コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ify up to 90% of reads in viral metagenomes (viromes).
2 erating viral metagenome sequence libraries (viromes).
3 longitudinal quasispecies complexity of the virome.
4 otypes' among this fraction of the human gut virome.
5 unprecedented opportunity to study the human virome.
6 into the effects of immune modulation on the virome.
7 : http://www.ark-genomics.org/bioinformatics/virome.
8 of ultrafilters, are part of the human blood virome.
9 ed with significant expansion of the enteric virome.
10 and functional potential of the Indian Ocean virome.
11 l of SIV-associated expansion of the enteric virome.
12 , the picorna-like viruses, dominate the RNA virome.
13 and how we vaccinate to limit or control our virome.
14 ittle-recognized part of our metagenome: our virome.
15 y understood members of the human-associated virome.
16 the emergence and evolution of the archaeal virome.
17 ss-sectional studies, changes in the enteric virome.
18 hould incorporate examination of the enteric virome.
19 to infect humans or to be part of the human virome.
20 art due to the lack of investigation of tick viromes.
21 nd phage sequences dominated the anoxic core viromes.
22 to sequences present in other environmental viromes.
23 dentify 7-38% of 'unknown' sequence space in viromes.
24 the first time to our knowledge within ssDNA viromes.
26 mammals is defined in part by our coevolved virome, a concept with profound implications for underst
35 s associated with alterations in the enteric virome and bacterial microbiome, which may contribute to
37 From birth to 2 years of age, the eukaryotic virome and the bacterial microbiome expanded, but this w
38 namic but metastable equilibrium between the virome and the host can be dangerous, benign, or even sy
40 Nonbacterial organisms, particularly the virome and the mycobiome, are important regulators of in
41 obiomes and, for the first time, 42 distinct viromes and show that there are strongly discriminatory
42 spite remarkable interpersonal variations in viromes and their encoded functions, intrapersonal diver
43 the viral taxonomic composition in simulated viromes and viral metagenomes from different benthic dee
44 n 'virobiota' and its associated genes (the 'virome'), and have fostered the emerging field of host-v
45 nded DNA (dsDNA) viral-fraction metagenomes (viromes) and whole viral community morphological data se
46 nomes and virioplankton shotgun metagenomes (viromes), and estimated to occur within >90% of the dsDN
47 ological dark matter extant in the human gut virome, and bring to light a population of potentially g
48 health and disease states of the respiratory virome, and drive a paradigm shift in how the practicing
50 yotic virus sequences dominated the oxycline viromes, and phage sequences dominated the anoxic core v
52 tly healthy cotwins in discordant pairs have viromes associated with, although not necessarily mediat
54 rvention was associated with a change in the virome community to a new state, in which individuals on
59 ess is known about the viral microbiome (or 'virome'), consisting of bacteriophages and eukaryotic RN
63 es (vSAGs) are more abundant in global ocean virome data sets than published metagenome-assembled vir
64 ication to 32 viromes from the Pacific Ocean Virome dataset identified clusters of samples broadly de
65 ons, and analyse the resulting 'global ocean virome' dataset to present a global map of abundant, dou
67 retained over the period surveyed, and with viromes dominated by a few temperate phages that exhibit
68 nderstanding of the bacterial microbiome and virome during early development, conditions that might i
70 y bowel diseases or solid-organ transplants, virome dynamics in allogeneic hematopoietic stem cell tr
71 inhabiting the intestine termed "the enteric virome." Enteric viruses have intimate functional and ge
72 abase, phage sequences dominated the surface viromes, eukaryotic virus sequences dominated the oxycli
74 tools (BLAST, MG-RAST, NBC, VMGAP, MetaVir, VIROME) for analysing the viral taxonomic composition in
76 ies, we characterized and compared the fecal viromes from 32 healthy animals, 31 animals with acute d
82 ead targeted hypervariation in the human gut virome, identify previously undescribed types of genes t
84 metagenomic approach, we surveyed the fecal virome in California sea lions of different ages and hea
85 Here, we report the landscape of the tomato virome in China, the leading country in tomato productio
87 eal an under-appreciated role of the enteric virome in HIV-associated gastroenteritis and pathogenesi
88 investigating the biological role of the gut virome in human physiology, and the importance of our vi
89 Our results demonstrate a complex urinary virome in kidney transplant patients with multiple virus
92 We describe here the metagenomics-derived virome in the feces of 24 healthy and 12 diarrheic pigle
94 human virome, the current literature on the virome in transplant recipients, and near-future applica
96 ng the role of these populations (the human "virome") in health and disease requires a much deeper un
97 ersity and composition of viral communities (viromes) in ballast and harbor waters using metagenomics
100 cell-free DNA in plasma to investigate drug-virome interactions in a cohort of organ transplant reci
109 Moreover, it is becoming clear that the virome is part of a dynamic network of microorganisms th
114 irus infection, a component of the mammalian virome, is regulated by the counterpoised actions of mul
115 yrosequencing of virus-enriched metagenomes (viromes) isolated from bovine rumen fluid and analysed t
116 rimetric microtiter plate (MTP) systems from ViroMed Laboratories, Inc. (PrimeCapture), CPG, Inc. (Qu
117 scribe the extent and nature of the mosquito virome, little is known about how these viruses persist,
118 data support a model in which changes in the virome may contribute to intestinal inflammation and bac
120 e presence of viruses in blood suggests that virome members can traverse mucosal barriers, as indeed
127 present preliminary characterization of the virome of three common North American bat species, inclu
133 y, we characterized six novel viruses in the viromes of laboratory fruit flies and wild populations o
134 natural freshwater systems but distant from viromes of marine and human designed/managed freshwater
135 erence between the two mosquito genera, with viromes of mosquitoes of the Aedes genus exhibiting subs
136 Great Lakes viromes were closely related to viromes of other cold natural freshwater systems but dis
137 gh-throughput sequencing to characterize the viromes of these tick species and identified the presenc
139 wever, the large viral population diversity (virome) of bats has been partially determined for only a
140 s-related pathology; thus, the impact of the virome on health and disease may be even more relevant i
142 and observed that changes in the intestinal virome over time differed between cases and controls.
143 dicate that the gut bacterial microbiome and virome play an important role in healthy infant developm
147 In this study we investigated the urine virome profile of BKV+ and BKV- kidney transplant recipi
149 , they generate compelling evidence that the virome provides protection from gut inflammatory conditi
150 R sequences and compared them with 2 588 172 virome reads in the saliva of four human subjects over 1
154 ETSP virome comparison with surface marine viromes (Sargasso Sea, Gulf of Mexico, Kingman Reef, Che
156 nmental viromes, tBLASTx, MetaVir, VMGAP and VIROME showed a similar efficiency of sequence annotatio
158 Species-specific recruitment patterns and virome simulation data suggest that vSAGs are highly mic
164 chnical considerations in studying the human virome, the current literature on the virome in transpla
165 is initial characterization of the bat guano virome, the first metagenomic analysis of viruses in wil
166 ight into the relationship between the human virome, the state of the immune system, and the effects
167 ired respiratory viruses and the respiratory virome to better understand the dynamics in acute infect
169 view of our current understanding of how the virome, together with other components of the microbiome
170 were shared between surface and anoxic core viromes using reciprocal BLASTn sequence comparison.
171 expansion and diversification of the enteric virome was secondary to changes in bacterial populations
172 robial metabolic capabilities encoded by the viromes was extensive, suggesting that they serve as a r
173 te the origin and evolution of the human gut virome, we analyzed the viral community of one adult ind
174 act of this population bottleneck on the AGM virome, we used metagenomics to compare the viral nuclei
176 t among the Great Lakes, and the Great Lakes viromes were closely related to viromes of other cold na
177 notation-independent comparisons showed that viromes were distinct among the Great Lakes, and the Gre
179 versity between the two genera, although the viromes were very similar among the three Culex species
180 e recombination events highlighted a dynamic virome where subpopulations of variants are in competiti
181 levels 4.2-fold higher than other published viromes, while carbohydrate and amino acids metabolisms
183 persistence of a small portion of the global virome within the gut of each individual and rapid evolu
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。