1 ance in clinical samples at the level of the
complete genome.
2 uence and RNA structural conservation of the
complete genome.
3 lay a very low frequency of cleavage even in
complete genomes.
4 ven their robustness in identifying genes in
complete genomes.
5 7,346 marine virome contigs that includes 44
complete genomes.
6 n was comparable to Glimmer and MetaGene for
complete genomes.
7 the compacted de Bruijn graph from a set of
complete genomes.
8 ns, highlighting the importance of obtaining
complete genomes.
9 sequencing have generated a large number of
complete genomes.
10 release 71), ranging from a single record to
complete genomes.
11 se provides orthology predictions among 1621
complete genomes (
1365 bacterial, 92 archaeal, and 164 e
12 This first
completed genome (
705 kb) for a human-associated TM7 phy
13 Complete genome analyses of 43 complete rotavirus genome
14 nts during bacterial infection, we performed
complete genome analysis on three newly isolated multidr
15 Using
complete genome analysis, we sequenced five bladder tumo
16 addition to presenting results of the first
complete-genome analysis of the breakthrough infections
17 hand, we performed phylogenetic analyses of
complete genome and VP1 capsid protein sequences.
18 demonstrated by an analysis of 555 Norovirus
complete genomes and 2500 sequence fragments, where a re
19 have found such DNPs and TNPs throughout two
complete genomes and eight exomes.
20 Here we assemble
complete genomes and large genomic fragments from both s
21 Here we describe the
complete genomes and metabolic contributions of these un
22 We recovered
complete genomes and up to 43% of the genome from sample
23 as EMBL-Bank and UniProt, and more than 2000
completed genomes and proteomes.
24 nonsupervised orthologous groups (NOGs) from
complete genomes,
and then applies a comprehensive chara
25 Complete genomes are attainable from 19(th) and early 20
26 Near-
complete genomes,
assembled de novo with paired-end and
27 With the ubiquitous generation of
complete genome assemblies for a variety of species, eff
28 Here we report near
complete genome assemblies for three Pneumocystis specie
29 e a web tool for genome assembly, SIMBA is a
complete genome assemblies project management system, wh
30 molecule sequencing promises to deliver more
complete genome assemblies with fewer gaps, concerns abo
31 ave a dual purpose: delivering a contiguous,
complete genome assembly and creating a full catalog of
32 Here, we present a
complete genome assembly of the skin commensal yeast Mal
33 These difficulties often delay the
complete genome assembly projects.
34 nformatic tools are ushering in an era where
complete genome assembly will become common for species
35 ncing of a deep aquifer, recovering two near-
complete genomes belonging to the archaeal phylum Bathya
36 Storing and transferring
complete genomes between computers for the purpose of ap
37 the genomic diversity of 433 isolates and 78
complete genomes (
CGs) from six continents.
38 miRNA, 3747 snRNA, gene sequences from 9282
complete genome chromosomes of all prokaryotes and eukar
39 Here, we report a nearly
complete genome co-assembly of three closely related sin
40 nt a protocol for generating coding-sequence-
complete genomes,
comprising an online primer design too
41 ddition to uneven ancient gene loss, the two
complete genomes contained within maize are differentiat
42 This may reflect limited
complete genome data available for red algae, currently
43 We apply this strategy to
complete genome data from 47 wild and domestic pigs from
44 the 1000 Genomes Project, and deep coverage
complete genome data from our own projects.
45 First, the near-
complete genome data generated with the in-house pipelin
46 With
complete genome data, it becomes possible to identify an
47 e, can align mixtures of assembled draft and
completed genome data, and is robust in identifying a ri
48 e on a global scale, however, information on
complete genomes (
DNA), transcriptomes (RNA) and proteom
49 Thus, numerous mechanisms exist to
complete genome duplication in the absence of a pristine
50 lls possess numerous tolerance mechanisms to
complete genome duplication in the presence of such impe
51 replication forks that may cause failure to
complete genome duplication or result in possibly catast
52 igins along eukaryotic chromosomes, ensuring
complete genome duplication within a single S-phase.
53 e and fires approximately 100,000 origins to
complete genome duplication.
54 is a tightly controlled process that ensures
complete genome duplication.
55 We have applied this method to the
complete genome for Escherichia coli strain K12 and look
56 Using the RNA-seq approach, we obtained a
complete genome for one sample, which contained a recomb
57 scriptomic sequencing recover the first near-
complete genomes for a novel methanogen species, and sho
58 rado River (USA) and reconstructed the first
complete genomes for Archaea using cultivation-independe
59 urface aquifer metagenomic samples to obtain
complete genomes for members of a new candidate phylum s
60 Here, we present
complete genomes for three distinct groups of viruses as
61 We acquired multiple near-
complete genomes for two bacterial species from human or
62 Assembling a
complete genome from a single bacterial cell, termed sin
63 he genome coverage to include representative
complete genomes from all bacterial and archaeal lineage
64 IMG integrates publicly available draft and
complete genomes from all three domains of life with a l
65 n-independent recovery of 49 partial to near-
complete genomes from an acetate-amended aquifer.
66 possibility of improving assemblies by using
complete genomes from closely related species/strains.
67 Recovery rates of
complete genomes from fragmented assemblies of single-ce
68 By sequencing 27
complete genomes from H1 and D8 genotype measles viruses
69 ults highlight the benefit of reconstructing
complete genomes from metagenomic data and demonstrate m
70 Near-
complete genomes from nine of these species show conserv
71 eline for EV-D68 that produced a total of 59
complete genomes from respiratory samples with a 95% suc
72 iversity of HPV6, using 724 isolates and 190
complete genomes from six continents, and the associatio
73 ine lakes and present analysis of two nearly
complete genomes from this group.
74 Complete genomes from two populations revealed a high de
75 Here, we report eight coding-
complete genomes from US serum samples from 1978-1979-ei
76 representing orders of millipedes for which
complete genomes had not been characterized.
77 The
complete genome has also greatly expanded our understand
78 sequencing of targeted regions, exomes, and
complete genomes has begun to dramatically increase the
79 tions of >80 million sequences covering 2414
complete genomes,
hundreds of meta-genomes, thousands of
80 y, the condition of possessing more than two
complete genomes in a cell, has intrigued biologists for
81 17 of which represented by complete or near-
complete genomes,
in two North American freshwater lakes
82 tion allele frequency of variants across the
complete genome,
including both coding and noncoding reg
83 The
complete genome is 7,551 nucleotides in length, with pol
84 o larger size ssRNAs are recruited until the
complete genome is packaging into the capsid.
85 In this study, we performed
complete-genome next-generation sequencing of 92 RSV iso
86 next-generation sequencing, we sequenced the
complete genome of 100 Salmonella Bareilly isolates obta
87 Elucidation of the
complete genome of a 1992 ST-1 strain revealed that this
88 We report a
complete genome of a filamentous tropical marine cyanoba
89 te, we have now discovered and sequenced the
complete genome of a third novel virus, Le Blanc virus,
90 ng and optical mapping approaches, a 24.1-Mb
complete genome of an industrial strain, Monascus purpur
91 We also sequenced the
complete genome of an isolate of DWV that covertly infec
92 ase (HN) and large polymerase (L) genes in a
complete genome of an NDV isolate from this geographical
93 The sequencing of the first
complete genome of an ST10 A. baumannii clinical strain
94 Here we report the
complete genome of Edwardsiella ictaluri 93-146.
95 wo distinct lineages, we sequenced the first
complete genome of F. philomiragia strain ATCC 25017, wh
96 , during our isolation and sequencing of the
complete genome of faustovirus, followed by the descript
97 The
complete genome of HPV-SD2 is 7,299 bp long (36.3% G/C)
98 he development of lymphoma, we sequenced the
complete genome of MneRV2 and identified 87 protein codi
99 from this individual also contained a nearly
complete genome of the archaeal commensal Methanobreviba
100 We sequenced the
complete genome of the DNA contained in the gourd at low
101 Here, we sequenced and assembled the
complete genome of the ET-743 producer, Candidatus Endoe
102 peptides of 15 to 350 amino acids across the
complete genome of the HPAI H7N7 A/Netherlands/33/03 vir
103 The coding-
complete genome of the new virus, named Kanyawara virus
104 To this end, we sequenced the first
complete genome of the obligate endosymbiont, Candidatus
105 In this report, we analyze the
complete genome of the prototype RBV, strain M64.
106 The
complete genome of this isolate, chicken/DominicanRepubl
107 Here, we describe the
complete genome of this microbe.
108 We reconstructed a nearly
complete genome of this phylotype from a soil metagenome
109 First, we sequenced the
complete genome of Wolbachia strain wOo, which revealed
110 The
complete genome of ZIKV was recovered from the fetal bra
111 logenies using homologous gene families from
complete genomes of 10 bacterial and archaeal groups.
112 Here, we sequenced the
complete genomes of 11 PHs, representing all founding li
113 We sequenced the
complete genomes of 123 IAV isolates and found 31 H1N1,
114 We analyzed the
complete genomes of 16 naturally occurring infectious P-
115 Our results identified the
complete genomes of 24 species of RNA viruses from a div
116 diversity of this parasite, we sequenced the
complete genomes of 42 B. microti samples from around th
117 utosomal (X/A) nucleotide diversity with the
complete genomes of 569 females from 14 populations.
118 We have sequenced the
complete genomes of 72 individuals affected with early-o
119 We further obtained
complete genomes of 8 Calycopis specimens: 3 C. cecrops
120 We sequenced
complete genomes of 92 DENV-3 clinical isolates to chara
121 Compared with 20 other
complete genomes of A. baumannii, LAC-4 genome harbors a
122 Here we report high-depth sequencing of 128
complete genomes of AJ controls.
123 WNV evolution and ecology, we sequenced the
complete genomes of approximately 300 avian isolates sam
124 Using LSA, we assemble partial and near-
complete genomes of bacterial taxa present at relative a
125 We present the
complete genomes of Bifidobacterium animalis subsp. lact
126 Comparison of
complete genomes of closely related species enables rese
127 The
complete genomes of each of the two variant strains were
128 conserved amino acids in dengue viruses, 120
complete genomes of each serotype were selected at rando
129 By analyzing the
complete genomes of five plants we generated a database
130 Here, we present the
complete genomes of nine present-day Yakutian horses and
131 We analyzed 89
complete genomes of polar bear and brown bear using popu
132 We have generated 27 complete or nearly
complete genomes of RSV from hospitalized children atten
133 We sequenced the
complete genomes of seven infectious MLVs isolated from
134 s consisted almost exclusively of phage, and
complete genomes of several phage were recovered, includ
135 We generated
complete genomes of the type strains G. apicola wkB1(T)
136 petitive sequence elements and assembled the
complete genomes of two co-extracted bacteria.
137 Reconstruction of near-
complete genomes of two cooccurring SUP05 populations in
138 ologous gene families shared across multiple
complete genomes of viruses that infect bacterial or arc
139 The system is built with 82
complete genomes organized into gene families and subfam
140 RNA splicing machinery for expression of its
complete genome potentially makes it vulnerable to modul
141 In trees built from
complete genomes rather than sets of core genes, we obse
142 On the basis of its reconstructed
complete genome,
RBG-1 is metabolically versatile.
143 Moreover, our sequencing data allowed near-
complete genome reconstruction of five bacterial species
144 ubmitted to NCBI for integration into RefSeq
complete genome records as link-out features, maximizing
145 s identified in T. monococcum, which lacks a
complete genome reference sequence, by mapping the enric
146 However, the routine resequencing of
complete genomes remains infeasible.
147 Failure to
complete genome replication and defective checkpoint sur
148 on of replication origins in yeasts promotes
complete genome replication even in the presence of irre
149 We show that the probability of
complete genome replication is maximized if replication
150 point, cds1Delta and mrc1Delta forks cannot
complete genome replication.
151 Here we focus on the recovery of a nearly
complete genome representing a novel strain of the perio
152 c sequencing led to the recovery of its near-
complete genome,
revealing the genes necessary for hydro
153 Analysis of the
complete genome reveals a putative iron-regulated surfac
154 The analysis identified 72 partial or
complete genome segments representing 66 previously unde
155 Its
complete genome sequence allows for an examination of th
156 In this study, we report the
complete genome sequence analysis of 58 RVs isolated fro
157 Blood, Morin et al report their findings on
complete genome sequence analysis of primary diffuse lar
158 Here we report the
complete genome sequence and annotation of the second po
159 Here we present the
complete genome sequence and the clinicopathological cha
160 Analysis of
complete genome sequence data from island foxes shows a
161 estimated allele effects in conjunction with
complete genome sequence data of the founder strains red
162 Analyses of publicly available
complete genome sequence data show that haplotype N shar
163 Due to a lack of
complete genome sequence data, there is only a limited u
164 The existence of a
complete genome sequence for C. elegans and draft genome
165 The publication of the
complete genome sequence for Mycobacterium tuberculosis
166 We report the
complete genome sequence of "Candidatus Mycoplasma haemo
167 We report the first
complete genome sequence of a lineage III isolate, HCC23
168 uired for RQ biosynthesis, we determined the
complete genome sequence of a mutant strain of R. rubrum
169 this study, we report the identification and
complete genome sequence of a novel enterovirus isolated
170 and HHV-7.IMPORTANCE Herein we describe the
complete genome sequence of a novel murine herpesvirus.
171 tis in the world; however, there is only one
complete genome sequence of a poultry strain to date.
172 Here we report the first
complete genome sequence of a serotype b non-JP2 strain
173 The
complete genome sequence of an African Newcastle disease
174 We report the first
complete genome sequence of an isolate (IND2004/01) of b
175 Here we report the first
complete genome sequence of an isolate belonging to the
176 The first
complete genome sequence of B. burgdorferi strain 31, av
177 Here, we report the
complete genome sequence of Blattabacterium (BNCIN) harb
178 We report here the
complete genome sequence of Borrelia sp. isolate SV1 fro
179 Here we report the
complete genome sequence of Brucella suis VBI22, which w
180 We report the finished
complete genome sequence of C. pecorum E58, the type str
181 We report the
complete genome sequence of canine papillomavirus type 1
182 We report the
complete genome sequence of canine papillomavirus type 9
183 A coding-
complete genome sequence of EBOV that was isolated durin
184 Here, we present the
complete genome sequence of F. columnare strain ATCC 495
185 Here, we report the
complete genome sequence of four BATV strains (MM2222, C
186 On the basis of analysis of the
complete genome sequence of Kutzneria, we now identify a
187 Towards this goal, we have determined the
complete genome sequence of LdCen (-/-) and its parent s
188 without DNA enrichment, we obtained the near-
complete genome sequence of M. lepromatosis present in a
189 The work presented here represents the first
complete genome sequence of NDV in the Dominican Republi
190 Herein, for the first time, the
complete genome sequence of newly identified porcine ast
191 Here we present the
complete genome sequence of Providencia stuartii MRSN 21
192 Here we report the
complete genome sequence of Rahnella aquatilis CIP 78.65
193 Here, we present the
complete genome sequence of S. mutans GS-5, a serotype c
194 We describe here the
complete genome sequence of S. Typhimurium UK-1.
195 We report the
complete genome sequence of soybean Putnam virus (SPuV),
196 Here we report the
complete genome sequence of strain JR.
197 However, the
complete genome sequence of the 68-1 BAC has not been de
198 We report the
complete genome sequence of the Blattabacterium sp. asso
199 Here we report the
complete genome sequence of the CaCV-1 strain NY214, whi
200 We report the
complete genome sequence of the first polyomavirus to be
201 Here we report the
complete genome sequence of the first strain of HEV from
202 e, real-time DNA sequencing to determine the
complete genome sequence of the German outbreak strain,
203 The
complete genome sequence of the isolate revealed that th
204 Reported herein is the
complete genome sequence of the M. putrefaciens type str
205 To this end, we characterized the
complete genome sequence of the M16917 isolate and perfo
206 We dissected the
complete genome sequence of the O1 serotype strain Vibri
207 By the time the
complete genome sequence of the soil bacterium Pseudomon
208 We describe the
complete genome sequence of this cellulose-degrading bac
209 Here, we announce the first
complete genome sequence of this organism.
210 Here we present the
complete genome sequence of this strain, the first avail
211 Comparison of the
complete genome sequence of X. axonopodis pv. citrumelo
212 g, and optical mapping were used to obtain a
complete genome sequence of X. axonopodis pv. citrumelo
213 s system, the complete cell lineage, and the
complete genome sequence provide a framework to phrase a
214 The
complete genome sequence reported here suggested that D.
215 The
complete genome sequence reveals a diverse set of carboh
216 The
complete genome sequence reveals a suite of carbohydrate
217 Here the
complete genome sequence, as well as DNA methylation pat
218 dictyBase houses the
complete genome sequence, ESTs, and the entire body of l
219 The availability of a
complete genome sequence, together with the ability to p
220 ce tags (ESTs) as the reference in lieu of a
complete genome sequence.
221 predictive breeding even in the absence of a
complete genome sequence.
222 Here we report its
complete genome sequence.
223 educing bacteria (DMRB) for which there is a
complete genome sequence.
224 s, a microarray was constructed based on the
completed genome sequence and annotation.
225 The
completed genome sequence reported here is the first for
226 r and Acidovorax genera for which there is a
completed genome sequence.
227 arding the evolution of WEEV, we analyzed 33
complete genome sequences and conducted comprehensive ph
228 at founded the global pandemic, and very few
complete genome sequences are available from patients in
229 technologies have the potential to generate
complete genome sequences at even higher rates.
230 With more than 70
complete genome sequences available, the mycobacteriopha
231 As more
complete genome sequences become available, bioinformati
232 Samples of multiple
complete genome sequences contain vast amounts of inform
233 The availability of
complete genome sequences for two bird species, the chic
234 Phylogenetic analysis of
complete genome sequences found evidence for two distinc
235 Each NGS method generated near-
complete genome sequences from more than 90% of samples.
236 sviruses, a notion supported by more than 60
complete genome sequences from multiple isolates and fol
237 hat for common bacterial species, where many
complete genome sequences from related strains have been
238 The availability of complete or nearly
complete genome sequences from several plant species per
239 dy present in the Upper Paleolithic, we used
complete genome sequences from Sunghir, a site dated to
240 g genomic information that can be partial or
complete genome sequences from the same or a related org
241 Here, we present high-quality
complete genome sequences from two woolly mammoths (Mamm
242 We analysed a data set of 334 near-
complete genome sequences from various risk groups, samp
243 We report here the
complete genome sequences of 138 new mycobacteriophages,
244 In this study, we report the nearly
complete genome sequences of 34 HSV-2 low-passage-number
245 We aligned
complete genome sequences of 8 disease-associated and 4
246 Here we analyze the
complete genome sequences of 863 human tumors from The C
247 We report the
complete genome sequences of B. valaisiana VS116, B. spi
248 we doubled the number of publicly available
complete genome sequences of EV-D68 by performing high-t
249 e information derived from over 1,300 (near-)
complete genome sequences of HCV available on public dat
250 This is the first report of
complete genome sequences of NDV strains isolated from c
251 Here we report the first
complete genome sequences of Ngari virus.
252 t-generation DNA sequencing has revealed the
complete genome sequences of numerous organisms, establi
253 The
complete genome sequences of several plant-associated ba
254 Thanks to the availability of
complete genome sequences of species representing import
255 We report the
complete genome sequences of the pathogenic strain M. my
256 Comparing the
complete genome sequences of the three dominant outbreak
257 Complete genome sequences of these 8 genetically diverse
258 Here we report two
complete genome sequences of this bacterium from the B a
259 We report the
complete genome sequences of TI0902, a highly virulent t
260 Here we report the
complete genome sequences of two ALSD strains of this ba
261 Here, we report the analysis of the first
complete genome sequences of two important B. megaterium
262 The
complete genome sequences of two NDV strains and the seq
263 and female germline mutation rates from the
complete genome sequences of two parent-offspring trios.
264 Analysis of
complete genome sequences or concatenated ORF1/ORF2 amin
265 The basal branching of some of the
complete genome sequences that we recovered suggests tha
266 A multiple alignment of the 32
complete genome sequences was filtered to remove mobile
267 Complete genome sequences were obtained from six of the
268 Complete genome sequences were obtained from three to de
269 n-dependent and -independent analyses of the
complete genome sequences, we identified 58 strain-speci
270 ass or in other monocotyledonous plants with
complete genome sequences.
271 organisms owing to the ready availability of
complete genome sequences.
272 he lack of a genetic manipulation system and
complete genome sequences.
273 plex mixed virus sample and the retrieval of
complete genome sequences.
274 The recently
completed genome sequences of several plant species have
275 several animals (genetic degeneration), and
complete genome sequencing confirms that the heterogamet
276 Complete genome sequencing demonstrated that PRV G9P[13]
277 Our results demonstrate the value of
complete genome sequencing in families.
278 Complete genome sequencing of all members of the genus a
279 Complete genome sequencing of five isolates confirmed th
280 Recent advances in transcriptomics and the
complete genome sequencing of mosquito vectors have incr
281 We developed a high-throughput
complete genome sequencing pipeline for EV-D68 that prod
282 Complete genome sequencing revealed that the isolate doe
283 Complete genome sequencing revealed the phage was a nove
284 tance, conifers seemed long out of reach for
complete genome sequencing, due in part to their enormou
285 ase and identified by using metagenomics and
complete genome sequencing.
286 in the DRC, we identified rare variants for
complete genome sequencing.
287 ed in the host interaction.In the absence of
complete genomes,
the metabolic capabilities of uncultur
288 genomic reads resulted in five novel, nearly
complete genomes,
three of which had features similar to
289 nome-scale operons for 2072 prokaryotes with
complete genomes,
three times the number of genomes cove
290 otprinting framework; (ii) 2125 species with
complete genomes to support the above five functions, co
291 they rely upon, and, because of the lack of
complete genomes,
to what extent.
292 e omics studies of R. opacus PD630 including
complete genome,
transcriptome and proteome analysis.
293 igate the deep evolutionary history of HPV58
complete genome variants.
294 y complete ( approximately 99%) and two near-
complete genomes were assembled for bacteria that compri
295 Near-
complete genomes were reconstructed for these bacteria.
296 Four high-quality (63-90%
complete) genomes were obtained from White Oak River est
297 NGS produced 14 new
complete genomes,
which included pure subtype C (n = 2),
298 We recovered near-
complete genomes,
whose phylogeny matched those of the p
299 r phenotypes; conduct follow up studies of a
completed genome-
wide association study; generate indepe
300 d Oxytricha macronuclear genome is the first
completed genome with such an unusual architecture.