Utility of X-chromosome SNPs in relationship testing

Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearchpeer-review

X-chromosome markers may complement the results obtained from other genetic markers in complex relationship cases. Until now, reports on relationship testing using X-chromosome markers have mainly included data of short tandem repeats (STRs) while little data on single nucleotide polymorphisms (SNPs) in relationship testing have been published. We selected 25 highly polymorphic biallelic SNPs distributed through the human X-chromosome. One 25-plex PCR reaction and one 25-plex single base extension (SNaPshot) reaction were developed. The maximum size of the PCR products was 120ábp and the size of the SBE primers varied between 18 and 85 nucleotides. We analyzed the allele and haplotype frequencies in 1078 unrelated males. All the SNPs were polymorphic and the lowest minor allele frequency was 0.103. All the haplotypes were unique. The forensic parameters were calculated in the Danish and Somali populations. In the Danish population (Ná=á93), the power of discrimination (PD) in females was one in 4.4áÎá109 individuals and the PD in males was one in 2.6áÎá106. The PD in Somalis (Ná=á91) was one in 2.7áÎá109 in females and one in 1.7áÎá106 in males. Finally, we present an example of how the 25 X-chromosome SNP-multiplex may help to solve a complex immigration case
Original languageEnglish
Title of host publicationProgress in Forensic Genetics 12 : Proceedings of the 22nd International ISFG Congress
EditorsNiels Morling
Volume1
PublisherElsevier
Publication date2008
Pages528-530
Publication statusPublished - 2008
Event22nd International ISFG Congress - Copenhagen, Denmark
Duration: 21 Aug 200725 Aug 2007

Conference

Conference22nd International ISFG Congress
LandDenmark
ByCopenhagen
Periode21/08/200725/08/2007
SeriesForensic Science International: Genetics Supplement Series
Number1
Volume1
ISSN1875-1768

ID: 14465725