Search results for "Sequencing"

showing 10 items of 1087 documents

Key roles for freshwater A ctinobacteria revealed by deep metagenomic sequencing

2014

Freshwater ecosystems are critical but fragile environments directly affecting society and its welfare. However, our understanding of genuinely freshwater microbial communities, constrained by our capacity to manipulate its prokaryotic participants in axenic cultures, remains very rudimentary. Even the most abundant components, freshwater Actinobacteria, remain largely unknown. Here, applying deep metagenomic sequencing to the microbial community of a freshwater reservoir, we were able to circumvent this traditional bottleneck and reconstruct de novo seven distinct streamlined actinobacterial genomes. These genomes represent three new groups of photoheterotrophic, planktonic Actinobacteria.…

DNA BacterialMolecular Sequence DatarhodopsinsFresh WaterCyanobacteria633 - Cultivos y producciones [CDU]GenomeFreshwater ecosystemActinobacteriaContig MappingPhylogeneticsRNA Ribosomal 16Slignin degradationGeneticsMicrococcineaePhylogenyEcology Evolution Behavior and SystematicsmetagenomicsbiologyEcologyHigh-Throughput Nucleotide SequencingSequence Analysis DNAbiology.organism_classificationfreshwater reservoirActinobacteriaSpainMetagenomicsMetagenomicsActinomycetalesWater MicrobiologyGenome BacterialGC-contentMolecular Ecology
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Whole genome sequencing analysis of intrapatient microevolution in Mycobacterium tuberculosis: potential impact on the inference of tuberculosis tran…

2013

Background. It has been accepted that the infection by Mycobacterium tuberculosis (M. tuberculosis) can be more heterogeneous than considered. The emergence of clonal variants caused by microevolution events leading to population heterogeneity is a phenomenon largely unexplored. Until now, we could only superficially analyze this phenomenon by standard fingerprinting (RFLP and VNTR).Methods. In this study we applied whole genome sequencing for a more in-depth analysis of the scale of microevolution both at the intrapatient and interpatient scenarios.Results. We found that the amount of variation accumulated within a patient can be as high as that observed between patients along a chain of t…

DNA BacterialTuberculosisSingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideDNA sequencingMycobacterium tuberculosisEvolution MolecularmedicineImmunology and AllergyCluster AnalysisHumansTuberculosisGeneticsWhole genome sequencingMolecular EpidemiologyTransmission (medicine)MicroevolutionMycobacterium tuberculosisSequence Analysis DNAbiology.organism_classificationmedicine.disease3. Good healthInfectious DiseasesRestriction fragment length polymorphismGenome BacterialThe Journal of infectious diseases
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Genome Sequence of the Methanotrophic Poly-β-Hydroxybutyrate Producer Methylocystis parvus OBBP

2012

-- PAGS 2 5709-5710

DNA Bacterialfood.ingredientOperonMethane monooxygenasePolyestersMolecular Sequence DataMethylocystisHydroxybutyratesmonooxigenasaMicrobiologyfoodmethylotrophOperonBotanyMolecular BiologyGeneGeneticsWhole genome sequencingbiologySequence Analysis DNAbiology.organism_classificationGenome AnnouncementsType speciesMethylocystisOxygenasesbiology.proteinMethylotrophMethylocystis parvusMethaneMethylocystaceaeGenome BacterialMetabolic Networks and PathwaysJournal of Bacteriology
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Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes

2006

AbstractImprinted genes are expressed from only one allele in a parent-of-origin-specific manner. We here describe a systematic approach to identify novel imprinted genes using quantification of allele-specific expression by Pyrosequencing, a highly accurate method to detect allele-specific expression differences. Sixty-eight candidate imprinted transcripts mapping to known imprinted chromosomal regions were selected from a recent expression profiling study of uniparental mouse embryos and analyzed. Three novel imprinted transcripts encoding putative non-protein-coding RNAs were identified on the basis of parent-of-origin-specific monoallelic expression in E11.5 (C57BL/6 × Cast/Ei)F1 and in…

DNA ComplementaryTranscription GeneticGenomic imprintingMouseParthenogenesisGene ExpressionGenomicsMice Inbred StrainsUniparental embryoBiologyPolymorphism Single NucleotideChromosomesMicePregnancyDatabases GeneticGeneticsAnimalsRNA MessengerAlleleGeneAllelesCrosses GeneticGeneticsModels GeneticChromosome MappingGenetic VariationPyrosequencingEmbryoParthenogenesisDNAEmbryo MammalianGene expression profilingGene expression profilingMice Inbred C57BLPyrosequencingRNAFemaleGenomic imprintingPrader-Willi SyndromeSoftwareGenomics
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Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana.

2000

Arabidopsis thaliana is an important model system for plant biologists. In 1996 an international collaboration (the Arabidopsis Genome Initiative) was formed to sequence the whole genome of Arabidopsis and in 1999 the sequence of the first two chromosomes was reported. The sequence of the last three chromosomes and an analysis of the whole genome are reported in this issue. Here we present the sequence of chromosome 3, organized into four sequence segments (contigs). The two largest (13.5 and 9.2 Mb) correspond to the top (long) and the bottom (short) arms of chromosome 3, and the two small contigs are located in the genetically defined centromere. This chromosome encodes 5,220 of the rough…

DNA PlantSequence analysisArabidopsisplantGenomeComplete sequenceArabidopsisGene DuplicationCentromerePlant genomics; model organismHumansgenomic structureGenemodel organismPlant ProteinsGeneticsMultidisciplinarybiologyChromosomeChromosome MappingSequence Analysis DNAbiology.organism_classificationPlant genomicsgenome sequencingChromosome 3plant; genome sequencing; genomic structureGenome Plant
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UVPAR: fast detection of functional shifts in duplicate genes.

2006

Abstract Background The imprint of natural selection on gene sequences is often difficult to detect. A plethora of methods have been devised to detect genetic changes due to selective processes. However, many of those methods depend heavily on underlying assumptions regarding the mode of change of DNA sequences and often require sophisticated mathematical treatments that made them computationally slow. The development of fast and effective methods to detect modifications in the selective constraints of genes is therefore of great interest. Results We describe UVPAR, a program designed to quickly test for changes in the functional constraints of duplicate genes. Starting with alignments of t…

DanioComputational biologyBiologylcsh:Computer applications to medicine. Medical informaticsBiochemistryDNA sequencingEvolution MolecularGenes DuplicateSequence Analysis ProteinStructural BiologySelection GeneticHox geneMolecular BiologyGenelcsh:QH301-705.5Selection (genetic algorithm)GeneticsNatural selectionApplied MathematicsProteinsSequence Analysis DNAbiology.organism_classificationComputer Science Applicationslcsh:Biology (General)lcsh:R858-859.7DNA microarraySequence AlignmentSoftwareAlgorithmsGenètica
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Shortcut nitrification-denitrification by means of autochthonous halophilic biomass in an SBR treating fish-canning wastewater

2017

Abstract Autochthonous halophilic biomass was cultivated in a sequencing batch reactor (SBR) aimed at analyzing the potential use of autochthonous halophilic activated sludge in treating saline industrial wastewater. Despite the high salt concentration (30 g NaCl L −1 ), biological oxygen demand (BOD) and total suspended solids (TSS), removal efficiencies were higher than 90%. More than 95% of the nitrogen was removed via a shortcut nitrification-denitrification process. Both the autotrophic and heterotrophic biomass samples exhibited high biological activity. The use of autochthonous halophilic biomass led to high-quality effluent and helped to manage the issues related to nitrogen removal…

DenitrificationEnvironmental EngineeringAutochthonous-halophilic bacteriaNitrogen0208 environmental biotechnologySequencing batch reactor02 engineering and technologyWastewater010501 environmental sciencesManagement Monitoring Policy and LawWaste Disposal Fluid01 natural sciencesFish-canning wastewaterIndustrial wastewater treatmentBioreactorsBiomassWaste Management and DisposalSBR0105 earth and related environmental sciencesTotal suspended solidsSewageSettore ICAR/03 - Ingegneria Sanitaria-AmbientaleChemistryGeneral MedicinePulp and paper industryNitrification020801 environmental engineeringActivated sludgeWastewaterDenitrificationSewage treatmentNitrificationSaline wastewaterShortcut nitrification-denitrification
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Characterization of denitrification gene clusters of soil bacteria via a metagenomic approach

2009

International audience; Denitrification is a microbial respiratory process contributing to the emission of greenhouse gas. The study of denitrifying bacteria, like that of others, is hindered by characteristics that can prevent up to 99% of soil bacteria from being cultivated in vitro. New approaches based on the direct extraction of DNA from the natural environment and PCR amplifications can overcome limitations due to bacterial unculturability, but until now their application to denitrification genes has led only to the recovery of partial sequences for some of these genes.Our goals in this study were to apply a metagenomic approach characterized by cloning of DNA extracted from soil and …

Denitrification[SDV]Life Sciences [q-bio]Microbial metabolismNIRKApplied Microbiology and Biotechnology[ SPI.NRJ ] Engineering Sciences [physics]/Electric powerGene OrderGene clusterPHYLOGENETIC ANALYSISNITROUS-OXIDE REDUCTASESoil MicrobiologyComputingMilieux_MISCELLANEOUS2. Zero hunger0303 health sciencesdenitrificationEcologyfood and beveragesFAMILYCOMMUNITYPCRMultigene Family[SDE]Environmental SciencesSoil microbiologyMetabolic Networks and PathwaysBiotechnologyDNA BacterialDOMAINSNitrogenMolecular Sequence DataComputational biologyBiologyMicrobial Ecologysoil03 medical and health sciencesmetagenomic;n-cycle;denitrification;soil Bacterial ProteinsOperonBotanymetagenomicNitrogen cycle030304 developmental biology[ SDE.BE ] Environmental Sciences/Biodiversity and EcologyNITRIC-OXIDEBacteriaSequence Homology Amino Acid030306 microbiology[SPI.NRJ]Engineering Sciences [physics]/Electric powerSequence Analysis DNAn-cyclebiology.organism_classificationDENITRIFYING PSEUDOMONAS-STUTZERIMetagenomicsPyrosequencing[SDE.BE]Environmental Sciences/Biodiversity and EcologyBacteria[SPI.NRJ] Engineering Sciences [physics]/Electric powerFood ScienceNOSZ GENES
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Sequencing ancient calcified dental plaque shows changes in oral microbiota with dietary shifts of the Neolithic and Industrial revolutions

2013

The importance of commensal microbes for human health is increasingly recognized, yet the impacts of evolutionary changes in human diet and culture on commensal microbiota remain almost unknown. Two of the greatest dietary shifts in human evolution involved the adoption of carbohydrate-rich Neolithic (farming) diets (beginning ∼10,000 years before the present) and the more recent advent of industrially processed flour and sugar (in ∼1850). Here, we show that calcified dental plaque (dental calculus) on ancient teeth preserves a detailed genetic record throughout this period. Data from 34 early European skeletons indicate that the transition from hunter-gatherer to farming shifted the oral m…

Dental PlaqueBiologyDental plaqueArticleCariogenic bacteriaOral MicrobiotaHuman healthGeneticsmedicineHumansIndustrybusiness.industryEcologyCalculus (dental)Mouth MucosaHigh-Throughput Nucleotide Sequencingmedicine.diseaseBiological EvolutionDietstomatognathic diseasesArchaeologyHuman evolutionAgricultureMetagenomicsMetagenomebusinessNature Genetics
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Congenital secretory diarrhoea caused by activating germline mutations in GUCY2C

2016

Objective Congenital sodium diarrhoea (CSD) refers to a form of secretory diarrhoea with intrauterine onset and high faecal losses of sodium without congenital malformations. The molecular basis for CSD remains unknown. We clinically characterised a cohort of infants with CSD and set out to identify disease-causing mutations by genome-wide genetic testing. Design We performed whole-exome sequencing and chromosomal microarray analyses in 4 unrelated patients, followed by confirmatory Sanger sequencing of the likely disease-causing mutations in patients and in their family members, followed by functional studies. Results We identified novel de novo missense mutations in GUCY2C, the gene encod…

DiarrheaMale0301 basic medicinemedicine.medical_specialtyReceptors PeptideColonGuanylinGuanosine MonophosphateMutation MissenseReceptors EnterotoxinGUANYLATE CYCLASEBiologyCHRONIC DIARRHOEAPathogenesis03 medical and health scienceschemistry.chemical_compoundsymbols.namesakeGermline mutationInternal medicineBACTERIAL ENTEROTOXINSmedicineHumansMissense mutationAbnormalities MultipleGenetic Predisposition to Disease1506Intestinal MucosaCyclic guanosine monophosphateSanger sequencingPAEDIATRIC DIARRHOEASodiumGastroenterologyInfantMolecular Reproduction Development & Genetics (formed by the merger of DBGL and CRBME)Molecular biologyIntestines030104 developmental biologyEndocrinologyIntestinal AbsorptionReceptors Guanylate Cyclase-CoupledchemistryINTESTINAL ION TRANSPORTsymbolsFemaleMetabolism Inborn ErrorsIntracellularUroguanylinGut
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