ライフサイエンスコーパス: hypervariable

1 their DNA structure and primary sequence are hypervariable.

2 In analogy with poliovirus, a hypervariable 5' untranslated region tract may affect vi

3 inical isolates by pyrosequencing within the hypervariable A region of the 16S rRNA gene was compared

4 ecies revealed that the N-terminal domain is hypervariable among species yet is conserved with regard

5 e NH2-terminal region of troponin T (TnT) is hypervariable among the muscle type-specific isoforms an

6 Numerous CD4(+) T cell epitopes in the hypervariable and conserved regions of MSP2 contribute t

7 In addition, we show that both hypervariable and conserved regions of pilin are not sup

8 pheral peptide residues and the roles of the hypervariable and germline CDR loops in engaging peptide

9 all, conserved functional sites on otherwise hypervariable antigens.

10 o the Xp/Yp telomere, each copy containing a hypervariable array of the DXYS14 minisatellite.

11 Using universal primers that amplify the hypervariable bacterial 16 S rRNA gene as a model system

12 thin filament proteins, and its sequence is hypervariable between fiber type and developmental isofo

13 The hypervariable C-terminal domain (HVD) of Rabs is posttra

14 e-directed mutagenesis now indicate that the hypervariable C-terminal region of beta5 plays no role i

15 of CG8486-specific genes mapping outside the hypervariable carbohydrate biosynthesis loci.

16 ung, as determined by deep sequencing of the hypervariable CD3RbetaVJ region of the TCR.

17 CD1d affinities are further modulated by the hypervariable CDR3 beta loop, thereby defining a functio

18 receptor then contacts the peptide using the hypervariable CDR3 loops as the transition state decays

19 C ligand derives largely from the juxtaposed hypervariable CDR3 regions on the TCRalpha and TCRbeta c

20 On average, the hypervariable CDRH3 region was four nucleotides shorter

21 , it is unclear if affinity mutations in the hypervariable CDRs generally impact antibody stability a

22 Using the hypervariable chloroplast ndhF-rpl32 sequences of 604 sa

23 variations and the presence and structure of hypervariable chromosomal elements indicate that there i

24 Hypervariable contingency loci and epigenetic switches i

25 tly capture all common variation (except the hypervariable D-loop).

26 R amplification and sequence analysis of the hypervariable D1/D2 region of the 26S rRNA gene for the

27 es that are specific to epitopes in both the hypervariable deletion and control proteins.

28 In contrast, the hypervariable deletion protein was unable to elicit an i

29 lular proteins are largely determined by the hypervariable domain (HVD) of nsP3.

30 ese nonstructural proteins, nsP3, contains a hypervariable domain (HVD), which demonstrates very low

31 of nsp2 (the PLP2 protease domain [OTU], the hypervariable domain [HV], the putative transmembrane do

32 The V4 hypervariable domain in clade C is shorter than that in

33 ylation, and amino acid sequence of the V1V2 hypervariable domain of gp120, while the recipient Envs

34 The hypervariable domain of the EEEV nsP3 protein interacts

35 A filaments and identified a surface-exposed hypervariable domain that contains the immunodominant Es

36 ar domains: a conserved N-terminal domain, a hypervariable domain, and an acidic C-terminal domain.

37 rved N-terminal domain of VP90 but lacks the hypervariable domain, which forms the capsid surface spi

38 those of other teams have demonstrated that hypervariable domains (HVDs) of the alphavirus nsP3 prot

39 e receptor and the surface (SU) glycoprotein hypervariable domains are required for binding affinity

40 t population turnover of the V1-V2 and V4-V5 hypervariable domains of the human immunodeficiency viru

41 tudy, acquisition of length in the Env gp120 hypervariable domains was shown to correlate with resist

42 zation, chimeras containing heterologous Rab hypervariable domains were generated, and their ability

43 acids in length, with large surface-exposed hypervariable domains.

44 ia their unstructured and membrane-anchored, hypervariable domains.

45 of Env is particularly striking in the V1/V2 hypervariable domains.

46 and gene copy number variation (CNV) at the hypervariable DRB locus within the MHC region to HPV ser

47 1918 and 2009 hemagglutinins, a site that is hypervariable due to immune selection.

48 mutations by acting like a blanket over the hypervariable epitope, thereby providing effective viral

49 In neutrophils, genes with hypervariable expression are found to be implicated in k

50 de a transmembrane receptor protein with two hypervariable extracellular regions similar to immunoglo

51 helping to control product chemistry in this hypervariable family of marine natural products.

52 We report a previously unidentified, hypervariable family of PDIs that represents the most di

53 re widely recognized than were extracellular hypervariable fragments.

54 three variable island regions, with the most hypervariable genes concentrated at one end of the genom

55 This novel family of hypervariable genes with conserved, repetitive, and alle

56 t strains identified, with (except for a few hypervariable genes) the EEHV2, EEHV3, and EEHV6 strains

57 by less than 1% within populations, even in hypervariable genome regions, and by 42-71% between popu

58 ndings uncover a novel and cryptic source of hypervariable genomic diversity with global regulatory c

59 sted by PCR for the presence or absence of 4 hypervariable genomic regions.

60 Specific mutations within the hypervariable herpes simplex virus (HSV) gene thymidine

61 We conclude that the hypervariable hinge region of the P protein plays an imp

62 the largely conserved HLA-A*0201-M158and the hypervariable HLA-B*3501-NP418antigens.

63 Kupffer cell interaction is mediated by the hypervariable (HVR) loops of the virus hexon protein, we

64 Adaptive immunity in humans is provided by hypervariable Ig-like molecules on the surface of B and

65 The described homopolymer is hypervariable in length, varying from 12 to 17 bp in the

66 These studies reveal sequences upstream, hypervariable in the human population (HVR3), and downst

67 Because residues 418 to 426 of the hypervariable influenza A virus nucleoprotein (NP(418-42

68 BorreliaBase allows online identification of hypervariable lipoprotein genes, potential regulatory el

69 Unexpectedly, other hypervariable loci in our data were in previously undesc

70 genome sequences have defined conserved and hypervariable loci in the C. jejuni genome.

71 Most of the hypervariable loci were linked to genes encoding RTs of

72 he capability to selectively bind and enrich hypervariable, long or repetitive sequences.

73 ns of Africa was therefore surprising as one hypervariable loop contains the entire collagen-binding

74 eir concave surface, in addition to a unique hypervariable loop in the C-terminal LRR capping module.

75 ht chains, the majority of CDR-L3 [the third hypervariable loop of the light chain variable domain (V

76 ally divergent face of the protein formed by hypervariable loop segments, confirming that TRIM5alpha

77 ity (together with the local dynamics of the hypervariable loop within domain 3) could facilitate rec

78 P.falciparum isolates demonstrates that the hypervariable loop within Stevor and Pfmc-2TM proteins p

79 ighlight the divergences observed within the hypervariable loop.

80 Neutralization epitopes localize to three hypervariable loops in the distal portion of the protrud

81 me the coding sequences for the two external hypervariable loops in the protein.

82 ity in structure is most apparent in the six hypervariable loops of the complementarity-determining r

83 ed of immunoglobulin (Ig) domains containing hypervariable loops that bind antigen.

84 Antibodies recognize antigens through six hypervariable loops, five of which have a limited set of

85 e heavy and light chain each providing three hypervariable loops, which are varied to generate divers

86 ndicated only for the CDR3alpha and CDR3beta hypervariable loops.

87 The haplotigs accurately characterized the hypervariable major histocompatability complex region as

88 creased combinations of the newly identified hypervariable microdomains.

89 Furthermore, these motifs are found in hypervariable minisatellites and are clustered in the br

90 Furthermore, these motifs are found in hypervariable minisatellites and are clustered in the br

91 study reveals that a previously undescribed hypervariable molecule bearing three extracellular domai

92 orphisms within the Helicobacter pylori CagL hypervariable motif (CagLHM) in gastric cancer-associate

93 ation sites or with deletions in the central hypervariable mucin region.

94 By exploiting the hypervariable nature of virulence genes and clustered re

95 These results suggest that the hypervariable NH2-terminal region modulates the conforma

96 Deletion of the TnT hypervariable NH2-terminus preserved binding to troponin

97 n-specific splice variant repertoires of the hypervariable pattern recognition receptor AgDscam.

98 al fusion of a reporter lacZ fragment to the hypervariable poly-Psi domain facilitated measurement of

99 We aligned time-stamped second hypervariable region (330 bp) of G-gene sequence data (g

100 e for viral replication, and the nsp2 middle hypervariable region (aa 324 to 813) tolerated 100-aa or

101 kines was localized to 40 amino acids in the hypervariable region (amino acids 301-340) of the protei

102 me of the hepatitis E virus (HEV) contains a hypervariable region (HVR) in ORF1 that tolerates small

103 rnesylated and positively charged C-terminal hypervariable region (HVR) is critical to its oncogenic

104 sed on chromosomal DNA fingerprints (CDF), a hypervariable region (HVR) of a 5.6-kb plasmid, the rRNA

105 man ribosomal protein S17 (RPS17) within the hypervariable region (HVR) of the HEV ORF1 protein.

106 A hypervariable region (HVR) previously identified in the

107 n, predominately against the surface-exposed hypervariable region (HVR) rather than against the invar

108 Between these two ends is a hypervariable region (HVR) that is only poorly conserved

109 Comparative sequence analysis revealed a hypervariable region (HVR) with extensive sequence varia

110 cently, insertions and rearrangements of the hypervariable region (HVR) within the HEV genome, allowi

111 -Ras4B is predominantly autoinhibited by its hypervariable region (HVR), whereas the GTP-bound state

112 Previous studies have shown that the first hypervariable region (V1 loop) is immunogenic on soluble

113 ies (NAbs) that primarily targeted the first hypervariable region (V1 loop) of gp120, although SF162g

114 ne hypervariable region of mtDNA, designated hypervariable region 1 (HV1).

115 amino acid quasispecies complexities of the hypervariable region 1 (HVR-1) were less in the responde

116 Hypervariable region 1 (HVR1) (amino acids [aa] 384 to 4

117 edly reduced binding when amino acids within hypervariable region 1 (HVR1) and at sites approximately

118 Hypervariable region 1 (HVR1) is genetically diverse and

119 Interestingly, the E2 hypervariable region 1 (HVR1) mutation T385P caused (i)

120 which we find maps to a specific site within hypervariable region 1 (HVR1) of AdV5 hexon, has no appa

121 f HCV and shielding of important epitopes by hypervariable region 1 (HVR1) of E2 are believed to be m

122 Hypervariable region 1 (HVR1) of hepatitis C virus (HCV)

123 Furthermore, replacement of hypervariable region 1 (HVR1) of the Ad capsid proteins

124 Evolutionary rates in the hypervariable region 1 (HVR1) region of the E2 gene were

125 Remarkably, sequences of hypervariable region 1 (HVR1) remained stable for up to

126 to Huh7.5 cells to produce a quasispecies of hypervariable region 1 (HVR1) that mimicked that circula

127 Hypervariable region 1 (HVR1) variability is frequently

128 Hypervariable region 1 (HVR1) within viral envelope prot

129 We obtained sequences from the HCV hypervariable region 1 (HVR1), using end-point limiting-

130 plotypes that had identical sequences in the hypervariable region 1 (HVR1).

131 s-immunoreactivity among variants of the HCV hypervariable region 1 (HVR1).

132 instead of the well-known immunodominant E2 hypervariable region 1 (HVR1).

133 d, ranging from high diversity (the envelope hypervariable region 1 [HVR1]) to almost no diversity (t

134 on of SR-BI governed by specific residues in hypervariable region 1 of E2 leading to enhanced cell en

135 terized epitopes on E1/E2, especially to the hypervariable region 1 of E2.

136 out the envelope genes, primarily within the hypervariable region 1 of E2.

137 is virus (VSV)/HCV pseudotype model that the hypervariable region 1 of the HCV E2 envelope glycoprote

138 o 986 present-day human sequences located in hypervariable region 1 of the mitochondrion to estimate

139 Hypervariable region 1 of the second envelope gene was a

140 Most NAbs recognize hypervariable region 1 on E2, which undergoes frequent m

141 equence revealed amino acid substitutions in hypervariable region 1 that were responsible for a drama

142 yethylene glycol to a specific site in hexon hypervariable region 1 yielded vector particles that wer

143 Deletion of hypervariable region 1, a region previously proposed to

144 s, suggesting purifying selection, except in hypervariable region 1, where positive selection pressur

145 nfectivity of J6(2a) and J8(2b) with deleted hypervariable region 1.

146 Sequencing of hypervariable region 4 poorly captures skin commensal mi

147 a single immunization of chimeric rAd5 hexon hypervariable region 48 (rAd5HVR48) vectors expressing S

148 igen (PA) as a model antigen to characterize hypervariable region 5 (HVR5) of hexon as a site for pep

149 MiSeq and Roche454 platforms using the V3-V4 hypervariable region also showed a high level of concord

150 ue to a mixture of P44 proteins with diverse hypervariable region amino acid sequences expressed by a

151 Neisserial mod alleles also contained a hypervariable region and all mod alleles exhibited varia

152 Analysis of the szp gene hypervariable region and the 16S-23S rRNA intergenic spa

153 The hemagglutinin (H) gene and hypervariable region between the fusion and matrix genes

154 3 million 16S rRNA sequences spanning the V4 hypervariable region by pyrosequencing.

155 While the hypervariable region CDR3 often mediates much of the spe

156 The hypervariable region D2 and D3 domains appear to stabili

157 We propose that this hypervariable region encodes the target recognition doma

158 lysis indicated that most sites outside this hypervariable region experienced strong negative selecti

159 extension containing a His- and Asp/Glu-rich hypervariable region followed by a highly conserved sequ

160 d for identification of the 16S rRNA gene V3 hypervariable region from Escherichia coli genomic DNA.

161 two primer pairs demonstrated that the V3-V4 hypervariable region had significantly better capture of

162 etion variants of UreG demonstrated that the hypervariable region has a minor impact on activation ef

163 -446 (epitope II), located downstream of the hypervariable region I within the HCV E2 protein.

164 60 million molecules) of human mitochondrial hypervariable region II amplicon was introduced into the

165 Here we show that the human mitochondrial hypervariable region II can function as a molecular fing

166 esent high-throughput sequencing analysis of hypervariable region II for spatial resolution of the co

167 the structural and physiological role of the hypervariable region in flagella assembly, stability and

168 ed sequence blocks throughout the MSP2 (P44) hypervariable region in reservoir hosts.

169 on-typeable H.influenzae isolates revealed a hypervariable region in the central portion of the mod g

170 e induction of Gal-3 expression requires the hypervariable region in the extracellular domain of beta

171 sitive to GM-CSF, mutations within the N-Ras hypervariable region induced N-Ras mislocalization and a

172 in primary structure within the immunogenic hypervariable region microdomains and tested whether the

173 ted nanoclustering of H-ras helix alpha4 and hypervariable region mutants that have different bona fi

174 .1 M bacterial pyrotag sequences from the V6 hypervariable region of 16S rRNA genes from 38 influent

175 human hepatoma cells when inserted into the hypervariable region of a genotype 1 strain, but this ch

176 plified by using primers specific for the V6 hypervariable region of bacterial 16s rRNA.

177 a crucial but commonly coded residue in the hypervariable region of CDR3 provide the basis for the s

178 anged p44Es revealed that the entire central hypervariable region of donor p44 pseudogenes or of dono

179 rough elevated signal produced to the unique hypervariable region of each - 2/114 in HL-60, 3/114 in

180 oduplex tracking assay targeted to the V1/V2 hypervariable region of env.

181 The hypervariable region of K-Ras4B binds specifically to th

182 tration calorimetry, we demonstrate that the hypervariable region of K-Ras4B contributes in a major w

183 histocompatibility antigens, we examined one hypervariable region of mtDNA, designated hypervariable

184 r results show that in the murine model, the hypervariable region of PilE is required to activate imm

185 nal structure-based antigen by replacing the hypervariable region of PilE with an aspartate-glutamine

186 ly bound to the CAAX motif in the C-terminal hypervariable region of Rac1, and then inhibited Rac1 me

187 zed by bar-coded pyrosequencing of the V3-V5 hypervariable region of the 16S rRNA gene, defining 662

188 ent study, using pyrosequencing of the V1-V2 hypervariable region of the 16S rRNA gene, reported find

189 We were able to assemble the D1-D2 hypervariable region of the 28S ribosomal RNA (rRNA) of

190 This virus was unusual in that the hypervariable region of the adapted virus contained a 17

191 idase subunit 1 gene of nematodes and the V3 hypervariable region of the bacterial 16 s ribosomal RNA

192 d a tag-sequencing strategy targeting the V6 hypervariable region of the bacterial small-subunit (16S

193 ndings indicate that sequence variation in a hypervariable region of the degron affects JAZ stability

194 s a 5-aa sequence motif in the third allelic hypervariable region of the HLA-DRbeta chain.

195 This residue is located in the C-terminal hypervariable region of the proteins and is not conserve

196 several single-nucleotide substitutions in a hypervariable region outside the SAM-binding core can al

197 g GC and AT rich motifs correlated well with hypervariable region recombination sites across the HAdV

198 The K-Ras4A hypervariable region sequence is positively charged, in

199 ing more than 1.7 million bacterial 16S rRNA hypervariable region sequences from 52 to 56 samples per

200 a gonorrhoeae and contains a surface-exposed hypervariable region thought to be one feature of pili t

201 had greater accuracy than sequencing of the hypervariable region V4 in determining genus and species

202 The 16S RNA hypervariable region V4 was sequenced on Illumina MiSeq.

203 sequencing based on the bacterial 16 S rRNA hypervariable region V4.

204 gG variants containing the EHV-1 hypervariable region were able to bind chemokines and we

205 -DR alleles sharing amino acids at the third hypervariable region with DRB1*0401(shared epitope) are

206 he majority of their genomes but contained a hypervariable region with extensive divergence.

207 e, and -f were mapped within the nsp2 middle hypervariable region, but no conserved cleavage sites co

208 terminal conserved region and P44-18 central hypervariable region, respectively.

209 Results obtained from the V3-V4 16S rRNA hypervariable region, sequencing on the MiSeq and Roche4

210 key changes to the lipidation pattern of the hypervariable region, suggest that dimerization is a gen

211 mice, suggesting that in the absence of the hypervariable region, the conserved regions of PilE alon

212 By looping out the hypervariable region, the porin structure is conserved a

213 The HCV E2 hypervariable region-1 was amplified using nested revers

214 nt cells, and we mapped this activity to the hypervariable region.

215 lyzed using 16S rRNA sequencing of the V3-V4 hypervariable region.

216 obility analysis of the second envelope gene hypervariable region.

217 arnesylated-methylated KRAS4b, including the hypervariable region.

218 ha and Vbeta chain usage, and throughout the hypervariable region.

219 ed flanking domains and the other within the hypervariable region.

220 A gene sequences by more than 80% for the V4 hypervariable region.

221 monella typhimurium phase 1 flagellin, this "hypervariable" region encodes two solvent-exposed domain

222 egments from multiple alleles to form unique hypervariable regions (HVR).

223 Replacing hypervariable regions (HVRs) 1, 2, 4, and 5 with the equ

224 ing antibodies typically recognize M protein hypervariable regions (HVRs) and confer narrow protectio

225 at CaM preferentially binds unfolded K-Ras4B hypervariable regions (HVRs) and not alpha-helical HVRs.

226 h substantial sequence homology in the hexon hypervariable regions (HVRs) and suppressed the immunoge

227 rface-exposed regions of the capsid, such as hypervariable regions (HVRs) I to IX of VP3.

228 maeric rAd5 vectors in which the seven short hypervariable regions (HVRs) on the surface of the Ad5 h

229 us catalytic domains and flexible C-terminal hypervariable regions (HVRs) that differ across Ras isof

230 (NAbs) directed primarily against the hexon hypervariable regions (HVRs).

231 FX binds to the adenovirus hexon hypervariable regions (HVRs).

232 to potential N-linked glycosylation sites in hypervariable regions (V1 to V3) of the env gene of HIV

233 We used DNA from hypervariable regions (V1-V2) of 16S bacteria rRNA to de

234 tes microbial communities, but sequencing of hypervariable regions 1-3 of the 16S rRNA gene provides

235 hanges both within the traditionally defined hypervariable regions and downstream, near the 3'-end of

236 r multiple markers such as the 16S rRNA gene hypervariable regions are available, MetAmp improves the

237 ts and the genes from the other intraspecies hypervariable regions contributes to a better assessment

238 Only the C-terminal hypervariable regions differ significantly.

239 cally infected individuals by sequencing the hypervariable regions encoding TCR alpha and beta polype

240 identified in at least two of five examined hypervariable regions for every virus, suggesting the ev

241 g it into our Ad5 vector containing all nine hypervariable regions from Ad43, Ad5.H(43m-43), increase

242 the specific amplification of 18s rRNA gene hypervariable regions from eukaryotic microbes: anneal-i

243 Pyrosequencing of amplicons for hypervariable regions in the 16S rRNA gene generated tax

244 16S rRNA per cells and also the presence of hypervariable regions in the genes.

245 unique, sexually dimorphic motifs in the TCR hypervariable regions in the SjS(S) mice.

246 ligonucleotide gold nanoprobe for one of the hypervariable regions of 16S rRNA gene.

247 nd ESPRIT-Tree, sequence data from different hypervariable regions of 16S rRNA were used and binning

248 serotype 5 (Ad5) vector containing the hexon hypervariable regions of Ad serotype 48 (Ad48) and expre

249 hexon-modified vector that carried the hexon hypervariable regions of Ad48, indicating that the SP mu

250 In these hybrid glycoproteins the hypervariable regions of EHV-1 gG, a vCKBP, and the clos

251 Finally, features of the first and second hypervariable regions of gp120 (V1V2) may be critical fo

252 oes is efficiently surveyed by sequencing of hypervariable regions of the 16s ribosomal RNA (rRNA) ge

253 lyzed by FLX+ pyrosequencing of the V1 to V4 hypervariable regions of the 16S rRNA gene and polymeras

254 Unique melt profiles generated from multiple hypervariable regions of the 16S rRNA gene for 100 clini

255 DNA was amplified with primer pairs covering hypervariable regions of the 16S rRNA gene: primers 63F

256 The rates of evolution within hypervariable regions of the FCV capsid gene in individu

257 an interaction between the FX Gla domain and hypervariable regions of the hexon surface.

258 Conventional genotyping methods target small hypervariable regions of the M. bovis genome and provide

259 is phosphorylated at sites clustered in two hypervariable regions of the protein.

260 ences between D1 domains are concentrated in hypervariable regions on the front sheet strands of the

261 s in the mtDNA control region, including the hypervariable regions typically sequenced in a forensic

262 two species by pyrosequencing the 16S V1-V3 hypervariable regions using the 454 GS FLX Titanium plat

263 pected microbial profiles, sequencing of the hypervariable regions V1-V3 of the 16S ribosomal RNA gen

264 The 16s rRNA hypervariable regions V3 and V6 were amplified from Kleb

265 analysis indicates that alternative 16S rRNA hypervariable regions will present similar challenges, w

266 s identified as phage morons were located in hypervariable regions within individual SVMs, indicating

267 l seven HAdV species, confirmed the uniquely hypervariable regions within species.

268 method also identified 18 other intraspecies hypervariable regions, such as the capsule and lipooligo

269 of hepatitis C virus (HCV) contains several hypervariable regions.

270 regions, including splice site acceptors and hypervariable regions.

271 not exclusively, directed against the hexon hypervariable regions.

272 is is further complicated by the presence of hypervariable regions.

273 The hypervariable reiterative repeat regions in the US1 and

274 Surprisingly, three different hypervariable repetitive regions in csd are present in t

275 Both are hypervariable rhoptry proteins that are secreted into th

276 As expected, the third hypervariable segment (CDR3), formed by the rearrangemen

277 amino acid, Thr(1068), in the evolutionarily hypervariable segment of beta'.

278 A hypervariable segment, residing between the atp6 and rrn

279 alyzed 815,377 autosomal SNPs, mitochondrial hypervariable segments I and II, and 36 Y-chromosome STR

280 r 32 lineage-defining mitochondrial SNPs and hypervariable sequence (HVS) 1, Tamil castes have higher

281 The custom database was generated using the hypervariable sequences of the internal transcribed spac

282 Neutrophil-specific DNA methylation hypervariable sites are enriched at dynamic chromatin re

283 Two 18S rDNA hypervariable sites, the V4 and V8-V9 regions, were ampl

284 However, exon variation within the hypervariable splice region resulted in significant diff

285 ison, deletion of loop 2, which contains the hypervariable splice region, did not reduce the ability

286 Hypervariable subregion 1 (HV-1) is localized to an inte

287 t clustered exclusively within HV-1 or other hypervariable subregions.

288 CBD uses the repetitive nature of hypervariable tag datasets and well-established compress

289 etween gastrointestinal tract microbiota 16S hypervariable tag datasets.

290 btained from carefully curated deep 16S rRNA hypervariable tag sequencing data.

291 composition through the use of 16S rRNA gene hypervariable tag sequencing has profound health implica

292 t microbial populations were generated using hypervariable tag sequencing of the V3-V5 region of the

293 aoperatively obtained samples using 16S rDNA hypervariable tag sequencing.

294 this family of genes are characterized by a hypervariable "toxin" region capable of encoding a wide

295 rived from next-generation sequencing of the hypervariable V3 region of the 16S ribosomal RNA gene sh

296 acer using two approaches, pyrosequencing of hypervariable V3-V5 regions of the 16S rRNA gene and who

297 f linear peptides corresponding to the third hypervariable (V3) loop of gp120 failed to inhibit serum

298 Pro(313)-Gly(314)-Arg(315) arch of the third hypervariable (V3) loop of the HIV-1 surface glycoprotei

299 associated multigene families, including the hypervariable var genes, is broadly conserved, but P. fa

300 les that serve as sequence templates for the hypervariable VLR repertoires.