DNA Commission of the International Society for Forensic Genetics (ISFG): Guidelines on the use of X-STRs in kinship analysis. (July 2017)

• Record Type: Journal Article
• Authors: Tillmar, Andreas O.; Kling, Daniel; Butler, John M.; Parson, Walther; Prinz, Mechthild; Schneider, Peter M.; Egeland, Thore; Gusmão, Leonor
• Is Part Of: Forensic science international. Volume 29(2017)
• Page Start: 269
• Page End: 275
• Publication Date: 2017-07
• Subjects: X chromosome -- Linkage -- Linkage disequilibrium -- Haplotype -- Recombination -- Paternity -- Kinship; Forensic genetics -- Periodicals; Génétique légale -- Périodiques; Forensic genetics; Electronic journals; Periodicals; 614.1
• DOI: 10.1016/j.fsigen.2017.05.005
• Languages: English
• ISSNs: 1872-4973

Abstract

Highlights: Guidelines for the use of X-chromosomal markers in kinship analysis are provided. Recommendations on how to account for linkage and LD are provided. A list of more than 150 publications presenting population frequency data is provided. Abstract: Forensic genetic laboratories perform an increasing amount of genetic analyses of the X chromosome, in particular to solve complex cases of kinship analysis. For some biological relationships X-chromosomal markers can be more informative than autosomal markers, and there are a large number of markers, methods and databases that have been described for forensic use. Due to their particular mode of inheritance, and their physical location on a single chromosome, some specific considerations are required when estimating the weight of evidence for X-chromosomal marker DNA data. The DNA Commission of the International Society for Forensic Genetics (ISFG) hereby presents guidelines and recommendations for the use of X-chromosomal markers in kinship analysis with a special focus on the biostatistical evaluation. Linkage and linkage disequilibrium (association of alleles) are of special importance for such evaluations and these concepts and the implications for likelihood calculations are described in more detail. Furthermore it is important to use appropriate computer software that accounts for linkage and linkage disequilibrium among loci, as well as for mutations. Even though some software exist, there is still a need for further improvement of dedicated software.