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Featured researches published by Mechthild Prinz.


International Journal of Legal Medicine | 1997

Evaluation of Y-chromosomal STRs: a multicenter study

Manfred Kayser; A. Caglià; Daniel Corach; Neale Fretwell; Christian Gehrig; G. Graziosi; F. Heidorn; S. Herrmann; B. Herzog; M. Hidding; Katsuya Honda; Mark A. Jobling; Michael Krawczak; K. Leim; S. Meuser; Eckhard Meyer; W. Oesterreich; Arpita Pandya; Walther Parson; G. Penacino; A. Perez-Lezaun; A. Piccinini; Mechthild Prinz; Cornelia Schmitt; Peter M. Schneider; Reinhard Szibor; J. Teifel-Greding; G. Weichhold; P. de Knijff; Lutz Roewer

Abstract A multicenter study has been carried out to characterize 13 polymorphic short tandem repeat (STR) systems located on the male specific part of the human Y chromosome (DYS19, DYS288, DYS385, DYS388, DYS389I/II, DYS390, DYS391, DYS392, DYS393, YCAI, YCAII, YCAIII, DXYS156Y). Amplification parameters and electrophoresis protocols including multiplex approaches were compiled. The typing of non-recombining Y loci with uniparental inheritance requires special attention to population substructuring due to prevalent male lineages. To assess the extent of these subheterogeneities up to 3825 unrelated males were typed in up to 48 population samples for the respective loci. A consistent repeat based nomenclature for most of the loci has been introduced. Moreover we have estimated the average mutation rate for DYS19 in 626 confirmed father-son pairs as 3.2 × 10–3 (95% confidence interval limits of 0.00041–0.00677), a value which can also be expected for other Y-STR loci with similar repeat structure. Recommendations are given for the forensic application of a basic set of 7 STRs (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393) for standard Y-haplotyping in forensic and paternity casework. We recommend further the inclusion of the highly polymorphic bilocal Y-STRs DYS385, YCAII, YCAIII for a nearly complete individualisation of almost any given unrelated male individual. Together, these results suggest that Y-STR loci are useful markers to identify males and male lineages in forensic practice.


International Journal of Legal Medicine | 1997

Chromosome Y microsatellites : population genetic and evolutionary aspects

P. de Knijff; Manfred Kayser; A. Caglià; Daniel Corach; Neale Fretwell; Christian Gehrig; G. Graziosi; F. Heidorn; S. Herrmann; B. Herzog; M. Hidding; Katsuya Honda; Mark A. Jobling; Michael Krawczak; K. Leim; S. Meuser; Eckhard Meyer; W. Oesterreich; Arpita Pandya; Walther Parson; G. Penacino; A. Perez-Lezaun; A. Piccinini; Mechthild Prinz; Cornelia Schmitt; Peter M. Schneider; Reinhard Szibor; J. Teifel-Greding; G. Weichhold; Lutz Roewer

Abstract By means of a multicenter study, a large number of males have been characterized for Y-chromosome specific short tandem repeats (STRs) or microsatellites. A complete summary of the allele frequency distributions for these Y-STRs is presented in the Appendix. This manuscript describes in more detail some of the population genetic and evolutionary aspects for a restricted set of seven chromosome Y STRs in a selected number of population samples. For all the chromosome Y STRs markedly different region-specific allele frequency distributions were observed, also when closely related populations were compared. Haplotype analyses using AMOVA showed that when four different European male groups (Germans, Dutch, Swiss, Italians) were compared, less than 10% of the total genetic variability was due to differences between these populations. Nevertheless, these pairwise comparisons revealed significant differences between most population pairs. Assuming a step-wise mutation model and a mutation frequency of 0.21%, it was estimated that chromosome Y STR-based evolutionary lines of descent can be reliably inferred over a time-span of only 1950 generations (or about 49000 years). This reduces the reliability of the inference of population affinities to a historical, rather than evolutionary time scale. This is best illustrated by the construction of a human evolutionary tree based on chromosome Y STRs in which most of the branches connect in a markedly different way compared with trees based on classical protein polymorphisms and/or mtDNA sequence variation. Thus, the chromosome Y STRs seem to be very useful in comparing closely related populations which cannot probably be separated by e.g. autosomal STRs. However, in order to be used in an evolutionary context they need to be combined with more stable Y-polymorphisms e.g. base-substitutions.


Forensic Science International | 2001

DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y- chromosome STRs

Peter Gill; Charles H. Brenner; B. Brinkmann; Bruce Budowle; Angel Carracedo; Mark A. Jobling; P. de Knijff; Manfred Kayser; Michael Krawczak; W. R. Mayr; Niels Morling; B. Olaisen; Vincenzo Lorenzo Pascali; Mechthild Prinz; Lutz Roewer; Peter M. Schneider; Antti Sajantila; Chris Tyler-Smith

During the past few years the DNA commission of the International Society of Forensic Genetics has published a series of documents providing guidelines and recommendations concerning the application of DNA polymorphisms to the problems of human identification. This latest report addresses a relatively new area, namely Y-chromosome polymorphisms, with particular emphasis on short tandem repeats (STRs). This report addresses nomenclature, use of allelic ladders, population genetics and reporting methods.


Forensic Science International-genetics | 2007

ISFG: Recommendations on biostatistics in paternity testing

David W. Gjertson; Charles H. Brenner; Max P. Baur; Angel Carracedo; Francois Guidet; Juan A. Luque; Rüdiger Lessig; Wolfgang R. Mayr; V. L. Pascali; Mechthild Prinz; Peter M. Schneider; Niels Morling

The Paternity Testing Commission (PTC) of the International Society for Forensic Genetics has taken up the task of establishing the biostatistical recommendations in accordance with the ISO 17025 standards and a previous set of ISFG recommendations specific to the genetic investigations in paternity cases. In the initial set, the PTC recommended that biostatistical evaluations of paternity are based on a likelihood ratio principle - yielding the paternity index, PI. Here, we have made five supplementary biostatistical recommendations. The first recommendation clarifies and defines basic concepts of genetic hypotheses and calculation concerns needed to produce valid PIs. The second and third recommendations address issues associated with population genetics (allele probabilities, Y-chromosome markers, mtDNA, and population substructuring) and special circumstances (deficiency/reconstruction and immigration cases), respectively. The fourth recommendation considers strategies regarding genetic evidence against paternity. The fifth recommendation covers necessary documentation, reporting details and assumptions underlying calculations. The PTC strongly suggests that these recommendations should be adopted by all laboratories involved in paternity testing as the basis for their biostatistical analysis.


Forensic Science International | 1997

Multiplexing of Y chromosome specific STRs and performance for mixed samples

Mechthild Prinz; Karen Boll; Howard R. Baum; Bob Shaler

A combination of four Y-specific polymorphic STR loci was amplified simultaneously using fluorescently labeled primers. Multiplex conditions required optimization to eliminate constant bands and amplification products for female DNA. A series of experiments was carried out for mixtures of DNA from two males, and from male and female individuals for the Y-specific STRs and an autosomal locus. For the male/male mixtures amplified with the Y specific system, and amplified for an autosomal locus, the minor component in the mixture could only be identified up to a ratio of 1:10, 1:50 respectively. In male/female DNA mixtures the Y STR alleles could be identified for the highest ratio tested, 400 pg male in DNA in 800 ng female DNA which amounts to a ratio of 1:2000.


International Journal of Legal Medicine | 2006

DNA Commission of the International Society of Forensic Genetics (ISFG): an update of the recommendations on the use of Y-STRs in forensic analysis

Leonor Gusmão; John M. Butler; Angel Carracedo; Peter Gill; Manfred Kayser; W. R. Mayr; Niels Morling; Mechthild Prinz; Lutz Roewer; Chris Tyler-Smith; Peter M. Schneider

The DNA Commission of the International Society of Forensic Genetics (ISFG) regularly publishes guidelines and recommendations concerning the application of DNA polymorphisms to the problems of human identification. A previous recommendation published in 2001 has already addressed Y-chromosome polymorphisms, with particular emphasis on short tandem repeats (STRs). Since then, the use of Y-STRs has become very popular, and numerous new loci have been introduced. The current recommendations address important aspects to clarify problems regarding the nomenclature, the definition of loci and alleles, population genetics and reporting methods.


Forensic Science International-genetics | 2011

ISFG: Recommendations regarding the use of non-human (animal) DNA in forensic genetic investigations

Adrian Linacre; Leonor Gusmão; W. Hecht; A.P. Hellmann; Wolfgang R. Mayr; Walther Parson; Mechthild Prinz; Peter M. Schneider; Niels Morling

The use of non-human DNA typing in forensic science investigations, and specifically that from animal DNA, is ever increasing. The term animal DNA in this document refers to animal species encountered in a forensic science examination but does not include human DNA. Non-human DNA may either be: the trade and possession of a species, or products derived from a species, which is contrary to legislation; as evidence where the crime is against a person or property; instances of animal cruelty; or where the animal is the offender. The first instance is addressed by determining the species present, and the other scenarios can often be addressed by assigning a DNA sample to a particular individual organism. Currently there is little standardization of methodologies used in the forensic analysis of animal DNA or in reporting styles. The recommendations in this document relate specifically to animal DNA that is integral to a forensic science investigation and are not relevant to the breeding of animals for commercial purposes. This DNA commission was formed out of discussions at the International Society for Forensic Genetics 23rd Congress in Buenos Aires to outline recommendations on the use of non-human DNA in a forensic science investigation. Due to the scope of non-human DNA typing that is possible, the remit of this commission is confined to animal DNA typing only.


International Journal of Legal Medicine | 2001

DNA commission of the International Society of Forensic Genetics: Recommendations on forensic analysis using Y-chromosome STRs

Peter Gill; Charles H. Brenner; B. Brinkmann; Bruce Budowle; E. Mayr; Mark A. Jobling; Peter de Knijff; Manfred Kayser; Michael Krawczak; Niels Morling; B. Olaisen; Vincenzo Lorenzo Pascali; Mechthild Prinz; Lutz Roewer; Peter M. Schneider; Antti Sajantila; Chris Tyler-Smith

Abstract During the past few years the DNA commission of the International Society of Forensic Genetics has published a series of documents providing guidelines and recommendations concerning the application of DNA polymorphisms to the problems of human identification. This latest report addresses a relatively new area, namely Y-chromosome polymorphisms, with particular emphasis on short tandem repeats (STRs). This report addresses nomenclature, use of allelic ladders, population genetics and reporting methods.


Forensic Science International-genetics | 2014

DNA Commission of the International Society for Forensic Genetics: Revised and extended guidelines for mitochondrial DNA typing

Walther Parson; Leonor Gusmão; Douglas R. Hares; Jodi A. Irwin; Wolfgang R. Mayr; Niels Morling; E. Pokorak; Mechthild Prinz; Antonio Salas; Peter M. Schneider; Thomas J. Parsons

The DNA Commission of the International Society of Forensic Genetics (ISFG) regularly publishes guidelines and recommendations concerning the application of DNA polymorphisms to the question of human identification. Previous recommendations published in 2000 addressed the analysis and interpretation of mitochondrial DNA (mtDNA) in forensic casework. While the foundations set forth in the earlier recommendations still apply, new approaches to the quality control, alignment and nomenclature of mitochondrial sequences, as well as the establishment of mtDNA reference population databases, have been developed. Here, we describe these developments and discuss their application to both mtDNA casework and mtDNA reference population databasing applications. While the generation of mtDNA for forensic casework has always been guided by specific standards, it is now well-established that data of the same quality are required for the mtDNA reference population data used to assess the statistical weight of the evidence. As a result, we introduce guidelines regarding sequence generation, as well as quality control measures based on the known worldwide mtDNA phylogeny, that can be applied to ensure the highest quality population data possible. For both casework and reference population databasing applications, the alignment and nomenclature of haplotypes is revised here and the phylogenetic alignment proffered as acceptable standard. In addition, the interpretation of heteroplasmy in the forensic context is updated, and the utility of alignment-free database searches for unbiased probability estimates is highlighted. Finally, we discuss statistical issues and define minimal standards for mtDNA database searches.


Forensic Science International | 2001

Allele sequences of six new Y-STR loci and haplotypes in the Chinese Han population.

Y. P. Hou; Jingquan Zhang; Youping Li; Jiagang Wu; S.Z. Zhang; Mechthild Prinz

Human chromosome Y-specific short tandem repeat (Y-specific STR) markers have useful properties for forensic applications. However, there is a need to develop more Y-specific STR markers, because the discriminating power of each STR locus is limited. In the present study, we describe our results on six new Y-specific STR markers that were initially located using sequence database information by Ayub et al. and were named DYS434, DYS435, DYS436, DYS437, DYS438 and DYS439. Our studies focused on the analysis of the DNA sequence for each allele at all six Y-specific STR loci in order to understand their structures in the human genome and to construct human allelic ladders, which are necessary for forensic DNA typing. In addition, the haplotype distribution for all six analyzed loci was studied in a Chinese Han population sample. The results indicate that DYS434, DYS435, DYS436, DYS437, DYS438 and DYS439 are useful Y-specific STR markers for forensic sciences.

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Niels Morling

University of Copenhagen

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Leonor Gusmão

Rio de Janeiro State University

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Theresa Caragine

Office of Chief Medical Examiner of the City of New York

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Walther Parson

Innsbruck Medical University

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John M. Butler

National Institute of Standards and Technology

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