Search results for "genomic library"

showing 10 items of 52 documents

No association between the cystatin C gene polymorphism and Alzheimer's disease: a case-control study in an Italian population.

2005

Cystatin C is an amyloidogenic protein found together with beta-amyloid in cerebral arteriolar walls of both patients with Alzheimer's Disease (AD) and conghopilic amyloid angiopathy. Several findings implicate cystatin C in the pathogenesis of vascular diseases. Recent genetic association studies proposed cystatin C gene (CST3) as a susceptibility factor for AD, although other reports did not replicate this finding. We conducted a case-control study including 192 probable AD cases and 192 age- and sex-matched controls to test the association between CST3 and AD. Possible interaction between CST3 and age at onset of AD or apolipoprotein E (APOE) was also examined. No significant differences…

MaleApolipoprotein EGenotypeDiseasePathogenesisApolipoproteins EAlzheimer DiseaseGenotypeHumansGenetic Predisposition to DiseaseCystatin CAllele frequencyAllelesAgedGenetic associationAged 80 and overGeneticsGenomic LibraryPolymorphism GeneticbiologyKeywords: Alzheimer’s disease cystatin C apolipoprotein E case-control study polymorphismGeneral NeuroscienceCase-control studyGeneral MedicineMiddle AgedCystatinsPsychiatry and Mental healthClinical PsychologyItalyCystatin CCase-Control StudiesImmunologybiology.proteinSettore MED/26 - NeurologiaFemaleGeriatrics and Gerontology
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Differential binding cell-SELEX method to identify cell-specific aptamers using high-throughput sequencing

2018

AbstractAptamers have in recent years emerged as a viable alternative to antibodies. High-throughput sequencing (HTS) has revolutionized aptamer research by increasing the number of reads from a few (using Sanger sequencing) to millions (using an HTS approach). Despite the availability and advantages of HTS compared to Sanger sequencing, there are only 50 aptamer HTS sequencing samples available on public databases. HTS data in aptamer research are primarily used to compare sequence enrichment between subsequent selection cycles. This approach does not take full advantage of HTS because the enrichment of sequences during selection can be due to inefficient negative selection when using live…

0301 basic medicineComputer scienceAptamerlcsh:MedicineGenomicsComputational biologyCell selexLigandsArticleDNA sequencingCell Line03 medical and health sciencessymbols.namesakeNegative selectionDrug Delivery Systems0302 clinical medicineCell Line TumorHumansGenomic librarylcsh:ScienceCarcinoma Renal CellSelection (genetic algorithm)Gene LibrarySanger sequencingMultidisciplinaryMolecular medicinelcsh:RSELEX Aptamer TechniqueHigh-throughput screeningComputational BiologyHigh-Throughput Nucleotide SequencingNucleotide MetabolismGenomicsAptamers NucleotideFlow CytometryMolecular medicineKidney Neoplasms030104 developmental biologyDrug DesignDrug deliverysymbolsNucleic Acid Conformationlcsh:QFunctional genomics030217 neurology & neurosurgerySystematic evolution of ligands by exponential enrichment
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Origin of the metazoan bodyplan: characterization and functional testing of the promoter of the homeobox gene EmH-3 from the freshwater sponge Ephyda…

1998

Porifera [sponges] represent the lowest metazoan phylum, probably already existing prior to the 'Cambrian explosion'. Based on amino acid sequences deduced from cDNAs that code for structural proteins, the monophyly of Metazoa was established. Now we analyzed for the first time a promoter of a sponge gene for its activity in a heterologous cell system from higher Metazoa. The promoter of the homeobox gene EmH-3 was cloned and sequenced from a genomic library of the freshwater sponge Ephydatia muelleri. For the determination of functional promoter activity, transient transfection experiments in mouse NIH 3T3 cells were performed; the promoter was fused with the luciferase reporter gene. The …

DNA ComplementaryClinical BiochemistryMolecular Sequence DataHeterologousBiochemistryMiceSequence Homology Nucleic AcidAnimalsGenomic libraryAmino Acid SequenceCloning MolecularPromoter Regions GeneticMolecular BiologyGeneTranscription factorPeptide sequenceCloningHomeodomain ProteinsbiologyBase SequenceSequence Homology Amino AcidGenes Homeobox3T3 Cellsbiology.organism_classificationMolecular biologyPoriferaSpongeHomeoboxBiological chemistry
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Cloning of a novel putative G-protein-coupled receptor (NLR) which is expressed in neuronal and lymphatic tissue.

1993

AbstractA novel G-protein-coupled receptor was isolated from mouse and rat neuronal and lymphatic tissues. The amino acid sequence of the rat receptor (rNLR) shows an overall homology of 80% to a recently cloned receptor from Burkitt's lymphoma cells (BLR1) which is exclusively expressed in lymphatic tissues [(1992) Eur. J. Immunol. 22, 2795]. Much less homology between rNLR and BLR1 was observed at the N-terminus (about 40%), whereas rNLR and the mouse homologue mNLR show 92% amino acid identity. Northern blot analysis of NLR revealed a predominant 5.5 kb mRNA species in various brain regions and neuronal cell lines, whereas in the spleen a 3 kb transcript is predominant. This distribution…

Restriction MappingInterleukin 8BiochemistryReceptors G-Protein-CoupledMiceStructural BiologyTumor Cells CulturedLymphocytesCloning MolecularReceptorPeptide sequencechemistry.chemical_classificationNeuronsGenomic LibraryBurkitt's lymphomaBrainBurkitt LymphomaPolymerase chain reactionAmino acidOligodeoxyribonucleotidesOrgan SpecificityG-protein-coupled receptorBLR1Molecular Sequence DataBiophysicsReceptors Cell SurfaceBiologyNLRGTP-Binding ProteinsComplementary DNAGeneticsmedicineAnimalsHumansNorthern blotAmino Acid SequenceRNA MessengerMolecular BiologyG protein-coupled receptorMessenger RNABase SequenceSequence Homology Amino AcidCell Biologymedicine.diseaseMolecular biologyIntronsRatsNG108-15 cellchemistryBurkitt's lymphomaFEBS letters
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Hybrid sequencing approach applied to human fecal metagenomic clone libraries revealed clones with potential biotechnological applications.

2012

Natural environments represent an incredible source of microbial genetic diversity. Discovery of novel biomolecules involves biotechnological methods that often require the design and implementation of biochemical assays to screen clone libraries. However, when an assay is applied to thousands of clones, one may eventually end up with very few positive clones which, in most of the cases, have to be "domesticated" for downstream characterization and application, and this makes screening both laborious and expensive. The negative clones, which are not considered by the selected assay, may also have biotechnological potential; however, unfortunately they would remain unexplored. Knowledge of t…

LibrarySequence analysisGene predictionApplied MicrobiologyClone (cell biology)lcsh:MedicineBiologyMicrobiologyMicrobial Ecology03 medical and health sciencesFecesOpen Reading FramesHumansIndustryGenomic libraryGenome Sequencinglcsh:ScienceBiology030304 developmental biologyGene LibraryGenetics0303 health sciencesMultidisciplinaryContigEcology030306 microbiologylcsh:RComputational BiologyMolecular Sequence AnnotationSequence Analysis DNAGenomicsEnzymesFunctional GenomicsMetagenomicsPyrosequencinglcsh:QMetagenomicsSequence AnalysisBiotechnologyResearch ArticlePloS one
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Making your own gene library

1997

Higher educationbusiness.industryLibrary scienceGenomic libraryBiologybusinessBiochemistryScience educationBiochemical Education
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Inducible metabolism of phenolic acids in Pediococcus pentosaceus is encoded by an autoregulated operon which involves a new class of negative transc…

2000

ABSTRACTPediococcus pentosaceusdisplays a substrate-inducible phenolic acid decarboxylase (PAD) activity onp-coumaric acid. Based on DNA sequence homologies between the three PADs previously cloned, a DNA probe of theLactobacillus plantarum pdcgene was used to screen aP. pentosaceusgenomic library in order to clone the corresponding gene of this bacteria. One clone detected with this probe displayed a low PAD activity. Subcloning of this plasmid insertion allowed us to determine the part of the insert which contains a 534-bp open reading frame (ORF) coding for a 178-amino-acid protein presenting 81.5% of identity withL. plantarumPDC enzyme. This ORF was identified as thepadAgene. A second O…

DNA BacterialTranscription GeneticOperonCarboxy-LyasesMolecular Sequence DataGenetics and Molecular BiologyBiologyMicrobiologyGene Expression Regulation EnzymologicPlasmidBacterial ProteinsSequence Homology Nucleic AcidOperonEscherichia coliHydroxybenzoatesGenomic libraryAmino Acid SequencePediococcusCloning MolecularMolecular BiologyGeneRegulator geneGeneticsBase SequenceSequence Homology Amino Acidfood and beveragesPromoterGene Expression Regulation BacterialSequence Analysis DNAMolecular biologyCulture MediaRepressor ProteinsOpen reading frameLactobacillusSubcloningGenes BacterialJournal of bacteriology
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FASTdoop: A versatile and efficient library for the input of FASTA and FASTQ files for MapReduce Hadoop bioinformatics applications

2017

Abstract Summary MapReduce Hadoop bioinformatics applications require the availability of special-purpose routines to manage the input of sequence files. Unfortunately, the Hadoop framework does not provide any built-in support for the most popular sequence file formats like FASTA or BAM. Moreover, the development of these routines is not easy, both because of the diversity of these formats and the need for managing efficiently sequence datasets that may count up to billions of characters. We present FASTdoop, a generic Hadoop library for the management of FASTA and FASTQ files. We show that, with respect to analogous input management routines that have appeared in the Literature, it offers…

0301 basic medicineFASTQ formatStatistics and ProbabilityComputer scienceSequence analysismedia_common.quotation_subjectInformation Storage and RetrievalBioinformaticscomputer.software_genreGenomeBiochemistryDomain (software engineering)03 medical and health sciencesComputational Theory and MathematicHumansGenomic libraryQuality (business)DNA sequencingFASTQ; NGS; FASTQ; DNA sequencingMolecular Biologymedia_commonGene LibrarySequenceDatabaseSettore INF/01 - InformaticaGenome HumanComputer Science Applications1707 Computer Vision and Pattern RecognitionGenomicsSequence Analysis DNAFASTQFile formatComputer Science ApplicationsStatistics and Probability; Biochemistry; Molecular Biology; Computer Science Applications1707 Computer Vision and Pattern Recognition; Computational Theory and Mathematics; Computational MathematicsComputational Mathematics030104 developmental biologyComputational Theory and MathematicsNGSDatabase Management Systemscomputer
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Isolation and characterization of nuclear microsatellite loci in the northern shrimp, Pandalus borealis

2012

Published version of an article published in the journal: Conservation Genetics Resources. Also available from the publisher at: http://dx.doi.org/10.1007/s12686-011-9486-4 We developed and characterized 20 microsatellite primer loci for the northern shrimp Pandalus borealis. All 20 loci were polymorphic with number of alleles ranging from 3 to 36 and with observed heterozygosity between 0.04 and 0.93. In addition, we tested the utility of these markers in three related shrimp species, P. montagui, Atlantopandalus propinqvus and Dichelopandalus bonnieri. These new markers will prove useful in the identification of stock structure and hence, assessment of the commercially important species P…

microsatelite primersPandalus borealismarine shrimpgenomic librarygenetic diversityVDP::Mathematics and natural science: 400::Basic biosciences: 470::Genetics and genomics: 474VDP::Agriculture and fishery disciplines: 900::Fisheries science: 920::Resource biology: 921
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The baculovirus display technology--an evolving instrument for molecular screening and drug delivery.

2008

High throughput screening is a core technology in drug discovery. During the past decade, several strategies have been developed to screen (poly)peptide libraries for diverse applications including disease diagnosis and profiling, imaging, as well as therapy. The recently established baculovirus display vector system (BDVS) represents a eukaryotic screening platform that combines the positive attributes of both cell and virus-based display approaches, allowing presentation of complex polypeptides on cellular and viral surfaces. Compared to microbial display systems, the BDVS has the advantage of correct protein folding and post-translational modifications similar to those in mammals, facili…

GlycosylationInsectaHigh-throughput screeningCellGenetic VectorsDrug Evaluation PreclinicalHeterologousComputational biologyBiologychemistry.chemical_compoundAdjuvants ImmunologicDrug DiscoverymedicineAnimalsHumansGenomic libraryGeneGene LibraryDrug discoveryOrganic ChemistryGene Transfer TechniquesGeneral MedicineMolecular biologyComputer Science Applicationsmedicine.anatomical_structurechemistryDrug deliveryBaculoviridaeCombinatorial chemistryhigh throughput screening
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