Search results for "Sequencing"

showing 10 items of 1087 documents

Complete Genome Sequence of “Candidatus Tremblaya princeps” Strain PCVAL, an Intriguing Translational Machine below the Living-Cell Status

2011

ABSTRACT The sequence of the genome of “ Candidatus Tremblaya princeps” strain PCVAL, the primary endosymbiont of the citrus mealybug Planococcus citri , has been determined. “ Ca . Tremblaya princeps” presents an unusual nested endosymbiosis and harbors a gammaproteobacterial symbiont within its cytoplasm in all analyzed mealybugs. The genome sequence reveals that “ Ca . Tremblaya princeps” cannot be considered an independent organism but that the consortium with its gammaproteobacterial symbiotic associate represents a new composite living being.

GeneticsWhole genome sequencingbiologyEndosymbiosisStrain (biology)Molecular Sequence Databiochemical phenomena metabolism and nutritionbiology.organism_classificationMicrobiologyHemipteraGenomeGenome AnnouncementsHemipteraHelicobacterCandidatus Tremblaya princepsBotanyPlanococcus citriAnimalsbacteriaMolecular BiologyGenome BacterialSequence (medicine)
researchProduct

Sequencing analysis of a 4·1 kb subtelomeric region from yeast chromosome IV identifiesHXT15, a new member of the hexose transporter family

1996

The DNA sequence of a 4·1 kb region of Saccharomyces cerevisiae chromosome IV was determined. This region contains a single open reading frame which codes for a member of the hexose transporter family. This new gene has been named HXT15 according to yeast gene data bases. The sequence has been entered in the EMBL data library under Accession Number X92891.

GeneticsbiologyAccession number (library science)Saccharomyces cerevisiaeChromosomeBioengineeringbiology.organism_classificationSubtelomereApplied Microbiology and BiotechnologyBiochemistryDNA sequencingYeastOpen reading frameGeneticsGeneBiotechnologyYeast
researchProduct

HLA typing from RNA-Seq sequence reads.

2012

We present a method, seq2HLA, for obtaining an individual's human leukocyte antigen (HLA) class I and II type and expression using standard next generation sequencing RNA-Seq data. RNA-Seq reads are mapped against a reference database of HLA alleles, and HLA type, confidence score and locus-specific expression level are determined. We successfully applied seq2HLA to 50 individuals included in the HapMap project, yielding 100% specificity and 94% sensitivity at a P-value of 0.1 for two-digit HLA types. We determined HLA type and expression for previously un-typed Illumina Body Map tissues and a cohort of Korean patients with lung cancer. Because the algorithm uses standard RNA-Seq reads and …

Geneticsbusiness.industryMethodRNA-SeqHuman leukocyte antigenHuman geneticsDNA sequencingGeneticsBiomarker (medicine)MedicineMolecular MedicineGenetics(clinical)International HapMap ProjectAllelebusinessMolecular BiologyGenetics (clinical)Sequence (medicine)Genome medicine
researchProduct

An approach to determining anthocyanin synthesis enzyme gene expression in an evolutionary context: an example from Erica plukenetii

2019

Abstract Background and Aims Floral colour in angiosperms can be controlled by variations in the expression of the genes of the anthocyanin pathway. Floral colour shifts influence pollinator specificity. Multiple shifts in floral colour occurred in the diversification of the genus Erica (Ericaceae), from plesiomorphic pink to, for example, red or white flowers. Variation in anthocyanin gene expression and its effects on floral colour in the red-, pink- and white-flowered Erica plukenetii species complex was investigated. Methods Next generation sequencing, reverse transcriptase PCR and real-time reverse transcriptase quantitative PCR were used to quantify anthocyanin gene expression. Key Re…

GeneticsfungiColorfood and beveragesContext (language use)FlowersOriginal ArticlesPlant ScienceBiologybiology.organism_classificationDNA sequencingAnthocyaninsWhite (mutation)DNA binding siteReverse transcription polymerase chain reactionErica plukenetiiGene Expression Regulation PlantGene expressionEricaceaeGene
researchProduct

Reliability of Restriction Enzyme Digestions of Genomic DNA for the Generation of DNA Fingerprints

1991

Since minisatellite DNA probes are used for the detection of hypervariable loci in eucaryotic genomes [1] the application of so called DNA fingerprints and DNA technology itself in paternity testing and forensic casework is critically discussed ([3]; Brinkmann et al., this volume). A particular problem is the possibility of obtaining partially digested genomic DNA in casework after treatment with restriction enzymes leading to inconclusive or even false results. This is even more important when multilocus DNA probes are used, since the total number of fragments in a given person is not known in advance. But also with single locus probes, where only two allelic fragments are usually detected…

Geneticsgenomic DNARestriction enzymeMinisatelliteRestriction mapDNA profilingGenomic libraryRestriction fragment length polymorphismBiologySequencing by ligation
researchProduct

PCR-Typing of the Human HLA-DQα Locus: Population Genetics and Application in Forensic Casework

1991

Multi- and single-locus probes recognizing highly polymorphic DNA sequences throughout the genome ([1–3]; C. Rittner, this volume) have become powerful tools for paternity testing and forensic stain analysis. In forensic casework, however, DNA probe technology can often not be applied, since genomic DNA extracted from stain material exposed to conditions of high temperatures and humidity is degraded. Also, the amount of DNA to be typed may not be sufficient to use DNA probe technology, e.g. if extracted from minute blood or sperm stains, from single hairs or from cell smears on microscope slides.

Geneticsgenomic DNAchemistry.chemical_compoundchemistryHybridization probePopulation geneticsLocus (genetics)BiologyGenomeStainDNA sequencingDNA
researchProduct

Molecular biology approaches utilized in preimplantation genetics: real-time PCR, microarrays, next-generation sequencing, karyomapping, and others

2020

Abstract Over the past few decades the development of new molecular technologies has revolutionized diagnosis in the reproductive medicine field, with the evaluation of the two main factors involved in a successful pregnancy: the embryo and the endometrium. The detection of genetically abnormal embryos, as well as the identification of an optimum endometrium using transcriptomics have become a priority in assisted reproductive treatments to increase pregnancy rates. This chapter provides an overview of the molecular techniques currently employed in assisted reproduction for embryo evaluation such as preimplantation genetic testing karyotyping, fluorescence in situ hybridization, polymerase …

Geneticsmedicine.diagnostic_testBiologyDNA sequencinglaw.inventionTranscriptomeReal-time polymerase chain reactionlawmedicineDNA microarrayPolymerase chain reactionComparative genomic hybridizationFluorescence in situ hybridizationGenetic testing
researchProduct

A novel approach to CFTR mutation testing by pyrosequencing-based assay panels adapted to ethnicities.

2009

Abstract Background: Cystic fibrosis (CF) is a common autosomal recessive genetic disorder caused by a variety of sequence alterations in the CFTR gene [cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)]. Because the relative prevalence of mutations strongly depends on the ethnic background, first-level testing of CF as defined by recent consensus recommendations ought to be adaptable to the ethnicity of patients. Methods: We therefore developed and implemented a diagnostic approach to first-level testing for CF based on published mutation frequencies and Pyrosequencing (PSQ) technology that we complemented with standard procedures of mutation…

Geneticsmedicine.diagnostic_testbiologyBase SequenceCystic FibrosisGenetic Carrier ScreeningBiochemistry (medical)Clinical BiochemistryGenetic disorderCystic Fibrosis Transmembrane Conductance RegulatorSequence Analysis DNAmedicine.diseaseCystic fibrosisPolymerase Chain ReactionCystic fibrosis transmembrane conductance regulatorCftr mutationCase-Control StudiesMutation (genetic algorithm)Mutationmedicinebiology.proteinPyrosequencingHumansGenotypingSweat testClinical chemistry
researchProduct

Molecular Genetics of Frontonasal Dysplasia

2018

Geneticsmedicine.medical_specialtyTeebi syndromebusiness.industryMolecular geneticsAcromelic Frontonasal DysostosisMedicinePAI SYNDROMEFrontonasal dysplasiabusinessmedicine.diseaseDNA sequencingExome sequencingeLS
researchProduct

Phylogenomic Analysis Reveals Deep Divergence and Recombination in an Economically Important Grapevine Virus

2015

The evolutionary history of the exclusively grapevine (Vitis spp.) infecting, grapevine leafroll-associated virus 3 (GLRaV-3) has not been studied extensively, partly due to limited available sequence data. In this study we trace the evolutionary history of GLRaV-3, focussing on isolate GH24, a newly discovered variant. GH24 was discovered through the use of next-generation sequencing (NGS) and the whole genome sequence determined and validated with Sanger sequencing. We assembled an alignment of all 13 available whole genomes of GLRaV-3 isolates and all other publicly available GLRaV-3 sequence data. Using multiple recombination detection methods we identified a clear signal for recombinat…

Genome evolutionSequence analysislcsh:MedicineGenome ViralBiologyGenomeDNA sequencingEvolution Molecularsymbols.namesakePhylogeneticsVitislcsh:SciencePhylogenyPlant DiseasesGeneticsSanger sequencingWhole genome sequencingRecombination GeneticMultidisciplinaryPhylogenetic treeModels Geneticlcsh:RGenetic VariationHigh-Throughput Nucleotide Sequencingsymbolslcsh:QResearch ArticleClosteroviridaePLoS ONE
researchProduct