Genomic Interventions in Medicine. Issue 12 (November 2018)

• Record Type: Journal Article
• Authors: Aworunse, Oluwadurotimi S; Adeniji, Oluwatomiwa; Oyesola, Olusola L; Isewon, Itunuoluwa; Oyelade, Jelili; Obembe, Olawole O
• Is Part Of: Bioinformatics and biology insights. Volume 2018:Issue 12(2018)
• Publication Date: 2018-11
• Subjects: Genomics -- Human Genome Project -- pharmacogenomics -- personalized medicine -- gene therapy -- diagnosis; Bioinformatics -- Periodicals; Biology -- Data processing -- Periodicals; 570.285
• DOI: 10.1177/1177932218816100
• Languages: English
• ISSNs: 1177-9322

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.