1. If a consumer version of the gene database was created, what additional features would it need to be user-friendly?
2. Do either of your diseases in part A (sickle cell anemia and down syndrome) have the same pattern of inheritance as the model of the colorblindness mutation? How do you know?
3. Do you think the genetic disorders you identified in part A or B (sickle cell anemia and down syndrome) would appear in a person’s DNA fingerprinting profile? Explain your reasoning.
4. In part A, you analyzed genes that contribute to two diseases (sickle cell anemia and down syndrome). How can scientists use this information to develop new treatments for these diseases? Based on your findings, do you think that scientists will need to develop multiple treatments to control symptoms of these diseases? Explain your reasoning.
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Ответ:
1) no harmful substances that will harm user, and no personal key information to other people
2)Sickle-cell anemia is caused by a point mutation in the β-globin chain of hemoglobin, causing the hydrophilic amino acid glutamic acid to be replaced with the hydrophobic amino acid valine at the sixth position. The β-globin gene is found on the short arm of chromosome 11
3) yes so it will help the user know what they have
4 unsure
Explanation:
Ответ:
I really don’t know you would have to actually break down the problem
Explanation:
Ответ:
antibodies to a disease bacterium
Explanation: