Exam 9: Functional and Comparative Genomics

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The genome of cancer cells tends to become unstable.

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Why is the Taq DNA polymerase well-suited for PCR?

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If you are setting up a PCR reaction,how much extension time per cycle should you allocate for the Taq DNA polymerase to amplify a 5-kb DNA fragment from a 10-kb template?

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A genomic region can rapidly become very common in a population due to

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RNA interference functions by

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Which of the following is not used in PCR amplification of DNA?

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Which of the following does not occur during PCR?

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The human-accelerated region 1 (HAR-1)gene

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What are the different methods by which we can assign function to particular genes?

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How can we explain the fact that the human genome contains far fewer genes than was predicted would be necessary for our survival?

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Sequence similarity between genes plays an important role in assigning gene function.

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Why are BLAST comparisons based on protein sequences often easier to interpret than those based on DNA sequences?

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Pharmacogenomics is the study of how

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The drug ________ is added to mouse cell cultures to select against transformants that do not have the desired gene knockout.

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Please select the best match for each term.
HAR-1
Fluorescent dye
shRNA
Small noncoding human RNA
Transgene
Artificially introduced DNA
Correct Answer:
Verified
Premises:
Responses:
HAR-1
Fluorescent dye
shRNA
Small noncoding human RNA
Transgene
Artificially introduced DNA
Cy5
Searches for sequence matches
BLAST
Transcript that has a stem and loop
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What does a large haplotype block suggest about a genomic region?

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Imagine that you are using random PCR primers to amplify fragments of DNA.Would you expect to get more amplification products if you set the PCR machine at a higher or lower annealing temperature and why?

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Why are the number of proteins in the eukaryotic proteome so much greater than the number of eukaryotic genes?

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The transcriptome is the complete set of polypeptides produced by an organism.

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After how many PCR cycles,starting from a single starting molecule,will fragments consisting of only the target DNA (the DNA between the primers)be generated?

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