Haplotyping of STR cluster DXS6801–DXS6809–DXS6789 on Xq21 provides a powerful tool for kinship testing

被引:8
|
作者
Reinhard Szibor
Sandra Hering
Eberhard Kuhlisch
Ines Plate
Susanne Demberger
Michael Krawczak
Jeanett Edelmann
机构
[1] Otto-von-Guericke-Universität Magdeburg,Institut für Rechtsmedizin
[2] Technische Universität Dresden,Institut für Rechtsmedizin
[3] Technische Universität Dresden,Institut für Medizinische Informatik und Biometrie
[4] Christian-Albrechts-Universität Kiel,Institut für Medizinische Informatik und Statistik
[5] Universität Leipzig,Institut für Rechtsmedizin
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关键词
Kinship testing; X chromosome; Haplotyping; Xq21; Linkage;
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摘要
Short tandem repeat (STR) markers DXS6801 (GATA41B11), DXS6809 (GATA69B129) and DXS6789 (GATA31F01) are located in a 3-Mb region on human chromosome Xq21, spanning approximately 3–6 cM. Theoretically, this cluster could give rise to 1,144 different haplotypes in the German population. In fact, genotyping of 806 males revealed the presence of 207 different haplotypes. Since the three STRs have been shown to be in strong linkage disequilibrium (LD), haplotype frequencies cannot be computed on the basis of single locus allele frequencies alone, but have to be estimated directly instead. In this work, we present data on linkage, haplotype frequencies and LD in the German population. To highlight the potential of the STR cluster for forensic analysis, we also report two examples of its successful application in pedigree-based kinship testing.
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页码:363 / 369
页数:6
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    Szibor, R
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    Kuhlisch, E
    Plate, I
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    Krawczak, M
    Edelmann, J
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