Purps J.,Charité - Medical University of Berlin |
Siegert S.,University of Cologne |
Willuweit S.,Charité - Medical University of Berlin |
Nagy M.,Charité - Medical University of Berlin |
And 165 more authors.
Forensic Science International: Genetics | Year: 2014
In a worldwide collaborative effort, 19,630 Y-chromosomes were sampled from 129 different populations in 51 countries. These chromosomes were typed for 23 short-tandem repeat (STR) loci (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393, DYS385ab, DYS437, DYS438, DYS439, DYS448, DYS456, DYS458, DYS635, GATAH4, DYS481, DYS533, DYS549, DYS570, DYS576, and DYS643) and using the PowerPlex Y23 System (PPY23, Promega Corporation, Madison, WI). Locus-specific allelic spectra of these markers were determined and a consistently high level of allelic diversity was observed. A considerable number of null, duplicate and off-ladder alleles were revealed. Standard single-locus and haplotype-based parameters were calculated and compared between subsets of Y-STR markers established for forensic casework. The PPY23 marker set provides substantially stronger discriminatory power than other available kits but at the same time reveals the same general patterns of population structure as other marker sets. A strong correlation was observed between the number of Y-STRs included in a marker set and some of the forensic parameters under study. Interestingly a weak but consistent trend toward smaller genetic distances resulting from larger numbers of markers became apparent. © 2014 The Authors.
Roby R.K.,Health Science Center |
Roby R.K.,Institute of Applied Genetics |
Sprouse M.,Health Science Center |
Phillips N.,Health Science Center |
And 4 more authors.
Current Protocols in Human Genetics | Year: 2014
This unit describes methods used in the analysis of mitochondrial DNA (mtDNA) for forensic and research applications. UNIT 14.7 describes procedures specifically for forensic casework where the DNA from evidentiary material is often degraded or inhibited. In this unit, protocols are described for quantification of mtDNA before amplification; amplification of the entire control region from high-quality samples as well as procedures for interrogating the whole mitochondrial genome (mtGenome); quantification of mtDNA post-amplification; and, post-PCR cleanup and sequencing. The protocols for amplification were developed for high-throughput databasing applications for forensic DNA testing such as reference samples and population studies. However, these same protocols can be applied to biomedical research such as age-related disease and health disparities research. © 2014 by JohnWiley & Sons, Inc.