Genetic Analysis: An Integrated Approach (2nd Edition)
Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Chapter 18, Problem 29P

If you were to compare your genome sequence with that of your parents, how would it differ? If you were to compare your genome sequence with another student’s in the class, how would it differ? What additional differencemight you see if your genome was compared with that of asub-Saharan African, or if you are of sub-Saharan Africandescent, with that of a non-African?

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How much of the human genomesequence is functional, and why is theremainder retained?
A scientist investigating the genome of two related individuals observes a difference of a few nucleotides in one individual compared to the other. The nucleotide differences are in a region of noncoding DNA on chromosome 1. Would these differences be considered a mutation? Why or why not? Yes, the difference in nucleotide sequences between the individuals is a mutation because it will affect the phenotype of the two individuals. Yes, any heritable variation in the nucleotide sequence is considered a mutation, even if that variation is in a noncoding region of DNA. Not enough information was provided to determine if this nucleotide difference is a mutation because the effect on phenotype is unknown. No, the change in nucleotide sequence doesn't appear in a coding region of the DNA and so can't be a mutation.
What does the future hold for genomes?  How will they be different in 100, 1,000, 1 million, or 1 billion years? Make this a long discussion.

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Genetic Analysis: An Integrated Approach (2nd Edition)

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