Tag Archives: african genomics


A landmark study led by researchers from University College London (UCL) and published in Science Advances reveals a previously hidden depth of genetic diversity, migration, and admixture within African populations. Titled “Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture,” the research analysed 1,333 genomes from over 150 ethnic groups across Cameroon, Ghana, Nigeria, Sudan, and the Republic of the Congo.





The findings challenge the often simplistic narratives about African genetic history. The study uncovered fine-scale genetic structure within single countries, showing that even neighbouring ethnic groups may carry distinct ancestral lineages. For instance, western Cameroonian groups exhibit unique ancestry signatures reflecting the region’s long history of local kingdoms and cultural interactions.





Researchers also traced long-distance admixture events, linking populations in northern Cameroon and Sudan with distant groups, suggesting centuries of movement through trade, migration, and empire expansion. In Ghana and Nigeria, they detected intermixing patterns dating back more than 2,000 years, likely connected to shifts in climate and vegetation that encouraged population mobility and contact.





Beyond uncovering these complex patterns, the study highlights an essential truth: Africa’s genomic diversity cannot be fully understood through limited or external data. It underscores the urgency of expanding and diversifying African genomic datasets to ensure equitable representation in global genetics research.





For MyAfroDNA, this research reaffirms our mission to strengthen African-centric molecular testing and biospecimen sourcing for both research and precision medicine. Understanding these fine-scale patterns helps scientists interpret genetic variation more accurately, improving ancestry insights and health-related findings for African communities.





As Africa continues to shape the global genomic landscape, studies like this remind us that every region, community, and ancestry carries its own genetic legacy, one that deserves to be studied, respected, and represented on its own terms.





Read the full research here.



Antimicrobial resistance (AMR) poses a major threat to global health, and Africa is no exception. As pathogens evolve, our ability to treat common infections is becoming increasingly limited.





A new study published in Scientific Reports provides valuable insight into the genetic basis of AMR in Africa, focusing on Staphylococcus aureus, one of the most widespread and clinically significant bacteria.What the Study FoundResearchers analyzed 95 whole genomes of S. aureus collected from 11 African countries. The majority of these samples were human-derived, taken from blood, pus, urine, and wound sites.





Through bioinformatic analysis, they identified 33 antimicrobial resistance genes.Key findings include:Efflux pump mechanisms were the dominant form of resistance, allowing bacteria to actively expel antibiotics.Other resistance strategies included enzyme-mediated inactivation, target alteration, protection, and replacement.West and East Africa emerged as hotspots for the distribution of resistance genes, signaling the need for stronger surveillance in these regions.





These findings highlight the urgent need to expand genomic surveillance systems across the continent. Despite covering 11 countries, the study was limited by small sample sizes and lack of data from many African nations. This gap emphasizes the importance of building local capacity for sequencing, data analysis, and sample collection.For African health systems, this research serves as a reminder that combating AMR requires both global collaboration and homegrown solutions. Without comprehensive genomic data, it will be difficult to design effective treatment guidelines, track the spread of resistance, or prepare for future outbreaks.





At MyAfroDNA, we believe genomic research should be powered by African data, African expertise, and African innovation. Our mission is to provide high-quality biospecimens and molecular testing services that enable researchers to generate the insights needed to safeguard public health.AMR is a collective challenge, but with better data and stronger collaboration, Africa can take the lead in finding solutions.









Read the full publication here: https://www.nature.com/articles/s41598-025-01398-0



A groundbreaking study published in Nature Communications has revealed novel genetic variants associated with carotid intima-media thickness (cIMT), a key marker of early atherosclerosis, among nearly 8,000 adults from sub-Saharan Africa. The research, part of the AWI-Gen project, included participants from Burkina Faso, Ghana, Kenya, and South Africa and marks one of the largest genome-wide association studies (GWAS) on cardiovascular risk in African populations.





Two previously unidentified loci, SIRPA and FBXL17, were found to be significantly associated with cIMT, offering new insight into biological pathways involved in vascular health. Notably, the study also identified sex-specific genetic signals: SNX29 in men, and LARP6 and PROK1 in women, the latter two being enriched for estrogen response genes. These findings suggest different genetic mechanisms for cardiovascular risk between men and women.





Many of the variants identified in this African cohort are either rare or absent in European populations, emphasizing the critical need for diversity in genomic research. This study not only deepens our understanding of cardiovascular disease in African communities but also underscores the importance of building inclusive datasets to drive precision medicine. At MyAfroDNA, we champion this kind of Africa-led genomic science.





Read more on this research here: https://www.nature.com/articles/s41467-022-28276-x