Search results for "genome analysis"

showing 10 items of 61 documents

Genome and phenotype microarray analyses of rhodococcus sp. BCP1 and rhodococcus opacus R7: Genetic determinants and metabolic abilities with environ…

2015

In this paper comparative genome and phenotype microarray analyses of Rhodococcus sp. BCP1 and Rhodococcus opacus R7 were performed. Rhodococcus sp. BCP1 was selected for its ability to grow on short-chain n-alkanes and R. opacus R7 was isolated for its ability to grow on naphthalene and on o-xylene. Results of genome comparison, includ- ing BCP1, R7, along with other Rhodococcus reference strains, showed that at least 30% of the genome of each strain presented unique sequences and only 50% of the predicted proteome was shared. To associate genomic features with metabolic capabilities of BCP1 and R7 strains, hundreds of different growth conditions were tested through Phenotype Microarray, b…

AROMATIC-COMPOUNDS; GENUS RHODOCOCCUS; HIGH-THROUGHPUT; PATHWAY; DEGRADATION; BIODEGRADATION; EQUI; PERFORMANCE; CATABOLISMGenomics RhodococcusGene predictionBacterial Proteinlcsh:MedicineBiologyGenomeXenobioticsRhodococcus opacusBacterial ProteinsRhodococcuslcsh:ScienceGenePhylogenyGeneticsComparative genomicsMultidisciplinarylcsh:RMetabolic Networks and PathwayPhenotype microarrayHigh-Throughput Nucleotide SequencingRhodococcus sp. BCP1 Rhodococcus opacus R7Genome analysisGene Expression Regulation BacterialGenomicsSequence Analysis DNAbiology.organism_classificationBIO/19 - MICROBIOLOGIA GENERALEBiodegradation EnvironmentalPhenotypeProteomeGenomiclcsh:QPhenotype MicroarrayRhodococcusMetabolic Networks and PathwaysRhodococcuhydrocarbon degradationResearch Article
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Logic programming applied to genome evolution in cancer?

2016

ASP; Cancer evolution; Genome analysis; Computer Science (all)ASPComputer Science (all)Genome analysisCancer evolution
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Transcriptome data reveal syndermatan relationships and suggest the evolution of endoparasitism in acanthocephala via an epizoic stage

2014

The taxon Syndermata comprises the biologically interesting wheel animals ("Rotifera": Bdelloidea + Monogononta + Seisonidea) and thorny-headed worms (Acanthocephala), and is central for testing superordinate phylogenetic hypotheses (Platyzoa, Gnathifera) in the metazoan tree of life. Recent analyses of syndermatan phylogeny suggested paraphyly of Eurotatoria (free-living bdelloids and monogononts) with respect to endoparasitic acanthocephalans. Data of epizoic seisonids, however, were absent, which may have affected the branching order within the syndermatan clade. Moreover, the position of Seisonidea within Syndermata should help in understanding the evolution of acanthocephalan endoparas…

Animal EvolutionScienceMolecular Sequence DataRotiferaAnimal PhylogeneticsTranscriptomesAcanthocephala570 Life sciencesGenome Analysis Toolsddc:570GeneticsAnimalsEvolutionary SystematicsParasitesBiologyPhylogenyTaxonomyEvolutionary BiologyLife Cycle StagesQRComputational BiologyGenomicsBiological EvolutionOrganismal EvolutionPhylogeneticsAnimal TaxonomyMedicineTranscriptomeAnimal GeneticsZoologyResearch Article570 Biowissenschaften
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Big Data in metagenomics: Apache Spark vs MPI.

2020

The progress of next-generation sequencing has lead to the availability of massive data sets used by a wide range of applications in biology and medicine. This has sparked significant interest in using modern Big Data technologies to process this large amount of information in distributed memory clusters of commodity hardware. Several approaches based on solutions such as Apache Hadoop or Apache Spark, have been proposed. These solutions allow developers to focus on the problem while the need to deal with low level details, such as data distribution schemes or communication patterns among processing nodes, can be ignored. However, performance and scalability are also of high importance when…

Big DataComputer and Information SciencesScienceBig dataMessage Passing InterfaceParallel computingResearch and Analysis MethodsComputing MethodologiesComputing MethodologiesComputer ArchitectureComputer SoftwareDatabase and Informatics MethodsSoftwareSpark (mathematics)GeneticsMammalian GenomicsMultidisciplinarybusiness.industryApplied MathematicsSimulation and ModelingQRBiology and Life SciencesComputational BiologySoftware EngineeringGenomicsDNAGenomic DatabasesGenome AnalysisComputer HardwareSupercomputerBiological DatabasesAnimal GenomicsPhysical SciencesScalabilityEngineering and TechnologyMetagenomeMedicineDistributed memoryMetagenomicsbusinessMathematicsAlgorithmsGenome BacterialSoftwareResearch ArticlePLoS ONE
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Assessing the impact of copy number variants on miRNA genes in autism by Monte Carlo simulation.

2014

Autism Spectrum Disorders (ASDs) are childhood neurodevelopmental disorders with complex genetic origins. Previous studies have investigated the role of de novo Copy Number Variants (CNVs) and microRNAs as important but distinct etiological factors in ASD. We developed a novel computational procedure to assess the potential pathogenic role of microRNA genes overlapping de novo CNVs in ASD patients. Here we show that for chromosomes # 1, 2 and 22 the actual number of miRNA loci affected by de novo CNVs in patients was found significantly higher than that estimated by Monte Carlo simulation of random CNV events. Out of 24 miRNA genes over-represented in CNVs from these three chromosomes only …

Clinical PathologyDNA Copy Number Variationsendocrine system diseasesChromosomes Human Pair 22ScienceGene regulatory networkGenomicsDevelopmental and Pediatric NeurologyBiologyPathology and Laboratory MedicinePediatricsGenomeMolecular GeneticsmiRNA Genes Monte Carlo Simulation AutismDiagnostic Medicinemental disordersGeneticsMedicine and Health SciencesmedicineHumansComputer SimulationGene Regulatory NetworksCopy-number variationAutistic DisorderGeneGeneticsMultidisciplinaryGenome HumanQRBiology and Life SciencesComputational BiologyGenomicsGenome Analysismedicine.diseaseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)MicroRNAsNeurologyChromosomes Human Pair 1Genetic LociAutism spectrum disorderChromosomes Human Pair 2AutismMedicineStructural GenomicsHuman genomeMonte Carlo MethodResearch ArticlePLoS ONE
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The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii

2007

Background Bacterial symbioses are widespread among insects. The early establishment of such symbiotic associations has probably been one of the key factors for the evolutionary success of insects, since it may have allowed access to novel ecological niches and to new imbalanced food resources, such as plant sap or blood. Several genomes of bacterial endosymbionts of different insect species have been recently sequenced, and their biology has been extensively studied. Recently, the complete genome sequence of Candidatus Carsonella ruddii, considered the primary endosymbiont of the psyllid Pachpsylla venusta, has been published. This genome consists of a circular chromosome of 159,662 bp and…

DNA BacterialCandidatus Carsonella ruddiiEvolutionBacterial genome sizeBiologyGenome analysis; Candidatus Carsonella ruddii; Circular chromosome of 159662 bpPolymerase Chain ReactionGenomeHemipteraOpen Reading FramesQH359-425AnimalsSymbiosisGeneEcology Evolution Behavior and SystematicsOrganism:CIENCIAS DE LA VIDA::Genética ::Otras [UNESCO]Whole genome sequencingGeneticsCircular bacterial chromosomefungiGenes rRNASequence Analysis DNAGenome analysisCircular chromosome of 159662 bpbiology.organism_classificationUNESCO::CIENCIAS DE LA VIDA::Genética ::OtrasCandidatus Carsonella ruddiiOpen reading frameGenes BacterialGammaproteobacteriaGenome BacterialResearch ArticleBMC Evolutionary Biology
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Sequencing, De Novo Assembly and Annotation of the Colorado Potato Beetle, Leptinotarsa decemlineata, Transcriptome

2012

Background. The Colorado potato beetle (Leptinotarsa decemlineata) is a major pest and a serious threat to potato cultivation throughout the northern hemisphere. Despite its high importance for invasion biology, phenology and pest management, little is known about L. decemlineata from a genomic perspective. We subjected European L. decemlineata adult and larval transcriptome samples to 454-FLX massively-parallel DNA sequencing to characterize a basal set of genes from this species. We created a combined assembly of the adult and larval datasets including the publicly available midgut larval Roche 454 reads and provided basic annotation. We were particularly interested in diapause-specific g…

Drug ResistanceGene Identification and AnalysisSequence assemblylcsh:MedicineGenes InsectDiapause InsectTranscriptomesTranscriptomeGenome Sequencinglcsh:ScienceLeptinotarsaPhylogenyvieraslajiGeneticsMultidisciplinarybiologytulokaslajitHigh-Throughput Nucleotide SequencingAgricultureGenomicsta4111ColeopteraLarvaInsect ProteinsSequence AnalysisResearch ArticlePesticide resistanceSequence analysisdiapaussiPolymorphism Single NucleotideDNA sequencingMolecular GeneticsGenome Analysis ToolsAnimalsPesticidesBiologySerpinsta1184Colorado potato beetlefungilcsh:RkoloradonkuoriainenComputational BiologyBayes TheoremMolecular Sequence AnnotationSequence Analysis DNA15. Life on landbiology.organism_classificationActinsdiapauseMicroRNAsGene OntologyPyrosequencingta1181lcsh:QPest ControltranskriptomiIntroduced SpeciesTranscriptomeZoologyEntomologyPLOS ONE
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Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia

2020

Introduction Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) occurs approximately 1 in 3.500 live births representing the most common malformation of the upper digestive tract. Only half a century ago, EA/TEF was fatal among affected newborns suggesting that the steady birth prevalence might in parts be due to mutational de novo events in genes involved in foregut development. Methods To identify mutational de novo events in EA/TEF patients, we surveyed the exome of 30 case-parent trios. Identified and confirmed de novo variants were prioritized using in silico prediction tools. To investigate the embryonic role of genes harboring prioritized de novo variants we perfor…

EmbryologyCandidate geneGene ExpressionTranscriptomeMiceDatabase and Informatics MethodsMedicine and Health SciencesExomeExomeExome sequencingGenetics0303 health sciencesMultidisciplinaryComputer-Aided Drug DesignQ030305 genetics & hereditySequence analysisRGenomicsCongenital AnomaliesDNA-Binding Proteinsembryonic structuresAmino Acid AnalysisMedicineTranscriptome AnalysisTracheoesophageal FistulaResearch ArticleDrug Research and DevelopmentBioinformaticsSequence analysisScienceIn silicoBiologyResearch and Analysis Methods03 medical and health sciencesExome SequencingGeneticsCongenital DisordersAnimalsHumansddc:610Molecular Biology TechniquesEsophageal AtresiaMolecular BiologyDNA sequence analysis030304 developmental biologyHomeodomain ProteinsPharmacologyMolecular Biology Assays and Analysis TechniquesGene Expression ProfilingEmbryosDNA HelicasesBiology and Life SciencesComputational BiologyEmbryo MammalianGenome AnalysisFANCBRepressor ProteinsGene expression profilingBiological DatabasesDrug DesignMutation DatabasesMutationDevelopmental Biology
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Paradigm of tunable clustering using Binarization of Consensus Partition Matrices (Bi-CoPaM) for gene discovery

2013

Copyright @ 2013 Abu-Jamous et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Clustering analysis has a growing role in the study of co-expressed genes for gene discovery. Conventional binary and fuzzy clustering do not embrace the biological reality that some genes may be irrelevant for a problem and not be assigned to a cluster, while other genes may participate in several biological functions and should simultaneously belong to multiple clusters. Also, these algorithms cannot generate tight cluster…

Fuzzy clusteringMicroarraysSingle-linkage clusteringGenes FungalGene Expressionlcsh:MedicineBiologyFuzzy logicSet (abstract data type)Molecular GeneticsEngineeringGenome Analysis ToolsYeastsConsensus clusteringMolecular Cell BiologyDatabases GeneticCluster (physics)GeneticsCluster AnalysisBinarization of Consensus Partition Matrices (Bi-CoPaM)Cluster analysislcsh:ScienceGene clusteringBiologyOligonucleotide Array Sequence AnalysisGeneticsMultidisciplinarybusiness.industryCell Cycleta111lcsh:RComputational BiologyPattern recognitionGenomicsgene discoveryPartition (database)tunable binarization techniquesComputingMethodologies_PATTERNRECOGNITIONGenesCell cyclesSignal Processinglcsh:QArtificial intelligencebusinessGenomic Signal ProcessingAlgorithmsResearch Articleclustering
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openSNP–A Crowdsourced Web Resource for Personal Genomics

2014

Genome-Wide Association Studies are widely used to correlate phenotypic traits with genetic variants. These studies usually compare the genetic variation between two groups to single out certain Single Nucleotide Polymorphisms (SNPs) that are linked to a phenotypic variation in one of the groups. However, it is necessary to have a large enough sample size to find statistically significant correlations. Direct-To-Consumer (DTC) genetic testing can supply additional data: DTC-companies offer the analysis of a large amount of SNPs for an individual at low cost without the need to consult a physician or geneticist. Over 100,000 people have already been genotyped through Direct-To-Consumer genet…

GenotypeScienceInformation Storage and RetrievalBiological Data ManagementGenome-wide association studyGenomicsBiologySocial and Behavioral SciencesPolymorphism Single NucleotideFormal CommentGenomic MedicineGenome Analysis Toolsddc:570Genetic variationGenome-Wide Association StudiesGenome DatabasesGeneticsmedicineHumansGenetic TestingPrecision MedicineBiologyGenetic Association StudiesInformation ScienceGenetic testingGenetic associationClinical GeneticsGeneticsInternetMultidisciplinarymedicine.diagnostic_testInformation DisseminationQPersonalized MedicineRComputational BiologyHuman GeneticsGenomicsGeneticistData scienceOpen dataPhenotypeGenetics of DiseaseMedicineCrowdsourcingSoftwareResearch ArticleGenome-Wide Association StudyPersonal genomicsPLoS ONE
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