Question: You determine that a particular gene in a peson with a genetic disease is the same size as that of a healthy individual. You suspect that the arises from a point mutation (a single nucleotide change that results in a defect in the protein.) Describe a how you could confirm this hypothesis.
Comment: We learned about Sanger Sequencing and Next Gen sequencing in class. Could you use either of these and if yes why would you use one over the other.
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