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Erschienen in: International Journal of Legal Medicine 5/2009

01.09.2009 | Original Article

Reduced-volume and low-volume typing of Y-chromosomal SNPs to obtain Finnish Y-chromosomal compound haplotypes

verfasst von: Marielle Heinrich, Tina Braun, Timo Sänger, Pekka Saukko, Sabine Lutz-Bonengel, Ulrike Schmidt

Erschienen in: International Journal of Legal Medicine | Ausgabe 5/2009

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Abstract

Single-nucleotide extension is a widespread method for typing Y-chromosomal single-nucleotide polymorphisms. In our study, we validated a multiplex minisequencing assay in a reduced-volume and in a low-volume approach. A four-plex assay was performed in a 6-µL multiplex reaction in 96-well microtiter reaction plates, which can be directly used for capillary electrophoresis. In a second approach, a six-plex assay was performed on a chemically structured glass slide. Both techniques have proven to be highly sensitive as well as time- and cost-saving, which makes them a valuable option not only for forensic purposes but also for population genetic studies where large sample numbers have to be analyzed. In the present paper, both techniques are compared and applied to analyze a population sample from the area of Turku, Finland. The most common haplogroup was found to be N1c*, which is nearly absent in western and central European populations. Additionally, 11 short tandem repeat markers were analyzed to further discriminate Y-chromosomal lineages.
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Metadaten
Titel
Reduced-volume and low-volume typing of Y-chromosomal SNPs to obtain Finnish Y-chromosomal compound haplotypes
verfasst von
Marielle Heinrich
Tina Braun
Timo Sänger
Pekka Saukko
Sabine Lutz-Bonengel
Ulrike Schmidt
Publikationsdatum
01.09.2009
Verlag
Springer-Verlag
Erschienen in
International Journal of Legal Medicine / Ausgabe 5/2009
Print ISSN: 0937-9827
Elektronische ISSN: 1437-1596
DOI
https://doi.org/10.1007/s00414-009-0358-3

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