Announcement of Population DataGenetic variability of 15 autosomal STR loci in Russian populations
Section snippets
Acknowledgements
This study was supported by the grant 07-04-01749 from the Russian Foundation of Basic Research. The authors are grateful to Promega Corporation for the gift of PowerPlex16 kit used in the study and to Dr. Olga Kurbatova for helpful remarks.
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Cited by (21)
Allele frequencies for 15 STR loci in the Ukrainian population
2017, Forensic Science International: GeneticsForensic and population genetic characteristics of 62 X chromosome SNPs revealed by multiplex PCR and MALDI-TOF mass spectrometry genotyping in 4 North Eurasian populations
2016, Legal MedicineCitation Excerpt :Current standard sets of DNA identity markers adopted in the United States (CODIS, Combined DNA Index System) and in Europe (European Standard Set) provide high and generally sufficient power of individual identification (MP = 3–5 × 10−16) [17]. In our previous work, it was shown that a set of 15 STR loci also provides a very high probability of discrimination of unrelated individuals in native populations of Russia (MP = 3.04 × 10−15–1.56 × 10−17) [15,18]. However, low multiplexing capacity and complexity of genotyping of STR loci, coupled with recent advances in sequencing and genotyping technologies obviously will lead to the replacement of STR markers by more simple and informative systems [2–4].
Korean population genetic data and concordance for the PowerPlex <sup>®</sup> ESX 17, AmpFlSTR Identifiler<sup>®</sup>, and PowerPlex<sup>®</sup> 16 systems
2013, Forensic Science International: GeneticsCitation Excerpt :Thus, the new kit is a valuable forensic tool and is suitable to extend the Korean population genetic data obtained with the two conventional kits. A population comparison based on the DSA values calculated from allele frequencies of the 17 STR markers in the AmpFlSTR Identifiler® and the PowerPlex® 16 kits, except for the amelogenin locus between the Korean population and other published populations is shown in supplementary Table S1 [18–47]. MDS plot of DSA based on the result of Table S1 is depicted in Fig. 1.