Genomic Interventions in Medicine.

Bioinform Biol Insights

Department of Biological Sciences, Covenant University, Ota, Nigeria.

Published: December 2018

AI Article Synopsis

  • Genomics is a rapidly advancing field focusing on the study of the human genome, which holds vital information about our origins, evolution, and health.
  • The Human Genome Project, started in 1990 and completed in 2003, aimed to sequence the 3 billion nucleotide base pairs in the human DNA, leading to significant breakthroughs in clinical applications.
  • The review discusses key discoveries that led to the HGP, its impact on clinical practice, challenges in implementing genomic medicine, especially in Africa, and potential solutions to these issues.

Article Abstract

Lately, the term "genomics" has become ubiquitous in many scientific articles. It is a rapidly growing aspect of the biomedical sciences that studies the genome. The human genome contains a torrent of information that gives clues about human origin, evolution, biological function, and diseases. In a bid to demystify the workings of the genome, the Human Genome Project (HGP) was initiated in 1990, with the chief goal of sequencing the approximately 3 billion nucleotide base pairs of the human DNA. Since its completion in 2003, the HGP has opened new avenues for the application of genomics in clinical practice. This review attempts to overview some milestone discoveries that paved way for the initiation of the HGP, remarkable revelations from the HGP, and how genomics is influencing a paradigm shift in routine clinical practice. It further highlights the challenges facing the implementation of genomic medicine, particularly in Africa. Possible solutions are also discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287307PMC
http://dx.doi.org/10.1177/1177932218816100DOI Listing

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