analysis showed a high degree of heterogeneity among

225 DNA analysis showed a smear pattern characteristic of ce

226 Mitochondrial DNA analysis showed multiple deletions in 90% of muscles

227 Buffy coat DNA analysis showed that 75-85% were EBV DNA-positive in

228 Sequential circulating tumor DNA analysis showed that changes to FGFRm correlated wit

229 s were then generated by Affymetrix GeneChip DNA Analysis Software.

230 ices may provide significant improvements in DNA analysis speed, portability, and cost.

231 Here, we present ancient DNA analysis, stable isotope data of oxygen, and radioge

232 In vitro protein/DNA analysis suggests that one of the sites is a TEF-2-l

233 Finally, ancient DNA analysis suggests the spring-run allele was abundant

234 olved and quantified by the high-performance DNA analysis system, a high-throughput, multichannel, mi

235 n successfully coupled to form an integrated DNA analysis system.

236 neration of low-power, portable microfluidic DNA analysis systems.

237 the possibility of more practical integrated DNA analysis systems.

238 Melt (HRM) is a versatile and rapid post-PCR DNA analysis technique primarily used to differentiate s

239 spective encourages use of rapidly advancing DNA analysis techniques to quantify mutational burden in

240 ymatic kinetics, and when coupled with other DNA analysis techniques, this could be used to construct

241 n subsequently be studied using conventional DNA analysis technologies.

242 solates appeared to be less heterogeneous by DNA analysis than isolates from other regions.

243 k genomic scanning (RLGS), a high-resolution DNA analysis that separates labeled NotI fragments in tw

244 ing a powerful new technology, environmental DNA analysis, that enabled us to characterize the site c

245 For single-cell genomic DNA analysis, the agarose-encapsulated DNA is physically

246 cpzUS) and have determined, by mitochondrial DNA analysis, the subspecies identity of all known SIVcp

247 On DNA analysis there was no evidence of meiotic recombinat

248 ent of semi-automated equipment to assist in DNA analysis, there has been a volley of articles on the

249 For DNA analysis, this technique apparently produces a more

250 DNA is more sensitive than circulating tumor DNA analysis to detect and monitor tumor burden in patie

251 models, agent-based simulations, and ancient DNA analysis to dissect and quantify the roles of cultur

252 h applications spanning from geolocation and DNA analysis to facial recognition and forensic identifi

253 istory of pancreatitis and one was proven by DNA analysis to have hereditary pancreatitis.

254 behavioral research coupled with historical DNA analysis to reveal that coevolution with hosts under

255 tracking and moth neurophysiology with fecal DNA analysis to show that the barbastelle, Barbastella b

256 le subjects submitted one stool specimen for DNA analysis, underwent standard Hemoccult II testing, a

257 In the present study, DNA analysis using COI confirms species identity as the

258 Interest in improving the speed of DNA analysis via capillary electrophoresis has led to ef

259 DNA analysis was carried out in 12 affected and 3 nonaff

260 quence-specific labeling and single-molecule DNA analysis was evaluated through chromatographic and o

261 , but a change of mutational status based on DNA analysis was found in only 4 matched tumors (3.0%).

262 enotype (with exception of families in which DNA analysis was not available).

263 DNA analysis was performed by direct automated sequencin

264 A genome-wide methylation DNA analysis was performed using microarray hybridizatio

265 present study, BOX-polymerase chain reaction DNA analysis was used to characterize nonserotypeable S.

266 t, according to random amplified polymorphic DNA analysis, was phylogenetically distant from the "J96

267 e spheres, relative to the four spheres with DNA analysis, we suspect that many of them were made by

268 Blood specimens for genomic DNA analysis were collected before random assignment in

269 information, family histories, and blood for DNA analysis were obtained from 263 women with breast ca

270 tance testing or subtype assessment based on DNA analysis, when HIV RNA genotypic assessment is not p

271 l analogous to that used for double-stranded DNA analysis, where fluorescent intercalating dyes are s

272 alpha-hemolysin pores, are commonly used for DNA analysis, whereas synthetic solid-state nanopores ha

273 This mutation (Ser131Cys) was confirmed by DNA analysis, which identified a single-base change of c

274 s for sex determination without resorting to DNA analysis, which requires good DNA survival and is ti

275 at disease progression for circulating tumor DNA analysis, which will be correlated with clinical out

276 while maximizing the likelihood that ancient DNA analysis will produce useable results.

277 Polymerase chain reaction DNA analysis with BOX primers demonstrated that 12 HIV-i

278 When comparing these results for DNA analysis with previously reported limits for protein

279 nica by using randomly amplified polymorphic DNA analysis with the primer DKU49.