0000000000409967

AUTHOR

Walter Bär

showing 5 related works from this author

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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Achievement of Interlaboratory Uniformity — A Summary of Work Carried out by the EDNAP Group

1992

This paper describes a collaborative exercise intended to demonstrate whether uniformity of DNA profiles results could be achieved between different European laboratories. It was shown that this goal would be obtained provided that a common protocol was followed (specifically the use of a common electrophoretic buffer is the most important parameter).

Full ProtocolProtocol (science)Computer architectureWork (electrical)Group (periodic table)Computer science
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STR analysis of artificially degraded DNA--results of a collaborative European exercise.

2003

Degradation of human DNA extracted from forensic stains is, in most cases, the result of a natural process due to the exposure of the stain samples to the environment. Experiences with degraded DNA from casework samples show that every sample may exhibit different properties in this respect, and that it is difficult to systematically assess the performance of routinely used typing systems for the analysis of degraded DNA samples. Using a batch of artificially degraded DNA with an average fragment size of approx. 200 bp a collaborative exercise was carried out among 38 forensic laboratories from 17 European countries. The results were assessed according to correct allele detection, peak heig…

DNA FragmentationBiologyPolymerase Chain ReactionPathology and Forensic Medicinelaw.inventionchemistry.chemical_compoundlawGenotypeHumansCooperative BehaviorAlleleAllelesPolymerase chain reactionGeneticsClinical Laboratory TechniquesDNADNA FingerprintingEuropeSTR analysisDNA profilingchemistryTandem Repeat SequencesMicrosatelliteLawDNATaq polymerase
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A report of an international collaborative experiment to demonstrate the uniformity obtainable using DNA profiling techniques

1992

This paper describes a collaborative exercise intended to demonstrate whether uniformity of DNA profile results could be achieved between different European laboratories. It was shown that this goal can be obtained provided that a common protocol is followed (specifically the use of a common electrophoretic buffer as being the most important parameter). Generally, lower molecular weight loci (with lower molecular weight fragments) such as YNH24 perform better than higher molecular weight loci such as MS43a. The results of the exercise are discussed in relation to the objectives of the European DNA profiling group (EDNAP).

GeneticsProtocol (science)Quality ControlElectrophoresis Agar GelDNA/bloodRestriction MappingComputational biologyDNABiologySettore MED/43 - MEDICINA LEGALEDNA FingerprintingPathology and Forensic MedicineDNA profilingMulticenter studyAutoradiographyHumansRestriction fragment length polymorphismLaboratoriesLawDNA Fingerprinting/standards
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Report of a european collaborative exercise comparing DNA typing results using a single locus VNTR probe

1991

A collaborative exercise was carried out in 1989 among 12 European forensic laboratories using the single locus VNTR probe pYNH24, the restriction enzyme HinfI, the same set of human genomic DNA samples, and a standardized DNA size marker. The objectives of the exercise were: (1) to study the degree of variation within and between laboratories, (2) to obtain information on requirements for technical standardization allowing the exchange of typing results and (3) to compare different approaches for the identification of allelic DNA fragments of unknown size. Each laboratory carried out up to 10 independent typing experiments using the same DNA samples. The results were analysed independently…

Restriction Mappingdata comparisonBiologyGenomePathology and Forensic Medicinechemistry.chemical_compoundVNTR probeRestriction mapforensic stain analysisHumansTypingAllelesGeneticsfragment size determinationNucleic Acid HybridizationReproducibility of ResultsDNAForensic MedicineSettore MED/43 - MEDICINA LEGALEEuropegenomic DNARestriction enzymechemistryGenetic markerDNA ProbesMolecular probeLawDNAForensic Science International
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