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Journal ArticleDOI

The y chromosome in forensic analysis and paternity testing

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TLDR
Y haplotyping is most likely to find application in special instances, such as deficiency cases in paternity testing and in the analysis of mixtures of male and female DNA, or in combination with autosomal markers.
Abstract
The male specificity of the human Y chromosome makes it potentially useful in forensic studies and paternity testing, and markers are now available which will allow its usefulness to be assessed in practice. However, while it can be used confidently for exclusions, the unusual properties of the Y mean that inclusions will be very difficult to make: haplotypes are confined within lineages, so population sub-structuring is a major problem, and many male relatives of a suspect will share his Y chromosome. Y haplotyping is most likely to find application in special instances, such as deficiency cases in paternity testing and in the analysis of mixtures of male and female DNA, or in combination with autosomal markers.

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Journal ArticleDOI

A nomenclature system for the tree of human Y-chromosomal binary haplogroups

Alan J. Redd
- 01 Oct 2002 - 
TL;DR: A simple set of rules was developed to unambiguously label the different clades nested within a single most parsimonious phylogeny, which supersedes and unifies past nomenclatures and allows the inclusion of additional mutations and haplogroups yet to be discovered.
BookDOI

Forensic DNA Evidence Interpretation

TL;DR: The Frequentist Approaches Bayesian Approaches Statistical Evaluation of Mixtures Low Copy Number and Interpretation Issues Associated with DNA Databases are discussed.
Journal ArticleDOI

Use of X-linked markers for forensic purposes.

TL;DR: The population genetic properties and forensic utility of selected ChrX markers are reviewed, and the problems and limitations arising with their practical use are discussed.
References
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Journal ArticleDOI

Mutation of human short tandem repeats

TL;DR: A total of 20,000 parent-offspring transfers of alleles were examined through the genotyping within 40 CEPH reference families of 28 short tandem repeat polymorphisms (STRPs) located on chromosome 19, and the average mutation rate was nearly four times higher than the average rate for dinucleotide STRPs.
Journal ArticleDOI

Forensic application of DNA 'fingerprints'.

TL;DR: It is shown that this technique can be used for forensic purposes; DNA of high relative molecular mass (Mr) can be isolated from 4-yr-old bloodstains and semen stains made on cotton cloth and digested to produce DNA fingerprints suitable for individual identification.
Journal ArticleDOI

Identification of the remains of the Romanov family by DNA analysis

TL;DR: The DNA evidence supports the hypothesis that the remains of the last Tsar, Tsarina, three of their five children, the Royal Physician and three servants are those of the Romanov family.
Journal ArticleDOI

Complex gene conversion events in germline mutation at human minisatellites

TL;DR: At MS32, high frequency mutation processes in sperm appear to be largely germline specific and to occur at a constant rate irrespective of allele size, which implies that germline instability is controlled by elements outside the tandem repeat array.
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