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Kenya is a diverse and populous nation that employs DNA evidence in its criminal justice system, and therefore requires reliable information on autosomal STR allele frequency variation across the country and in its many ethnic groups. In order to provide reference data and to assess population structure, we analysed the 21 autosomal STRs in the GlobalFiler multiplex in a sample of 510 indigenous Kenyans representing the country's eight former provinces, 43 of its 47 counties, three main linguistic families and all 29 ethnic groups that each comprise >0.5% of the 2019 census population. The indigenous population originated from successive migrations of Cushitic, Nilotic and Bantu speaking groups who settled in regions that suited their distinctive sustenance lifestyles. Consequently, they now largely reside in a patchwork of communities with strong associations with particular counties and provinces and limited degrees of inter-group marriage, as shown by DNA donors' ancestry details. We found significant genetic differentiation between the three Nilotic language sub-families, with Western Nilotes (the Luo ethnic group) showing greater similarity to the Bantu than the Southern and Eastern Nilotes which themselves showed closer affinity to the Cushitic speakers. This concurs with previous genetic, linguistic and social studies. Comparisons with other African populations also showed that linguistic affiliation is a stronger factor than geography. This study revealed several rare off-ladder alleles whose structure was determined by Sanger sequencing. Among the unusual features that could affect profile interpretation were a deletion of Amelogenin Y but no other forensic marker (autosomal or Y-chromosomal), a triallelic pattern at TPOX and an extremely short SE33 allele falling within the expected size range of D7S820. Compared with the currently implemented Identifiler multiplex, Random Match Probabilities decreased from 6.4 × 10 to 3.9 × 10. The appreciation of local population structure provided by the geographically and ethnically representative sample in this study highlights the structured genetic landscape of Kenya.
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http://dx.doi.org/10.1016/j.fsigen.2021.102535 | DOI Listing |
Sci Justice
September 2025
School of Life Sciences, University of KwaZulu-Natal, Private Bag X54001, Westville, Durban 4000, South Africa. Electronic address:
A compound marker integrates two or more genetic markers into a single assay. The application of compound markers enhances the predictive accuracy of genetic testing by leveraging the strengths of different genetic variations while mitigating the limitations of individual markers. Compound markers include SNP-SNPs, SNP-STRs, DIP-SNPs, DIP-STRs, Multi-In/Dels, CpG-SNPs, CpG-STRs/CpG-In/Del, and Methylation-Microhaplotypes.
View Article and Find Full Text PDFForensic Sci Int
August 2025
Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an 710004, China; Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou
Complex kinship testing presents significant challenges due to the complexity of genetic information among individuals and the lack of systematic exploration of genetic markers' effectiveness. This study developed an R package named KinshipLR to optimize biomarker selection for complex kinship testing, evaluating the efficacy of autosomal STRs, SNPs, and X-STRs across various scenarios. Using allele frequency data from Chinese four populations, 10,000 simulations were conducted for each scenario to analyze the factors influencing testing accuracy, including relationship type, population background, genetic marker type, and evaluation algorithms.
View Article and Find Full Text PDFForensic Sci Int Genet
January 2026
Institute of Legal Medicine, University of Münster, Röntgenstr. 23, Münster 48149, Germany. Electronic address:
TrACE (Trace Analysis Collaborative Exercise) represents a novel, strictly expert driven and transparent concept of external quality control based on a combination of proficiency testing and interlaboratory comparisons. TrACE is an official proficiency test scheme of the German Stain Commission and acts in accordance with the recommendations for proficiency testing issued by this commission and outlined in DIN EN ISO 17025. TrACE offers modules on all aspects of forensic genetics that address challenges encountered in real casework.
View Article and Find Full Text PDFForensic Sci Int Synerg
December 2025
Kenya Medical Research Institute, P.O. Box 54840 00200 off Raila Odinga Way, Nairobi, Kenya.
Forensic genetic frequency databases (FGFD) are used in estimating the probability of a DNA match in forensic investigations. They provide reference population data that can be used for statistical estimation for the rarity of a genotype, haplotype or a DNA profile in a population hence giving probative value for forensic evidence. Currently, three FGFD databases are recommended by the International Society for Forensic Genetics (ISFG) for forensic use; the Y-Chromosome Haplotype Reference Database (YHRD), the EDNAP Mitochondrial DNA Population Database (EMPOP), and the STRs for Identity ENFSI Reference Database (STRidER).
View Article and Find Full Text PDFLeg Med (Tokyo)
September 2025
Forensic Programme, School of Health Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian 16150, Kelantan, Malaysia. Electronic address:
In this study, we genotyped 21 autosomal STRs plus three loci located on the sex chromosomes in DNA samples collected from unrelated Melanau and Murut subjects using Globalfiler Express PCR amplification kits. A total of 94 and 81 blood samples were respectively collected from individuals living in Sarawak and Sabah. They were all healthy and had no history of intermixing with other ethnic groups for at least the three most recent generations.
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