Search results for "mapping"

showing 10 items of 1508 documents

New epicardial mapping electrode with warming/cooling function for experimental electrophysiology studies

2010

Cardiac electrical activity is influenced by temperature. In experimental models, the induction of hypothermia and/or hyperthermia has been used for the study of mechanisms of cardiac arrhythmia. A system that allows for localized, controlled induction, besides simultaneously recording electrical activity in the same induced area, needs to be developed ad hoc. This article describes the construction and application of a new system capable of locally modifying the epicardial temperature of isolated hearts and of carrying out cardiac mapping with sufficient spatial resolution. The system is based on a thermoelectric refrigerator and an array of 128 stainless steel unipolar electrodes in encap…

Epicardial MappingMaterials scienceCardiac electrophysiologyHeart VentriclesTemperatureBiomedical EngineeringBiophysicsCardiac arrhythmiamedicine.diseaseQT intervalElectrophysiological PhenomenaElectrophysiologymedicine.anatomical_structureHeart RateVentricleVentricular FibrillationElectrodeVentricular fibrillationmedicineAnimalsVentricular FunctionSinus rhythmRabbitsBiomedical engineeringMedical Engineering & Physics
researchProduct

Applications of alignment-free methods in epigenomics

2013

Epigenetic mechanisms play an important role in the regulation of cell type-specific gene activities, yet how epigenetic patterns are established and maintained remains poorly understood. Recent studies have supported a role of DNA sequences in recruitment of epigenetic regulators. Alignment-free methods have been applied to identify distinct sequence features that are associated with epigenetic patterns and to predict epigenomic profiles. Here, we review recent advances in such applications, including the methods to map DNA sequence to feature space, sequence comparison and prediction models. Computational studies using these methods have provided important insights into the epigenetic reg…

EpigenomicsSupport Vector MachineDNA sequenceSequence alignmentComputational biologyBiologyDNA sequencingEpigenesis GeneticArtificial IntelligenceSequence comparisonHumansNucleosomeEpigeneticsMolecular BiologyGeneEpigenomicsSequence (medicine)GeneticsModels GeneticSettore INF/01 - InformaticanucleosomeChromosome MappingComputational BiologySequence Analysis DNAmachine learningPapersSequence Alignmentepigeneticalignment-free methodInformation SystemsBriefings in Bioinformatics
researchProduct

Isolation and characterization of a cDNA encoding rat liver cytosolic epoxide hydrolase and its functional expression in Escherichia coli.

1993

A cDNA of 1992 base pairs encoding the complete rat liver cytosolic epoxide hydrolase has been isolated using a polymerase chain reaction-derived DNA fragment (Arand, M., Knehr, M., Thomas, H., Zeller, H. D., and Oesch, F. (1991) FEBS Lett. 294, 19-22) known to represent the 3'-end of the cytosolic epoxide hydrolase mRNA. Sequence analysis revealed an open reading frame of 1662 nucleotides corresponding to 554 amino acids (M(r) = 62,268). The DNA sequence obtained did not display significant homology to the sequences of microsomal epoxide hydrolase or leukotriene A4 hydrolase or to any other DNA included in the EMBL Data Bank (release 32). On Northern blotting of rat liver RNA, a single mRN…

Epoxide hydrolase 2Male1303 BiochemistryBase pairMolecular Sequence DataRestriction Mapping10050 Institute of Pharmacology and Toxicology610 Medicine & healthBiologyBiochemistryLeukotriene-A4 hydrolase1307 Cell BiologyRats Sprague-Dawleychemistry.chemical_compoundCytosolFenofibrateComplementary DNA1312 Molecular BiologyEscherichia coliAnimalsAmino Acid SequenceCloning MolecularEpoxide hydrolaseMolecular BiologyPeroxisomal targeting signalEpoxide HydrolasesBase SequenceCell BiologyDNABlotting NorthernMolecular biologyRatschemistryBiochemistryLiverMicrosomal epoxide hydrolase570 Life sciences; biologyDNAThe Journal of biological chemistry
researchProduct

The Role of Geographic Technologies in the Measure of Spatial Equity. Twenty-First Century Solutions for Old Geographical Issues

2019

In Western societies, the development of the Welfare State has been accompanied by the proposal of different models of spatial organisation that help to improve spatial equity, this being a priority object of all public policy because it clearly contributes to the achievement of a greater social cohesion. Geography has contributed, from Christaller to the present, to propose territorial models that help to optimise the location of activities and services, using spatial statistics and digital cartography. At present, the study of spatial equity is again receiving the attention of the academy, in particular as regards the provision of public services and facilities in urban and metropolitan a…

Equity (economics)InequalityDigital mappingEmerging technologiesmedia_common.quotation_subjectRegional sciencePublic policyWelfare stateMetropolitan areaSpatial analysismedia_common
researchProduct

On the power and the systematic biases of the detection of chromosomal inversions by paired-end genome sequencing

2013

One of the most used techniques to study structural variation at a genome level is paired-end mapping (PEM). PEM has the advantage of being able to detect balanced events, such as inversions and translocations. However, inversions are still quite difficult to predict reliably, especially from high-throughput sequencing data. We simulated realistic PEM experiments with different combinations of read and library fragment lengths, including sequencing errors and meaningful base-qualities, to quantify and track down the origin of false positives and negatives along sequencing, mapping, and downstream analysis. We show that PEM is very appropriate to detect a wide range of inversions, even with …

Evolutionary GeneticsChromosome Structure and Functionlcsh:MedicineComputational biologyBiologyGenomeDNA sequencingStructural variation03 medical and health sciences0302 clinical medicineGenetic MutationGeneticsFalse positive paradoxHumansComputer SimulationFalse Positive ReactionsGenomic libraryGenome Sequencinglcsh:ScienceBiologyGenome EvolutionFalse Negative Reactions030304 developmental biologyChromosomal inversionSegmental duplicationGeneticsEvolutionary Biology0303 health sciencesMultidisciplinaryChromosome Biologylcsh:RBreakpointMutation TypesComputational BiologyChromosome MappingGenomic EvolutionGenomicsSequence Analysis DNAComparative GenomicsChromosomes Human Pair 1Chromosome Inversionlcsh:QStructural GenomicsSequence AnalysisAlgorithms030217 neurology & neurosurgeryResearch Article
researchProduct

Critical comments on EEG sensor space dynamical connectivity analysis

2019

Many different analysis techniques have been developed and applied to EEG recordings that allow one to investigate how different brain areas interact. One particular class of methods, based on the linear parametric representation of multiple interacting time series, is widely used to study causal connectivity in the brain. However, the results obtained by these methods should be interpreted with great care. The goal of this paper is to show, both theoretically and using simulations, that results obtained by applying causal connectivity measures on the sensor (scalp) time series do not allow interpretation in terms of interacting brain sources. This is because (1) the channel locations canno…

FOS: Computer and information sciencesComputer scienceSocial SciencesTransfer functionStatistics - Applications050105 experimental psychology03 medical and health sciences0302 clinical medicinegranger causalityMVARHumansApplications (stat.AP)Computer Simulation0501 psychology and cognitive sciencesRadiology Nuclear Medicine and imagingBrain connectivityEEGTime domainSpurious relationshipRepresentation (mathematics)Mixing (physics)Parametric statisticsBrain MappingRadiological and Ultrasound TechnologySeries (mathematics)05 social sciencesbrain connectivitysource modellingElectroencephalographyNeurologyFOS: Biological sciencesFrequency domainQuantitative Biology - Neurons and CognitionSettore ING-INF/06 - Bioingegneria Elettronica E InformaticaGranger causalityDirected transfer functionNeurons and Cognition (q-bio.NC)Neurology (clinical)AnatomyAlgorithm030217 neurology & neurosurgery
researchProduct

Innovation Initiatives in Large Software Companies : A Systematic Mapping Study

2018

Context: To keep the competitive advantage and adapt to changes in the market and technology, companies need to innovate in an organised, purposeful and systematic manner. However, due to their size and complexity, large companies tend to focus on the structure in maintaining their business, which can potentially lower their agility to innovate.Objective:The aims of this study are to provide an overview of the current research on innovation initiatives and to identify the challenges of implementing those initiatives in the context of large software companies.Method: The investigation was primarily performed using a systematic mapping approach of published literature on corporate innovation …

FOS: Computer and information sciencesKnowledge managementCorporate innovationinnovation initiatives02 engineering and technologyentrepreneurshipCorporate innovationinnovationsComputer Science - Software EngineeringSoftwareohjelmistoala0502 economics and business0202 electrical engineering electronic engineering information engineeringLarge software companiescorporatesInnovationtietotekniikkayrityksetta113business.industry05 social sciencessystematic mapping study050301 education020207 software engineeringsoftware companiesyrittäjyysComputer Science ApplicationsinnovaatiotSoftware Engineering (cs.SE)Innovation initiativeCorporate entrepreneurshipSystematic mappingbusiness0503 educationSoftware050203 business & managementInformation Systems
researchProduct

Bayesian Analysis of Population Health Data

2021

The analysis of population-wide datasets can provide insight on the health status of large populations so that public health officials can make data-driven decisions. The analysis of such datasets often requires highly parameterized models with different types of fixed and random effects to account for risk factors, spatial and temporal variations, multilevel effects and other sources on uncertainty. To illustrate the potential of Bayesian hierarchical models, a dataset of about 500,000 inhabitants released by the Polish National Health Fund containing information about ischemic stroke incidence for a 2-year period is analyzed using different types of models. Spatial logistic regression and…

FOS: Computer and information sciencesmedicine.medical_specialtyComputer scienceGeneral MathematicsBayesian probabilitydisease mappingPopulation healthbayesian inference; disease mapping; integrated nested Laplace approximation; spatial models; survival modelsBayesian inferenceLogistic regressionStatistics - Applications01 natural sciences010104 statistics & probability03 medical and health sciences0302 clinical medicineStatisticsComputer Science (miscellaneous)medicineApplications (stat.AP)spatial models0101 mathematicsEngineering (miscellaneous)Socioeconomic statusbayesian inferencesurvival modelslcsh:MathematicsPublic healthintegrated nested Laplace approximationlcsh:QA1-939Random effects modelSpatial variability030217 neurology & neurosurgeryMathematics
researchProduct

Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.

2001

Clinical and molecular studies are reported on a family (MRX73) of five males with non-specific X-linked mental retardation (XLMR). A total of 33 microsatellite and RFLP markers was typed. The gene for this XLMR condition was been linked to DXS1195, with a lod score of 2.36 at theta = 0. The haplotype and multipoint linkage analyses suggest localization of the MRX73 locus to an interval of 2 cM defined by markers DXS8019 and DXS365, in Xp22.2. This interval contains the gene of Coffin-Lowry syndrome (RSK2), where a missense mutation has been associated with a form of non-specific mental retardation. Therefore, a search for RSK2 mutations was performed in the MRX73 family, but no causal muta…

Family HealthMaleGeneticscongenital hereditary and neonatal diseases and abnormalitiesCoffin–Lowry syndromeX ChromosomeGenetic LinkageHaplotypeChromosome MappingLocus (genetics)Biologymedicine.diseasePedigreeGenetic linkageIntellectual DisabilitymedicineHumansMissense mutationMicrosatelliteFemaleLod ScoreRestriction fragment length polymorphismGenetics (clinical)X chromosomeMicrosatellite Repeats
researchProduct

Student Author of the Year Award 2009

2009

The ‘‘Student author of the Year Award’’ is made for an outstanding paper in which an undergraduate or graduate student played a key role in the research and publication. The recipient of this award for 2009 is Ruben Diez Fernandez for his contribution, co-authored with Jose R. Martinez Catalan 3D Analysis of an Ordovician igneous ensemble: A complex magmatic structure hidden in a polydeformed allochthonous Variscan unit Journal of Structural Geology, Volume 31, Issue 3, March 2009, Pages 222–236. The Editors have selected this paper out of many student submissions in 2009. The basis of this paper is detailed field mapping, metamorphic petrology and structural analysis. These clearly establ…

Felsic3d analysisLibrary scienceGeologyFold (geology)Engineering physicslanguage.human_languageIgneous rockOrdovicianlanguageField mappingCatalanStructural geologyGeologyJournal of Structural Geology
researchProduct