Overview of the human genome

dc.contributor.authorOyelade, Jelili
dc.contributor.authorIsewon, Itunuoluwa
dc.contributor.authorOgunlana, Olubanke
dc.contributor.authorworunse, Oluwadurotimi A
dc.contributor.authorOyesola, Olusola
dc.contributor.authorAromolaran, Olufemi
dc.contributor.authorDokumu, Titilope
dc.contributor.author\uwagun, Ibitayo Adem
dc.contributor.authorIheagwam, Franklyn
dc.contributor.authorBabatunde, Eunice
dc.contributor.authorDania, Omoremime Elizabeth
dc.contributor.authorObembe, Olawole
dc.date.accessioned2026-03-03T12:49:20Z
dc.date.issued2025
dc.description.abstractThe human genome is composed of deoxyribonucleic acid (DNA) organized into 23 pairs of chromosomes in the nucleus of human cells, as well as the small DNA found inside individual mitochondria. Complete sequencing of the 3 billion base pairs that make up the human genome has made available a deluge of information that has enhanced our understanding of evolution, physiology, causality of disease, and association between heredity and environment in humans. This chapter discusses discoveries in genetics that spawned the field of human genomics. It further highlights the role of human genome in disease susceptibility, as well as its prospects for the future of healthcare.
dc.identifier.issnhttps://doi.org/10.1016/B978-0-12-817819-5.00002-4Get rights and content
dc.identifier.urihttps://repository.covenantuniversity.edu.ng/handle/123456789/50645
dc.language.isoen
dc.publisherTranslational and Applied Genomics
dc.titleOverview of the human genome
dc.title.alternativeGenome Plasticity in Health and Disease -Book
dc.typeBook chapter

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