Towards diversity in genomics: The emergence of neurogenomics in Africa?
There is a high burden of mental and neurological disorders in Africa. Nevertheless, there appears to be an under-representation of African ancestry populations in large-scale genomic studies. Here, we evaluated the extent of under-representation of Africans in neurogenomic studies in the GWAS Catal...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 2018-01, Vol.110 (1), p.1-9 |
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Zusammenfassung: | There is a high burden of mental and neurological disorders in Africa. Nevertheless, there appears to be an under-representation of African ancestry populations in large-scale genomic studies. Here, we evaluated the extent of under-representation of Africans in neurogenomic studies in the GWAS Catalog. We found 569 neurogenomic studies, of which 88.9% were exclusively focused on people with European ancestry and the remaining 11.1% having African ancestry cases included. In terms of population, only 1.2% of the total populations involved in these 569 GWAS studies were of African descent. Further, most of the individuals in the African ancestry category were identified to be African-Americans/Afro-Caribbeans, highlighting the huge under-representation of homogenous African populations in large-scale neurogenomic studies. Efforts geared at establishing strong collaborative ties with European/American researchers, maintaining freely accessible biobanks and establishing comprehensive African genome data repositories to track African genome variations are critical for propelling neurogenomics/precision medicine in Africa.
•There is a high burden of mental and neurological disorders in Africa.•African populations are hugely under-represented in neurogenomic studies in the GWAS Catalog (11.1% representation).•Population-wise, only 1.2% of the examined studies included participants of African ancestry.•Large-scale African-centered studies are needed for establishing variations associated with neurological disorders.•Including African populations in neurogenomic studies would be instrumental for fine mapping. |
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ISSN: | 0888-7543 1089-8646 1089-8646 |
DOI: | 10.1016/j.ygeno.2017.07.009 |