Exam 18: Recombinant DNA Technology
Exam 1: Genetics of Bacteria and Bacteriophages42 Questions
Exam 2: Variations in Chromosome Structure and Number43 Questions
Exam 3: Advanced Gene Mapping in Eukaryotes44 Questions
Exam 4: Gene Mapping in Eukaryotes41 Questions
Exam 5: Quantitative Genetics43 Questions
Exam 6: Extensions of Mendelian Genetic Principles41 Questions
Exam 7: Chromosomal Basis of Inheritance43 Questions
Exam 8: Molecular Evolution43 Questions
Exam 9: Population Genetics41 Questions
Exam 10: Non-Mendelian Inheritance43 Questions
Exam 11: Genetics of Cancer44 Questions
Exam 12: Genetic Analysis of Development42 Questions
Exam 13: Regulation of Gene Expression in Eukaryotes43 Questions
Exam 14: Mendelian Genetics43 Questions
Exam 15: Regulation of Gene Expression in Bacteria and Bacteriophages42 Questions
Exam 16: Genomics43 Questions
Exam 17: Applications of Recombinant DNA Technology44 Questions
Exam 18: Recombinant DNA Technology43 Questions
Exam 19: DNA Mutation, DNA Repair, and Transposable Elements43 Questions
Exam 20: Gene Expression: Translation33 Questions
Exam 21: Gene Expression: Transcription43 Questions
Exam 22: Gene Control of Proteins43 Questions
Exam 23: DNA Replication44 Questions
Exam 24: DNA: The Genetic Material43 Questions
Exam 25: Genetics: an Introduction41 Questions
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Genetic distances associated with genetic maps are generally obtained
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Announcement of the first draft sequence of the complete human genome was a monumental moment in the history of genetics. This announcement was made
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Sequencing involves PCR reactions using Taq polymerase, which we learned in the previous chapter can introduce errors because it lacks a mismatch repair mechanism. What precaution can be taken in genomic sequencing projects, or other sequencing projects, to minimize the possibility of erroneous sequence?
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Genome analysis has confirmed findings based on DNA sequences of single genes that prokaryotes are divided into two great lineages: the eubacteria and archaea. The latter may be more closely related to the Eukarya. Recount the lines of evidence these statements are based on.
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Explain the basic differences in goal and approach of functional, structural, and comparative genomics.
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Clone contigs are a set of contiguous, partially overlapping sequences that collectively cover a whole chromosome or chromosome region without gaps.
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Highly variable (polymorphic) short tandem repeats are considered the best kind of markers for constructing sequence tagged site (STS) maps. Why?
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The first eukaryote to have its genome completely sequenced is a fungus.
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"Knock-out" mutants involve eliminating gene activity, a useful strategy to see what effect the gene has in physiology, development, etc.
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A key issue being considered by the bioethics program ELSI is
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In a sequenced genome, candidate protein-encoding genes are identified by searching for
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In a clone-contig mapping experiment, four clones were obtained with the following STS markers: Clone 1: O P G E Clone 2: A C D M Clone 3: X O P Clone 4: D M N X O The order of the markers in this part of the genome is:
(Multiple Choice)
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Genome projects are usually justified by scientists to the public on the basis of providing knowledge of (and potential cures for) human disease. Do you think this argument is necessary? Do genome projects have to be justified in terms of curing human disease? Is the promise too ambitious?
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Which type of cloning vector is commonly used in the construction of contig maps?
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