ライフサイエンスコーパス: gene sequence

1 xtensively in terms of both gene content and gene sequence.

2 and finding the least-repetitive synonymous gene sequence.

3 ndependent of genomic locus, gene length and gene sequence.

4 identified only from their 16S ribosomal RNA gene sequence.

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

6 ed within 36 of the differentially expressed gene sequences.

7 ure and functional interactions of these RNA gene sequences.

8 thin Rpb1--induces transcription of silenced gene sequences.

9 ween the single guide RNA and the non-target gene sequences.

10 sirtuin 1 or sirtuin 2, onto GluA1 and GluA2 gene sequences.

11 and 0.7 +/- 0.2 despite a high similarity in gene sequences.

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

13 ic classification of any phylogenetic marker gene sequences.

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

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

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

17 fied to the species level using housekeeping gene sequencing.

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

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

20 ) disruption experiments and variable region gene sequencing.

21 00 d using qPCR and high-throughput 16S rRNA gene sequencing.

22 ridization copy number profiling and deep AR gene sequencing.

23 ns using whole-exome sequencing and targeted gene sequencing.

24 cal analysis of muscle biopsy, and candidate gene sequencing.

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

26 Samples were analyzed by 16S ribosomal RNA gene sequencing.

27 osatellite instability, PTEN status, and 487-gene sequencing.

28 and 150 days of age was assessed by 16S rDNA gene sequencing.

29 anges, including both direct counts and rRNA gene sequencing.

30 tide modification steps, followed by PCR and gene sequencing.

31 by phenotypic tests, mass spectrometry, and gene sequencing.

32 ass spectrometry (MALDI-TOF MS) and 16S rRNA gene sequencing.

33 , identified using whole exome and candidate gene sequencing.

34 stoma fasciculatum) using large subunit rRNA gene sequencing.

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

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

37 ommunities were characterized using 16S rRNA gene sequencing.

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

39 microbiota by 16S ribosomal ribonucleic acid gene sequencing.

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

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

42 no deleterious mutations in any of the eight genes sequenced.

43 159 case patients who had an HIV type 1 pol gene sequence, 157 (98.7%) had sequences that were highl

44 We used 16S rRNA gene sequencing, 1H nuclear magnetic resonance (NMR) met

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

46 Owing to divergent 16S ribosomal RNA (rRNA) gene sequences, 50-100% of organisms sampled from specif

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

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

49 n the infected mouse GI tract using 16S rRNA gene sequence analysis of bacterial DNA prepared from in

50 Comparative 16S rRNA gene sequencing analysis revealed 98.6% similarity to S.

51 Gene sequence and expression data from four major organs

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

53 DNA-DNA hybridization, variation in 16S rRNA gene sequence and phenotypic characteristics.

54 uestion, ABL capabilities are encoded by its gene sequence and that molecular blueprint designs this

55 res, in an unprecedented scope based on both gene sequence and tissue expression analyses.

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

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

58 Both gene sequences and complete plastid genome sequences wer

59 to identify the most phylogenetically unique gene sequences and molecules associated with these genes

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

61 orders has come about by novel techniques in gene sequencing and bioinformatics.

62 Candidate gene sequencing and chromosomal microarray established a

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

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

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

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

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

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

69 We performed whole-exome and targeted gene sequencing and phenotypic and functional analyses o

70 ected at all locations tested using 16S rRNA gene sequencing and quantification of hydrazine oxidored

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

72 16S rRNA gene sequencing and quantitative PCR of cecal and fecal

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

74 vestigated via protein studies and candidate gene sequencing and remained undiagnosed.

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

76 (as defined by their unique T cell receptor gene sequence) and by tracking clones that enter the mem

77 C. difficile-positive samples using 16S rRNA gene sequencing, and C. difficile was detected in 86.3%

78 lution, gradient diffusion (Etest), 23S rRNA gene sequencing, and cfr PCR.

79 nical phenotyping, whole exome and candidate gene sequencing, and functional validations.

80 taxonomic level by secA1 analysis, 16S rRNA gene sequencing, and matrix-assisted laser desorption io

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

82 (qPCR) from a research laboratory, 16S rRNA gene sequencing, and metagenomic shotgun sequencing (MSS

83 ultured colonies were identified by 16S rRNA gene sequencing, and purity was confirmed by sequencing

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

85 ols to query, mine and visualize large-scale gene sequences, annotations and transcriptome profiles.

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

87 Single-nucleotide polymorphisms (SNPs) in a gene sequence are markers for a variety of human disease

88 These findings indicate that ASGR-BBML gene sequences are highly conserved across the Paniceae

89 ts, but analyses of liver histology and full gene sequencing are required to identify patients with r

90 entified differences in cpsM, cpsO, and cpsI gene sequences as responsible for the differentiation be

91 bial composition was assessed using 16S rRNA gene sequencing at three specific time periods (baseline

92 icated this result in a second dataset of 57 genes sequenced at 127.5x in 3,124 individuals.

93 iant calling methods on exonic data from 202 genes sequenced at 24x in 7,842 individuals.

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

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

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

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

98 We analyzed the HBV precore/core gene sequences by cloning method in 33 chronic HBV-infec

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

100 We combine resistance (R) gene sequence capture (RenSeq) with single-molecule real

101 16S ribosomal RNA gene sequencing characterized the microbiota.

102 10(1) copies of Salmonella typhimurium InvA gene sequences (cloned in E. coli and after 30-cycle PCR

103 ore resistant AOB and NOB sharing functional gene sequences close to those of, respectively, Nitrosom

104 Gene sequence comparisons reveals very strong purifying

105 type, supporting the inference that specific gene sequences confer susceptibility to ICP27.

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

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

108 umour DNA encoding the clonal immunoglobulin gene sequence could be detected in the serum of patients

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

110 ed second hypervariable region (330 bp) of G-gene sequence data (global, n = 483; and Ontario, n = 60

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

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

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

114 nalyze host transcriptomic data and 16S rRNA gene sequencing data from paired biopsies from IPAA pati

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

116 yses of urine metabonomics data and 16S rRNA gene sequencing data to investigate the functional relat

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

118 ANGPTL3 gene sequencing demonstrated that approximately 1 in 309

119 16S ribosomal RNA gene sequencing detected diverse bacterial DNA signature

120 which is instrumental in gene discovery and gene sequence determination.

121 rican and 198 white HA subjects and their F8 gene sequences determined.

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

123 cular epidemiology studies analyse viral pol gene sequences due to their availability, but whole geno

124 e show evidence of convergent evolution of G gene sequence duplication and fixation over time, which

125 without a recently reported 72-nucleotide G gene sequence duplication.

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

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

128 systems rely on the production of a specific gene sequence encoding one therapeutic product.

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

130 it can be difficult to assign identities to gene sequences, especially from non-model organisms.

131 he evaluation of the impact of metabolism on gene sequence evolution and show that it is possible to

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

133 ity lipoprotein cholesterol (after candidate gene sequencing excluded known genetic causes for high l

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

135 Our method fully takes into account the gene sequence features and the miRNA and mRNA expression

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

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

138 ular and subcellular levels is complementing gene sequencing for pathway discovery and metabolic engi

139 was directly compared with that of 16S rRNA gene sequencing for the evaluation of 297 mycobacteria i

140 queried to extract the 53 ribosomal protein gene sequences from 44 genomes from diverse species.

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

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

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

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

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

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

147 ms multiple analyses based on comparisons to gene sequences from large databases.

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

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

150 We extracted all subtype B HIV-1 pol gene sequences from treatment-naive patients within the

151 BAP1 gene sequencing from blood samples of patients with uvea

152 n to be encoded by a multitude of synonymous gene sequences, has an important role in regulating prot

153 Gene sequence homology predicts that the sioxanthin bios

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

155 1.5) sites in Spain and UK that are 16S rRNA gene sequence-identical with 'G-plasma'.

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

157 ing negative for BRCA1/2 mutations, multiple-gene sequencing identified 16 potentially pathogenic mut

158 23S rRNA gene sequencing identified mutations previously associat

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

160 cterial flow cytometry coupled with 16S rRNA gene sequencing (IgA-Seq) in murine models of immunodefi

161 Inference of gene sequences in ancestral species has been widely used

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

163 compared and analysed the homologous coding gene sequences in genomic and transcriptomic data from 2

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

165 Analyses of gene sequences in various closely related prokaryotic gr

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

167 d, we profiled gut microbiota using 16s rRNA gene sequencing in a panel of 110 diverse inbred strains

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

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

170 sequencing, Zap-70 methylation, and targeted gene sequencing in these patients are identical at basel

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

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

173 in resistance was detected in 3 eyes by rpoB gene sequencing, in 3 eyes by the MTBDRplus assay, and i

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

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

176 from the order Chlorobiales prevailed, with gene sequences indicating members of the genera Chlorobi

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

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

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

180 (LAMP) assays targeting the L. loa-specific gene sequences LLMF72 and LLMF342 were developed for the

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

182 However, these results suggest that multiple-gene sequencing may benefit appropriately selected patie

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

184 broad range of applications such as targeted gene sequencing, metagenomics, small genome sequencing a

185 design, and a workflow of 16S ribosomal RNA gene sequencing methodology, primarily for investigators

186 Recent advanced gene-sequencing methods have facilitated the discovery o

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

188 Prion protein gene sequence, molecular, and neuropathological studies

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

190 Full genome (n = 17) or spike gene sequences (n = 82) were obtained from 99 individual

191 Five primers specific for the N gene sequence of PEDV were used for the cross-priming am

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

193 analysis of HAdV-D capsid genes, fiber knob gene sequences of HAdV-D types associated with EKC forme

194 Minimal polymorphism was detected in BmAMA1 gene sequences of parasite isolates from six babesiosis

195 through the analyses of partial N-gene and F-gene sequences of the virus.

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

197 h FVIII2194-2213 T-cell receptor beta (TCRB) gene sequencing of 15 T-cell clones from the severe HA s

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

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

200 o detected by using high-throughput antibody gene sequencing of blood samples, nasal mucosal samples,

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

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

203 From gene sequencing of patients known or suspected to have o

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

205 biota was determined using 16S ribosomal RNA gene sequencing of stool samples.

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

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

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

209 ormed genetic linkage analysis and candidate gene sequencing on 13 patients from a large consanguineo

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

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

212 breaks on the basis of the nucleoprotein (N) gene sequence only, as the diversity of circulating MeV

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

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

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

216 With advances in next-generation gene sequencing, progress in deep phenotyping and a grea

217 sis) and molecular data (prion protein [PrP] gene sequencing, PrPSc type).

218 tive abundance of C. difficile from 16S rRNA gene sequencing (r(2) = -0.60) and MSS (r(2) = -0.55).

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

220 valuation of pyrosequencing-derived 16S rRNA gene sequences recovered from incubations revealed the d

221 matically survey primer fidelity in SSU rRNA gene sequences recovered from over 6,000 assembled metag

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

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

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

225 Our gene sequencing results of gut microbiota showed that th

226 sedimentation, as many prokaryotic 16S rRNA gene sequences retrieved from the extracted DNA are phyl

227 Analysis of 16S rRNA gene sequences revealed that methanogens closely related

228 ed genus-specific primers targeting 16S rRNA gene sequences revealed the presence of a Dehalogenimona

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

230 Illumina 16S rRNA gene sequencing revealed a complex community of bacteria

231 16S-rRNA gene sequencing revealed a differential abundance of 71

232 Gene sequencing revealed a phenylalanine-->isoleucine mu

233 16S rRNA gene sequencing revealed diverse microbial communities i

234 d by whole-genome amplification and 16S rRNA gene sequencing revealed previously unrecognized interac

235 16S rRNA gene sequencing revealed that diazinon exposure signific

236 primary uRCC, incorporating targeted cancer gene sequencing, RNA sequencing, single-nucleotide polym

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

238 t of CRISPR loci and cas (CRISPR-associated) genes: sequence segments of invaders are incorporated in

239 ilocus sequence analysis (MLSA) and 16S rRNA gene sequence showed that most equine isolates could als

240 In this study, gene sequences showed the presence of two PaLAR3 allelic

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

242 . azotoformans NBRC 15712(T) (96.3% 16S rRNA gene sequence similarity) is the closest Bacillus specie

243 d showed 100% 16S rRNA, rpoB, sodA, and recN gene sequence similarity.

244 have seldom been applied to microbial marker gene sequencing studies, which have mostly relied on nov

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

246 e forma specialis harbour identical effector gene sequences, supporting horizontal transfer of geneti

247 Using a synthetic BCR-ABL fusion gene sequence target, we examined samples containing bet

248 In particular, the 16S ribosomal RNA gene sequencing technique has played an important role i

249 The other splice site is co-opted from the gene sequence that is duplicated upon transposon inserti

250 Accurate detection of 16S rRNA gene sequences that include intragenomic variations can

251 yotic genome projects have reported multiple gene sequences that were much more similar to homologues

252 3-3 and tau proteins, and together with PRNP gene sequencing the test allows the major prion subtypes

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

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

255 ut collections are invaluable for connecting gene sequence to function, yet traditionally, their cons

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

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

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

259 of each HIV molecular form together with CD3 gene sequences to precisely measure cell input.

260 microbiome research is moving from 16S rDNA gene sequencing to a more comprehensive genomic and func

261 gmental glomerulosclerosis were confirmed by gene sequencing to bear dominant-negative MC1R mutations

262 with positive results were subjected to rpoB gene sequencing to demonstrate rifampicin resistance.

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

264 action for RV to judge viral load along with gene sequencing to identify strains of RV.

265 anscriptomics, quantitative PCR and 16S rRNA gene sequencing to study the changes in community compos

266 The EIII gene sequence typically encodes epitopes recognized by v

267 001 Genomes Consortium, we characterize rRNA gene sequence variation within and among accessions.

268 gene based on mechanisms dependent on subtle gene sequence variation.

269 grams, basecaller software frequently missed gene sequence variations or could not identify variant b

270 eases, yet it has been difficult to identify gene sequence variations that underlie this heritability

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

272 The PrP gene sequence was significantly associated with decline

273 ulating EBV latent membrane protein 1 (LMP1) gene sequences was observed between cellular and oral wa

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

275 16s RNA gene sequencing was performed on acellular bronchoalveol

276 -control strategy for this disease, 16S rRNA gene sequencing was used to assess the microbial communi

277 16S ribosomal RNA gene sequencing was used to characterize the microbiota

278 Single-molecule real-time gene sequencing was used to quantify enrichment of mutan

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

280 he complementary determining region 3 (CDR3) gene sequence, we found no significant differences in th

281 thousands of shared single-copy orthologous gene sequences, we fully reconstruct, for the first time

282 Based on genome and relevant gene sequences, we infer that the sweet, umami, and bitt

283 Using 16S-rRNA gene sequencing, we characterized 260 seaweed-associated

284 Using high-throughput 16S rRNA gene sequencing, we characterized the most abundant bact

285 icant isolates from the VGS group by16S rRNA gene sequencing, we identified 14 S. tigurinus isolates

286 gosity mapping and whole-exome and candidate gene sequencing, we identified ten families carrying six

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

288 The HBV basal core promoter and precore/core gene sequences were also evaluated in subjects with and

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

290 Bacterial 16S rRNA gene sequences were characterized, and microbial diversi

291 Several nsLTPs-encoding cDNA and gene sequences were cloned from Coffea arabica and Coffe

292 A total of 8,263,982 16S rRNA gene sequences were obtained, which were affiliated to 5

293 Moreover, similar morphotypes and 16S gene sequences were retrieved from samples collected fro

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

295 Full exome and candidate gene sequencing were carried out in a family with A1ATD

296 he anode of all three SAPs based on 16S rRNA gene sequencing were Geobacter, Smithella and Syntrophob

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

298 The set of cold genes, which were 21% of the genes sequenced, were further winnowed down by examining

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

300 Resistance to pyrazinamide was assessed by gene sequencing with the detection of resistance-conferr