Search results for "DNA profiling"

showing 10 items of 64 documents

Molecular typing of clinical Candida strains using random amplified polymorphic DNA and contour-clamped homogenous electric fields electrophoresis.

2009

Aims:  This report describes an investigation into the genetic profiles of 38 Candida albicans and 19 Candida glabrata strains collected from a dental hospital of Monastir (Tunisia) and the Laboratory of Parasitology, Farhat Hached Hospital of Sousse (Tunisia), using two typing methods: random amplified polymorphic DNA (RAPD) and contour-clamped homogenous electric fields (CHEF). Methods and Results:  The two methods (RAPD and CHEF electrophoresis) were able to identify clonal-related isolates from different patients. RAPD method using two primers (CA1 and CA2) exhibited the highest discriminatory power by discriminating 22 genotypes for C. albicans with CA1 oligonucleotides and 19 genotype…

GeneticsElectrophoresisPolymorphism GeneticTunisiaCandida glabratabiologyCandidiasisCandida glabrataGeneral Medicinebacterial infections and mycosesbiology.organism_classificationApplied Microbiology and BiotechnologyGenetic analysisRAPDRandom Amplified Polymorphic DNA TechniqueDNA profilingParasitologyGenotypeCandida albicansHumansTypingCandida albicansBiotechnologyDNA PrimersJournal of applied microbiology
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Forensic validation of the SNPforID 52-plex assay.

2007

The advantages of single nucleotide polymorphism (SNP) typing in forensic genetics are well known and include a wider choice of high-throughput typing platforms, lower mutation rates, and improved analysis of degraded samples. However, if SNPs are to become a realistic supplement to current short tandem repeat (STR) typing methods, they must be shown to successfully and reliably analyse the challenging samples commonly encountered in casework situations. The European SNPforID consortium, supported by the EU GROWTH programme, has developed a multiplex of 52 SNPs for forensic analysis, with the amplification of all 52 loci in a single reaction followed by two single base extension (SBE) react…

GeneticsForensic GeneticsAnalysis of VarianceGenotypeDNABiologySingle-base extensionDNA FingerprintingPolymorphism Single NucleotideSensitivity and SpecificityPathology and Forensic MedicineEuropeDNA profilingSTR analysisGeneticsMicrosatelliteHumansMultiplexTypingCooperative BehaviorLow copy numberLaboratoriesAllelesSNP arrayMicrosatellite RepeatsForensic science international. Genetics
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Forensic typing of autosomal SNPs with a 29 SNP-multiplex--results of a collaborative EDNAP exercise.

2008

We report the results of an inter-laboratory exercise on typing of autosomal single nucleotide polymorphisms (SNP) for forensic genetic investigations in crime cases. The European DNA Profiling Group (EDNAP), a working group under the International Society for Forensic Genetics (ISFG), organised the exercise. A total of 11 European and one US forensic genetic laboratories tested a subset of a 52 SNP-multiplex PCR kit developed by the SNPforID consortium. The 52 SNP-multiplex kit amplifies 52 DNA fragments with 52 autosomal SNP loci in one multiplex PCR. The 52 SNPs are detected in two separate single base extension (SBE) multiplex reactions with 29 and 23 SNPs, respectively, using SNaPshot …

GeneticsForensic GeneticsGenotypeElectrophoresis CapillarySingle-nucleotide polymorphismBiologySingle-base extensionDNA FingerprintingPolymerase Chain ReactionPolymorphism Single NucleotideUnited StatesPathology and Forensic MedicineSNP genotypingEuropeDNA profilingBlood StainsMultiplex polymerase chain reactionGeneticsSNPHumansMultiplexTypingLaboratoriesAllelesRepetitive Sequences Nucleic AcidForensic science international. Genetics
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Report of the European DNA profiling group (EDNAP)-an investigation of the hypervariable STR loci ACTBP2, APOAI1 and D11S554 and the compound loci D1…

1999

This paper describes the results of three collaborative exercises which continues the EDNAP theme to explore whether uniformity of DNA profiling results could be achieved between European laboratories using STRs. In an earlier exercise, complex hypervariable AAAG-repeat STR loci were investigated, but reproducibility was found to be poor because of the variation of techniques used by participating laboratories. In the exercise reported here, an internal allelic ladder composed of ACTBP2 and D11S554 fragments was distributed. This ladder was used to size ACTBP2 analysed by a "singleplex" PCR amplification and D11S554 combined with APOAI1 in a separate "duplex" reaction. Laboratories were ask…

GeneticsInternational CooperationBlood StainsImmunoglobulin Variable RegionReproducibility of ResultsMinisatellite RepeatsDNA SatelliteBiologyDNA FingerprintingPolymerase Chain ReactionPathology and Forensic Medicinelaw.inventionEuropeDNA profilingMulticenter studylawGenetic markerStr lociHumansMicrosatelliteLawAllelesSocieties MedicalPolymerase chain reactionForensic Science International
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Considerations from the European DNA profiling group (EDNAP) concerning STR nomenclature

1997

(1) The nomenclature of any STR follows from comparison with a control allelic ladder; availability of reference allelic ladders is central to any scheme. The components of an allelic ladder should be sequenced. (2) The DNA commission recommended a nomenclature based upon the number of repeat sequences present in an allele. Whereas this method is suitable for typing simple STRs, complex hypervariable repeats such as ACTBP2 do not conform to a simple repeating structure. We propose that designation of complex STR repeats such as ACTBP2, D11S554 and APOAI1 follows from the size of specific alleles. Because the size is dependant upon the primers utilised, the size is not definitive (it may als…

GeneticsLocus (genetics)DNASequence Analysis DNAForensic MedicineBiologyActinsPathology and Forensic MedicineEuropeType (biology)DNA profilingGenetic markerPolymorphism (computer science)Terminology as TopicHumansMicrosatelliteTypingAlleleLawSocieties MedicalRepetitive Sequences Nucleic AcidForensic Science International
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Forensics of birds of prey by DNA fingerprinting with 32P-labeled oligonucleotide probes.

1991

Paternity tests on confiscated families of eight species of birds of prey were carried out successfully by DNA fingerprinting with 32P-labeled oligonucleotide probes. Variations in the number of hybridized fragments, depending on the species of birds, are observed using the same probe, as well as differences of polymorphism by hybridizing the DNA samples with several oligonucleotide probes.

GeneticsMaleBase CompositionBase SequenceOligonucleotideClinical BiochemistryPhosphorus IsotopesBiologyBiochemistryDNA FingerprintingAnalytical ChemistryPredationBirdschemistry.chemical_compoundchemistryDNA profilingPolymorphism (computer science)Paternity testsAnimalsBase sequenceMolecular probeOligonucleotide ProbesDNAPolymorphism Restriction Fragment LengthRepetitive Sequences Nucleic AcidElectrophoresis
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Results of collaborative study regarding the standardization of the Y-linked STR system DYS385 by the European DNA Profiling (EDNAP) group.

1999

Y-chromosome linked short tandem repeat (STR) loci are inherited as a closely linked haplotype, which appears to remain stable in a given paternal lineage over many generations. In forensic cases, Y-linked STRs are particularly useful for the identification of human remains as well as in rape cases with mixed male/female stain samples. DYS385 is derived from tandemly duplicated segments of the Y chromosome thus giving rise to two fragments of variable length which do not behave like alleles but genotypes. The European DNA Profiling (EDNAP) group has carried out a collaborative exercise among 14 participating laboratories using DYS385 for typing of five unknown bloodstains and a control samp…

GeneticsMaleGenetic LinkageSTR multiplex systemInternational CooperationHaplotypeReproducibility of ResultsMinisatellite RepeatsBiologyY chromosomeBlood Protein ElectrophoresisDNA FingerprintingPathology and Forensic MedicineEuropeGenetics PopulationDNA profilingBlood StainsY ChromosomeGenotypeY linkageMicrosatelliteHumansTypingLawForensic science international
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Biostatistical basis of individualization and segregation analysis using the multilocus DNA probe MZ 1.3: results of a collaborative study.

1992

A collaborative study using the multilocus minisatellite DNA probe MZ 1.3 was carried out to investigate segregation information, mutation rate, DNA fragment frequencies as well as band sharing characteristics. The fingerprint patterns of 393 children as well as 694 unrelated individuals were analysed after digestion of DNA with the restriction enzyme HinfI. A mutation rate of 1% per meiosis or 0.04% per band was found with a mean number of 26 bands/individual. It was shown that maternal and paternal fragments are inherited in equal proportions. Population frequencies of restriction fragments demonstrated a distribution with increasing frequencies in the small fragment size range below 10 k…

GeneticsMaleMutation rateeducation.field_of_studyBiometrybiologyHybridization probePopulationPaternityDNA FingerprintingPathology and Forensic MedicineRestriction fragmentRestriction enzymeMinisatelliteDNA profilingData Interpretation Statisticalbiology.proteinHumansFemaleeducationMolecular probeChildDNA ProbesLawProbabilityForensic science international
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Results of a collaborative study of the EDNAP group regarding mitochondrial DNA heteroplasmy and segregation in hair shafts.

2004

Abstract A collaborative exercise was carried out by the European DNA Profiling Group (EDNAP) in order to evaluate the distribution of mitochondrial DNA (mtDNA) heteroplasmy amongst the hairs of an individual who displays point heteroplasmy in blood and buccal cells. A second aim of the exercise was to study reproducibility of mtDNA sequencing of hairs between laboratories using differing chemistries, further to the first mtDNA reproducibility study carried out by the EDNAP group [Forensic Sci. Int. 97 (1998) 165]. Laboratories were asked to type 2 sections from each of 10 hairs, such that each hair was typed by at least two laboratories. Ten laboratories participated in the study, and a to…

GeneticsMitochondrial DNATransition (genetics)integumentary systemBuccal swabGenetic VariationSequence Analysis DNABiologyDNA MitochondrialHeteroplasmyPathology and Forensic MedicineDNA profilingMutationHumansTypingLawHairForensic science international
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Natural hybrids of S. cerevisiae×S. kudriavzevii share alleles with European wild populations of Saccharomyces kudriavzevii

2010

Saccharomyces kudriavzevii, a yeast species described from a pair of strains isolated from decayed leaves in Japan, has recently been isolated from oak barks in Portugal. Some data suggest that these European S. kudriavzevii populations could be closely related to the S. kudriavzevii genetic background present in natural hybrids isolated from wines and beers in different regions of Europe. However, a more exhaustive study of European S. kudriavzevii natural populations is necessary to confirm this observation. In this study, new S. kudriavzevii isolates were recovered from oak trees in different areas in Spain, and identified and characterized according to their molecular and physiological …

GeneticsNuclear geneStrain (biology)Fungal geneticsGeneral MedicineBiologybiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyDNA profilingPhylogeneticsBotanyGenotypeSaccharomyces kudriavzeviiHybridFEMS Yeast Research
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