This difference has been explained by (i) the smaller effective population size of Y chromosomes causing stronger genetic drift,

GW786034 and (ii) haplotype clustering due to widespread patrilocality. Therefore, population structure, will be more pronounced in Y-chromosomal genetic databases and must be taken into account when database counts are used to quantify the evidential value of matches in forensic casework [38]. It has been shown, however, that so-called meta-populations may be constructed for Y-STRs that have low haplotypic variation among population groups within a meta-population, but large variation between meta-populations [39]. If necessary, such meta-populations can be defined ab initio using geography as a proxy of genetic relatedness, or by taking ethnic or linguistic data into account. For all five forensic marker sets studied here, samples of African ancestry were clearly separated genetically from all other continental meta-populations. Pairwise genetic distances, measured by RST, between Africa and the four non-African meta-populations were of similar magnitude.

These results confirm a previous study of 40,669 haplotypes from 339 populations typed only for the nine markers of the MHT panel [39]. Moreover, genetic distances between non-African meta-populations were comparatively small. While North and South America still differed to some degree in the first MDS component, Eastern and Western Asia showed notable differences only in the second component. However, since the study here lacked samples from large parts of Northern and Central Asia, reasonable inference about the population structure in HDAC inhibitor Asia

as a whole was not possible. Europe was the most intensively sampled continent in the present study and made up ∼60% of the overall sample size. A separate MDS analysis of samples of European residency and ancestry recapitulated the outcome of previous studies with smaller marker sets [32] and [40]. In particular, Depsipeptide a clear East–West divide became evident in the first component of the MDS analysis for all five forensic marker sets. Finland and some regions of the Balkans (Croatia, Bosnia–Herzegovina) showed consistently large differences to other European populations in the second MDS component. It must be emphasized that this population genetic analysis was based upon marker sets that were designed for forensic purposes, and that shared several markers. That all five sets yielded a similar picture of the geographic distribution of Y-STR haplotypes may therefore indicate that, in terms of population structure, the effects of markers included in the MHT (which are common to all five sets) dominate those of more mutable markers, such as PPY23-specific STRs DYS576, DYS570 and DYS481. Indeed, it has been shown recently that haplotypes comprising only rapidly mutating markers lack strong signals of population history (Ballantyne et al., submitted for publication).