Answer:
Explanation:
Sequencing the human genome is the function of the human genome project with the goal of determining the base pairs/order of DNA nucleotides that make up human genome, and also identifying and mapping all of the genes of the human genome both from the physical level and its functions in molecular medicine. The benefits in this field could allow for better diagnosis of disease, early detection of certain diseases, and gene therapy and control systems for drugs.
Inborn errors of metabolism are rare genetic (inherited) disorders where the body cannot properly digest and turn food into energy through the normal pathway. The disorders are usually caused by mutations in specific enzymes that help in the break down of these foods.
Through the study of the human genome, sequences involved in these mutations giving rise to these disorders are identified and mapped to their variuos locations. This can help in the early diagnosis of the disorders and effective control system for drugs and gene therapy against these disorders.
1.
C. Genus and species
Binominal nomenclature: a formal system of naming species of living things, such as humans which are <em>homo sapiens.</em>
2.
A. carbohydrates
any of a large group of organic compounds occurring in foods and living tissues and including sugars, starch, and cellulose.
3.
C. work with other cells
one unicellular organism would quickly die if was not within a colony of very similar unicellular organisms.
4.
C. Bacteria
bacteria are able to cause contagious diseases seeing as a virus, (which can be a contagious disease) is a form of bacteria.
By performing controlled experiment that are tested by gathering more data based on observations
