1 predictive breeding even in the absence of a
complete genome sequence.
2 Here we report its
complete genome sequence.
3 educing bacteria (DMRB) for which there is a
complete genome sequence.
4 rward and reverse genetics, and we present a
complete genome sequence.
5 ould be greatly assisted through access to a
complete genome sequence.
6 e is limited despite the availability of the
complete genome sequence.
7 nase (CCD) genes have been identified in the
complete genome sequence.
8 ce tags (ESTs) as the reference in lieu of a
complete genome sequence.
9 he lack of a genetic manipulation system and
complete genome sequences.
10 ogenicity in HPAI H5N1 strains comprising 69
complete genome sequences.
11 plex mixed virus sample and the retrieval of
complete genome sequences.
12 Ts and full-length cDNAs to their respective
complete genome sequences.
13 distributes annotation of ncRNAs in over 200
complete genome sequences.
14 ass or in other monocotyledonous plants with
complete genome sequences.
15 organisms owing to the ready availability of
complete genome sequences.
16 pendent Fe(II) oxidizer for which there is a
completed genome sequence.
17 r and Acidovorax genera for which there is a
completed genome sequence.
18 in the DRC, we identified rare variants for
complete genome sequencing.
19 duals whose HIV-1 infection was evaluated by
complete genome sequencing.
20 hylogenetic signal could be captured without
complete genome sequencing.
21 ase and identified by using metagenomics and
complete genome sequencing.
22 in 1996, there has been a large increase in
complete genome sequences,
accompanied by great advances
23 Its
complete genome sequence allows for an examination of th
24 The availability of a
complete genome sequence allows the detailed study of in
25 In this study, we report the
complete genome sequence analysis of 58 RVs isolated fro
26 Blood, Morin et al report their findings on
complete genome sequence analysis of primary diffuse lar
27 We present the
complete genome sequence and a molecular characterizatio
28 As a result of the recent release of the
complete genome sequence and a wide variety of new genom
29 Here we report the
complete genome sequence and annotation for a low-passag
30 Here we report the
complete genome sequence and annotation of the second po
31 The availability of the
complete genome sequence and the ability of the parasite
32 Here we present the
complete genome sequence and the clinicopathological cha
33 In recent years, the
complete genome sequence and thousands of single nucleot
34 We present here the
complete genome sequence and transcription map of a rhab
35 ractive visualisation of comparisons between
complete genome sequences and associated annotations.
36 arding the evolution of WEEV, we analyzed 33
complete genome sequences and conducted comprehensive ph
37 Analysis of five
complete genome sequences and PCR genotyping of 42 H. py
38 s, a microarray was constructed based on the
completed genome sequence and annotation.
39 We utilized the
completed genome sequence and optimized methods for homo
40 cesses at a holistic level, made possible by
completed genome sequences and integrated with detailed
41 at founded the global pandemic, and very few
complete genome sequences are available from patients in
42 d outer membrane channels in organisms whose
complete genome sequences are available.
43 Apicomplexa from other eukaryotes for which
complete genome sequences are available.
44 mbrane transport proteins in organisms whose
complete genome sequences are available.
45 Complete genome sequences are now available for two geog
46 Here the
complete genome sequence,
as well as DNA methylation pat
47 ionally been under-represented in studies of
complete genome sequences,
as have microbes from the mar
48 technologies have the potential to generate
complete genome sequences at even higher rates.
49 There are
complete genome sequences available for five additional
50 vivirus strains) and compared them to the 11
complete genome sequences available in GenBank.
51 With more than 70
complete genome sequences available, the mycobacteriopha
52 As more
complete genome sequences become available, bioinformati
53 To make effective use of the growing host of
complete genome sequences,
biologists must have easy-to-
54 ioning pairs of closely related species with
complete genome sequences by average population size of
55 An analysis of recombination among
complete genome sequences by computation of a phylogenet
56 The availability of
complete genome sequences combined with the likelihood t
57 me comparative analysis with other available
complete genome sequences confirms the close relationshi
58 several animals (genetic degeneration), and
complete genome sequencing confirms that the heterogamet
59 In the absence of a
complete genome sequence,
considerable insight into geno
60 Samples of multiple
complete genome sequences contain vast amounts of inform
61 g a similar mAGP and the availability of the
complete genome sequence,
Corynebacterium glutamicum has
62 Analysis of
complete genome sequence data from island foxes shows a
63 estimated allele effects in conjunction with
complete genome sequence data of the founder strains red
64 Analyses of publicly available
complete genome sequence data show that haplotype N shar
65 Due to a lack of
complete genome sequence data, there is only a limited u
66 Complete genome sequencing demonstrated that PRV G9P[13]
67 tance, conifers seemed long out of reach for
complete genome sequencing,
due in part to their enormou
68 The availability of
complete genome sequences enables the statistical analys
69 It houses the
complete genome sequence,
ESTs and the entire body of li
70 dictyBase houses the
complete genome sequence,
ESTs, and the entire body of l
71 The
complete genome sequence for a number of organisms is av
72 The existence of a
complete genome sequence for C. elegans and draft genome
73 With the availability of
complete genome sequence for Drosophila melanogaster, on
74 The publication of the
complete genome sequence for Mycobacterium tuberculosis
75 The availability of the
complete genome sequence for Shewanella oneidensis MR-1
76 me possible to test this notion by searching
complete genome sequence for signs of ancient duplicatio
77 The availability of
complete genome sequences for a large variety of organis
78 Recently, with the availability of
complete genome sequences for many organisms, very-high-
79 sance that coincides with the acquisition of
complete genome sequences for multiple organisms and an
80 The multiple available
complete genome sequences for other motile and immotile
81 We have determined
complete genome sequences for the remaining 22 HEV-B ser
82 We have determined the
complete genome sequences for the remaining nine HEV-C s
83 The availability of
complete genome sequences for two bird species, the chic
84 tic history of human influenza B virus using
complete genome sequences for which the date (day) of is
85 Phylogenetic analysis of
complete genome sequences found evidence for two distinc
86 The availability of
complete genome sequence from 12 Drosophila species pres
87 The availability of
complete genome sequence from multiple organisms, as wel
88 ined, representing the fourth species with a
complete genome sequence from the Chlamydiaceae family o
89 The availability of nearly
complete genome sequences from a variety of organisms ha
90 ole genome sequencing falls, anticipation of
complete genome sequences from divergent species, reflec
91 Each NGS method generated near-
complete genome sequences from more than 90% of samples.
92 sviruses, a notion supported by more than 60
complete genome sequences from multiple isolates and fol
93 hat for common bacterial species, where many
complete genome sequences from related strains have been
94 The availability of complete or nearly
complete genome sequences from several plant species per
95 dy present in the Upper Paleolithic, we used
complete genome sequences from Sunghir, a site dated to
96 g genomic information that can be partial or
complete genome sequences from the same or a related org
97 in this organism coupled with the release of
complete genome sequences from two strains.
98 Here, we present high-quality
complete genome sequences from two woolly mammoths (Mamm
99 We analysed a data set of 334 near-
complete genome sequences from various risk groups, samp
100 s, as well as those predicted to occur in 46
completed genome sequences from all three domains of lif
101 composition in an NTHI strain for which the
complete genome sequence has been determined.
102 The
complete genome sequence has revealed an unusual breadth
103 To date, the
complete genome sequences have been reported for only tw
104 With
complete genome sequences in hand, understanding the epi
105 Our results demonstrate the value of
complete genome sequencing in families.
106 Here, we report on the use of
complete-genome sequencing in the characterization of sp
107 Here we present
complete genome sequences,
including a comparative analy
108 few years will see even more progress as the
complete genome sequence is available and genomic and pr
109 Though its
complete genome sequence is available, little is underst
110 boratory-passaged Rd KW20 strain for which a
complete genome sequence is available.
111 With the advent of
complete genome sequences,
large-scale functional analys
112 sms (SNP) in cattle, but the current lack of
complete genome sequence limits this approach in swine.
113 We report the
complete genome sequence of "Candidatus Mycoplasma haemo
114 Here we report its
complete genome sequence of 2.97 Mb, which is contained
115 We describe here the
complete genome sequence of a common clone of Mycobacter
116 of a PE-2 derived diploid (JAY270), and the
complete genome sequence of a haploid derivative (JAY291
117 We report the first
complete genome sequence of a lineage III isolate, HCC23
118 uired for RQ biosynthesis, we determined the
complete genome sequence of a mutant strain of R. rubrum
119 this study, we report the identification and
complete genome sequence of a novel enterovirus isolated
120 and HHV-7.IMPORTANCE Herein we describe the
complete genome sequence of a novel murine herpesvirus.
121 In recent years the
complete genome sequence of a number of Y. pestis strain
122 tis in the world; however, there is only one
complete genome sequence of a poultry strain to date.
123 Here we report the first
complete genome sequence of a serotype b non-JP2 strain
124 Analysis of the
complete genome sequence of A. actinomycetemcomitans (ww
125 Here we report the
complete genome sequence of A. vinelandii DJ, which has
126 Here we announce the
complete genome sequence of Algoriphagus sp. PR1 and ini
127 The
complete genome sequence of an African Newcastle disease
128 in bifidobacteria cultures, we obtained the
complete genome sequence of an intestinal isolate, Bifid
129 We report the first
complete genome sequence of an isolate (IND2004/01) of b
130 Here we report the first
complete genome sequence of an isolate belonging to the
131 rovided the plant science community with the
complete genome sequence of Arabidopsis thaliana and ric
132 The
complete genome sequence of B. bacteriovorus has recentl
133 The first
complete genome sequence of B. burgdorferi strain 31, av
134 To facilitate such studies, we used the
complete genome sequence of B. melitensis 16M, the speci
135 Accordingly, the
complete genome sequence of Bifidobacterium longum subsp
136 Here, we report the
complete genome sequence of Blattabacterium (BNCIN) harb
137 We report here the
complete genome sequence of Borrelia sp. isolate SV1 fro
138 We report the
complete genome sequence of Brucella abortus field isola
139 Here we report the
complete genome sequence of Brucella suis VBI22, which w
140 The
complete genome sequence of Burkholderia mallei ATCC 233
141 es encoding soluble guanylyl cyclases in the
complete genome sequence of C. elegans.
142 We report the
complete genome sequence of C. parvum, type II isolate.
143 We report the finished
complete genome sequence of C. pecorum E58, the type str
144 We report the
complete genome sequence of canine papillomavirus type 1
145 We report the
complete genome sequence of canine papillomavirus type 9
146 We determined the
complete genome sequence of Clostridium difficile strain
147 The
complete genome sequence of cultivated rice (Oryza sativ
148 A coding-
complete genome sequence of EBOV that was isolated durin
149 We report the
complete genome sequence of enterobacteriophage SP6, whi
150 The
complete genome sequence of Enterococcus faecalis V583,
151 Here, we present the
complete genome sequence of F. columnare strain ATCC 495
152 Here, we report the
complete genome sequence of four BATV strains (MM2222, C
153 to meiotic and molecular genetic analysis; A
complete genome sequence of G. zeae should soon be avail
154 The
complete genome sequence of Geobacter sulfurreducens, a
155 Insert DNA was sequenced and compared to the
complete genome sequence of H. influenzae strain Rd.
156 xibility of many anoxygenic phototrophs, the
complete genome sequence of H. modesticaldum reveals an
157 Here we announce the
complete genome sequence of H. pylori strain G27, which
158 On the basis of analysis of the
complete genome sequence of Kutzneria, we now identify a
159 Towards this goal, we have determined the
complete genome sequence of LdCen (-/-) and its parent s
160 Computational and PCR-based analysis of the
complete genome sequence of M. avium subsp. paratubercul
161 without DNA enrichment, we obtained the near-
complete genome sequence of M. lepromatosis present in a
162 We present the
complete genome sequence of Mycoplasma hyopneumoniae, an
163 The
complete genome sequence of N. risticii Illinois consist
164 The work presented here represents the first
complete genome sequence of NDV in the Dominican Republi
165 Herein, for the first time, the
complete genome sequence of newly identified porcine ast
166 Here we report the
complete genome sequence of P. mirabilis HI4320, a repre
167 Here we present the
complete genome sequence of Providencia stuartii MRSN 21
168 The
complete genome sequence of PsHV-1 has been determined a
169 Here we present the
complete genome sequence of R. typhi (1,111,496 bp) and
170 Here we report the
complete genome sequence of Rahnella aquatilis CIP 78.65
171 Here, we present the
complete genome sequence of S. mutans GS-5, a serotype c
172 We describe here the
complete genome sequence of S. Typhimurium UK-1.
173 We present the 4.8-Mb
complete genome sequence of Salmonella enterica serovar
174 Here we report the
complete genome sequence of serotype c strain D11S-1, wh
175 We determined the
complete genome sequence of Shigella flexneri serotype 2
176 We report the
complete genome sequence of soybean Putnam virus (SPuV),
177 Here we report the
complete genome sequence of strain JR.
178 We report here on the
complete genome sequence of strain PXO99A and its compar
179 This study describes the
complete genome sequence of that original isolate, deriv
180 However, the
complete genome sequence of the 68-1 BAC has not been de
181 We report the
complete genome sequence of the Blattabacterium sp. asso
182 Here we report the
complete genome sequence of the CaCV-1 strain NY214, whi
183 We report the
complete genome sequence of the deep-sea gamma-proteobac
184 We report the
complete genome sequence of the first polyomavirus to be
185 Here we report the
complete genome sequence of the first strain of HEV from
186 e, real-time DNA sequencing to determine the
complete genome sequence of the German outbreak strain,
187 Here, we present the
complete genome sequence of the Gram-negative anaerobe B
188 The
complete genome sequence of the isolate revealed that th
189 However, despite determination of the
complete genome sequence of the lethal species Plasmodiu
190 Reported herein is the
complete genome sequence of the M. putrefaciens type str
191 To this end, we characterized the
complete genome sequence of the M16917 isolate and perfo
192 The
complete genome sequence of the malarial parasite, Plasm
193 We report the
complete genome sequence of the model bacterial pathogen
194 We dissected the
complete genome sequence of the O1 serotype strain Vibri
195 By the time the
complete genome sequence of the soil bacterium Pseudomon
196 The
complete genome sequence of the T4-like, broad-host-rang
197 The
complete genome sequence of Thiobacillus denitrificans A
198 We describe the
complete genome sequence of this cellulose-degrading bac
199 Here, we announce the first
complete genome sequence of this organism.
200 for over 20 years as an important cause, the
complete genome sequence of this serotype has yet to be
201 Here we present the
complete genome sequence of this strain, the first avail
202 Availability of the
complete genome sequence of two K-12 strains allows comp
203 The
complete genome sequence of two strains of H. pylori has
204 types and sources of viruses, obtaining near
complete genome sequence of viruses ranging in size from
205 Comparison of the
complete genome sequence of X. axonopodis pv. citrumelo
206 g, and optical mapping were used to obtain a
complete genome sequence of X. axonopodis pv. citrumelo
207 We report here the
complete genome sequences of 138 new mycobacteriophages,
208 The
complete genome sequences of 2 closely related plaque-de
209 f seven resequencing GeneChips, based on the
complete genome sequences of 24 strains of smallpox viru
210 In this study, we report the nearly
complete genome sequences of 34 HSV-2 low-passage-number
211 Based on the alignments of the
complete genome sequences of 40 ecologically and biologi
212 ogs of all flagellar proteins encoded in the
complete genome sequences of 41 flagellated species from
213 We aligned
complete genome sequences of 8 disease-associated and 4
214 Here we analyze the
complete genome sequences of 863 human tumors from The C
215 We have determined the
complete genome sequences of a host-promiscuous Salmonel
216 Recently, the
complete genome sequences of a large number of important
217 Here we present the
complete genome sequences of an indigenous hunter-gather
218 We report the
complete genome sequences of B. valaisiana VS116, B. spi
219 The
complete genome sequences of Clostridium perfringens str
220 we doubled the number of publicly available
complete genome sequences of EV-D68 by performing high-t
221 he identification of 17 small sHSPs from the
complete genome sequences of five diverse algae: Chlamyd
222 The
complete genome sequences of five GII.4 noroviruses (thr
223 Here we report the
complete genome sequences of four additional members of
224 The
complete genome sequences of four evolved plasmids with
225 The availability of two
complete genome sequences of H. pylori represents a uniq
226 were carried out on all available published
complete genome sequences of HBV.
227 e information derived from over 1,300 (near-)
complete genome sequences of HCV available on public dat
228 This is the first report of
complete genome sequences of NDV strains isolated from c
229 Here we report the first
complete genome sequences of Ngari virus.
230 t-generation DNA sequencing has revealed the
complete genome sequences of numerous organisms, establi
231 To date, however, the
complete genome sequences of only 17 marine phage are kn
232 The increasing availability of
complete genome sequences of RNA viruses has the potenti
233 In the time since the
complete genome sequences of several members of the arch
234 The
complete genome sequences of several plant-associated ba
235 Thanks to the availability of
complete genome sequences of species representing import
236 We report the
complete genome sequences of the pathogenic strain M. my
237 Comparing the
complete genome sequences of the three dominant outbreak
238 Using the (near)
complete genome sequences of the yeasts Candida albicans
239 Complete genome sequences of these 8 genetically diverse
240 Here we report two
complete genome sequences of this bacterium from the B a
241 Nearly
complete genome sequences of three novel RNA viruses wer
242 tive pdf genes, pdfA, pdfB, and pdfC, in the
complete genome sequences of three strains of L. pneumop
243 We report the
complete genome sequences of TI0902, a highly virulent t
244 Here we report the
complete genome sequences of two ALSD strains of this ba
245 Here, we report the analysis of the first
complete genome sequences of two important B. megaterium
246 The
complete genome sequences of two NDV strains and the seq
247 and female germline mutation rates from the
complete genome sequences of two parent-offspring trios.
248 nship, we have taken advantage of the nearly
complete genome sequences of two rice subspecies to gene
249 The availability of the
complete genome sequences of two subspecies of the Asian
250 The
complete genome sequences of two Sulfolobus spindle-shap
251 Complete genome sequencing of all members of the genus a
252 Complete genome sequencing of CG8486 revealed a 1.65-Mb
253 Complete genome sequencing of five isolates confirmed th
254 Recent advances in transcriptomics and the
complete genome sequencing of mosquito vectors have incr
255 Analysis of the recently
completed genome sequence of Methanosaeta thermophila co
256 rometry, which in conjunction with the newly
completed genome sequence of P. mirabilis HI4320, was us
257 The
completed genome sequence of Syntrophus aciditrophicus S
258 Aided by the availability of the partially
completed genome sequence of the simian malaria parasite
259 Analysis of eight
completed genome sequences of rickettsial species reveal
260 The recently
completed genome sequences of several plant species have
261 Taken together, the availability of the
complete genome sequence offers a foundation for the stu
262 Analysis of
complete genome sequences or concatenated ORF1/ORF2 amin
263 Complete genome sequences permit the construction of poo
264 proteins of P. falciparum predicted from the
completed genome sequence,
permitting facile identificat
265 We developed a high-throughput
complete genome sequencing pipeline for EV-D68 that prod
266 For 14 plant species with emerging or
complete genome sequence,
PlantGDB's genome browsers (xG
267 s were virtually ignored in all but the most
complete genome sequencing projects, and the full extent
268 Although the list of
completed genome sequencing projects has expanded rapidl
269 s system, the complete cell lineage, and the
complete genome sequence provide a framework to phrase a
270 Completed genome sequences provide templates for the des
271 CoGe, a platform of multiple whole or near-
complete genome sequences,
provides an integrative Web-b
272 The
complete genome sequence reported here suggested that D.
273 The
completed genome sequence reported here is the first for
274 Using a data set of 32
complete genome sequences representing all four viral se
275 Complete genome sequences revealed 404 and 299 base subs
276 Complete genome sequencing revealed that the E. canis ge
277 Complete genome sequencing revealed that the isolate doe
278 Complete genome sequencing revealed the phage was a nove
279 The
complete genome sequence reveals a diverse set of carboh
280 The
complete genome sequence reveals a suite of carbohydrate
281 The
complete genome sequence showed that T. fusca has a sing
282 ly used as phylogenetic markers, analyses of
complete genome sequences showed that global measures of
283 The basal branching of some of the
complete genome sequences that we recovered suggests tha
284 For the increasing number of species with
complete genome sequences,
the task of elucidating their
285 ia parasite Plasmodium falciparum, despite a
completed genome sequence,
there are no experimental dat
286 the evolution of microbes, and thousands of
complete genome sequences to help formulate and refine o
287 ctrometry, in combination with the partially
completed genome sequence,
to detect and identify a tota
288 The availability of a
complete genome sequence,
together with the ability to p
289 The availability of
complete genome sequences,
together with various genomic
290 successful high-throughput generation of the
complete genome sequence was achieved for 33 diverse RVF
291 The
complete genome sequence was determined and shows a high
292 first plant pathogenic bacterium for which a
complete genome sequence was determined, much progress h
293 A multiple alignment of the 32
complete genome sequences was filtered to remove mobile
294 Using
complete genome sequences,
we analysed the intron conten
295 n-dependent and -independent analyses of the
complete genome sequences,
we identified 58 strain-speci
296 In addition,
complete genome sequences were obtained from RNAs extrac
297 Complete genome sequences were obtained from six of the
298 Complete genome sequences were obtained from three to de
299 ious issue has been fuelled by the influx of
complete genome sequences,
which has allowed for a more
300 A
complete genome sequence will provide an effective ances