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Neurogenomics: An opportunity to integrate neuroscience genomics and bioinformatics research in Africa

机译:神经基因组学:非洲整合神经科学基因组学和生物信息学研究的机会

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摘要

Modern genomic approaches have made enormous contributions to improving our understanding of the function, development and evolution of the nervous system, and the diversity within and between species. However, most of these research advances have been recorded in countries with advanced scientific resources and funding support systems. On the contrary, little is known about, for example, the possible interplay between different genes, non-coding elements and environmental factors in modulating neurological diseases among populations in low-income countries, including many African countries. The unique ancestry of African populations suggests that improved inclusion of these populations in neuroscience-related genomic studies would significantly help to identify novel factors that might shape the future of neuroscience research and neurological healthcare. This perspective is strongly supported by the recent identification that diseased individuals and their kindred from specific sub-Saharan African populations lack common neurological disease-associated genetic mutations. This indicates that there may be population-specific causes of neurological diseases, necessitating further investigations into the contribution of additional, presently-unknown genomic factors. Here, we discuss how the development of neurogenomics research in Africa would help to elucidate disease-related genomic variants, and also provide a good basis to develop more effective therapies. Furthermore, neurogenomics would harness African scientists' expertise in neuroscience, genomics and bioinformatics to extend our understanding of the neural basis of behaviour, development and evolution.
机译:现代基因组学方法为增进我们对神经系统的功能,发展和进化以及物种内和物种间多样性的理解做出了巨大贡献。但是,大多数研究进展已在拥有先进科学资源和资金支持系统的国家中记录。相反,人们对例如低收入国家(包括许多非洲国家)的人群中调节神经系统疾病的不同基因,非编码元件和环境因素之间可能存在的相互作用知之甚少。非洲人口的独特血统表明,将这些人口纳入神经科学研究相关的基因组研究中,将大大有助于确定可能塑造神经科学研究和神经医疗保健未来的新因素。最近发现,患病的个体及其来自撒哈拉以南非洲特定人群的血统缺乏与神经疾病相关的常见基因突变,这一观点得到了有力支持。这表明可能存在特定人群的神经系统疾病原因,因此有必要进一步研究其他目前未知的基因组因素的贡献。在这里,我们讨论了非洲神经基因组学研究的发展如何帮助阐明与疾病相关的基因组变异,并为开发更有效的疗法提供了良好的基础。此外,神经基因组学将利用非洲科学家在神经科学,基因组学和生物信息学方面的专业知识来扩展我们对行为,发展和进化的神经基础的理解。

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