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The ends of chromosomes are called _________.


A) telomeres
B) centromeres
C) caps
D) DNA termini

E) C) and D)
F) A) and B)

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Traditionally,toxicology studies have involved numerous bioassays on rodents.However,a more reliable and reproducible approach to study the genome-wide effects of a toxin,one could use


A) a protein microarray.
B) functional genomics.
C) a yeast two-hybrid screen.
D) a DNA microarray.

E) A) and B)
F) A) and D)

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After years of work,a researcher identified a novel protein that binds to serotonin receptors in mouse brain.Which of the following explanations regarding gene patents is most appropriate in this case?


A) The researcher has clearly defined the function of the gene.The gene itself can be patented.
B) The researcher has not yet clearly defined the function of the gene.However,when the function is clearly identified,the gene itself can be patented.
C) The researcher has clearly defined the function of the gene.Thus,the use of the gene can be patented.
D) The researcher has not yet clearly defined the function of the gene.However,when the function is clearly identified,the use of the gene can be patenteD.

E) A) and D)
F) B) and C)

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As the director of a new non-profit functional genomics research center,it is your job to oversee the set up of laboratories necessary to achieve the research goals of the center.Therefore,you plan to include all of the following,except a


A) DNA microarray facility.
B) proteomics laB.
C) sequence annotation facility.
D) mutagenesis facility.

E) C) and D)
F) None of the above

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What is the most significant research finding from the rice genome project?


A) The similarity between the rice genome and other cereal crops will help scientists to move faster to develop genome data for other cereal crops.
B) The rice genome was found to be larger than that of humans.
C) The development of Golden Rice.
D) The genome data can be used to develop more nutritional rice.

E) B) and D)
F) None of the above

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Non-coding DNA regions within a gene are referred to as


A) introns.
B) exons.
C) templates.
D) transposons.
E) pseudogenes.

F) None of the above
G) All of the above

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Some regions of chromosomes remain highly condensed,tightly coiled,and untranscribed throughout the cell cycle.These regions are referred called


A) transposable elements.
B) single sequence repeats.
C) non-coding DNA.
D) short interspersed elements.
E) constitutive heterchromatin.

F) B) and E)
G) D) and E)

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As a scientist working for an antibioterrorism task force,you are asked to evaluate some biological samples for presence of Yersinia pestis,the organism that causes plague.After confirming that the samples did,indeed,contain Y.pestis,you instruct your team to begin sequencing the strain.Given that the genome sequence of Y.pestis is already known,why did you instruct your team to sequence this strain?


A) to confirm the original genome sequence and gather possible information on the origin of the strain
B) to establish the course of infection and determine whether the strain has been genetically engineered
C) to gather possible information on the origin of the strain and determine whether the strain has been genetically engineered
D) to establish the SNPs necessary to confirm infection from this strain

E) A) and D)
F) A) and C)

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All of the following would be useful in an effort to construct a physical map of a genome except


A) BAC end sequences.
B) BLAST data.
C) ESTs.
D) STS markers.

E) B) and D)
F) C) and D)

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________ are silent copies of genes that have been inactivated by mutations.


A) Pseudogenes
B) Clones
C) Exons
D) Introns

E) A) and B)
F) B) and C)

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To be classed as a polymorphism,a SNP must be present in


A) every draft sequence of the species being investigated.
B) every finished sequence of the species being investigated.
C) at least one genome of the species being investigated.
D) at least 1% of the population of the species being investigateD.

E) None of the above
F) All of the above

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Sequences of DNA assembled by identifying overlaps among smaller DNA segments are known as


A) single strand polymorphisms.
B) synteny.
C) draft sequences.
D) proteone.
E) contig.

F) A) and D)
G) C) and D)

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Mobile bits of DNA that can jump from one location on a chromosome to another location are called


A) simple sequence repeats.
B) transposons.
C) exons.
D) introns.
E) pseudogenes.

F) B) and D)
G) A) and D)

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Inactive genes that have lost their function due to mutations are called


A) introns.
B) exons.
C) templates.
D) transposons.
E) pseudogenes.

F) C) and D)
G) B) and D)

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Which of the following statements regarding genomes is true?


A) In general,eukaryotic genomes are larger than prokaryotic genomes.
B) In general,eukaryotic genomes are smaller than prokaryotic genomes.
C) The size of the organism determines the size of the genome.
D) Larger and more complex organisms have more genes than smaller,less complex organisms.

E) None of the above
F) A) and D)

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_________ is another term used to describe genome science.


A) Genomics
B) Proteomics
C) Chromosomics
D) Dianetics

E) B) and D)
F) A) and B)

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A transgene is


A) hard to destroy once inserted into a genome.
B) hard to study because of its transposons.
C) created by several of the DNA motifs.
D) an inserted foreign gene.
E) a result of endosymbiosis.

F) None of the above
G) C) and E)

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Which of the following organisms has the greatest number of genes?


A) rice
B) human
C) fruit fly
D) yeast

E) A) and D)
F) B) and D)

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You can do all of the following using comparative genomics except


A) draw particular conclusions about species.
B) draw general conclusions about evolution.
C) infer function about an unsequenced genome using synteny.
D) develop a haplotype map.

E) A) and C)
F) None of the above

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Homologous regions of DNA can vary slightly in base-pair composition among individuals in a population.When a homologous stretch of DNA is cut with restriction enzymes in different individuals,fragments of different lengths are produced.These fragments are called


A) landmarks of DNA sequencing.
B) contig fragments.
C) single length polymorphisms.
D) restriction fragments length polymorphisms.
E) sequence-tagged site fragments.

F) B) and C)
G) All of the above

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