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Africa: Continent of genome contrasts with implications for biomedical research and health

Journal

FEBS LETTERS
Volume 586, Issue 18, Pages 2813-2819

Publisher

WILEY
DOI: 10.1016/j.febslet.2012.07.061

Keywords

African populations; Genetic variation; Genomics; Epigenetics; Health transition

Funding

  1. National Health Laboratory Service Research Trust
  2. South African National Research Foundation
  3. University of the Witwatersrand

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The genomic architecture of African populations is poorly understood and there is considerable variation between ethno-linguistic groups. Genome-wide approaches have been extensively applied to search for genetic associations to complex traits in Europeans, but rarely in Africans. This is largely attributed to lower levels of funding, poor infrastructure and public health systems, and to the small pool of trained scientists. High levels of genetic variation and underlying population structure in Africans present significant challenges, but lower levels of linkage disequilibrium provide an opportunity for more effective localisation of causal variants. High throughput technologies, including dense genotyping arrays, genome sequencing and epigenome studies, together with plummeting costs, are making research more affordable, even for African scientists. Understanding the interactions between genome structure and environmental influences is essential to interpreting their contributions to the increase in infectious diseases and non-communicable diseases, exacerbated by adverse environments and lifestyle choices. The unique genome dynamics in African populations have an important role to play in understanding human health and susceptibility to disease. (c) 2012 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.

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