1 In total, 528 sequences were used in
phylogenetic analysis.
2 ructural conservation, thus supporting prior
phylogenetic analysis.
3 s the prediction of substrate specificity by
phylogenetic analysis.
4 n the Israeli and Palestinian populations by
phylogenetic analysis.
5 in several tissues and sequenced for further
phylogenetic analysis.
6 ndary structure through chemical probing and
phylogenetic analysis.
7 atural reservoir, as illustrated through our
phylogenetic analysis.
8 ed four nuclear gene regions and performed a
phylogenetic analysis.
9 ene coevolution information with large-scale
phylogenetic analysis.
10 t back DNA sequences required for subsequent
phylogenetic analysis.
11 d at least three distinct times according to
phylogenetic analysis.
12 oneous frame-shifts, suitable for subsequent
phylogenetic analysis.
13 s the alternative "well behaved" markers for
phylogenetic analysis,
3) applying site heterogeneous mi
14 In support of RNA mutation and
phylogenetic analysis,
a web server (RNA-TVcurve) was de
15 nked to large-scale whole-genome sequencing,
phylogenetic analysis and computational modelling that d
16 Using a combination of sequence-based
phylogenetic analysis and conservation of local chromoso
17 We used
phylogenetic analysis and heterologous reconstitution of
18 Phylogenetic analysis and mathematical modeling suggest
19 Phylogenetic analysis and phenotyping of multiple patien
20 e developed a one-step design strategy using
phylogenetic analysis and Rosetta atomistic calculations
21 Phylogenetic analysis and synteny studies suggest that b
22 use the CLE domain is too short for reliable
phylogenetic analysis and the pre-propeptide is too vari
23 llum from the United States using multilocus
phylogenetic analysis and their in vitro susceptibilitie
24 ctinorhizal tree Casuarina glauca using both
phylogenetic analysis and transgenic plants expressing e
25 c and/or genomic sequence search, subsequent
phylogenetic analysis,
and detailed biochemical and gene
26 were performed with hierarchical clustering,
phylogenetic analysis,
and principal component analysis.
27 cator orthologs identified from an extensive
phylogenetic analysis,
and type III effector translocati
28 SGS, together with mathematical modeling and
phylogenetic analysis,
as a novel strategy to infer T/F
29 Phylogenetic analysis at the genome level provides convi
30 Our
phylogenetic analysis based on 2148 orthologous gene clu
31 Phylogenetic analysis based on 397 concatenated core gen
32 A
phylogenetic analysis based on protein sequences showed
33 Phylogenetic analysis based on the protease domain sugge
34 Phylogenetic analysis based on the protease domain sugge
35 Phylogenetic analysis based on whole-genome sequencing o
36 otton species, Gossypium arboreum, including
phylogenetic analysis,
chromosome location, gene duplica
37 A
phylogenetic analysis combined with an analysis of the s
38 Anonymized
phylogenetic analysis compared couples' HIV-1 polymerase
39 Phylogenetic analysis confirmed that the virus is a maca
40 Sequencing-based
phylogenetic analysis confirmed the presence of distinct
41 Phylogenetic analysis confirms that the isolates reflect
42 Phylogenetic analysis demonstrated high similarity with
43 A genome-wide
phylogenetic analysis demonstrated in detail the relatio
44 Phylogenetic analysis demonstrated that 58% (7 of 12) of
45 Phylogenetic analysis demonstrated that all hospitals fr
46 Phylogenetic analysis demonstrated that cluster 4 and th
47 Phylogenetic analysis demonstrated that SPI is associate
48 Bayesian
phylogenetic analysis demonstrated that the influenza C
49 Phylogenetic analysis demonstrated that the majority of
50 Phylogenetic analysis demonstrated that the mobile cox1
51 Phylogenetic analysis demonstrates that evolution of the
52 e heterotrophic bacterium Eudoraea adriatica
Phylogenetic analysis demonstrates that the E. adriatica
53 However, according to chemical
phylogenetic analysis developed for kinetic data, severa
54 sequencing of 70 type IV GBS and subsequent
phylogenetic analysis elucidated the localization of typ
55 Phylogenetic analysis found close clustering of strains
56 roject is to identify orthologs suitable for
phylogenetic analysis from next-generation transcriptome
57 Phylogenetic analysis further suggests a history of dupl
58 Phylogenetic analysis further supports the chondrichthya
59 Phylogenetic analysis grouped CrANT with other non-seed-
60 Phylogenetic analysis grouped these isoforms into distin
61 ion of new evidence and modern approaches to
phylogenetic analysis has now resolved the affinities of
62 Whereas
phylogenetic analysis has revealed M. tuberculosis sprea
63 Phylogenetic analysis identified a clade of MHC-B, defin
64 Phylogenetic analysis identified a flux of distinct ST 2
65 A
phylogenetic analysis identified four LDI-like proteins
66 A
phylogenetic analysis identified PmC11 orthologues in ba
67 Phylogenetic analysis identifies P. meiomenus as a basal
68 This combination of characters, supported by
phylogenetic analysis,
identifies Tullimonstrum as a ver
69 The results of a new
phylogenetic analysis,
in which both Savannasaurus and D
70 Phylogenetic analysis indicated that baculoviruses have
71 Moreover,
phylogenetic analysis indicated that BAM2 is the ancestr
72 Phylogenetic analysis indicated that dissemination from
73 Comparative
phylogenetic analysis indicated that elmo2 originated up
74 Phylogenetic analysis indicated that L1 52/55-kDa DNA pa
75 Phylogenetic analysis indicated that MHHAV groups with k
76 Phylogenetic analysis indicated that pioneers occur more
77 Sequence homology and
phylogenetic analysis indicated that predicted proteins
78 Phylogenetic analysis indicated that rhodopsins have ada
79 Phylogenetic analysis indicated that Rv2633c is a member
80 Our
phylogenetic analysis indicated that six of the phylotyp
81 Phylogenetic analysis indicated that the viral-encoded n
82 Phylogenetic analysis indicates that Krishnatermes are i
83 Our
phylogenetic analysis indicates that marsupials or their
84 Phylogenetic analysis indicates that the outbreak was ca
85 Phylogenetic analysis indicates that this topology is as
86 novel approach to this problem, performing a
phylogenetic analysis indicating that family living is a
87 Our comparative
phylogenetic analysis involved single-cell transcriptome
88 Phylogenetic analysis is now an important tool in the st
89 Additionally, as indicated by a
phylogenetic analysis,
it appears that Cfr did not diver
90 and viruses in uncharacterized DNA samples,
phylogenetic analysis,
large-scale comparative genomics
91 leotide dataset, implying that probabilistic
phylogenetic analysis methods are needed.
92 Phylogenetic analysis,
nucleotide distances, and rates o
93 Phylogenetic analysis of >400 plant species in 41 genera
94 We performed whole-genome sequencing and
phylogenetic analysis of 108 strains isolated from sympt
95 surgery were analyzed by means of molecular
phylogenetic analysis of 16S rDNA pyrosequences.
96 full genomic sequences, insertion sites and
phylogenetic analysis of 28 prophages found in H. pylori
97 Here, we performed a whole-genome
phylogenetic analysis of 368 IAV circulating in swine fr
98 Our
phylogenetic analysis of 37 GET3 orthologs from 18 diffe
99 Genome sequencing and
phylogenetic analysis of 387 isolates, representing the
100 Phylogenetic analysis of 62 craniodental characters plac
101 history of symbiotic palaemonids based on a
phylogenetic analysis of 87 species belonging to 43 gene
102 ps (GI, GII, GIV, and GV) were identified by
phylogenetic analysis of a partial VP1 gene.
103 ure history, and whole-genome sequencing and
phylogenetic analysis of all available MRSA isolates (n
104 Phylogenetic analysis of all coding genes showed a close
105 rm a fish-specific monophyletic group in the
phylogenetic analysis of all three hepadnaviral genes.
106 Phylogenetic analysis of alveolate lineages demonstrates
107 Phylogenetic analysis of amphibactin biosynthetic genes
108 Phylogenetic analysis of apple bHLH (MdbHLH) genes and t
109 cal contact tracing of patients and Bayesian
phylogenetic analysis of bacterial WGS data were used to
110 Phylogenetic analysis of both the V1/V2 and C2/V3 region
111 nce of driver mutations can be inferred from
phylogenetic analysis of cancer chronograms, guiding dev
112 Phylogenetic analysis of CCOs in all kingdoms of life co
113 This
phylogenetic analysis of CFTR structure and function dem
114 Phylogenetic analysis of complete genome sequences found
115 Phylogenetic analysis of concatenated sequences of the e
116 capacity of urban soil environments using a
phylogenetic analysis of conserved NP biosynthetic genes
117 Through
phylogenetic analysis of contemporary swIAVs in the Unit
118 As suggested by our
phylogenetic analysis of CPAS genes, identified in our s
119 A
phylogenetic analysis of cwlM implies that localization
120 Moreover,
phylogenetic analysis of DNA replication proofreading in
121 angiosperms and gymnosperms were used for a
phylogenetic analysis of end wall types, calculation of
122 Phylogenetic analysis of EPS biosynthesis proteins sugge
123 nd CISD3, Miner2) as our guides to conduct a
phylogenetic analysis of eukaryotic NEET proteins and th
124 Here we use molecular
phylogenetic analysis of four genetic markers to describ
125 Phylogenetic analysis of full-genome sequences of these
126 he North American Rocky Mountains, combining
phylogenetic analysis of fungi and bacteria with shotgun
127 Phylogenetic analysis of genome sequences showed that re
128 We performed
phylogenetic analysis of genotype 4 NS5A sequences from
129 However the detailed
phylogenetic analysis of GH5_4 members did not delineate
130 Phylogenetic analysis of H10 and related viruses showed
131 In a comprehensive
phylogenetic analysis of HAdV-D capsid genes, fiber knob
132 We performed
phylogenetic analysis of high-grade serous ovarian cance
133 Phylogenetic analysis of key methylotrophy functions rev
134 Phylogenetic analysis of metagenome sequences indicated
135 Phylogenetic analysis of MF myosin domains suggests that
136 Phylogenetic analysis of mitochondrial coding sequences
137 eover, the structure of the virus genome and
phylogenetic analysis of multiple genes strongly suggest
138 V RNA at follow-up week 24) and used refined
phylogenetic analysis of multiple HCV genes to distingui
139 The
phylogenetic analysis of NucS indicates a complex evolut
140 Phylogenetic analysis of our Chytridiomycota clones plac
141 Phylogenetic analysis of our isolates replicated the dis
142 Kingdom-wide
phylogenetic analysis of over 400 CYP716s from over 200
143 HTS and
phylogenetic analysis of paired specimens confirmed shed
144 Phylogenetic analysis of phytobacterial T6SS clusters sh
145 Phylogenetic analysis of Plasmodium parasites has indica
146 Phylogenetic analysis of plastid and mitochondrial genes
147 Phylogenetic analysis of RDR genes present in potato and
148 We used PARIS-determined helices to guide
phylogenetic analysis of RNA structures and discovered c
149 eted of sequences from the genus Bacteroides
Phylogenetic analysis of sequence data indicates that F.
150 Transmission chains were inferred by
phylogenetic analysis of sequence data.
151 Finally, by
phylogenetic analysis of serial TGCTs that emerge with c
152 Phylogenetic analysis of SNAP genes from 22 diverse plan
153 Here we undertake an expansive
phylogenetic analysis of swIAV sequence data and demonst
154 Phylogenetic analysis of the algal fermentative enzyme s
155 Systematic
phylogenetic analysis of the alveolate PAT family reveal
156 Phylogenetic analysis of the cloned sequences demonstrat
157 Phylogenetic analysis of the complete coding sequence sh
158 Phylogenetic analysis of the data obtained revealed a hi
159 Temporal
phylogenetic analysis of the emergence of ST69 and ST131
160 Phylogenetic analysis of the endoglucanases revealed thr
161 Phylogenetic analysis of the eradicated European P. viva
162 amplified from the original lung tissue, and
phylogenetic analysis of the full-length L, M and S segm
163 Phylogenetic analysis of the new genomes demonstrated th
164 Phylogenetic analysis of the nucleotide sequence of two
165 Phylogenetic analysis of the RdRp domain clearly indicat
166 island integrated at the leuX locus, and the
phylogenetic analysis of the TgtA5 family is consistent
167 Phylogenetic analysis of the two elements demonstrated t
168 Phylogenetic analysis of the viral genome showed that SF
169 Phylogenetic analysis of the virus genome showed that EP
170 Phylogenetic analysis of the WGS data indicated that the
171 Phylogenetic analysis of the whole genome identified a c
172 Our
phylogenetic analysis of these genes and a related TNFSF
173 Phylogenetic analysis of these two novel avian influenza
174 Phylogenetic analysis of translation system components,
175 Phylogenetic analysis of WGS data revealed a common orig
176 Phylogenetic analysis of whole skin microbiome at differ
177 A
phylogenetic analysis placed the split between Plasmodiu
178 Phylogenetic analysis places Gurbanodelta as the sister
179 ct picorna-like viruses, and structure-based
phylogenetic analysis places HAV between typical picorna
180 Phylogenetic analysis places Meemannia as an early-diver
181 A
phylogenetic analysis places the new species at the base
182 Phylogenetic analysis places this new taxon as the siste
183 A
phylogenetic analysis predicts that OsONS1 branches off
184 A new comprehensive
phylogenetic analysis provides strong support for the le
185 Phylogenetic analysis recovers Teyujagua as the sister t
186 Traditionally,
phylogenetic analysis relies on alignments of orthologs,
187 A
phylogenetic analysis resolves E. rarus as a stem-group
188 Our
phylogenetic analysis resolves the new arthropod as a st
189 Phylogenetic analysis revealed a common origin of the me
190 Phylogenetic analysis revealed a moderate to significant
191 Phylogenetic analysis revealed a temporally dependent mo
192 Phylogenetic analysis revealed conservative evolutionary
193 Phylogenetic analysis revealed multigene family associat
194 Phylogenetic analysis revealed recent viral spread betwe
195 Intriguingly, our
phylogenetic analysis revealed rodent lineage-specific C
196 Phylogenetic analysis revealed six Mates in teleost fish
197 A
phylogenetic analysis revealed six more novel-type TrxR
198 Phylogenetic analysis revealed that all enterovirus D68
199 Phylogenetic analysis revealed that all NPC-EBV genomes
200 A
phylogenetic analysis revealed that amoebal TPSs are evo
201 Phylogenetic analysis revealed that EV71 belonged to the
202 Phylogenetic analysis revealed that HbXIPs clustered int
203 Phylogenetic analysis revealed that NRT1.1B diverges bet
204 Molecular
phylogenetic analysis revealed that power-amplified chel
205 Phylogenetic analysis revealed that SbFT1 clusters with
206 Phylogenetic analysis revealed that the abundances of 65
207 Phylogenetic analysis revealed that the isolate belonged
208 Phylogenetic analysis revealed that the sequence of the
209 Metagenomic binning and
phylogenetic analysis revealed that two anammox populati
210 Phylogenetic analysis revealed the evolutionary division
211 Phylogenetic analysis revealed the existence of higher s
212 Phylogenetic analysis revealed the presence of a high nu
213 Additionally, the
phylogenetic analysis revealed the two terpene synthase
214 Phylogenetic analysis revealed these HRSVB sequences clu
215 Global
phylogenetic analysis revealed two HPV11 variant lineage
216 servoir, most likely bats, into humans, with
phylogenetic analysis revealing the co-circulation of se
217 A
phylogenetic analysis reveals a relationship to Bartonel
218 Phylogenetic analysis reveals AMPA, kainate, and NMDA re
219 Phylogenetic analysis reveals AtBZR1-like genes are high
220 Phylogenetic analysis reveals congruent evolutionary his
221 Phylogenetic analysis reveals important discrepancies wi
222 Phylogenetic analysis reveals other bacterial species si
223 Phylogenetic analysis reveals that 4CL1, 4CL2, and 4CL4
224 Phylogenetic analysis reveals that contemporary epidemic
225 Phylogenetic analysis reveals that GCNA proteins emerged
226 Phylogenetic analysis reveals that H5N6 arose from reass
227 Finally,
phylogenetic analysis reveals that the genes correspondi
228 Phylogenetic analysis reveals that these genes are highl
229 Furthermore, comparative
phylogenetic analysis reveals that this phenotype is a f
230 Phylogenetic analysis reveals the sustained transmission
231 Phylogenetic analysis reveals this bear to be basal to m
232 Phylogenetic analysis,
sequence alignment and site-direc
233 Phylogenetic analysis sheds light on the evolutionary or
234 Phylogenetic analysis showed distinct GII.4 variants in
235 Phylogenetic analysis showed most of the HRSVA sequences
236 Phylogenetic analysis showed that 291 of 293 isolates re
237 ructures of Puccinia graminis f. sp. tritici
Phylogenetic analysis showed that CBM32s appended to chi
238 Phylogenetic analysis showed that disease flares were as
239 Phylogenetic analysis showed that evolution of pathogen
240 Sequence and
phylogenetic analysis showed that EVs of the C species (
241 Phylogenetic analysis showed that in the structural regi
242 Phylogenetic analysis showed that MV is most closely rel
243 Additional
phylogenetic analysis showed that Pta and MaeB sequences
244 Finally,
phylogenetic analysis showed that some microbial groups
245 Phylogenetic analysis showed that the K. pneumoniae ST27
246 e for two patients in the CE-high group, and
phylogenetic analysis showed that the prevalent clonal p
247 Phylogenetic analysis showed that the TBX5-NuRD interact
248 Phylogenetic analysis showed that the ZIKVs belonged to
249 These findings were further supported by
phylogenetic analysis showing that GPV-QH15 evolved from
250 very low sequence identity, structure-based
phylogenetic analysis shows that all poxvirus Bcl-2 prot
251 Our
phylogenetic analysis shows that the FliW-mediated regul
252 Furthermore, a novel
phylogenetic analysis shows the new dinosaur as the most
253 Phylogenetic analysis shows two divergent groups for G.
254 ons so they can be used as input to existing
phylogenetic analysis software packages.
255 some transmission fidelity 4 (Ctf4) based on
phylogenetic analysis,
structural similarities, physical
256 ural and mechanistic insights, together with
phylogenetic analysis,
suggest convergent evolution of p
257 Phylogenetic analysis suggested that SbCYP82D2 might hav
258 Phylogenetic analysis suggested that the producer of the
259 ances to Eocene African anthropoids, and our
phylogenetic analysis suggests a relationship with Afric
260 Phylogenetic analysis suggests that at least two regulat
261 Phylogenetic analysis suggests that CVDE evolved from an
262 t simplified reovirus described to date, and
phylogenetic analysis suggests that it arose from a more
263 Phylogenetic analysis suggests that LGC-35 evolved from
264 Our
phylogenetic analysis suggests that the ileS1 and ileS2
265 Phylogenetic analysis suggests that the viral E6 gene wa
266 Our
phylogenetic analysis suggests that this may be common a
267 Phylogenetic analysis suggests that this mechanism was p
268 Phylogenetic analysis suggests that V. fordii is a siste
269 Phylogenetic analysis suggests that wild poliovirus stra
270 Phylogenetic analysis supported close relationships amon
271 We further show through a timescaled
phylogenetic analysis that a cross-species transmission
272 its relationships by designing an inclusive
phylogenetic analysis that broadly incorporates definiti
273 We confirm through
phylogenetic analysis that hub interfaces are strongly c
274 In a
phylogenetic analysis,
the PsTPS enzymes and PsIDS3 were
275 Based on a
phylogenetic analysis,
the three vertebrate TLR architec
276 Together with a
phylogenetic analysis,
these results highlight the diver
277 Combined with a
phylogenetic analysis,
these results suggest that amino
278 ugh several hepcidin genes were found, after
phylogenetic analysis they could be clustered in two gro
279 o do so, we conducted the most comprehensive
phylogenetic analysis to date, examined CHIKV evolution
280 Then, using a
phylogenetic analysis to examine actin evolution, we sho
281 Phylogenetic analysis to identify lineages of sequences
282 t was necessary to employ bioinformatics and
phylogenetic analysis to identify orthologs related to m
283 We present the first
phylogenetic analysis to include musculoskeletal data ob
284 We used whole-genome sequencing and
phylogenetic analysis to investigate the patterns of glo
285 Here, Grabowski and Jungers use comparative
phylogenetic analysis to reconstruct the likely size of
286 ain current techniques for viral sequencing,
phylogenetic analysis,
transmission reconstruction, and
287 Detailed in silico and
phylogenetic analysis unraveled that the biosynthesis in
288 A
phylogenetic analysis using 803 sequences places the thr
289 a platform-independent software package for
phylogenetic analysis using multi-copy gene trees.
290 The accuracy of
phylogenetic analysis was 100%.
291 elatedness between the isolated sequences, a
phylogenetic analysis was conducted.
292 bserved KS selectivity and that predicted by
phylogenetic analysis was seen.
293 Phylogenetic analysis was used to infer the relationship
294 In this study, based on homology search and
phylogenetic analysis,
we identified three homologs of A
295 Based on a comprehensive
phylogenetic analysis,
we propose that one of the HCP su
296 -genome single nucleotide polymorphism (SNP)
phylogenetic analysis,
which accurately discriminated be
297 A new
phylogenetic analysis (
with updates on a quarter of the
298 classified into four classes (I-IV) based on
phylogenetic analysis,
with ARFs in classes I-III and AR
299 SNP3.0, a program for SNP identification and
phylogenetic analysis without genome alignment or the re
300 Based on multilocus
phylogenetic analysis,
YSLV6 shows a close evolutionary