1 clinical interventions using virological and
phylogenetic analysis.
2 of VacA, m1 and m2, can be distinguished by
phylogenetic analysis.
3 TCRdelta (but not IgH) rearrangements in our
phylogenetic analysis.
4 viral genome was sequenced and subjected to
phylogenetic analysis.
5 combination of distance-based clustering and
phylogenetic analysis.
6 nto 2, 4 and 2 cluster respectively based on
phylogenetic analysis.
7 ic acid gyrase (gyrB) genes and conducting a
phylogenetic analysis.
8 position is robustly supported by multigene
phylogenetic analysis.
9 T-PCR-positive individual and assessed using
phylogenetic analysis.
10 rus deep-sequenced at sufficient quality for
phylogenetic analysis.
11 uous synapomorphies for clades identified by
phylogenetic analysis.
12 carcinoids and myriapods recovered in recent
phylogenetic analysis.
13 Pol region consensus sequences were used for
phylogenetic analysis.
14 ) are subdivided into type I and II based on
phylogenetic analysis.
15 on these features and results of a multigene
phylogenetic analysis,
a new genus and species, Emydomyc
16 In support of RNA mutation and
phylogenetic analysis,
a web server (RNA-TVcurve) was de
17 In our
phylogenetic analysis,
acquisition of the definitive mam
18 Phylogenetic analysis across different kingdoms shows th
19 Systematic
phylogenetic analysis allowed us to propose similar regu
20 The
phylogenetic analysis also showed that strains involved
21 Phylogenetic analysis and ancestral fruit-type reconstru
22 orphic sites to RR and SR was assessed using
phylogenetic analysis and Bayesian network methods.
23 logous Bacillus subtilis CopL, together with
phylogenetic analysis and chemical-shift perturbation ex
24 Ligands of SLC22A15 were proposed based on
phylogenetic analysis and comparative modeling.
25 sequences were available for well-supported
phylogenetic analysis and could provide valuable resourc
26 Based on a
phylogenetic analysis and enzymatic assays, we propose t
27 IGEs from 2168 genomes, along with integrase
phylogenetic analysis and gene inactivation tests, revea
28 Phylogenetic analysis and genetic distance indices resol
29 Using
phylogenetic analysis and molecular dynamics simulations
30 ional evolution of MS5 homologs in plants by
phylogenetic analysis and molecular genetic experiments.
31 o the Saccharum and Erianthus genera through
phylogenetic analysis and principle component analysis (
32 Our analysis is illustrated by
phylogenetic analysis and publicly available gene expres
33 Phylogenetic analysis and ribosome binding experiments i
34 e-origin" variant influenza viruses based on
phylogenetic analysis and sequence comparison methods.
35 ter I through IV, in the GII.P7 RdRp gene by
phylogenetic analysis and the GII.14[P7] variants report
36 use the CLE domain is too short for reliable
phylogenetic analysis and the pre-propeptide is too vari
37 Phylogenetic analysis and the presence of consensus moti
38 to two subtypes (DTEW and DTEF) according to
phylogenetic analysis and the presence of highly conserv
39 c and/or genomic sequence search, subsequent
phylogenetic analysis,
and detailed biochemical and gene
40 were performed with hierarchical clustering,
phylogenetic analysis,
and principal component analysis.
41 for splicing prediction, sequence alignment,
phylogenetic analysis,
and structure prediction.
42 cator orthologs identified from an extensive
phylogenetic analysis,
and type III effector translocati
43 expression profiling, allelic diversity and
phylogenetic analysis,
as well as local association stud
44 -scale microbial genome characterization and
phylogenetic analysis at multiple levels of resolution.
45 Phylogenetic analysis based on 79 craniodental and 20 po
46 Phylogenetic analysis based on ITS2 and COX1 genes revea
47 A
phylogenetic analysis based on protein sequences showed
48 Phylogenetic analysis based on whole-genome sequencing o
49 HRV-positive samples were sequenced for
phylogenetic analysis by targeting the 5' noncoding regi
50 Thus, in practice,
phylogenetic analysis can broadly identify functional de
51 Phylogenetic analysis can provide valuable information t
52 A
phylogenetic analysis combined with an analysis of the s
53 Phylogenetic analysis comparing these 28 new encapsulin
54 ehensive, vertebrate-wide gene sampling, our
phylogenetic analysis complemented with synteny analyses
55 Phylogenetic analysis confirmed infection with the donor
56 Phylogenetic analysis confirmed that these two Peromyscu
57 Our
phylogenetic analysis confirmed the position of R. micro
58 This
phylogenetic analysis contributes to growing evidence fo
59 Relaxed molecular clock
phylogenetic analysis demonstrated a molecular evolution
60 Phylogenetic analysis demonstrated high similarity with
61 A genome-wide
phylogenetic analysis demonstrated in detail the relatio
62 Phylogenetic analysis demonstrated that 2019 diagnoses w
63 Phylogenetic analysis demonstrated that 58% (7 of 12) of
64 Phylogenetic analysis demonstrated that all hospitals fr
65 Additionally, sequence similarity and
phylogenetic analysis demonstrated that different bacter
66 Phylogenetic analysis demonstrated that GPC4 is most clo
67 The
phylogenetic analysis demonstrated the lack of clonal ev
68 e heterotrophic bacterium Eudoraea adriatica
Phylogenetic analysis demonstrates that the E. adriatica
69 Phylogenetic analysis determined a close relationship be
70 Phylogenetic analysis determined that Rph1 clustered sep
71 he genomic dynamics of OROV that encompasses
phylogenetic analysis,
evolutionary rate estimates, infe
72 Phylogenetic analysis found close clustering of strains
73 monella serovar detected in L. olivacea, and
phylogenetic analysis from whole genome sequencing showe
74 Phylogenetic analysis grouped CrANT with other non-seed-
75 Retrospective
phylogenetic analysis has shown that recombination betwe
76 Phylogenetic analysis identified a clade of MHC-B, defin
77 Phylogenetic analysis identified two strains of S Enteri
78 Phylogenetic analysis identifies MARVs that are similar
79 Our
phylogenetic analysis implicates NusG-dependent pausing
80 Phylogenetic analysis implies a recent origination of th
81 Phylogenetic analysis implies CRESS viruses infecting mu
82 Our results from
phylogenetic analysis,
in vitro enzymatic assays, X-ray
83 A
phylogenetic analysis including the new taxon recovers G
84 Here, we discuss the major steps of
phylogenetic analysis,
including identification of ortho
85 Comparative genomics and
phylogenetic analysis indicate it is a new species of Ga
86 Genetic mapping and
phylogenetic analysis indicate that the duplications giv
87 Phylogenetic analysis indicated that Rv2633c is a member
88 Last, while
phylogenetic analysis indicates a bat origin of 2019-nCo
89 Phylogenetic analysis indicates ancestral polymorphic ar
90 Phylogenetic analysis indicates that the outbreak was ca
91 Phylogenetic analysis indicates that the San genetic lin
92 Our
phylogenetic analysis indicates that Y. biscarpa is a st
93 novel approach to this problem, performing a
phylogenetic analysis indicating that family living is a
94 Finally, OrthoFinder's comprehensive
phylogenetic analysis is achieved with equivalent speed
95 Phylogenetic analysis is complicated by interspecific ge
96 In
phylogenetic analysis,
Kongonaphon is recovered as a mem
97 amics characterizing these processes while a
phylogenetic analysis let us identify a candidate vitell
98 the airway field and NSCLCs were assessed by
phylogenetic analysis.
Measurements and Main Results: Gen
99 leotide dataset, implying that probabilistic
phylogenetic analysis methods are needed.
100 Using detailed time-resolved
phylogenetic analysis,
most of these gene segments likel
101 Bayesian clock-based
phylogenetic analysis nests this genus (Ucayalipithecus)
102 Phylogenetic analysis of >400 plant species in 41 genera
103 Phylogenetic analysis of 102 UPMC Citrobacter genomes sh
104 osteric regulation is broadly conserved, and
phylogenetic analysis of 264 vertebrates shows the long
105 Here, we performed a whole-genome
phylogenetic analysis of 368 IAV circulating in swine fr
106 Our
phylogenetic analysis of 37 GET3 orthologs from 18 diffe
107 Genome sequencing and
phylogenetic analysis of 387 isolates, representing the
108 Whole-genome sequencing and
phylogenetic analysis of 388 samples across 18 individua
109 The
phylogenetic analysis of 54 strains showed 3 distinct cl
110 Phylogenetic analysis of 84 distinct SARS-CoV-2 genomes
111 A
phylogenetic analysis of 87 men who have sex with men re
112 Phylogenetic analysis of a concatenation of main OM comp
113 Subsequent
phylogenetic analysis of a pericentromeric endogenous re
114 Phylogenetic analysis of all coding genes showed a close
115 Phylogenetic analysis of all IncHI2 plasmids carrying mc
116 Phylogenetic analysis of apple bHLH (MdbHLH) genes and t
117 Our structure-based
phylogenetic analysis of arenaviral GP1s provides a blue
118 cal contact tracing of patients and Bayesian
phylogenetic analysis of bacterial WGS data were used to
119 Phylogenetic analysis of cancer-associated alleles and a
120 Phylogenetic analysis of CEK orthologs in Brassicaceae s
121 A
phylogenetic analysis of class I RNRs suggests that acti
122 of the new family is supported by molecular
phylogenetic analysis of COI and 18S datasets.
123 In a
phylogenetic analysis of coleopteran and lepidopteran ar
124 crophiarin gene cluster into a comprehensive
phylogenetic analysis of echinocandin gene clusters indi
125 angiosperms and gymnosperms were used for a
phylogenetic analysis of end wall types, calculation of
126 This was supported by
phylogenetic analysis of Env sequences from viral-outgro
127 nd CISD3, Miner2) as our guides to conduct a
phylogenetic analysis of eukaryotic NEET proteins and th
128 Phylogenetic analysis of genome sequences identified two
129 y across the genus and present a comparative
phylogenetic analysis of GS evolution in diploid Heliant
130 In recent years,
phylogenetic analysis of HIV sequence data has been used
131 In agreement with ancient DNA findings, our
phylogenetic analysis of HV12 and HV14, the two exclusiv
132 We undertook an epidemiological and
phylogenetic analysis of isolates from all cases of shig
133 Phylogenetic analysis of metagenome sequences indicated
134 Phylogenetic analysis of more than 4000 annotated bacter
135 Phylogenetic analysis of morphological data proceeds fro
136 Our
phylogenetic analysis of NCLDV metabolic genes and their
137 The
phylogenetic analysis of NucS indicates a complex evolut
138 Phylogenetic analysis of our Chytridiomycota clones plac
139 Kingdom-wide
phylogenetic analysis of over 400 CYP716s from over 200
140 HTS and
phylogenetic analysis of paired specimens confirmed shed
141 Comparative genomics and
phylogenetic analysis of phage isolates facilitated the
142 Phylogenetic analysis of phytobacterial T6SS clusters sh
143 lishing, through delayed time to viremia and
phylogenetic analysis of plasma virus, that treatment of
144 Phylogenetic analysis of plastid and mitochondrial genes
145 Phylogenetic analysis of pol and env sequences grouped 3
146 Phylogenetic analysis of pol sequences from 445 index pa
147 Phylogenetic analysis of pol sequences showed a cluster
148 Phylogenetic analysis of published datasets identified s
149 to other Ebola viruses in DR Congo, we did a
phylogenetic analysis of representative complete Ebola v
150 l ribosome presented here now allow a deeper
phylogenetic analysis of ribosomal components including
151 Phylogenetic analysis of SNAP genes from 22 diverse plan
152 r, and metastatic samples in 2 cases, enable
phylogenetic analysis of spatial features of clonal expa
153 Phylogenetic analysis of the algal fermentative enzyme s
154 A comprehensive
phylogenetic analysis of the CBF/DREB1 family members in
155 addressed this by performing a comprehensive
phylogenetic analysis of the Cdc14 family and comparing
156 Phylogenetic analysis of the corresponding melanin polyk
157 Here we present a large-scale,
phylogenetic analysis of the distribution and determinan
158 Phylogenetic analysis of the DUF231 family revealed that
159 Temporal
phylogenetic analysis of the emergence of ST69 and ST131
160 ntharia and any other cnidarian lineage, but
phylogenetic analysis of the genes contained in the mito
161 Phylogenetic analysis of the genes of the echinocandin b
162 Phylogenetic analysis of the nanopore- and Sanger-derive
163 Phylogenetic analysis of the operon revealed that Kpi be
164 Here we describe the identification and
phylogenetic analysis of the Ptr1 gene.
165 However,
phylogenetic analysis of the RdRPs supports the previous
166 Phylogenetic analysis of the risk variants reveals a uni
167 Phylogenetic analysis of the whole genome identified a c
168 Results from
phylogenetic analysis of these datasets differ substanti
169 Phylogenetic analysis of these genomes and 1011 genomes
170 evisiae scaffolds from pulque, and performed
phylogenetic analysis of these sequences along with a co
171 Phylogenetic analysis of this new haplotype suggests tha
172 Phylogenetic analysis of thrips mitochondrial sequence d
173 Phylogenetic analysis of translation system components,
174 The aim of this study was to carry out a
phylogenetic analysis of tuberculosis in Wales, United K
175 We performed
phylogenetic analysis of viral genomes obtained from inf
176 Phylogenetic analysis of whole skin microbiome at differ
177 The
phylogenetic analysis of whole-genome sequences from eac
178 Phylogenetic analysis on 12 microsatellite loci and 1715
179 Phylogenetic analysis on the eight reconstructed genomes
180 Phylogenetic analysis placed the majority of fungal and
181 Phylogenetic analysis placed tonsil-derived IAV in clust
182 Phylogenetic analysis places Dineobellator within Veloci
183 Phylogenetic analysis places Irisosaurus at the very bas
184 Phylogenetic analysis places Ptr1 in a distinct clade co
185 Phylogenetic analysis places SFV in a basal position amo
186 Our
phylogenetic analysis places the majority of these genom
187 However, new fossil-calibrated
phylogenetic analysis places their appearance at ~115 mi
188 HPG in multiple pteropid bat species, while
phylogenetic analysis places these bat viruses as the ba
189 Phylogenetic analysis pointed to adaptations of enzyme r
190 A
phylogenetic analysis predicts that OsONS1 branches off
191 Phylogenetic analysis provided further evidence that fun
192 The
phylogenetic analysis provides compelling evidence that
193 Phylogenetic analysis provides further indications that
194 In contrast to PFGE, WGS
phylogenetic analysis refuted an epidemiological link be
195 In contrast to PFGE, WGS
phylogenetic analysis refuted an epidemiological link be
196 Phylogenetic analysis revealed 20 OsPLDalpha1 cDNA varia
197 Phylogenetic analysis revealed 3 clusters suggestive of
198 Phylogenetic analysis revealed an ascarid-specific Pgp l
199 Phylogenetic analysis revealed four separate emergences
200 Genomic-based similarity and a
phylogenetic analysis revealed multiple clusters (n = 16
201 In addition,
phylogenetic analysis revealed multiple independent line
202 Phylogenetic analysis revealed several new or rare subli
203 Phylogenetic analysis revealed that 3 (PhFT1, PhFT2 and
204 Phylogenetic analysis revealed that all NPC-EBV genomes
205 Phylogenetic analysis revealed that enriched microbial p
206 Phylogenetic analysis revealed that GH5_4 consists of th
207 Phylogenetic analysis revealed that lamprey GHR and PRLR
208 Phylogenetic analysis revealed that mollusc alpha-CA evo
209 Importantly, a
phylogenetic analysis revealed that most change has occu
210 Phylogenetic analysis revealed that most MDR/XDR isolate
211 generated the same phylogenetic signals, and
phylogenetic analysis revealed that P. ovata formed a si
212 Phylogenetic analysis revealed that the ancient duplicat
213 Phylogenetic analysis revealed that the GAST-Cysteine Ri
214 Phylogenetic analysis revealed that the hemagglutinin (H
215 widely distributed in eukaryotic organisms,
phylogenetic analysis revealed that their protein domain
216 Maximum likelihood
phylogenetic analysis revealed that these YFV sequences
217 Phylogenetic analysis revealed that they can be classifi
218 Phylogenetic analysis revealed that this apparently punc
219 Phylogenetic analysis revealed that this glycine-arginin
220 Phylogenetic analysis revealed that this virus branches
221 Metagenomic binning and
phylogenetic analysis revealed that two anammox populati
222 The 16S rDNA sequencing and the
phylogenetic analysis revealed the close evolutionary re
223 Phylogenetic analysis revealed the expansion of an indig
224 Phylogenetic analysis reveals a wide distribution of RIT
225 n cranial morphology of G. auaritae, and the
phylogenetic analysis reveals an unexpected power of res
226 Phylogenetic analysis reveals host specificity within ne
227 Phylogenetic analysis reveals that apicomplexan-like par
228 Phylogenetic analysis reveals that contemporary epidemic
229 Phylogenetic analysis reveals this bear to be basal to m
230 protein of the modification pathway, as our
phylogenetic analysis reveals.
231 The
phylogenetic analysis showed a complex clustering patter
232 Phylogenetic analysis showed Asp t 36 to be highly conse
233 Phylogenetic analysis showed distinct GII.4 variants in
234 Phylogenetic analysis showed most of the HRSVA sequences
235 Phylogenetic analysis showed that 291 of 293 isolates re
236 Phylogenetic analysis showed that AmeloD belongs to the
237 Phylogenetic analysis showed that disease flares were as
238 Phylogenetic analysis showed that divergent US DWV genot
239 Sequence and
phylogenetic analysis showed that EVs of the C species (
240 A multi-gene
phylogenetic analysis showed that H. sacchari and the ce
241 Phylogenetic analysis showed that in the structural regi
242 Phylogenetic analysis showed that RtAstV and RTCV groupe
243 Phylogenetic analysis showed that SHMT genes are divided
244 Phylogenetic analysis showed that the polymerase genes o
245 Phylogenetic analysis showed that, with one exception, s
246 Phylogenetic analysis showed this recent increase in S.
247 A
phylogenetic analysis shows that FabIs fall into four di
248 Phylogenetic analysis shows that POLGARF evolved ~160 mi
249 Phylogenetic analysis shows the triad emerged in GPR65,
250 Congruent with our
phylogenetic analysis,
slowly evolving residues were ide
251 some transmission fidelity 4 (Ctf4) based on
phylogenetic analysis,
structural similarities, physical
252 ural and mechanistic insights, together with
phylogenetic analysis,
suggest convergent evolution of p
253 Phylogenetic analysis suggested that SbCYP82D2 might hav
254 Phylogenetic analysis suggested that the CAB domain was
255 Phylogenetic analysis suggested that VvAHGD and its homo
256 Finally, we present a
phylogenetic analysis suggesting a likely origin for SAR
257 Phylogenetic analysis suggests a highly conserved nature
258 the events involved in such changes, and our
phylogenetic analysis suggests a possible change from fe
259 The
phylogenetic analysis suggests that *Lessiniabatis gen.
260 Phylogenetic analysis suggests that AcMYB123 or AcbHLH42
261 Phylogenetic analysis suggests that ERF12 is conserved a
262 Phylogenetic analysis suggests that MYC function first a
263 Phylogenetic analysis suggests that the nematodes origin
264 Phylogenetic analysis suggests that the transition from
265 Phylogenetic analysis supported close relationships amon
266 Finally, a
phylogenetic analysis supported the notion that ZgAgaC h
267 A comprehensive
phylogenetic analysis supports the placement of A. botto
268 its relationships by designing an inclusive
phylogenetic analysis that broadly incorporates definiti
269 We include a
phylogenetic analysis that predicted that many other ins
270 Here, we present a comprehensive
phylogenetic analysis that revealed deep-branching clade
271 Likewise, through
phylogenetic analysis,
the evolutionary relationship of
272 several N. neivai salivary proteins and use
phylogenetic analysis to compare with Old- and New-World
273 ly predict drug susceptibility profiles, and
phylogenetic analysis to detect transmission between cas
274 Then, using a
phylogenetic analysis to examine actin evolution, we sho
275 We present the first
phylogenetic analysis to include musculoskeletal data ob
276 We used whole-genome sequencing and
phylogenetic analysis to investigate the patterns of glo
277 Here, Grabowski and Jungers use comparative
phylogenetic analysis to reconstruct the likely size of
278 Here, we combine structural modeling with
phylogenetic analysis to shed light on archaeal histone
279 robe, Galvez et al. employed metagenomic and
phylogenetic analysis to systemically characterize murin
280 By conducting
phylogenetic analysis,
transcomplementation studies, and
281 A
phylogenetic analysis uncovered MrfAB homologs in divers
282 Phylogenetic analysis using full genome sequences is mor
283 The accuracy of
phylogenetic analysis was 100%.
284 Phylogenetic analysis was conducted using whole genomes
285 elatedness between the isolated sequences, a
phylogenetic analysis was conducted.
286 rred in the HIV-negative partner, anonymised
phylogenetic analysis was done to compare HIV-1 pol and
287 Phylogenetic analysis was performed to assess microbial
288 osen for whole-genome sequencing (WGS) and a
phylogenetic analysis was performed to detect clustering
289 fy correlates of prevalent HCV, and Bayesian
phylogenetic analysis was used to examine genetic cluste
290 Phylogenetic analysis was used to infer partial HIV tran
291 d a C-D region "latch." Interestingly, using
phylogenetic analysis,
we found that these features evol
292 Through
phylogenetic analysis,
we found that these genes likely
293 In this study, based on homology search and
phylogenetic analysis,
we identified three homologs of A
294 Using
phylogenetic analysis,
we inferred that the newly identi
295 The
phylogenetic analysis were done using BEAST v2.3.0 [1] .
296 to circumvent the limitations of traditional
phylogenetic analysis when studying the relationship bet
297 hy images were used to perform an exhaustive
phylogenetic analysis where most of the extant and fossi
298 hesis was supported by a 16S rRNA gene-based
phylogenetic analysis,
which identified at least one arc
299 We combine
phylogenetic analysis with Bayesian inference under an e
300 mma) and Type-II (32 MIKCc, 2 MIKC*) through
phylogenetic analysis with orthologs in Arabidopsis and