Search results for " Nucleic Acid"

showing 10 items of 272 documents

Monte Carlo simulation of DNA electrophoresis

1989

This paper describes an attempt to study the electrophoresis mobility of a DNA molecule in a gel by means of a Monte Carlo simulation. We find that the electrophoresis mobility mu can be well described by the empirical equation mu v kappa 1/N + kappa 2E2 with N being the number of monomers of the model chain and E being the applied field. For small E the data can merge into the linear response result mu = kappa 1/N. The paper also discusses necessary extensions of the present approach.

ElectrophoresisPhysicsQuantitative Biology::BiomoleculesGel electrophoresis of nucleic acidsClinical BiochemistryMonte Carlo methodMarkov chain Monte CarloDNABiochemistryAnalytical ChemistryMolecular WeightHybrid Monte CarloElectrophoresissymbols.namesakeModels ChemicalsymbolsDynamic Monte Carlo methodComputer SimulationStatistical physicsGelsKappaMonte Carlo molecular modelingElectrophoresis
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Comparing analytical methods to detect SARS-CoV-2 in wastewater

2021

Wastewater based epidemiology (WBE) has emerged as a reliable strategy to assess the coronavirus disease 2019 (COVID-19) pandemic. Recent publications suggest that SARS-CoV-2 detection in wastewater is technically feasible; however, many different protocols are available and most of the methods applied have not been properly validated. To this end, different procedures to concentrate and extract inactivated SARS-CoV-2 and surrogates were initially evaluated. Urban wastewater seeded with gamma-irradiated SARS-CoV-2, porcine epidemic diarrhea virus (PEDV), and mengovirus (MgV) was used to test the concentration efficiency of an aluminum-based adsorption-precipitation method and a polyethylene…

Environmental Engineering010504 meteorology & atmospheric sciencesSwineMicrobiologiaWastewater010501 environmental sciences01 natural sciencesArticleWHO World Health OrganizationAigües residuals MicrobiologiaAluminum-based adsorption-precipitationSpin column-based nucleic acid purificationPEG ratioAnimalsHumansEnvironmental ChemistryPandemicsWaste Management and DisposalPEG polyethylene glycol0105 earth and related environmental sciencesDetection limitCOVID-19 Coronavirus disease 2019ChromatographybiologySARS-CoV-2MgV MengovirusWBE wastewater-based epidemiologyChemistryPorcine epidemic diarrhea virusRT-qPCRExtraction (chemistry)COVID-19Contaminationbiology.organism_classificationSalut públicaPollutionEcologiaPolyethylene glycol precipitationSARS-CoV-2 Severe Acute Respiratory Syndrome Coronavirus 2WastewaterRNAEC European CommissionRNA extractionPorcine epidemic diarrhea virusPEDV Porcine Epidemic Diarrhea virusWastewater based epidemiologyScience of The Total Environment
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Losing DNA methylation at repetitive elements and breaking bad

2021

Abstract Background DNA methylation is an epigenetic chromatin mark that allows heterochromatin formation and gene silencing. It has a fundamental role in preserving genome stability (including chromosome stability) by controlling both gene expression and chromatin structure. Therefore, the onset of an incorrect pattern of DNA methylation is potentially dangerous for the cells. This is particularly important with respect to repetitive elements, which constitute the third of the human genome. Main body Repetitive sequences are involved in several cell processes, however, due to their intrinsic nature, they can be a source of genome instability. Thus, most repetitive elements are usually meth…

EpigenomicsGenome instabilityHeterochromatinSatellitesReviewRepetitive DNABiologyQH426-47003 medical and health sciencesLINE-10302 clinical medicineDNA hypomethylationGeneticsHumansEpigeneticsAutism spectrum disorderRepeated sequenceMolecular BiologyRepetitive Sequences Nucleic Acid030304 developmental biologyCancerGenetics0303 health sciencesHereditary diseasesDNA MethylationChromatinChromatinSettore BIO/18 - GeneticaLong Interspersed Nucleotide ElementsICF syndromeDNA methylationHuman genomeAlzheimer’s disease030217 neurology & neurosurgeryNeuropsychiatric disordersDNA hypomethylationEpigenetics & Chromatin
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Tandem repeats lead to sequence assembly errors and impose multi-level challenges for genome and protein databases

2019

AbstractThe widespread occurrence of repetitive stretches of DNA in genomes of organisms across the tree of life imposes fundamental challenges for sequencing, genome assembly, and automated annotation of genes and proteins. This multi-level problem can lead to errors in genome and protein databases that are often not recognized or acknowledged. As a consequence, end users working with sequences with repetitive regions are faced with ‘ready-to-use’ deposited data whose trustworthiness is difficult to determine, let alone to quantify. Here, we provide a review of the problems associated with tandem repeat sequences that originate from different stages during the sequencing-assembly-annotatio…

FOS: Computer and information sciencesBioinformatics[SDV]Life Sciences [q-bio]Sequence assemblyGenomics[SDV.BC]Life Sciences [q-bio]/Cellular BiologyComputational biologyBiologyGenome03 medical and health sciencesAnnotation0302 clinical medicineTandem repeatGeneticsAnimalsSurvey and SummaryDatabases ProteinGeneComputingMilieux_MISCELLANEOUS030304 developmental biology0303 health sciencesEnd user572: BiochemieDNASequence Analysis DNAGenomics[SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM]WorkflowComputingMethodologies_PATTERNRECOGNITIONGadus morhuaTandem Repeat SequencesScientific Experimental Error[INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]Databases Nucleic Acid030217 neurology & neurosurgery
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Large-scale compression of genomic sequence databases with the Burrows-Wheeler transform

2012

Motivation The Burrows-Wheeler transform (BWT) is the foundation of many algorithms for compression and indexing of text data, but the cost of computing the BWT of very large string collections has prevented these techniques from being widely applied to the large sets of sequences often encountered as the outcome of DNA sequencing experiments. In previous work, we presented a novel algorithm that allows the BWT of human genome scale data to be computed on very moderate hardware, thus enabling us to investigate the BWT as a tool for the compression of such datasets. Results We first used simulated reads to explore the relationship between the level of compression and the error rate, the leng…

FOS: Computer and information sciencesStatistics and ProbabilityBurrows–Wheeler transformComputer scienceData_CODINGANDINFORMATIONTHEORYBurrows-Wheeler transformcomputer.software_genreBiochemistryBurrows-Wheeler transform; Data Compression; Next-generation sequencingComputer Science - Data Structures and AlgorithmsEscherichia coliCode (cryptography)HumansOverhead (computing)Data Structures and Algorithms (cs.DS)Computer SimulationQuantitative Biology - GenomicsMolecular BiologyGenomics (q-bio.GN)Genome HumanString (computer science)Search engine indexingSortingGenomicsSequence Analysis DNAConstruct (python library)Data CompressionComputer Science ApplicationsComputational MathematicsComputational Theory and MathematicsFOS: Biological sciencesNext-generation sequencingData miningDatabases Nucleic AcidcomputerAlgorithmsData compression
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desat1: A Swiss army knife for pheromonal communication and reproduction?

2012

International audience; The desat1 gene possesses an extraordinary-maybe unique-feature in the control of sensory communication systems: it codes for the two principal and complementary aspects-the emission and the reception-of Drosophila sex pheromones. These two complex aspects depend on separate genetic control indicating that desat1 pleiotropically acts on pheromonal communication. This gene also control other characters either related to reproduction and to osmoregulation. Such a functional pleiotropy may be related to the molecular structure of desat1 gene which combines a highly conserved coding region with fast evolving regulatory regions: It produces at least five transcripts all g…

Fatty Acid DesaturasesMaleGeneticsReproductionmedia_common.quotation_subject[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionGenetic PleiotropyRegulatory Sequences Nucleic AcidBiologyAlternative SplicingDrosophila melanogasterPleiotropyRegulatory sequenceInsect ScienceSex pheromoneAnimalsDrosophila ProteinsCoding regionFemaleSex AttractantsReproductionGene[SDV.AEN]Life Sciences [q-bio]/Food and Nutritionmedia_common
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The FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations.

2009

International audience; Congenital contractural arachnodactyly (CCA) is an extremely rare disease, due to mutations in the FBN2 gene encoding fibrillin-2. Another member of the fibrillin family, the FBN1 gene, is involved in a broad phenotypic continuum of connective-tissue disorders including Marfan syndrome. Identifying not only what is in common but also what differentiates these two proteins should enable us to better comprehend their respective functions and better understand the multitude of diseases in which these two genes are involved. In 1995 we created a locus-specific database (LSDB) for FBN1 mutations with the Universal Mutation Database (UMD) tool. To facilitate comparison of …

Fibrillin-2MESH : Polymorphism GeneticFibrillin-1DNA Mutational AnalysisMESH : Genotype[SDV.GEN] Life Sciences [q-bio]/Geneticscomputer.software_genreMESH: Genotype0302 clinical medicineGenotypeDatabases GeneticMissense mutationCongenital contractural arachnodactylyMESH: DNA Mutational AnalysisGenetics (clinical)MESH: Databases GeneticRegulation of gene expressionGenetics0303 health sciencesDatabaseMESH : Gene Expression RegulationMicrofilament ProteinsPhenotypeMESH: Gene Expression RegulationBeals-Hecht syndrome3. Good healthINCMESH : PhenotypePhenotypeMESH : MutationFibrillinmusculoskeletal diseasesMESH: MutationGenotypeMESH : Microfilament Proteinsdatabase OFFICIAL JOURNAL wwwhgvsorg & 2008 WILEY-LISSLocus (genetics)fibrillinMESH : DNA Mutational AnalysisBiologyFibrillinsMESH: PhenotypeMESH: Sequence Homology Nucleic Acidcongenital contractural arachnodactyly03 medical and health sciencesMESH: Microfilament ProteinsSequence Homology Nucleic AcidMESH: Polymorphism GeneticGeneticsmedicineHumansMESH : Sequence Homology Nucleic AcidFBN2CCAMESH : Databases GeneticGene030304 developmental biology[SDV.GEN]Life Sciences [q-bio]/GeneticsPolymorphism GeneticMESH: HumansMESH : Humansmedicine.diseaseGene Expression RegulationMutation[ SDV.GEN ] Life Sciences [q-bio]/Geneticscomputer030217 neurology & neurosurgery
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Improved resolution power of electrophoretic fractionation of DNA using a voltage gradient up and down application

2004

The improved resolution power of electrophoretic fractionation of DNA in a wide range of molecular masses is demonstrated using an "up and down" application of voltage gradient gel electrophoresis (VGGE). This application also allows separation of different DNA fragments which are poorly fractionated in conventional electrophoresis.

Free-flow electrophoresisGel electrophoresisElectrophoresisDNA fractionationChromatographyGel electrophoresis of nucleic acidsResolution (mass spectrometry)Voltage gradient gel electrophoresisChemistryClinical BiochemistryAnalytical chemistryFractionationDNABiochemistryELECTROPHORESIS INSTRUMENTATIONAnalytical Chemistrychemistry.chemical_compoundElectrophoresisIndicators and ReagentsDNA
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Regulated expression and phosphorylation of the 23-26-kDa ras protein in the sponge Geodia cydonium.

1990

We have cloned, sequenced and examined the sponge Geodia cydonium cDNA encoding a protein homologous to ras proteins. The sponge ras protein has a more conserved N-terminal region and a less conserved C-terminal region, especially in comparison to Dictyostelium discoideum; the similarity to human c-Ha-ras-1 and to Saccharomyces cerevisiae is less pronounced. The sponge ras cDNA comprises five TAG triplets; at the translational level these UAG termination codons are suppressed by a Gln-tRNA. The sponge ras protein was isolated and partially purified (23-26 kDa) and found to undergo phosphorylation at a threonine moiety, when dissociated cells were incubated in the presence of a homologous ag…

GTP'Saccharomyces cerevisiaeMolecular Sequence DataGTPaseBiochemistryDictyostelium discoideumProto-Oncogene Proteins p21(ras)Complementary DNASequence Homology Nucleic AcidAnimalsInsulinNCK1Amino Acid SequenceThreonineCloning MolecularPhosphorylationGene LibrarybiologyBase SequenceDNAbiology.organism_classificationMolecular biologyPoriferaMolecular WeightKineticsBiochemistryGene Expression RegulationPhosphorylationEuropean journal of biochemistry
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Orthogonal electrophoretic fractionation of DNA in agarose gels.

2008

We developed an electrophoretic procedure, using Voltage Gradient Gel Electrophoresis (VGGE), which allows to obtain both an improvement of the resolution power of the system in orthogonal fractionation of DNA and, mainly, an about fourfold enhancement of hybridization signals in Southern blotting applications.

Gel electrophoresisElectrophoresis Agar GelChromatographyGel electrophoresis of nucleic acidsCell BiologyFractionationDNABiologyMolecular biologyInterleukin-10chemistry.chemical_compoundElectrophoresischemistryAgaroseRNA MessengerMolecular BiologyDNATemperature gradient gel electrophoresisSouthern blotMolecular and cellular probes
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