Search results for "Genome"

showing 10 items of 1913 documents

Historical and biological determinants of genetic diversity in the highly endemic triploid sea lavender Limonium dufourii (Plumbaginaceae)

2007

14 páginas, 5 figuras, 2 tablas.

GenotypePopulationBiologyPlant conservationGenetic diversityEvolution MolecularCritically endangeredPlumbaginaceaeHalophytesAlloploidyGenetic variationGeneticsAlleleMicrosatelliteseducationAllelesEcology Evolution Behavior and Systematicseducation.field_of_studyGenetic diversityGeographyEcologyGenetic VariationSequence Analysis DNASpainGenetic markerEvolutionary biologyGenetic structureHybridization GeneticMicrosatelliteApomixisGenome PlantMicrosatellite RepeatsMolecular Ecology
researchProduct

Genotypic analysis at multiple loci across Kaposi's sarcoma herpesvirus (KSHV) DNA molecules: clustering patterns, novel variants and chimerism

2001

Abstract Background: the genomes of human Kaposi's sarcoma-associated herpesvirus (KSHV) display several levels of DNA sequence heterogeneity and subgrouping that show distinctive clustering patterns in related human populations. The four major subtype patterns for the hypervariable ORF-K1 protein correlate closely with the principal diasporas resulting from the migration of modern humans out of East Africa and suggest that KSHV is an ancient human virus that is transmitted primarily in a familial fashion with consequent very low recombination rates. However, chimeric genomes have also been detected, especially with regard to the presence of P versus M alleles of the ORF-K15 gene. Objective…

GenotypePopulationMolecular Sequence DataGenome ViralBiologyGenomeDNA sequencingMiddle EastOpen Reading FramesAfrica NorthernViral Envelope ProteinsVirologyGenotypemedicineHumansAmino Acid SequenceAlleleeducationCladeKaposi's sarcomaGeneSarcoma KaposiAllelesPhylogenyGeneticsRecombination Geneticeducation.field_of_studyAcquired Immunodeficiency SyndromeKoreaMembrane Proteinsmedicine.diseaseEuropeInfectious DiseasesHerpesvirus 8 HumanNorth AmericaSequence Alignment
researchProduct

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
researchProduct

The sf32 unique gene of Spodoptera frugiperda multiple nucleopolyhedrovirus (SfMNPV) is a non-essential gene that could be involved in nucleocapsid o…

2013

A recombinant virus lacking the sf32 gene (Sf32null), unique to the Spodoptera frugiperda multiple nucleopolyhedrovirus (SfMNPV), was generated by homologous recombination from a bacmid comprising the complete viral genome (Sfbac). Transcriptional analysis revealed that sf32 is an early gene. Occlusion bodies (OBs) of Sf32null contained 62% more genomic DNA than viruses containing the sf32 gene, Sfbac and Sf32null-repair, although Sf32null DNA was three-fold less infective when injected in vivo. Sf32null OBs were 18% larger in diameter and contained 17% more nucleocapsids within ODVs than those of Sfbac. No significant differences were detected in OB pathogenicity (50% lethal concentration)…

GenotypevirusesScienceGenome ViralSpodopteraSpodopteraVirus ReplicationOcclusion-derived virionsRecombinant virusHomology (biology)VirusViral Proteins03 medical and health sciencesAnimalsNucleocapsidSpodoptera frugiperda multiple nucleopolyhedrovirus (SfMNPV)Gene030304 developmental biology0303 health sciencesGenes Essential[SDV.BA.MVSA]Life Sciences [q-bio]/Animal biology/Veterinary medicine and animal HealthMultidisciplinaryNucleocapsid organizationbiology030306 microbiologyfungiQVirionRbiology.organism_classificationVirologyNucleopolyhedroviruses3. Good healthViral replicationEssential geneLarvaDNA Viral[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyMedicinesf32Homologous recombinationResearch ArticlePLoS ONE
researchProduct

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.

2014

Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with breast cancer risk. To clarify the role of CASP8 in breast cancer susceptibility, we carried out dense genotyping of this region in the Breast Cancer Association Consortium (BCAC). Single-nucleotide polymorphisms (SNPs) spanning a 1 Mb region around CASP8 were genotyped in 46 450 breast cancer cases and 42 600 controls of European origin from 41 studies participating in the BCAC as part of a custom genotyping array experiment (iCOGS). Missing genotypes and SNPs were imputed and, after quality exclusions, 501 typed and 1232 imputed SNPs were included in logistic regressionmodels adjusting for stud…

Genotyping TechniquesResearch Support U.S. Gov't P.H.S.CASP8 and FADD-Like Apoptosis Regulating ProteinGenome-wide association studyP.H.S.Medical and Health SciencesBreast and Ovarian Cancer Susceptibility (BOCS) StudyMedizinische FakultätGenetics(clinical)Non-U.S. Gov'tGenetics (clinical)GeneticsGenetics & HeredityvariantsCaspase 8Research Support Non-U.S. Gov'tAssociation Studies ArticlesGeneral MedicineBiological Sciencesddc:Chromosomes Human Pair 2kConFab InvestigatorsFemaleGENICA NetworkAustralian Ovarian Cancer Study GroupEuropean Continental Ancestry GroupNon-P.H.S.Single-nucleotide polymorphismBreast Neoplasms-BiologyResearch SupportPolymorphism Single NucleotideWhite PeopleN.I.H.Breast cancerResearch Support N.I.H. ExtramuralSDG 3 - Good Health and Well-beingmedicineGeneticsJournal ArticleHumansGenetic Predisposition to Diseaseddc:610geneGenotyping TechniquesGenotypingMolecular BiologyGenetic associationdiseaseExtramuralProteinsOdds ratiomedicine.diseasesusceptibility lociMinor allele frequencyCase-Control Studiesgenome-wide associationenhancersU.S. Gov'tcasp8Research Support U.S. Gov't Non-P.H.S.Genome-Wide Association Study
researchProduct

Genome-Wide SNP-Genotyping Array to Study the Evolution of the Human Pathogen Vibrio vulnificus Biotype 3

2014

Vibrio vulnificus is an aquatic bacterium and an important human pathogen. Strains Of V. vulnificus are classified into three different biotypes. The newly emerged biotype 3 has been found to be clonal and restricted to Israel. In the family Vibrionaceae , horizontal gene transfer is the main mechanism responsible for the emergence of new pathogen groups. To better understand the evolution of the bacterium, and in particular to trace the evolution of biotype 3, we performed genome-wide SNP genotyping of 254 clinical and environmental V. vulnificus isolates with worldwide distribution recovered over a 30-year period, representing all phylogeny groups. A custom single-nucleotide polymorphism …

GenotypingGenome evolutionlcsh:MedicineMarine and Aquatic SciencesGenome ViralVibrio vulnificusPolymorphism Single NucleotideMicrobiologyGenomeEvolution MolecularMolecular GeneticsGeneticslcsh:ScienceMolecular Biology TechniquesCladeVibrio vulnificusMolecular BiologyGenotypingComparative genomicsGeneticsEvolutionary BiologyBacterial EvolutionMultidisciplinarybiologyPhylogenetic treelcsh:REcology and Environmental SciencesBiology and Life SciencesAquatic Environmentsbiology.organism_classificationOrganismal EvolutionSNP genotypingHaplotypesBacteris patògensMicrobial EvolutionEarth Scienceslcsh:QPopulation GeneticsResearch ArticlePLoS ONE
researchProduct

Population genetic analysis of bi-allelic structural variants from low-coverage sequence data with an expectation-maximization algorithm

2014

Background Population genetics and association studies usually rely on a set of known variable sites that are then genotyped in subsequent samples, because it is easier to genotype than to discover the variation. This is also true for structural variation detected from sequence data. However, the genotypes at known variable sites can only be inferred with uncertainty from low coverage data. Thus, statistical approaches that infer genotype likelihoods, test hypotheses, and estimate population parameters without requiring accurate genotypes are becoming popular. Unfortunately, the current implementations of these methods are intended to analyse only single nucleotide and short indel variation…

GenotypingGenotypePopulation geneticsPopulationPopulation geneticsBiologyBiochemistryReference biasStructural variation03 medical and health sciences0302 clinical medicineStructural BiologyGenotypeStatisticsHumans1000 Genomes ProjecteducationMolecular BiologyAlleles030304 developmental biologySampling biasGenetic associationGeneticsLikelihood Functions0303 health scienceseducation.field_of_studyGenomePolymorphism GeneticGenètica de poblacionsApplied MathematicsHigh-Throughput Nucleotide SequencingGenomicsComputer Science ApplicationsGenotype frequencyGenetics PopulationStructural variationSoftwareAlgorithms030217 neurology & neurosurgeryMaximum likelihood
researchProduct

Modificazioni germinali del patrimonio genetico e biodiritto. I paradossi della de-differenziazione tra bioetica e biodiritto

2021

Il presente lavoro, incominciato nel novembre del 2017, è partito con l'ambizione di ricostruire la risposta che il sistema giuridico fornisce innanzi alle nuove tecniche di ingegneria genetica che, a fronte della loro applicabilità sugli esseri umani, hanno prodotto, negli ultimi anni, il sorgere di nuovi stakeholders e, ancor prima, di nuovi interessi meritevoli di tutela. Se fino a qualche anno fa pareva impensabile modificare il genoma umano e, men che meno, farlo in maniera precisa, efficiente ed economica, oggi grazie al sistema di modificazione genetica CRISPR/Cas9 è possibile, intervenendo sulla linea germinale degli embrioni umani, prevenire la contrazione di odiose malattie geneti…

Germ-line gene editingSettore IUS/20 - Filosofia Del Dirittogene editinghuman right:CIENCIAS JURÍDICAS Y DERECHO [UNESCO]philosophy of lawUNESCO::CIENCIAS JURÍDICAS Y DERECHObiolawsociology of lawdignitybioethicGeneticseugeniccrisprbioethicsGenome editing
researchProduct

Ploidy manipulation and citrus breeding, genetics and genomics

2020

Polyploidy appears to have played a limited role in citrus germplasm evolution. However, today, ploidy manipulation is an important component of citrus breeding strategies. For varieties, the main objective is to develop triploid seedless cultivars. For rootstock, the aim is to cumulate interesting traits in tetraploid hybrids and to improve adaptation to biotic and abiotic stresses. This chapter starts with a review of the recent knowledge acquired on the natural mechanisms of citrus polyploidization and tetraploid meiosis. Chromosome doubling of nucellar cells is frequent in apomictic citrus and results in tetraploid seedling production. Unreduced gametes are also frequently produced, mai…

GermplasmCitrusGenomicsBiologyGenomeF30 - Génétique et amélioration des plantesgénomiquehttp://aims.fao.org/aos/agrovoc/c_49902PolyploidApomixisCitrus Genome BreedingGénétiquehttp://aims.fao.org/aos/agrovoc/c_3222Hybridamélioration génétiqueGeneticshttp://aims.fao.org/aos/agrovoc/c_1637fungihttp://aims.fao.org/aos/agrovoc/c_6094food and beverageshttp://aims.fao.org/aos/agrovoc/c_92382PolyploïdieAmélioration des plantesSettore AGR/03 - Arboricoltura Generale E Coltivazioni Arboreehttp://aims.fao.org/aos/agrovoc/c_5956Doubled haploidyPloidy
researchProduct

Rapid adaptation of signaling networks in the fungal pathogen Magnaporthe oryzae

2019

Abstract Background One fundamental question in biology is how the evolution of eukaryotic signaling networks has taken place. “Loss of function” (lof) mutants from components of the high osmolarity glycerol (HOG) signaling pathway in the filamentous fungus Magnaporthe oryzae are viable, but impaired in osmoregulation. Results After long-term cultivation upon high osmolarity, stable individuals with reestablished osmoregulation capacity arise independently from each of the mutants with inactivated HOG pathway. This phenomenon is extremely reproducible and occurs only in osmosensitive mutants related to the HOG pathway – not in other osmosensitive Magnaporthe mutants. The major compatible so…

GlycerolMagnaportheved/biology.organism_classification_rank.speciesMutantGenomeSalt StressTranscriptome0302 clinical medicineOsmoregulationLoss of Function MutationGene Expression Regulation FungalGene Regulatory NetworksSuppressorReestablishment of osmoregulation0303 health sciencesbiologyMagnaporthe oryzaeRewiringAdaptation PhysiologicalRapid adaptationCell biologyMagnaportheOsmoregulationEpigeneticsGenome FungalBiotechnologySignal TransductionResearch Articlelcsh:QH426-470lcsh:BiotechnologyDioxolesFungal Proteins03 medical and health sciencesDrug Resistance Fungallcsh:TP248.13-248.65GeneticsPyrrolesModel organismGene030304 developmental biologyPlant DiseasesOsmotic concentrationved/biologyGene Expression ProfilingEvolution of signaling networksHOG pathwayOryzabiology.organism_classificationlcsh:Genetics030217 neurology & neurosurgery
researchProduct