scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1036869843 |
P356 | DOI | 10.1038/ISMEJ.2013.144 |
P932 | PMC publication ID | 3869020 |
P698 | PubMed publication ID | 24030599 |
P5875 | ResearchGate publication ID | 256541062 |
P50 | author | Edward F. DeLong | Q5342553 |
Sangita Ganesh | Q85946688 | ||
Frank J Stewart | Q91181976 | ||
Darren J Parris | Q125270827 | ||
P2860 | cites work | The Sorcerer II Global Ocean Sampling expedition: northwest Atlantic through eastern tropical Pacific | Q21092763 |
Genome divergence in two Prochlorococcus ecotypes reflects oceanic niche differentiation | Q21994463 | ||
Genome Streamlining in a Cosmopolitan Oceanic Bacterium | Q22065795 | ||
Integrative analysis of environmental sequences using MEGAN4 | Q24604814 | ||
QIIME allows analysis of high-throughput community sequencing data | Q24616873 | ||
Microbial community gene expression in ocean surface waters | Q24651959 | ||
Endosymbiotic associations within protists | Q24652962 | ||
The subsystems approach to genome annotation and its use in the project to annotate 1000 genomes | Q24817116 | ||
Microbial oceanography of anoxic oxygen minimum zones | Q27025471 | ||
Environmental genome shotgun sequencing of the Sargasso Sea | Q27860605 | ||
The Planctomycetes, Verrucomicrobia, Chlamydiae and sister phyla comprise a superphylum with biotechnological and medical relevance | Q28240583 | ||
The global, ppGpp-mediated stringent response to amino acid starvation in Escherichia coli | Q28277451 | ||
Fast growth increases the selective advantage of a mutation arising recurrently during evolution under metal limitation | Q28476065 | ||
Denitrifying alphaproteobacteria from the Arabian Sea that express nosZ, the gene encoding nitrous oxide reductase, in oxic and suboxic waters | Q28709129 | ||
A deeply branching thermophilic bacterium with an ancient acetyl-CoA pathway dominates a subsurface ecosystem | Q28732372 | ||
Selfish genetic elements, genetic conflict, and evolutionary innovation | Q28742794 | ||
Downward flux of particulate organic matter in the ocean: a particle decomposition paradox | Q29035781 | ||
Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences | Q29547172 | ||
UniFrac: a new phylogenetic method for comparing microbial communities | Q29547435 | ||
Community genomics among stratified microbial assemblages in the ocean's interior | Q29614711 | ||
Mesophilic Crenarchaeota: proposal for a third archaeal phylum, the Thaumarchaeota | Q29618150 | ||
Effect of oxygen minimum zone formation on communities of marine protists | Q30521402 | ||
Correlating microbial community profiles with geochemical data in highly stratified sediments from the Arctic Mid-Ocean Ridge | Q30571625 | ||
Biodiversity of denitrifying and dinitrogen-fixing bacteria in an acid forest soil | Q30839798 | ||
Transporter genes expressed by coastal bacterioplankton in response to dissolved organic carbon | Q30905477 | ||
Microbial community phylogenetic and trait diversity declines with depth in a marine oxygen minimum zone | Q31087253 | ||
Marine actinobacteria: perspectives, challenges, future directions | Q31149321 | ||
Pirellula and OM43 are among the dominant lineages identified in an Oregon coast diatom bloom | Q33251973 | ||
Potential interactions of particle-associated anammox bacteria with bacterial and archaeal partners in the Namibian upwelling system | Q33285812 | ||
Microbial population structures in the deep marine biosphere | Q33301618 | ||
Bacterial diversity in the oxygen minimum zone of the eastern tropical South Pacific | Q33320874 | ||
Phylogenetic analyses of ribosomal DNA-containing bacterioplankton genome fragments from a 4000 m vertical profile in the North Pacific Subtropical Gyre | Q33336810 | ||
An assessment of actinobacterial diversity in the marine environment | Q33337416 | ||
A microdiversity study of anammox bacteria reveals a novel Candidatus Scalindua phylotype in marine oxygen minimum zones | Q33338603 | ||
Genomic patterns of recombination, clonal divergence and environment in marine microbial populations | Q33346822 | ||
Revising the nitrogen cycle in the Peruvian oxygen minimum zone | Q33414079 | ||
Comparative metagenomic analysis of a microbial community residing at a depth of 4,000 meters at station ALOHA in the North Pacific subtropical gyre | Q33471287 | ||
Abundant transposases encoded by the metagenome of a hydrothermal chimney biofilm | Q33477310 | ||
Microbial community structure in the North Pacific ocean | Q33485828 | ||
Antagonistic activity of bacteria isolated from organic aggregates of the German Wadden Sea. | Q33497529 | ||
New insights into the diversity of marine picoeukaryotes | Q33507276 | ||
Microbial community dynamics in a seasonally anoxic fjord: Saanich Inlet, British Columbia | Q33507410 | ||
Development and quantitative analyses of a universal rRNA-subtraction protocol for microbial metatranscriptomics | Q33539537 | ||
Phylogeographic separation of marine and soil myxobacteria at high levels of classification. | Q33623358 | ||
The interconnection between biofilm formation and horizontal gene transfer | Q37996597 | ||
Pseudomonas aeruginosa twitching motility: type IV pili in action | Q38022664 | ||
Heterotrophic bacteria and bacterivorous protozoa in oceanic macroaggregates | Q39099293 | ||
Comparison of cell-specific activity between free-living and attached bacteria using isolates and natural assemblages. | Q39135578 | ||
The hydrogenases and formate dehydrogenases of Escherichia coli | Q40523829 | ||
A 'rare biosphere' microorganism contributes to sulfate reduction in a peatland | Q41114375 | ||
Biomass production and assimilation of dissolved organic matter by SAR11 bacteria in the Northwest Atlantic Ocean | Q41988095 | ||
Influence of nutrients and currents on the genomic composition of microbes across an upwelling mosaic | Q42109589 | ||
High-temperature-induced transposition of insertion elements in burkholderia multivorans ATCC 17616 | Q42122691 | ||
Detoxification of sulphidic African shelf waters by blooming chemolithotrophs | Q42606052 | ||
Ecological consequences of bacterioplankton lifestyles: changes in concepts are needed | Q43809551 | ||
Metagenome of a versatile chemolithoautotroph from expanding oceanic dead zones | Q44095131 | ||
Autonomous observations of in vivo fluorescence and particle backscatteringin an oceanic oxygen minimum zone | Q44436390 | ||
Treponema denticola biofilm-induced expression of a bacteriophage, toxin-antitoxin systems and transposases. | Q45875456 | ||
Resource partitioning and sympatric differentiation among closely related bacterioplankton. | Q45899249 | ||
Dominance of Mycoplasma in the guts of the Long-Jawed Mudsucker, Gillichthys mirabilis, from five California salt marshes. | Q45957253 | ||
A mannose-sensitive haemagglutinin (MSHA)-like pilus promotes attachment of Pseudoalteromonas tunicata cells to the surface of the green alga Ulva australis. | Q46027837 | ||
Comparison of free-living and particle-associated bacterial communities in a coastal lagoon | Q46136356 | ||
Transposition is modulated by a diverse set of host factors in Escherichia coli and is stimulated by nutritional stress | Q46680790 | ||
Compositional differences in particle-associated and free-living microbial assemblages from an extreme deep-ocean environment. | Q46692278 | ||
Selective enrichment and molecular characterization of a previously uncultured Nitrospira-like bacterium from activated sludge | Q46944612 | ||
Detection of methanogenic archaea in seawater particles and the digestive tract of a marine fish species | Q47968894 | ||
Nitrous oxide reductase (nosZ) gene-specific PCR primers for detection of denitrifiers and three nosZ genes from marine sediments | Q48038054 | ||
Free-living and aggregate-associated Planctomycetes in the Black Sea. | Q48052883 | ||
Niche partitioning among Prochlorococcus ecotypes along ocean-scale environmental gradients. | Q51242132 | ||
A cryptic sulfur cycle in oxygen-minimum-zone waters off the Chilean coast. | Q51615041 | ||
PERSPECTIVE: TRANSPOSABLE ELEMENTS, PARASITIC DNA, AND GENOME EVOLUTION | Q56267651 | ||
Characteristics, dynamics and significance of marine snow | Q56444396 | ||
Intense hydrolytic enzyme activity on marine aggregates and implications for rapid particle dissolution | Q56973729 | ||
Bacterial chemolithotrophy in the ocean is associated with sinking particles | Q57201655 | ||
Heterogeneous archaeal communities in the particle-rich environment of an arctic shelf ecosystem | Q57211560 | ||
Archaeaplankton in the Columbia River, its estuary and the adjacent coastal ocean, USA | Q57272534 | ||
Antibacterial Activity of Marine Culturable Bacteria Collected from a Global Sampling of Ocean Surface Waters and Surface Swabs of Marine Organisms | Q57639488 | ||
Oxygen minimum zones in the eastern tropical Atlantic and Pacific oceans | Q58400067 | ||
Identification of putative methylotrophic and hydrogenotrophic methanogens within sedimenting material and copepod faecal pellets | Q58773987 | ||
Major role of bacteria in biogeochemical fluxes in the ocean's interior | Q59075184 | ||
Interactions between marine snow and heterotrophic bacteria: aggregate formation and microbial dynamics | Q59221472 | ||
Diel and seasonal variations in abundance, activity, and community structure of particle-attached and free-living bacteria in NW Mediterranean Sea | Q79898406 | ||
Mycoplasma-like organisms: occurrence with the larvae and adults of a marine bryozoan | Q81071370 | ||
Domain evolution and functional diversification of sulfite reductases | Q81401521 | ||
Microbial ecology of organic aggregates in aquatic ecosystems | Q106407046 | ||
Biogenesis, architecture, and function of bacterial type IV secretion systems | Q34449723 | ||
Metagenomic exploration of viruses throughout the Indian Ocean | Q34451821 | ||
Co-occurring anammox, denitrification, and codenitrification in agricultural soils | Q34453818 | ||
Marine microbes see a sea of gradients | Q34464187 | ||
A microbial consortium couples anaerobic methane oxidation to denitrification | Q34513437 | ||
Microbial behavior in a heterogeneous world | Q34633475 | ||
Can microscale chemical patches persist in the sea? Microelectrode study of marine snow, fecal pellets | Q34683969 | ||
A novel delta-subdivision proteobacterial lineage from the lower ocean surface layer | Q35199702 | ||
Nitrite oxidation in the Namibian oxygen minimum zone | Q35979328 | ||
Diversify or die: generation of diversity in response to stress. | Q36178618 | ||
Transcription profiling of the stringent response in Escherichia coli | Q36421860 | ||
Rapid chemotactic response enables marine bacteria to exploit ephemeral microscale nutrient patches | Q36670227 | ||
Contribution of particle-bound bacteria to total microheterotrophic activity in five ponds and two marshes | Q36705690 | ||
Endogenous oxidative stress produces diversity and adaptability in biofilm communities | Q36858633 | ||
Genetic basis of evolutionary adaptation by Escherichia coli to stressful cycles of freezing, thawing and growth | Q36873735 | ||
Contrasting genomic properties of free-living and particle-attached microbial assemblages within a coastal ecosystem | Q36889579 | ||
The genomic basis of trophic strategy in marine bacteria | Q37337800 | ||
Self-generated diversity produces "insurance effects" in biofilm communities | Q37621081 | ||
Vertical stratification of microbial communities in the Red Sea revealed by 16S rDNA pyrosequencing | Q33644220 | ||
baySeq: empirical Bayesian methods for identifying differential expression in sequence count data | Q33653650 | ||
Planctomycetes dominate biofilms on surfaces of the kelp Laminaria hyperborea | Q33719848 | ||
Microbial metatranscriptomics in a permanent marine oxygen minimum zone. | Q33787220 | ||
IS elements as constituents of bacterial genomes | Q33836581 | ||
Diversity and dynamics of free-living and particle-associated Betaproteobacteria and Actinobacteria in relation to phytoplankton and zooplankton communities | Q33902660 | ||
Enzymology and bioenergetics of respiratory nitrite ammonification. | Q33960681 | ||
Diversity of free-living and attached bacteria in offshore Western Mediterranean waters as depicted by analysis of genes encoding 16S rRNA | Q33984205 | ||
Phylogenetic analysis of particle-attached and free-living bacterial communities in the Columbia river, its estuary, and the adjacent coastal ocean. | Q33985477 | ||
Bacterial community assembly based on functional genes rather than species | Q33985559 | ||
Natural assemblages of marine proteobacteria and members of the Cytophaga-Flavobacter cluster consuming low- and high-molecular-weight dissolved organic matter | Q33987014 | ||
Structured multiple endosymbiosis of bacteria and archaea in a ciliate from marine sulfidic sediments: a survival mechanism in low oxygen, sulfidic sediments? | Q33990279 | ||
Antagonistic interactions among marine pelagic bacteria | Q33990588 | ||
Multiple bacterial symbionts in two species of co-occurring gutless oligochaete worms from Mediterranean sea grass sediments. | Q34013611 | ||
The phylogenetic diversity of metagenomes | Q34017552 | ||
Transposases are the most abundant, most ubiquitous genes in nature. | Q34020170 | ||
Potential for chemolithoautotrophy among ubiquitous bacteria lineages in the dark ocean. | Q34028365 | ||
The metagenome of the marine anammox bacterium 'Candidatus Scalindua profunda' illustrates the versatility of this globally important nitrogen cycle bacterium | Q34031865 | ||
A Nitrospira metagenome illuminates the physiology and evolution of globally important nitrite-oxidizing bacteria | Q34067963 | ||
Metabolic strategies of free-living and aggregate-associated bacterial communities inferred from biologic and chemical profiles in the Black Sea suboxic zone | Q34069781 | ||
Nitrite-driven anaerobic methane oxidation by oxygenic bacteria | Q34106608 | ||
Biogeography and phylogenetic diversity of a cluster of exclusively marine myxobacteria | Q34108069 | ||
Structure, fluctuation and magnitude of a natural grassland soil metagenome. | Q34148568 | ||
Untangling genomes from metagenomes: revealing an uncultured class of marine Euryarchaeota | Q34149345 | ||
Nitrogen cycle of the open ocean: from genes to ecosystems. | Q34165219 | ||
Intensive nitrogen loss over the Omani Shelf due to anammox coupled with dissimilatory nitrite reduction to ammonium | Q34179753 | ||
Perspective: transposable elements, parasitic DNA, and genome evolution | Q34192362 | ||
Extreme genome reduction in symbiotic bacteria | Q34230656 | ||
Antagonistic interactions among marine bacteria impede the proliferation of Vibrio cholerae | Q34232416 | ||
Microbial ecology of expanding oxygen minimum zones | Q34266951 | ||
Experimental incubations elicit profound changes in community transcription in OMZ bacterioplankton | Q34277761 | ||
Evaluation of 16S rDNA-based community profiling for human microbiome research | Q34312366 | ||
The Genome of Nitrospina gracilis Illuminates the Metabolism and Evolution of the Major Marine Nitrite Oxidizer | Q34329676 | ||
Oxygen minimum zones harbour novel viral communities with low diversity | Q34435061 | ||
P433 | issue | 1 | |
P921 | main subject | metagenomics | Q903778 |
P304 | page(s) | 187-211 | |
P577 | publication date | 2013-09-12 | |
P1433 | published in | The ISME Journal | Q7741240 |
P1476 | title | Metagenomic analysis of size-fractionated picoplankton in a marine oxygen minimum zone | |
P478 | volume | 8 |
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