ライフサイエンスコーパス: next-generation sequencing

1 the methylation patterns were visualized by Next Generation Sequencing.

2 es that this strategy might prove useful for next generation sequencing.

3 virus genes were identified via metagenomic next generation sequencing.

4 of methylome, transcriptome and miRNA using Next Generation Sequencing.

5 use of FFPET for heritable CV disorders via next-generation sequencing.

6 tors can now be profiled on a large scale by next-generation sequencing.

7 S who underwent kidney transplantation using next-generation sequencing.

8 temperature gradient gel electrophoresis and next-generation sequencing.

9 ates the design of multiplex PCR primers for next-generation sequencing.

10 otide synthesis, yeast display screening and next-generation sequencing.

11 apping, Sanger sequencing, and gene-targeted next-generation sequencing.

12 ethod to quantify errors in synthetic DNA by next-generation sequencing.

13 ions in 25 cancer susceptibility genes using next-generation sequencing.

14 vealed in model plants using high-throughput next-generation sequencing.

15 NA is eluted from the TF and sequenced using next-generation sequencing.

16 g genome-wide chemical mutagenesis allied to next-generation sequencing.

17 ntification of each mutant's abundance using next-generation sequencing.

18 carcinoma (ccRCC) has been uncovered through next-generation sequencing.

19 ant collections by combinatorial pooling and next-generation sequencing.

20 via multiplexed assembly and sequenced using next-generation sequencing.

21 framework that is based on gene capture and "next-generation" sequencing.

22 the present study, which was facilitated by next-generation sequencing, 96 SHFV body TRSs were ident

23 This report demonstrates that metagenomic next generation sequencing allows for unbiased pathogen

24 Extensive multiplexing in combination with next-generation sequencing allows affordable ultra-deep

25 Serial next-generation sequencing analysis of 28 genes in 16 pa

26 Next-generation sequencing analysis of chromosomal copy

27 a sample of our co-location intervals using next generation sequencing and functional annotation, in

28 ' SHAPE data is now routinely collected with next generation sequencing and/or capillary sequencers.

29 d transposon insertion library combined with next-generation sequencing and a mouse model of infectio

30 The introduction of next-generation sequencing and array-based technologies

31 We provide an overview of the main next-generation sequencing and array-based technologies

32 enome sequences was initially obtained using next-generation sequencing and completed with Sanger seq

33 3 cases previously characterized by targeted next-generation sequencing and copy number array.

34 The quality of the library was assessed by next-generation sequencing and detailed bioinformatics a

35 We applied genetic linkage analysis and next-generation sequencing and functional analyses of NF

36 filed MYC and BCL2 genetic alterations using next-generation sequencing and high-resolution SNP array

37 Here, we used next-generation sequencing and quantitative real-time PC

38 proach that integrates sequencing reads from next-generation sequencing and single-molecule sequencin

39 r rat lungs and whole blood were analyzed by next-generation sequencing and the changes by radiation

40 n a recent study, Mareschal et al. performed next-generation sequencing and whole-exome sequencing, i

41 method uses manual 4D combinatorial pooling, next-generation sequencing, and a Bayesian inference alg

42 By expression analysis, next-generation sequencing, and immunohistochemical exam

43 esign multiplex PCR experiments suitable for next-generation sequencing, and simplifies retooling tar

44 rmation of variant identity by barcoding and next-generation sequencing, and stratification of cancer

45 genetic pathogenesis in this family using a next generation sequencing approach.

46 olecule overlapping reads (SMOR), a targeted next-generation sequencing approach that dramatically re

47 e Bemisia puparium are characterised using a Next-Generation Sequencing approach.

48 Moreover, next generation sequencing approaches are more accurate

49 ng strategy to facilitate future coupling to next generation sequencing approaches.

50 Emergent data from cultivation and next-generation sequencing approaches continue to provid

51 Here we use next-generation sequencing approaches to examine and qua

52 Here we have used next-generation sequencing approaches to identify de nov

53 With the development of next-generation sequencing approaches, biochemical and g

54 marriages, we have developed a gene-targeted next generation sequencing array consisting of 38 genes

55 ity of tumour genomic LOH, quantified with a next-generation sequencing assay, to predict response to

56 ts in 2016 were obtained using a metagenomic next-generation sequencing assay.

57 lopment of "OG-Seq" to sequence OG sites via next-generation sequencing at approximately 0.15-kb reso

58 cular genetic approaches, including targeted next-generation sequencing, autozygosity mapping, and ap

59 xpress and GenBoard enable broad adoption of next generation sequencing based inquiries by the Dictyo

60 We used next-generation sequencing-based techniques to identify

61 Next generation sequencing, bioinformatics, and segregat

62 Metagenomic next generation sequencing can identify unusual or novel

63 yndrome, and sequencing of specific genes or next-generation sequencing can determine or confirm the

64 ouse limbs at embryonic day 12.5 followed by next-generation sequencing (ChIP-seq).

65 tool for handling all studies which include next generation sequencing data.

66 ying patient-specific tumor neoantigens from next generation sequencing data.

67 characterize these variations accurately in next generation sequencing data.

68 introduce Germline Mutation Scoring Tool fOr Next-generation sEquencing data (GeMSTONE), a cloud-base

69 h respect to the incorporation of -omics and next-generation sequencing data and continual improvemen

70 Based on use of next-generation sequencing data for characterizing epige

71 gration site analysis web server, to analyze next-generation sequencing data for retroviral vector in

72 identification of microbial genomes based on next-generation sequencing data is a challenging problem

73 Analysis of next-generation sequencing data often results in a list

74 e methods makes them particularly useful for next-generation sequencing data processing and analysis.

75 The next-generation sequencing data provided a previously un

76 Next-generation sequencing data were generated using the

77 dissimilarity between two long sequences or Next-Generation Sequencing data with the Markov models o

78 for identifying novel cancer risk loci from next-generation sequencing data, with iterative data ana

79 l to identify rare variants in heterogeneous next-generation sequencing data.

80 purpose software framework for management of next-generation sequencing data.

81 sequencing or facilitating interpretation of next-generation sequencing data.

82 to locate deletions at base pair level using next-generation sequencing data.

83 ns in allele fraction and read coverage from next-generation sequencing data.

84 pe with the high sequencing depth of current next-generation sequencing datasets.

85 l HIV-1 variants were determined by means of next-generation sequencing (False Positive Rate (FPR), 3

86 utations, we developed a pipeline that takes next-generation sequencing fastq files as input, calls o

87 of extracting, clustering and analyzing raw next generation sequencing files derived from pooled scr

88 To date, most de novo discovery through next-generation sequencing focused on congenital heart d

89 cell responses, including approaches to use next generation sequencing for antibody lineage tracing

90 We performed targeted next-generation sequencing for 120 genes associated with

91 In this study, we performed next-generation sequencing for 82 unrelated PFAPA patien

92 has benefited mightily from the adoption of next-generation sequencing for genomics and transcriptom

93 k to PAH pathophysiology was investigated by next-generation sequencing, functional studies in cultur

94 While next-generation sequencing has accelerated the discovery

95 The development of molecular barcoding for next-generation sequencing has greatly enhanced the sens

96 ecificities was intriguing and more recently Next-Generation Sequencing has identified wide-ranging u

97 Next-generation sequencing has revealed recurring somati

98 Although next-generation sequencing has revolutionized the abilit

99 tion using statistical algorithms.IMPORTANCE Next-generation sequencing has revolutionized the study

100 Next-generation sequencing has substantially enhanced ou

101 ometry-based proteomics, and, more recently, next-generation sequencing have contributed to greatly e

102 ency and ease of data production afforded by next-generation sequencing have created new opportunitie

103 Advances in genome profiling and next-generation sequencing have led to the classificatio

104 Newer MRD detection methods that use next-generation sequencing have yielded promising result

105 ecular technologies, such as microarrays and next-generation sequencing, have identified gene express

106 Next-generation sequencing holds the potential for early

107 medical histories consistent with KS in whom next generation sequencing identified the same novel c.2

108 The mutation was identified by next-generation sequencing in 14 patients with HAEnCI be

109 Biomarker discovery was done using next-generation sequencing in a discovery set of 18 surg

110 Targeted next-generation sequencing in inherited congenital catar

111 identified in a cancer gene panel that used next-generation sequencing in pretreatment biopsies from

112 To determine the role of targeted next-generation sequencing in resolving these minor vari

113 ranscription factor Tbx20) variants found by next-generation sequencing in two siblings with LQTS in

114 avigation, requiring only basic computer and next generation sequencing knowledge.

115 thod called "mutate-and-map read out through next-generation sequencing" (M2-seq) that takes advantag

116 DNA studies are almost completely reliant on next-generation sequencing, making evaluations of these

117 Targeted next-generation sequencing may offer the ability to circ

118 ht into the cutaneous microbiome in HS using next-generation sequencing may provide novel data on the

119 as being directly silenced by SPL13 based on Next Generation Sequencing-mediated transcriptome analys

120 The Next Generation Sequencing methodologies are considered

121 Metagenomic next-generation sequencing (mNGS) is increasingly used f

122 Metagenomic next-generation sequencing (mNGS) was conducted when >/=

123 es were (re)sequenced using a research-based next-generation sequencing multigene panel.

124 In the past decade, next-generation sequencing ( NGS) technologies were impr

125 Employing deep next generation sequencing (NGS) analysis of nucleotide

126 d topics on 3D genomics structural analysis, next generation sequencing (NGS) analysis, computational

127 We used Next Generation Sequencing (NGS) and CLC Genomics Workbe

128 anterior myocardial regions were analyzed by next generation sequencing (NGS) and post-processing wit

129 th of data but utilization of microarray and next generation sequencing (NGS) data for analysis can b

130 lidating putatively pathogenic variants from next generation sequencing (NGS) data.

131 ertainty in genotype-calling associated with Next Generation Sequencing (NGS) data.

132 Next generation sequencing (NGS) discovered age-related

133 large number of samples is made possible by next generation sequencing (NGS) due to its multiplexing

134 rpretation of mtDNA genomic data coming from next generation sequencing (NGS) experiments.

135 scriptome profiling of plasma-derived EVs by next generation sequencing (NGS) from limited quantities

136 Next generation sequencing (NGS) has been increasingly a

137 Next Generation Sequencing (NGS) has been widely impleme

138 Next generation sequencing (NGS) of the TCRs can be used

139 ontained description of genomic variation in Next Generation Sequencing (NGS) results.

140 Next Generation Sequencing (NGS) strategies, like RNA-Se

141 Recent genomics studies using next generation sequencing (NGS) technique have identifi

142 ) occupancy, or histone modification through next generation sequencing (NGS) technologies.

143 creasingly important with the development of next generation sequencing (NGS) technologies.

144 Next Generation Sequencing (NGS) was subsequently done t

145 Next generation sequencing (NGS) was used to define the

146 We combine next generation sequencing (NGS), capillary electrophore

147 cing technology, collectively referred to as next generation sequencing (NGS), mean the entire cancer

148 Established and emerging next generation sequencing (NGS)-based technologies allo

149 set, baseline samples were re-analyzed using next generation sequencing (NGS).

150 entified; 4 cases met inclusion criteria for next-generation sequencing (NGS) analysis.

151 t-associated genes were screened by targeted next-generation sequencing (NGS) and then validated by S

152 Next-generation sequencing (NGS) approaches are commonly

153 Next-generation sequencing (NGS) approaches to parasite

154 he purpose of this study was to test whether next-generation sequencing (NGS) can be a solution for t

155 Next-generation sequencing (NGS) can overcome some of th

156 novo assembly of whole genome shotgun (WGS) next-generation sequencing (NGS) data benefits from high

157 Here we analyzed next-generation sequencing (NGS) data for small RNAs in

158 Variant calling from next-generation sequencing (NGS) data is susceptible to

159 Short-Pair is best used for next-generation sequencing (NGS) data that lack referenc

160 t step in many variant calling pipelines for next-generation sequencing (NGS) data.

161 eedy algorithm for targeted STR profiling in next-generation sequencing (NGS) data.

162 The application of next-generation sequencing (NGS) genomic testing for som

163 Targeted next-generation sequencing (NGS) has been widely used as

164 The wide application of next-generation sequencing (NGS) has provided an enormou

165 Enhancements in clinical-grade next-generation sequencing (NGS) have fueled the advance

166 Barcoding of DNA template molecules early in next-generation sequencing (NGS) library construction pr

167 iral-associated disease were processed using next-generation sequencing (NGS) methodologies by target

168 Next-generation sequencing (NGS) of complete STLV genome

169 Next-generation sequencing (NGS) provides a broad invest

170 in index-contact pairs, and as confirmed if next-generation sequencing (NGS) revealed clonality of s

171 o reduce this overflow of false positives in next-generation sequencing (NGS) screens, we developed D

172 In many next-generation sequencing (NGS) studies, multiple sampl

173 ress has been made towards the adaptation of next-generation sequencing (NGS) techniques to decipheri

174 Advances in next-generation sequencing (NGS) technologies allow comp

175 low to yield new insights, but the advent of next-generation sequencing (NGS) technologies has altere

176 Next-generation sequencing (NGS) technologies have drive

177 Cheaper and faster next-generation sequencing (NGS) technologies have taken

178 With the advent of high-throughput, next-generation sequencing (NGS) technologies, a deeper

179 ations in many species thanks to advances in next-generation sequencing (NGS) technologies.

180 Recent advances in next-generation sequencing (NGS) technology enable resea

181 The tools of next-generation sequencing (NGS) technology, such as tar

182 n using a compartmented platform followed by next-generation sequencing (NGS) technology, we find tha

183 MS)-PCR, Sanger sequencing, and longitudinal next-generation sequencing (NGS) to determine their prof

184 Genomic interaction studies use next-generation sequencing (NGS) to examine the interact

185 olymerase, followed by PCR amplification and next-generation sequencing (NGS) to generate genome-wide

186 lies with pediatric VTE followed by targeted next-generation sequencing (NGS) to identify causative m

187 he ecology of denitrifying bacteria by using next-generation sequencing (NGS) to survey the diversity

188 Expanded mutational testing, such as next-generation sequencing (NGS), often identifies mutat

189 Next-generation sequencing (NGS)-based circulating tumor

190 Using a next-generation sequencing (NGS)-powered genomic scan, w

191 hods in FFPE cancer specimens using targeted next-generation sequencing (NGS).

192 th polymorphism of STR loci in the genome by next-generation sequencing (NGS).

193 than 2 million A-to-I RNA editing sites from next-generation sequencing (NGS).

194 ostic technology, particularly the advent of next-generation sequencing (NGS).

195 ing, where appropriate genetic testing using next-generation sequencing (NGS).

196 re identified in 576 of the families without next-generation sequencing (NGS).

197 Various methods have been developed to mine "next-generation" sequencing (NGS) data to detect deletio

198 Metagenomic next generation sequencing of his cerebrospinal fluid an

199 Next generation sequencing of Kupffer cell miRNA identif

200 Here we used Next Generation Sequencing of microRNAs to identify nega

201 Ultra-deep targeted next generation sequencing of pretreatment plasma cfDNA

202 To study this, we performed next generation sequencing of the livers of Sprague-Dawl

203 cal information, we focused on incorporating next-generation sequencing of B-cell transcripts to dete

204 ents with CUP using targeted clinical-grade, next-generation sequencing of circulating tumor DNA (ctD

205 We advocate that technological advances in next-generation sequencing of circulating, tumor-derived

206 Methods for next-generation sequencing of DNA are producing a wealth

207 erformance characteristics were observed for next-generation sequencing of FFPET, whole blood, and dr

208 By next-generation sequencing of infected tissue homogenate

209 Isolation and next-generation sequencing of MIWI2-positive multiciliat

210 icators of disease and can be measured using next-generation sequencing of RNA (RNA-seq).

211 Mutations were identified through next-generation sequencing of saliva or blood samples, a

212 Next-generation sequencing of tumors and matched normal

213 Next-generation sequencing of tumors as part of clinical

214 Recently, we performed next generation sequencing on patients with a spectrum o

215 Through next-generation sequencing on a cohort of patients with

216 Next-generation sequencing overcomes this drawback by un

217 Our next generation sequencing panel incorporated 38 inherit

218 tation screening was done using a customized next generation sequencing panel targeting 105 genes imp

219 associated genes using a customized targeted next-generation sequencing panel (Miseq).

220 of principle for the application of targeted next-generation sequencing panels in countries with limi

221 In contrast to other available next-generation sequencing platforms, PacBio single-mole

222 nd B virus-positive specimens using multiple next-generation sequencing platforms.

223 We therefore present two novel Next Generation Sequencing protocols (with freeware) cap

224 Advances in next-generation sequencing provide a route to therapeuti

225 Next generation sequencing provides a count of RNA molec

226 hain reaction, to check for concordance with next-generation sequencing results.

227 Results Targeted next-generation sequencing revealed that the genotype of

228 ified by RNA immunoprecipitation followed by next-generation sequencing (RIP-seq), and the diversity

229 and 90 asymptomatic controls were tested by next-generation sequencing (RNA-seq) and pan viral group

230 pisomal genomes (NIKS16) were compared using next-generation sequencing (RNA-Seq).

231 In next generation sequencing runs, higher proportions of a

232 c landscape of this tumor type, we performed next generation sequencing studies for mutational and co

233 nally conducted a literature review of prior next generation sequencing studies in this disease and c

234 Next-generation sequencing studies are highly dependent

235 Next-generation sequencing studies have identified chrom

236 ifferent microbiomes were investigated using next-generation sequencing targeting 16S and 18S ribosom

237 We compare two next-generation sequencing techniques - amplicon and sho

238 Using next-generation sequencing techniques and GeneMatcher, w

239 Using high-throughput next-generation sequencing techniques optimized for the

240 We used next-generation sequencing techniques to examine chromos

241 Advances in Next Generation Sequencing technologies have enabled the

242 Next generation sequencing technologies have enabled the

243 ecent breakthroughs in molecular biology and next generation sequencing technologies have led to the

244 Further studies using next generation sequencing technologies should be instru

245 Next generation sequencing technologies such as exome an

246 Next-generation sequencing technologies embedded in auto

247 The advent of next-generation sequencing technologies enables research

248 sequencing using short-read (e.g., <150 bp), next-generation sequencing technologies has reinvigorate

249 Next-generation sequencing technologies have allowed us

250 sequencing was first introduced in 1977, and next-generation sequencing technologies have been availa

251 Next-generation sequencing technologies have greatly inc

252 Recently, next-generation sequencing technologies have provided ge

253 In recent years next-generation sequencing technologies have revolutioni

254 However, recent advances in next-generation sequencing technologies provide new ways

255 Coupled with next-generation sequencing technologies, it becomes real

256 With the advent of next-generation sequencing technologies, the homozygous

257 Using next-generation-sequencing technologies, we demonstrated

258 The advent of high-throughput next generation sequencing technology has greatly promot

259 Although recent development of next generation sequencing technology suggests RNA-seq a

260 Recent breakthroughs in next-generation sequencing technology and complementary

261 seq can be practiced using widely accessible next-generation sequencing technology and does not requi

262 portunity to harness the tremendous power of next-generation sequencing technology in applied avian m

263 quantitative method using DNA barcodes and a next-generation sequencing technology), and quantitative

264 es for germ line and somatic mutations using next-generation sequencing technology.

265 DNA walking system to Pacific Bioscience(R) Next-generation sequencing technology.

266 ined in global peptide profiles generated by next generation sequencing, the large number of cancer a

267 Results were validated by probe capture next generation sequencing; the data from which also pro

268 an genome, transposon insertion profiling by next-generation sequencing (TIPseq).

269 ificant technical (sampling) bias when using next generation sequencing to determine clonal compositi

270 e the potential role of lncRNAs, we employed next generation sequencing to examine the transcriptome

271 We utilized next generation sequencing to examine transcriptional re

272 We used next-generation sequencing to barcode sedDNA retrieved f

273 m the same fibroblast population and applied next-generation sequencing to compare genomic variations

274 nfished reef, and (3) used metabarcoding and next-generation sequencing to determine diet composition

275 en array technology (PathoChip) coupled with next-generation sequencing to establish microbial signat

276 we report the first study utilizing targeted next-generation sequencing to identify single-nucleotide

277 We performed next-generation sequencing to obtain single-nucleotide r

278 Here we use next-generation sequencing to probe how this paradigm re

279 fy novel regulators of this process, we used next-generation sequencing to profile changes in microRN

280 mbination of in situ sampling techniques and next-generation sequencing to study the biological filtr

281 We recommend the use of next-generation sequencing to validate standards in clin

282 ent of EBV DNA by hybridization, followed by next-generation sequencing, to reveal sequence diversity

283 Next-generation sequencing ultimately guided therapy in

284 use of the environment, provide even novice next-generation sequencing users with the ability to per

285 ied blood spot) specimens underwent targeted next-generation sequencing using a custom panel of 101 C

286 loyed tumor genetic profiling via high-depth next-generation sequencing using a panel to assay affect

287 dian age: 24 years; 65% males) who underwent next-generation sequencing using an extended panel of 77

288 d and anaplastic thyroid cancers screened by next-generation sequencing using the MSK-IMPACT panel of

289 Targeted amplicon, next-generation sequencing was performed using primers t

290 tegy, based on PCR amplification followed by next-generation sequencing, was used to investigate a no

291 Using metagenomic next generation sequencing, we detected nucleic acid seq

292 Using next generation sequencing, we identified VDV1 in honey

293 Using next-generation sequencing, we discovered a novel ledant

294 zing genome-wide transcription and repair by next-generation sequencing, we identified locations of e

295 Subsequently, using next-generation sequencing, we identified the bacterial

296 With next-generation sequencing, we investigated how mites in

297 ng chromatin immunoprecipitation followed by next-generation sequencing, we show that ATF3 is bound t

298 (ORR) and minimal residual disease (MRD) by next-generation sequencing were secondary end points.

299 cancer and known somatic mutation status by next-generation sequencing who underwent hepatectomy for

300 ons in the LDLR, APOB, and PCSK9 genes using next generation sequencing, with results confirmed by Sa