ライフサイエンスコーパス: gene sequence

1 ied to any protein drug based on a conserved gene sequence.

2 yme analysis and ribosomal and mitochondrial gene sequences.

3 nly performed using 16S ribosomal RNA (rRNA) gene sequences.

4 ase catalogs, names and distributes microRNA gene sequences.

5 was based on both nuclear and mitochondrial gene sequences.

6 llumina) sequencing of partial (V4) 16S rRNA gene sequences.

7 ic classification of any phylogenetic marker gene sequences.

8 ds for each gene, to parameters derived from gene sequences.

9 ic) mutations at numerous non-immunoglobulin gene sequences.

10 ed within 36 of the differentially expressed gene sequences.

11 ure and functional interactions of these RNA gene sequences.

12 ommunity composition assessed using 16S rRNA gene sequences.

13 20-40 codons long and occur in about 10% of gene sequences.

14 ng the standard molecular method of 16S rRNA gene sequencing.

15 ThinPrep system and then underwent 16S rRNA gene sequencing.

16 f flight mass spectrometry (MALDI-TOF MS) or gene sequencing.

17 e gut microbiota was profiled using 16S rRNA gene sequencing.

18 l centrifuged sediment culture, and 16S rRNA gene sequencing.

19 d, and microbiomes were analyzed by 16S rRNA gene sequencing.

20 es were recovered and identified by 16S rRNA gene sequencing.

21 ommunity composition was studied by 16S rRNA gene sequencing.

22 complete 16S rRNA, rpoB region V, and hsp65 gene sequencing.

23 obiome analysis was performed using 16S rRNA gene sequencing.

24 d by using high-throughput 16S ribosomal DNA gene sequencing.

25 e isolated from biopsies and analyzed by 16S gene sequencing.

26 fied to the species level using housekeeping gene sequencing.

27 olled trial was determined by using 16S rRNA gene sequencing.

28 E), polymerase chain reaction, and pertactin gene sequencing.

29 ment and 5 days after treatment for 16S rRNA gene sequencing.

30 y and analyzed fecal microbiomes by 16S sRNA gene sequencing.

31 ommunities were characterized using 16S rRNA gene sequencing.

32 rol subjects were profiled by using 16S rRNA gene sequencing.

33 microbiota by 16S ribosomal ribonucleic acid gene sequencing.

34 y and weekly during gestation using 16S rRNA gene sequencing.

35 eeks of life were analyzed by using 16S rRNA gene sequencing.

36 s in the bone marrow using flow cytometry or gene sequencing.

37 All protozoa were identified by 18S rRNA gene sequencing.

38 collected and analyzed by 16S ribosomal RNA gene sequencing.

39 combined approach of (RAPD)-PCR and 16S rRNA gene sequencing.

40 non-CA and CA individuals based on 16S rRNA gene sequencing.

41 microbiota was characterized using 16S rRNA gene sequencing.

42 ients of allo-HCT and analyzed using 16SrRNA gene sequencing.

43 ged <= 6 years, were analyzed using 16S rRNA gene sequencing.

44 rom the same geographic location by 16S rRNA gene sequencing.

45 bial profiles were obtained through 16S rRNA gene sequencing.

46 l body) microbial communities using 16S rRNA gene sequencing.

47 s assessed through metagenomics and 16S rRNA gene sequencing.

48 week 12 and profiled using 16S ribosomal RNA gene sequencing; 122 patients had paired stool microbiom

49 Based on gene sequencing, 44/62 of the isolates were determined t

50 e studied the expression of Hag/MID, hag/mid gene sequences, adherence to human cells, and autoaggreg

51 rm led to recovery near-full-length 16S rRNA gene sequences allowing accurate identification of micro

52 microbiota by culture and 16S ribosomal RNA gene sequencing.Among the 3161 enrolled preterm infants,

53 associated with Populus deltoides using rRNA gene sequence analyses and how these vary with tree and

54 rior work has demonstrated the value of dnaJ gene sequence analysis in resolving different members of

55 16S rRNA gene sequence analysis revealed diverse gut communities

56 AART to an HIV-negative group using 16S rRNA gene sequence analysis.

57 We performed 16S ribosomal RNA gene sequencing analysis of stool samples from 1795 volu

58 Gene sequence and expression data from four major organs

59 me in a plant pathology study, we discovered gene sequence and gene expression variants across a gene

60 the conserved off-target free partial HaCHI gene sequence and was used to generate several HaCHI-RNA

61 Initiative (6,177 near full-length 16S rRNA gene sequences and 9.4 million high-quality 16S V1-V2 am

62 Using faecal 16S ribosomal RNA gene sequences and host genotype data from the Flemish G

63 We reanalyzed raw 16S ribosomal RNA (rRNA) gene sequences and metadata from published studies to ex

64 generate double-strand breaks in the target gene sequences and then utilize DNA repair mechanisms to

65 accompanied without any detectable change in gene sequences and thus suggest that chromosomal translo

66 ngival microbiome was evaluated via 16S rRNA gene sequencing and 8 selected inflammatory markers meas

67 Using 16S ribosomal RNA gene sequencing and a clustering approach, infants with

68 Small subunit 18S rRNA gene sequencing and accessory pigment analysis displayed

69 We used 16S rRNA gene sequencing and bacterial cell sorting to evaluate g

70 collected and analyzed by 16S ribosomal RNA gene sequencing and bacterial community analyses.

71 as Bacillus mojavensis based on the 16S rRNA gene sequencing and biochemical properties.

72 ep toward standardizing methods for 16S rRNA gene sequencing and bioinformatics analysis of vaginal m

73 were identified by 16S ribosomal RNA (rRNA) gene sequencing and compared with validly described spec

74 on was characterized using 16S ribosomal RNA gene sequencing and culture.

75 microbiota composition by 16S ribosomal RNA gene sequencing and fecal/urinary metabolites by 1H-NMR

76 Vaccine-virus relatedness was assessed by gene sequencing and hemagglutination inhibition assay.

77 Bacterial profiling through 16S rRNA gene sequencing and histology showed no bacterial taxa l

78 We used high-throughput antibody gene sequencing and identification of allergen-specific

79 Both 16S rRNA gene sequencing and Lactobacillus species-specific (L. i

80 pa zea larvae using 16S ribosomal RNA (rRNA) gene sequencing and matrix-assisted laser desorption/ion

81 obiome assembly outcomes using fungal marker gene sequencing and measured susceptibility of the colon

82 nt ID and mecA results were resolved by rpoB gene sequencing and mecA gene sequencing, respectively.

83 aches, including bacterial 16S ribosomal RNA gene sequencing and metagenomic shotgun sequencing, have

84 main approaches: linkage analysis, candidate gene sequencing and most recently, exome and genome sequ

85 Results from 16S rRNA gene sequencing and qPCR showed that, compared with suck

86 -based) microbiota were analysed by 16S rRNA gene sequencing and qPCR.

87 10(8) cells per g of soil based on 16S rRNA gene sequencing and quantification.

88 on was analysed by a combination of 16S rRNA gene sequencing and quantitative PCR (qPCR).

89 Using 16S rRNA gene sequencing and quantitative PCR, we characterized t

90 16S rRNA gene sequencing and RNA-Seq analyses identified composit

91 rium were identified by rpoB, sodA and hsp65 gene sequencing and strain typed using variable number t

92 The HMP used both 16S ribosomal RNA gene sequencing and whole-genome metagenomic sequencing

93 ion of selected isolates based on partial S1 gene sequences, and the full genome characterization of

94 s well, many research assays, including PCR, gene sequencing, and melt curve analysis, have been deve

95 act with soil was analyzed by using 16S rRNA gene sequencing, and the data were combined with immune

96 gment-length polymorphism analysis, targeted gene sequencing, and whole-genome sequencing.

97 i et al. reveals that a recently evolved SRY gene sequence antagonizes SRY protein stability, necessi

98 utations in the CTLA-4 pathway identified by gene-sequencing approaches.

99 onment, but also specifically which cultivar gene sequences are absent or ubiquitous.

100 em, microRNAs are special because individual gene sequences are conserved across the animal kingdom.

101 P1, P2, and P3, were identified by 16S-rRNA gene sequencing as Bacillus subtilis, Bacillus thuringie

102 their composition by multiparallel 16S rRNA gene sequencing as well as the density of bacteria in st

103 stipation and evaluated by 16S ribosomal RNA gene sequencing (average, 49,186 reads/sample).

104 t digestive tract were subjected to 16S rRNA gene sequencing-based analysis to determine the baseline

105 st co-evolution is imprinted within promoter gene sequences before transcript or protein interactions

106 on untargeted mass spectrometry and 16S rRNA gene sequencing, both stress and Test diet altered the f

107 rate knockout mouse models by disrupting the gene sequence, but its efficiency for creating models th

108 y, allowing a reduction of mosquito 18s rRNA gene sequences by more than 80% for the V4 hypervariable

109 chniques such as phylogenetic and functional gene sequencing, can provide more insights into the mech

110 status, major technological advancements in gene sequencing capability and a shift towards personali

111 High selectivity against nonspecific gene sequences characteristic of potential interfering s

112 10(1) copies of Salmonella typhimurium InvA gene sequences (cloned in E. coli and after 30-cycle PCR

113 One genotype B3 cluster based on the N gene sequence contained epidemiologically unrelated viru

114 rsity studies using small subunit (SSU) rRNA gene sequences continue to advance our understanding of

115 g an integrated approach, including targeted gene sequencing, copy-number arrays, and gene expression

116 Partial gene sequences could also be retrieved in some cases, fr

117 nd Pachycerianthus magnus, the mitochondrial gene sequences could not be assembled into a single circ

118 hesized that the use of ultra-deep, targeted gene sequencing could detect somatic mutations in uterin

119 d RV-C), nasopharyngeal microbiome (16S rRNA gene sequencing), cytokine, and metabolome (liquid chrom

120 eams, we predicted metagenomes from 16s rRNA gene sequence data using PICRUSt and identified function

121 ores, DACE clustered the Lake Taihu 16S rRNA gene sequencing data ( approximately 316M reads, 30 GB)

122 min, and the Ocean TARA Eukaryotic 18S rRNA gene sequencing data ( approximately 500M reads, 88 GB)

123 associated with coronary heart disease using gene sequencing data from the Myocardial Infarction Gene

124 mic levels multivariate analysis of 16S rRNA gene sequencing data showed diet affected faecal microbi

125 roarray, HLA high-resolution typing and AQP4 gene sequencing data to analyze genetic ancestry and to

126 tional Taxonomic Units from16S ribosomal RNA gene sequencing data.

127 Among 58 469 participants with CETP gene-sequencing data available, average age was 51.5 yea

128 ANGPTL3 gene sequencing demonstrated that approximately 1 in 309

129 16S ribosomal RNA gene sequencing detected diverse bacterial DNA signature

130 acterized bacterial communities using marker gene sequencing, determined N(2) -fixation rates using s

131 sfers on CM and H2 , Acetobacterium 16S rRNA gene sequences dominated the culture and the DCM-degrade

132 Large-scale gene sequencing efforts and functional studies have faci

133 taxonomic classification tools for 16S rRNA gene sequences either do not provide species-level class

134 imeric protein selected from native envelope gene sequences (envs) induced neutralizing Abs against T

135 a given gene family; this pipeline can model gene sequence evolution, gene duplication-loss, gene tra

136 are ubiquitous, but the discovery of new RNA gene sequences far outpaces the research on the structur

137 single-molecule translation dynamics of any gene sequence for any of these assays and for different

138 entric diatom Cyclotella cryptica to analyze gene sequences for putative light-harvesting proteins in

139 We integrated the exome data with targeted gene sequencing for 1,321 genes selected for their invol

140 onomic unit [OTU] abundances) using 16S rRNA gene sequencing for co-occurring Plethodon salamander sp

141 f genomic DNA with PCR-identifiable 18S rRNA gene sequence from single cells was low (15% of aplastid

142 he 5,097 bp of the concatenated housekeeping gene sequence from the patient were 99.0% identical to a

143 ferent subunits) and 5250 miRNA, 3747 snRNA, gene sequences from 9282 complete genome chromosomes of

144 cently, tools and methods for inferring such gene sequences from AIRR-seq datasets have become availa

145 Viral gene sequences from an enlarged set of about 200 Epstein

146 We apply our new framework to a set of gene sequences from an epidemic of rabies virus in North

147 Bacterial 16S ribosomal RNA gene sequences from each sample were amplified, sequence

148 Bacterial 16S ribosomal RNA gene sequences from each sample were amplified, sequence

149 in multiple hosts are in fact different, but gene sequences from formally described species remain a

150 The retrieved 16S rRNA gene sequences from magnetically-enriched magnetotactic

151 ss clustering to reconstruct full-length 16S gene sequences from metagenomic sequencing data with hig

152 lored the genetic diversity of 125 Bm86 cDNA gene sequences from R. microplus from 10 endemic areas o

153 We analysed 735 G gene sequences from samples collected from paediatric pa

154 n extended Greengenes database including 16S gene sequences from vaginal bacteria not already present

155 We also recovered symbiont-specific gene sequences from water collected near hosts, suggesti

156 ng effort, we analysed the 16S ribosomal RNA gene sequences from ~1,200 activated sludge samples take

157 Env gene sequencing from NAb-resistant viruses was used to a

158 hing of data describing the complete sets of gene sequences (genotypes and haplotypes) inferred from

159 The rapidly decreasing cost of gene sequencing has resulted in a deluge of genomic data

160 Haemagglutinin (HA) and neuraminidase (NA) gene sequencing have traditionally been used to identify

161 GAS candidate antigens for gene carriage and gene sequence heterogeneity.

162 ygmaea and Roccella fuciformis with SSU rRNA gene sequences identical to the type strain of Streptomy

163 me housed Micromonospora, and using 16S rRNA gene sequence identification, we verified that the reiso

164 not in immune-evasive Yp Analysis of Yp pagP gene sequences identified a single-nucleotide polymorphi

165 Gene sequencing identifies a pathogenic or likely pathog

166 three named species that share 99% 16S rRNA gene sequence identity.

167 c resistance gene changes employing 16S rRNA gene sequencing (Illumina-Miseq) and quantitative polyme

168 Whole-exome and direct gene sequencing, immunohistochemistry, real-time PCR, EL

169 x gene expression and binds Col3a1 and Postn gene sequences in cultured cardiac fibroblasts after ind

170 in widely used as methods for characterizing gene sequences in many varieties of crops.

171 first realizes the access to full-length 16S gene sequences in the near-terabase-scale metagenomic sh

172 Analyses of gene sequences in various closely related prokaryotic gr

173 dy, we profile gut microbiota using 16S rRNA gene sequencing in 531 well-phenotyped Finnish men from

174 in an sbds-negative SDS family and candidate gene sequencing in additional SBDS-negative SDS cases or

175 Oral bacteria were assessed using 16S rRNA gene sequencing in prediagnostic mouthwash samples from

176 Using 16S rRNA gene sequencing in two model NHP species, we show that a

177 ty (small subunit (SSU) ribosomal RNA (rRNA) gene sequences) in field samples.

178 leted and 29 polymorphisms were found in the gene sequence, including two novel exonic mutations: R25

179 detected based on partial nitrogenase (nifH) gene sequences, including the four most commonly detecte

180 vo function of beta-actin is provided by the gene sequence independent of the encoded protein isoform

181 tracts used for transcribing and translating gene sequences into proteins as well as the products of

182 Added contributions of cytogenetic and gene sequencing investigations were determined.

183 This study aims to identify the role of gene sequences involved in daylength-regulated bulb form

184 SGR occurs when a gene sequence is cut and recombined within a single cell

185 iota as profiled by high-throughput 16S rRNA gene sequencing is predictive of ECC onset.

186 By analyzing bacterial 16S rRNA gene sequences isolated from clinical samples, we used a

187 merase chain reaction, and 16S ribosomal RNA gene sequencing; lamina propria and mesenteric lymph nod

188 highly repetitive nature of the LRP reporter gene sequence leads to DNA recombination events and the

189 and found that mutation rates may differ by gene sequence length but not by host, gene, strain, an e

190 e the bacteria with high-resolution 16S rRNA gene sequencing, linking these community data to geochem

191 We performed whole-exome and targeted gene sequencing, lymphocyte characterization, molecular

192 ressive in MPn metabolism and their 16S rRNA gene sequences matched 35% of the Illumina PMEZ Pseudomo

193 We used a combination of 16S rRNA gene sequencing, metagenomics sequencing, and mass spect

194 urveillance in Hong Kong SAR, China, and new gene sequencing methods has been used in this study to a

195 not yet addressed by the CLSI and molecular (gene sequencing) methods associated with the detection o

196 IMS), and Minimum Information about a Marker Gene Sequence (MIMARKS).

197 The samples were analyzed using 16S rRNA-gene sequencing (MiSeq-Illumina) and QIIME pipeline.

198 Envelope gene sequences (n = 661) from 11 DENV genotypes in 10 en

199 ied utilizing 16S rRNA rapid next-generation gene sequencing (NGS) and expanded quantitative urine cu

200 We used next-generation 16S rRNA gene sequencing (NGS16S) to determine how often cultivat

201 Using whole-genome sequences or individual gene sequences obtained from IMD isolates or clinical sp

202 We present the complete gene sequence of the Mpi locus and quantify nucleotide p

203 l-experienced patients and that based on env gene sequence of the viruses in the patients.

204 Included studies reported 16S rRNA gene sequences of fecal samples from HIV+ patients.

205 A total of 209 partial pol gene sequences of HIV-1 CRF55_01B were sampled during 20

206 Further analysis of the MeV-N gene sequences of these 2 groups confirmed that they rep

207 The HA gene sequences of viruses recovered after the fifth pass

208 Marker gene sequencing of 16S ribosomal genes revealed that the

209 In the second pair, targeted gene sequencing of 25 genes known to be associated with

210 ns in both health and disease using 16S rRNA gene sequencing of 410 individuals from across the world

211 We conducted 16S ribosomal RNA gene sequencing of an ICU admission swab and >=1 additio

212 Analysis of 16S ribosomal RNA gene sequencing of cervicovaginal lavage clustered each

213 m 100 Lynch syndrome patients using 16S rRNA gene sequencing of colon biopsies, coupled with metageno

214 V4 16S rRNA gene sequencing of fecal DNA demonstrated minimal shifts

215 otope signatures from fin clips and 18S rRNA gene sequencing of fecal samples identified the smalltoo

216 sease, emphasis should be placed in targeted gene sequencing of genes known to cause adRP, such as RH

217 16S rRNA gene sequencing of SIgA-coated/uncoated bacteria (IgA-Bi

218 Here, using high-throughput marker gene sequencing of soils collected from 18 sites through

219 ication of PC intake, together with 16S rRNA gene sequencing of the gut microbiota, and faecal and pl

220 which extended to 18 months) using 16S rRNA gene sequencing of the V4 region.

221 Full-length 16S rRNA gene sequencing of these isolates identified nine discre

222 e genetic group, based on hemagglutinin (HA) gene sequences, of influenza A(H3N2) viruses from patien

223 In application to gene sequences on the papaya X chromosome and protein-co

224 We performed 16S rRNA gene sequencing on 333 infants' stool samples.

225 For cases, we also used targeted gene sequencing on bone marrow samples and investigated

226 Therefore, we performed 16S rRNA gene sequencing on rectal swab samples from 381 men who

227 16S rRNA and nifH gene sequencing on single sorted cells allowed us to ide

228 Differential analysis of 16S rRNA gene sequencing or L. murinus-specific qPCR of DNA from

229 both, with M. chimaera diagnosed by culture, gene sequencing, or both.

230 d to a number of key findings: (i) VH and VL gene sequences pair in a combinatorial fashion without d

231 we recombinantly expressed a bacterial GH161 gene sequence (PapP) from the Gram-positive bacterium Pa

232 ng high-resolution metabolomics and 16S rRNA gene sequencing, plasma/urine metabolomes and the fecal

233 probes were designed to detect a specific L-gene sequence present in the five most common Ebola spec

234 ptomyces, strain de-replication based on SSU gene sequences prior to screening for bioactive molecule

235 PCRs and a telomere-sequence to single-copy-gene-sequence ratio method to determine telomere length

236 The full-length 16S gene sequences recovered by our approach allowed Escheri

237 llected time series data of 16S and 18S rRNA gene sequences, recovered from 29 planktonic shotgun met

238 Species-level classification for 16S rRNA gene sequences remains a serious challenge for microbiom

239 V3-V4 and V4 regions of the 16S and 18S rRNA gene sequences, respectively.

240 re resolved by rpoB gene sequencing and mecA gene sequencing, respectively.

241 ase-aided de novo MS/MS and 100% matched the gene sequencing result, except for two amino acids with

242 16S V3 and V4 gene sequencing results from fecal samples of patients t

243 Additionally, 16S rRNA gene sequencing results showed that anammox bacteria, n-

244 Unsupervised clustering of 16S rRNA gene sequences revealed three clusters (subtypes), one o

245 Gene sequencing revealed a phenylalanine-->isoleucine mu

246 16S rRNA gene sequencing revealed diverse microbial communities i

247 16S rRNA gene sequencing revealed that diazinon exposure signific

248 Analysis of HIV-1 gene sequences sampled longitudinally from infected indi

249 We applied 16S ribosomal RNA gene sequencing, shotgun metagenomic sequencing, in vitr

250 population bottleneck, whereas BeHV envelope gene sequences showed strong population genetic substruc

251 Furthermore, 16S rRNA gene sequencing showed that TA@RAs could increase the di

252 enrichment shared 98.6%, and 98.5% 16S rRNA gene sequence similarities to Sulfurospirillum multivora

253 RNaseq identified eight candidate catabolic genes, sequence similarity networks, and genome neighbor

254 Gene sequencing studies on stored ICV-positive clinical

255 ne have been identified in large-scale human gene sequencing studies.

256 ustering analyses of microsatellite and Chd1 gene sequences support two divergent clusters separating

257 Remarkable advancements in high-throughput gene sequencing technologies have led to an exponential

258 In addition, the assay includes detection of gene sequences that confer antimicrobial resistance.

259 3-3 and tau proteins, and together with PRNP gene sequencing the test allows the major prion subtypes

260 the metabolic predictions based on 16S rRNA gene sequences, the relative abundance of functional gen

261 thod comprised of urine culture and 16S rRNA gene sequencing, the sensitivity, specificity, positive

262 protected from MazF activity by recoding the gene sequence to eliminate recognition sites, while pres

263 m nasal wash samples was amplified and the F gene sequenced to monitor presatovir resistance.

264 enable bacterial and archaeal ribosomal RNA gene sequences to be followed across multiple studies an

265 t-generation Illumina sequencing of 16S rRNA gene sequences to characterize symbiont communities.

266 We used sets of barley and wheat orthologous gene sequences to compare discrete parts of the Ae. mark

267 wn to enable "shuffling" of antigen-encoding gene sequences to vastly increase antigen diversity and

268 We applied 16S rRNA gene sequencing to all nasal swabs.

269 NAseq of the citrus host responses, 16S rRNA gene sequencing to characterize citrus-associated microb

270 We conducted 16S ribosomal RNA gene sequencing to characterize intestinal microbiota of

271 ows, we used high-resolution 16S rRNA marker gene sequencing to examine outcomes in our mouse model o

272 We used 16S rRNA gene sequencing to identify the dominant bacteria in spu

273 bgingival samples were subjected to 16S rRNA gene sequencing to investigate the microbiota compositio

274 The EIII gene sequence typically encodes epitopes recognized by v

275 nd tomato samples were profiled by 16 S rRNA gene sequencing (V1-V3) in the days surrounding two rain

276 001 Genomes Consortium, we characterize rRNA gene sequence variation within and among accessions.

277 leeding phenotypes and often do not have VWF gene sequence variations.

278 The pol gene sequence was amplified to ascertain the HIV-1 subty

279 the present study, 16S ribosomal RNA (rRNA) gene sequencing was applied to saliva samples that were

280 The predictive value of 16S ribosomal RNA gene sequencing was not superior to the simpler and less

281 16S ribosomal RNA target gene sequencing was performed and taxonomy assignments w

282 (VWF) laboratory testing and full-length VWF gene sequencing was performed for all index cases and he

283 16S rRNA gene sequencing was performed in a cohort of 83 biopsy-p

284 16S ribosomal RNA gene sequencing was performed on DNA extracted from vagi

285 16S ribosomal RNA gene sequencing was performed on sputum from 253 clinica

286 High-throughput 16S rRNA gene sequencing was used to identify the bacterial commu

287 16S rRNA gene sequencing was utilized to determine microbiota com

288 icrobial composition, determined by 16S rRNA gene sequencing, was predictive of the metabolome, indic

289 Using 16 S rRNA gene sequencing we demonstrated that microbiota ecology

290 Using 16S rRNA gene sequencing, we analyzed the tumor microbiome compos

291 Using 16S rRNA gene sequencing, we found that selenate exposure altered

292 ampled per species whereas, with advances in gene sequencing, we now have access to multiple samples

293 Using 16S rRNA gene sequencing, we observed that phylum Proteobacteria

294 A total of 752 VP1 gene sequences were analyzed (413 generated in this stud

295 ng the pilot season (2017-2018), 410 RSV G-F gene sequences were obtained from 476 RSV-positive nasal

296 Forty-two available D4 genotype gene sequences were subsequently analyzed and divided in

297 Culture and 16 S rRNA gene sequencing were performed on nasopharyngeal specime

298 DNA extraction and 16S rRNA gene sequencing were undertaken.

299 tor tube (MGIT) were confirmed by using rpoB gene sequencing, which raised the sensitivity of Xpert M

300 g bacteria were characterized using 16S rRNA gene sequencing with novel techniques optimized for low-