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Ch. 15 - Recombinant DNA Technology and Its Applications
Chapter 15, Problem 5

Explain the meaning of 'identity by descent' in the context of identifying genealogical relationship between individuals. In these analyses, why are segments of chromosomes (haplotypes) rather than individual STRs used to identify genetic relationships?

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Understand that 'identity by descent' (IBD) refers to segments of DNA that are inherited from a common ancestor without recombination.
Recognize that IBD segments are used to identify genealogical relationships because they provide evidence of shared ancestry.
Consider that haplotypes, which are groups of genes inherited together from a single parent, are more informative than individual short tandem repeats (STRs) because they cover larger segments of the genome.
Acknowledge that using haplotypes allows for the detection of longer stretches of shared DNA, increasing the accuracy of identifying genetic relationships.
Realize that haplotypes can reveal more about the genetic history and relatedness of individuals, as they are less likely to be broken up by recombination compared to individual STRs.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Identity by Descent (IBD)

Identity by descent refers to the genetic relationship between individuals who inherit the same segment of DNA from a common ancestor. This concept is crucial in genealogical studies as it helps determine how closely related two individuals are based on shared genetic material. IBD segments can indicate familial connections and are essential for understanding inheritance patterns in populations.
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Haplotypes

A haplotype is a group of genes or DNA variations that are inherited together from a single parent. In genetic analyses, haplotypes are preferred over individual Short Tandem Repeats (STRs) because they provide a more comprehensive view of genetic relationships. By examining larger segments of chromosomes, researchers can better identify shared ancestry and the extent of genetic similarity between individuals.

Chromosomal Segments vs. STRs

Using segments of chromosomes, or haplotypes, rather than individual STRs allows for a more accurate assessment of genetic relationships. STRs can vary significantly among individuals and may not reflect shared ancestry effectively. In contrast, haplotypes encompass multiple genetic markers, providing a clearer picture of lineage and enhancing the reliability of genealogical analyses.
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Segmentation Genes
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Textbook Question

What is the statistical principle underlying genetic health risk assessment? Why are these assessments not predictive of disease occurrence?

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Textbook Question
You have constructed four different libraries: a genomic library made from DNA isolated from human brain tissue, a genomic library made from DNA isolated from human muscle tissue, a human brain cDNA library, and a human muscle cDNA library. Which of these would have the greatest diversity of sequences?
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Textbook Question
You have constructed four different libraries: a genomic library made from DNA isolated from human brain tissue, a genomic library made from DNA isolated from human muscle tissue, a human brain cDNA library, and a human muscle cDNA library. Would the sequences contained in each library be expected to overlap completely, partially, or not at all with the sequences present in each of the other libraries?
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Textbook Question
Using the genomic libraries in Problem 4, you wish to clone the human gene encoding myostatin, which is expressed only in muscle cells. Assuming the human genome is 3x10⁹ and that the average insert size in the genomic libraries is 100 kb, how frequently will a clone representing myostatin be found in the genomic library made from muscle?
218
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Textbook Question
Using the genomic libraries in Problem 4, you wish to clone the human gene encoding myostatin, which is expressed only in muscle cells. How frequently will a clone representing myostatin be found in the genomic library made from brain?
212
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Textbook Question
Using the genomic libraries in Problem 4, you wish to clone the human gene encoding myostatin, which is expressed only in muscle cells. How frequently will a clone representing myostatin be found in the cDNA library made from muscle?
272
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