{"id":757,"date":"2017-08-02T18:37:16","date_gmt":"2017-08-02T18:37:16","guid":{"rendered":"http:\/\/www.besthealthsciencedegree.com\/?page_id=757"},"modified":"2017-08-02T18:37:39","modified_gmt":"2017-08-02T18:37:39","slug":"what-is-genomics","status":"publish","type":"page","link":"http:\/\/www.besthealthsciencedegree.com\/faq\/what-is-genomics\/","title":{"rendered":"What Is Genomics"},"content":{"rendered":"

Genomics – an offshoot science of molecular biology – is a science that concerns itself principally with the genomes of various species. In addition to mapping genome structure, the study of genomics also involves studying potential evolutions of species genomes and how those genomes function in nature.<\/p>\n

A genome is a complete layout of a single organism or species’ DNA and genetic identity markers<\/a> – a complete picture of the raw material of that individual or group. Understanding the human genome – or the genome of any other species – helps us not only to understand that species’ ecological niche, but how to better treat conditions and diseases that begin at the cellular and genetic levels, such as cancer.<\/p>\n

Why It’s Important<\/h3>\n

The Human Genome Project completed its work of mapping the human genome, providing billions of terabytes of raw data to geneticists, hospitals, doctors and disease study and control centers. Biomedical centers and practitioners have utilized this data to advance studies in the management and treatment of genetically-linked diseases, such as cancer, hemophilia, sickle-cell anemia and many others.<\/p>\n