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Volume 3, Issue 1, Pages 37-41 (December 2008)


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Analysis of linkage and linkage disequilibrium for eight X-STR markers

Andreas O. TillmaraCorresponding Author Informationemail address, Petter Mostadb, Thore Egelandcd, Bertil Lindbloma, Gunilla Holmlunda, Kerstin Monteliusa

Received 30 April 2008; received in revised form 21 August 2008; accepted 16 September 2008. published online 27 October 2008.

Abstract 

X-chromosomal short tandem repeats (X-STR) have proven to be informative and useful in complex relationship testing. The main feature of X-STR markers, compared to autosomal forensic markers, is that all loci are located on the same chromosome. Thus, linkage and linkage disequilibrium may occur. The aim of this work was to study population genetic parameters of eight X-STR markers, located in four linkage groups. We present haplotype frequencies, based on 718 Swedish males, for the four linkage groups included in the Argus X-8 kit. Forensic efficiency parameters have been calculated as well as the allelic association between the tested markers for detection of linkage disequilibrium. To study the occurrences of recombination between the loci, both Swedish and Somali families were typed. A mathematical model for the estimation of recombination frequencies is presented and applied on the family samples. Our study showed that the tested markers all have highly informative forensic values and that there is a significant degree of linkage disequilibrium between the STR markers within the four linkage groups. Furthermore, based on the tested families, we also demonstrated that two of the linkage groups are partially linked. A consequence of these findings is that both linkage and linkage disequilibrium should be accounted for when producing likelihood ratios in relationship testing with X-STR markers.

a National Board of Forensic Medicine, Department of Forensic Genetics and Forensic Toxicology, Artillerigatan 12, SE-58758, Linköping, Sweden

b Mathematical Sciences, Chalmers University of Technology, and Mathematical Sciences Göteborg University, Göteborg, Sweden

c Department of Medical Genetics, Ullevaal University Hospital, Oslo, Norway

d Oslo University College, PO Box 4, St Olavs Plass, N-0130 Oslo, Norway

Corresponding Author InformationCorresponding author. Tel.: +46 13 25 21 43; fax: +46 13 13 60 05.

PII: S1872-4973(08)00137-3

doi:10.1016/j.fsigen.2008.09.006


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