Deck 18: Genomics

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Question
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.
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Question
All of the RNA present in a cell or tissue at a specific time is called the

A)proteome.
B)spliceosome.
C)nucleosome.
D)RNA motif.
E)transcriptomE.
Question
Long interspersed elements (LINES)are a type of

A)pseudogene.
B)proteone.
C)exon.
D)intron.
E)transposon.
Question
______ maps are generated using actual landmarks within DNA sequences.

A)Genetic
B)DNA
C)Physical
D)Chromosomal
Question
Chloroplasts can replicate independently because

A)of synteny.
B)it has its own genome.
C)of its repetitive DNA sequences.
D)of its ability to use restriction enzymes.
E)it has several contigs.
Question
The sequence 5' CGGCGGCGGCGGCGGCGGCGGCGGCGGCGG 3' represents a ______________.

A)fragment
B)complex sequence
C)molecule of mRNA
D)simple sequence repeat
Question
Mitochondria and chloroplasts are bacterial relatives living within eukaryotes as a result of

A)synteny.
B)exosymbiosis.
C)endosymbiosis.
D)draft sequencing of the proteomes of the mitochondria and chloroplasts by the nucleosome.
E)contiguous base pairing.
Question
A genome sequence with minimal gaps,with the sequences in the correct order,and having no more that 1% error in 10,000 nucleotides would be considered a

A)PCR sequence.
B)draft sequence.
C)finished sequence.
D)shotgun sequence.
E)clone by clone sequencE.
Question
Conserved arrangements of segments of DNA in related genomes are referred to as

A)synteny.
B)homology.
C)analogous DNA.
D)a contig.
E)a comparative genomE.
Question
Distances on a genetic map are measured in _____ units.

A)centromere
B)DNA
C)dalton
D)centimorgan
Question
Following transcription of eukaryotic genes,introns are removed and exons are spliced together.This process is referred to as______.

A)translation
B)splicing
C)mRNA modification
D)coupling
Question
The ends of chromosomes are called _________.

A)telomeres
B)centromeres
C)caps
D)DNA termini
Question
Draft sequences have

A)many gaps in regions of highly repetitive DNA.
B)less than 1 error in 10,000 nucleotides.
C)been found in various proteomes across the eukaryote life forms.
D)been produced by alternative splicing.
E)several problems,the main one being their contiguous DNA fragments.
Question
_________ is another term used to describe genome science.

A)Genomics
B)Proteomics
C)Chromosomics
D)Dianetics
Question
A _____ consists of all of the DNA in a nucleus of a cell.

A)genome
B)chromosome
C)gene
D)protein
Question
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.
Question
A human gene is composed of numerous fragments of protein-encoding information known as ______.

A)DNA
B)mRNA
C)exons
D)introns
Question
________ are silent copies of genes that have been inactivated by mutations.

A)Pseudogenes
B)Clones
C)Exons
D)Introns
Question
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.
Question
______ maps show the relative location of genes on a chromosome as determined by recombination frequencies.

A)DNA
B)Genetic
C)Chromosomal
D)Physical
Question
Microarrays are created by

A)robotically placing DNA on to a microscope slide and probing with RNA from the tissue of interest.
B)robotically placing DNA on to a microscope slide and probing with another DNA from the tissue of interest.
C)robotically placing DNA on to a microscope slide and probing with SNPs from the tissue of interest.
D)robotically placing DNA on to a microscope slide and probing with STSs from the tissue of interest.
E)clone by clone sequencing.
Question
Groups of related,but distinctly different,genes that appear to have arisen from a single ancestral gene are referred to as

A)segmental duplications.
B)pseudogenes.
C)tandem clusters.
D)multigene families.
E)expressed sequences.
Question
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.
Question
The sequencing method that cuts the DNA of an entire chromosome into small fragments and then clones these fragments is called

A)shotgun sequencing.
B)clone by clone sequencing.
C)RFLP sequencing.
D)consensus sequencing.
Question
Non-coding DNA regions within a gene are referred to as

A)introns.
B)exons.
C)templates.
D)transposons.
E)pseudogenes.
Question
The majority of DNA in a human is

A)composed of short interspersed elements.
B)non-coding.
C)simple sequence repeats.
D)segmental duplications.
E)structural.
Question
Inactive genes that have lost their function due to mutations are called

A)introns.
B)exons.
C)templates.
D)transposons.
E)pseudogenes.
Question
Linkage disequilibrium is

A)the tendency of genes to be totally randomized during meiosis.
B)the tendency of genes not to be randomized during meiosis.
C)the tendency of genes of single nucleotides polymorphisms to be rearranged during meiosis because of crossing over.
D)the tendency of genes to link together within certain blocks along the chromosome.
E)the tendency of contigs being so randomized that mapping becomes an issue for gene sequencing.
Question
Identical copies of genes that can be transcribed simultaneously are called

A)segmental duplications.
B)pseudogenes.
C)tandem clusters.
D)multigene families.
E)expressed sequences.
Question
Rice and its grain relatives,maize,barley,and wheat,diverged from a common ancestor 50 million years ago,however the chromosomes of these plants demonstrate extensive conserved arrangements of segments.This phenomenon is called

A)a linkage disequilibrium.
B)a single nucleotide polymorphisms.
C)a contig.
D)synteny.
E)expressed sequence equilibrium.
Question
The majority (45%)of the human genome is composed of

A)introns.
B)exons.
C)templates.
D)transposons.
E)pseudogenes.
Question
Your research project involves the characterization of a novel protein.To learn more about its function you perform a yeast two-hybrid screen to identify potential interacting proteins.In your first screening attempt,you isolate one clone.You send the clone to be sequenced at the local sequencing facility.After translating the sequencing data,what should you do to (i)find out what type of protein this clone encodes,and (ii)get an idea about its possible function?

A)Run a blast search.
B)Identify the intron/exon organization.
C)Localize the gene to a specific chromosomal region.
D)Search the human genome sequence for your clone.
Question
Recombination frequency between genes can used to generate a

A)genetic map.
B)physical map.
C)restriction map.
D)haplotype map.
Question
To avoid confusion,and to allow ease of data interruption,researchers working on cloned DNA from the same species use

A)restriction fragment length polymorphisms.
B)shotgun sequencing.
C)sequenced-tagged sites.
D)clone by clone sequencing.
E)consensus sequencing.
Question
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.
Question
A private company has been hired by the parliament of ______ to create a data base from pooled medical,genetic,and genealogical information.

A)Nova Scotia
B)Iceland
C)Gibraltar
D)Portugal
E)Galapagos
Question
The sequencing method that cuts DNA segments into fragments,arranges those fragments based on overlapping nucleotide sequences,and then clones these fragments is called

A)shotgun sequencing.
B)clone by clone sequencing.
C)RFLP sequencing.
D)consensus sequencing.
Question
A transgene is an

A)inserted exon.
B)inserted intron.
C)inserted nucleosome.
D)inserted foreign gene.
E)inserted transcriptomE.
Question
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.
Question
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.
Question
In vertebrates,the family of myogenic regulatory factors (MFRs)plays a major role in muscle development.This family consists of four related genes,including MyoD,MRF4,myogenin,and myf5,each of which have distinct,but overlapping functions.Interestingly,this gene family is represented by only a single gene called nautilus in Drosophila.You want to determine if nautilus functions as the sum of the vertebrate factors,or rather,if it functions in a manner similar to that of one particular gene.Eventually,you plan to examine the loss-of-function phenotype of nautilus mutants.However,first you should

A)compare the DNA and protein sequences of all the genes to determine if nautilus is more closely related to one MRF than another.
B)perform a DNA microarray to compare gene activation patterns between nautilus and the MRFs.
C)compare the proteome of a cell expressing nautilus to the proteomes of cells expressing each of the MRFs in turn.
D)generate four transgenic Drosophila strains that express the MRFs.
Question
Which of the following techniques can be used to detect chromosomal abnormalities?

A)EST
B)FISH
C)STS
D)SNP
Question
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.
Question
Why do segmental duplications pose a logistical challenge in the proper alignment of DNA sequences?

A)Segmental duplications are inherently repetitive.
B)Segmental duplications contain large numbers of LINEs,which interfere with sequence annotation.
C)Segmental duplications interfere with BLAST analysis.
D)Segmental duplications are often found in areas of constitutive heterochromatin.
Question
Your research group has recently determined the complete genomic sequence of the organism Examus biologisium.You instruct your group to begin sequence annotation,which involves

A)shotgun cloning.
B)the alignment of contigs.
C)the identification of open reading frames.
D)the construction of a genetic map.
Question
How is the study of genomics expected to influence future health care?

A)The study of genomics is expected to provide insight into the relationship between genes and the environment,and why certain people get sick while others remain healthy.It should enable us to learn more about the causes and effects of various diseases,illnesses,and infections.Such information will help us to identify ways to improve health care and prevent disease.
B)The study of genomics will allow us to treat,with the use of genetic engineering,various diseases of genetic origin.It is just a matter of time before we are able to treat all diseases of genetic origin with this technique.
C)The study of genomics will allow us to use bacteria and viruses to create vaccinations for virually all diseases of genetic origin.
Question
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
Question
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.
Question
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.
Question
In the early 1980s,a number of clones encoding highly-related forms of actin were isolated from a human cDNA library.Given the information that (i)the restriction enzyme maps of the coding regions were dissimilar,and (ii)each clone contained sufficient coding region to encode all or most of an entire actin gene,you would conclude that

A)multiple actin genes arose as a result of a segmental duplication.
B)the various forms of actin are a result of alternative splicing.
C)actin proteins are encoded by genes found in a tandem cluster.
D)actin proteins are encoded by a multigene family.
Question
Given an ideal sequencing reaction of approximately 500 successive nucleotides (excluding overlap),how many sequencing reactions would be needed to determine the complete human genome?

A)3.2 billion
B)12.5 million
C)12.8 million
D)6.4 million
Question
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.
Question
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.
Question
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.
Question
A catalog of common genetic variants that occur in humans is called a

A)haplotype map.
B)restriction map.
C)genomic map.
D)SNP map.
Question
Which of the following statements regarding pseudogenes is false?

A)Pseudogenes may have some gene-like features such as a promoter and splice sites.
B)Pseudogenes encode proteins,but the translated proteins are non-functional.
C)Pseudogenes can provide insight into the evolutionary history of the related functional gene.
D)Every pseudogene has a similar DNA sequence to some functional gene.
Question
Which of the following organisms has the largest genome?

A)rice
B)human
C)fruit fly
D)yeast
Question
Which of the following organisms has the greatest number of genes?

A)rice
B)human
C)fruit fly
D)yeast
Question
A pharmaceutical company is trying to develop a new drug to help combat a rare disease.To facilitate the identification of new drug targets,they could

A)search the sequenced human genome for mutations involved in the development of the disease,and design drugs that bind to the mutated proteins.
B)employ protein microarray technology to evaluate the binding of drugs to various proteins.
C)test new drugs in transgenic organisms that display disease characteristics.
D)use antibodies to screen a DNA microarray.
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Deck 18: Genomics
1
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.
E
2
All of the RNA present in a cell or tissue at a specific time is called the

A)proteome.
B)spliceosome.
C)nucleosome.
D)RNA motif.
E)transcriptomE.
E
3
Long interspersed elements (LINES)are a type of

A)pseudogene.
B)proteone.
C)exon.
D)intron.
E)transposon.
E
4
______ maps are generated using actual landmarks within DNA sequences.

A)Genetic
B)DNA
C)Physical
D)Chromosomal
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
5
Chloroplasts can replicate independently because

A)of synteny.
B)it has its own genome.
C)of its repetitive DNA sequences.
D)of its ability to use restriction enzymes.
E)it has several contigs.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
6
The sequence 5' CGGCGGCGGCGGCGGCGGCGGCGGCGGCGG 3' represents a ______________.

A)fragment
B)complex sequence
C)molecule of mRNA
D)simple sequence repeat
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
7
Mitochondria and chloroplasts are bacterial relatives living within eukaryotes as a result of

A)synteny.
B)exosymbiosis.
C)endosymbiosis.
D)draft sequencing of the proteomes of the mitochondria and chloroplasts by the nucleosome.
E)contiguous base pairing.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
8
A genome sequence with minimal gaps,with the sequences in the correct order,and having no more that 1% error in 10,000 nucleotides would be considered a

A)PCR sequence.
B)draft sequence.
C)finished sequence.
D)shotgun sequence.
E)clone by clone sequencE.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
9
Conserved arrangements of segments of DNA in related genomes are referred to as

A)synteny.
B)homology.
C)analogous DNA.
D)a contig.
E)a comparative genomE.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
10
Distances on a genetic map are measured in _____ units.

A)centromere
B)DNA
C)dalton
D)centimorgan
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
11
Following transcription of eukaryotic genes,introns are removed and exons are spliced together.This process is referred to as______.

A)translation
B)splicing
C)mRNA modification
D)coupling
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
12
The ends of chromosomes are called _________.

A)telomeres
B)centromeres
C)caps
D)DNA termini
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
13
Draft sequences have

A)many gaps in regions of highly repetitive DNA.
B)less than 1 error in 10,000 nucleotides.
C)been found in various proteomes across the eukaryote life forms.
D)been produced by alternative splicing.
E)several problems,the main one being their contiguous DNA fragments.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
14
_________ is another term used to describe genome science.

A)Genomics
B)Proteomics
C)Chromosomics
D)Dianetics
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
15
A _____ consists of all of the DNA in a nucleus of a cell.

A)genome
B)chromosome
C)gene
D)protein
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Unlock Deck
k this deck
16
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.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
17
A human gene is composed of numerous fragments of protein-encoding information known as ______.

A)DNA
B)mRNA
C)exons
D)introns
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Unlock Deck
k this deck
18
________ are silent copies of genes that have been inactivated by mutations.

A)Pseudogenes
B)Clones
C)Exons
D)Introns
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Unlock Deck
k this deck
19
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.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
20
______ maps show the relative location of genes on a chromosome as determined by recombination frequencies.

A)DNA
B)Genetic
C)Chromosomal
D)Physical
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
21
Microarrays are created by

A)robotically placing DNA on to a microscope slide and probing with RNA from the tissue of interest.
B)robotically placing DNA on to a microscope slide and probing with another DNA from the tissue of interest.
C)robotically placing DNA on to a microscope slide and probing with SNPs from the tissue of interest.
D)robotically placing DNA on to a microscope slide and probing with STSs from the tissue of interest.
E)clone by clone sequencing.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
22
Groups of related,but distinctly different,genes that appear to have arisen from a single ancestral gene are referred to as

A)segmental duplications.
B)pseudogenes.
C)tandem clusters.
D)multigene families.
E)expressed sequences.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
23
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.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
24
The sequencing method that cuts the DNA of an entire chromosome into small fragments and then clones these fragments is called

A)shotgun sequencing.
B)clone by clone sequencing.
C)RFLP sequencing.
D)consensus sequencing.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
25
Non-coding DNA regions within a gene are referred to as

A)introns.
B)exons.
C)templates.
D)transposons.
E)pseudogenes.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
26
The majority of DNA in a human is

A)composed of short interspersed elements.
B)non-coding.
C)simple sequence repeats.
D)segmental duplications.
E)structural.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
27
Inactive genes that have lost their function due to mutations are called

A)introns.
B)exons.
C)templates.
D)transposons.
E)pseudogenes.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
28
Linkage disequilibrium is

A)the tendency of genes to be totally randomized during meiosis.
B)the tendency of genes not to be randomized during meiosis.
C)the tendency of genes of single nucleotides polymorphisms to be rearranged during meiosis because of crossing over.
D)the tendency of genes to link together within certain blocks along the chromosome.
E)the tendency of contigs being so randomized that mapping becomes an issue for gene sequencing.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
29
Identical copies of genes that can be transcribed simultaneously are called

A)segmental duplications.
B)pseudogenes.
C)tandem clusters.
D)multigene families.
E)expressed sequences.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
30
Rice and its grain relatives,maize,barley,and wheat,diverged from a common ancestor 50 million years ago,however the chromosomes of these plants demonstrate extensive conserved arrangements of segments.This phenomenon is called

A)a linkage disequilibrium.
B)a single nucleotide polymorphisms.
C)a contig.
D)synteny.
E)expressed sequence equilibrium.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
31
The majority (45%)of the human genome is composed of

A)introns.
B)exons.
C)templates.
D)transposons.
E)pseudogenes.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
32
Your research project involves the characterization of a novel protein.To learn more about its function you perform a yeast two-hybrid screen to identify potential interacting proteins.In your first screening attempt,you isolate one clone.You send the clone to be sequenced at the local sequencing facility.After translating the sequencing data,what should you do to (i)find out what type of protein this clone encodes,and (ii)get an idea about its possible function?

A)Run a blast search.
B)Identify the intron/exon organization.
C)Localize the gene to a specific chromosomal region.
D)Search the human genome sequence for your clone.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
33
Recombination frequency between genes can used to generate a

A)genetic map.
B)physical map.
C)restriction map.
D)haplotype map.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
34
To avoid confusion,and to allow ease of data interruption,researchers working on cloned DNA from the same species use

A)restriction fragment length polymorphisms.
B)shotgun sequencing.
C)sequenced-tagged sites.
D)clone by clone sequencing.
E)consensus sequencing.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
35
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.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
36
A private company has been hired by the parliament of ______ to create a data base from pooled medical,genetic,and genealogical information.

A)Nova Scotia
B)Iceland
C)Gibraltar
D)Portugal
E)Galapagos
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
37
The sequencing method that cuts DNA segments into fragments,arranges those fragments based on overlapping nucleotide sequences,and then clones these fragments is called

A)shotgun sequencing.
B)clone by clone sequencing.
C)RFLP sequencing.
D)consensus sequencing.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
38
A transgene is an

A)inserted exon.
B)inserted intron.
C)inserted nucleosome.
D)inserted foreign gene.
E)inserted transcriptomE.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
k this deck
39
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.
Unlock Deck
Unlock for access to all 59 flashcards in this deck.
Unlock Deck
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40
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.
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41
In vertebrates,the family of myogenic regulatory factors (MFRs)plays a major role in muscle development.This family consists of four related genes,including MyoD,MRF4,myogenin,and myf5,each of which have distinct,but overlapping functions.Interestingly,this gene family is represented by only a single gene called nautilus in Drosophila.You want to determine if nautilus functions as the sum of the vertebrate factors,or rather,if it functions in a manner similar to that of one particular gene.Eventually,you plan to examine the loss-of-function phenotype of nautilus mutants.However,first you should

A)compare the DNA and protein sequences of all the genes to determine if nautilus is more closely related to one MRF than another.
B)perform a DNA microarray to compare gene activation patterns between nautilus and the MRFs.
C)compare the proteome of a cell expressing nautilus to the proteomes of cells expressing each of the MRFs in turn.
D)generate four transgenic Drosophila strains that express the MRFs.
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42
Which of the following techniques can be used to detect chromosomal abnormalities?

A)EST
B)FISH
C)STS
D)SNP
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43
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.
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44
Why do segmental duplications pose a logistical challenge in the proper alignment of DNA sequences?

A)Segmental duplications are inherently repetitive.
B)Segmental duplications contain large numbers of LINEs,which interfere with sequence annotation.
C)Segmental duplications interfere with BLAST analysis.
D)Segmental duplications are often found in areas of constitutive heterochromatin.
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45
Your research group has recently determined the complete genomic sequence of the organism Examus biologisium.You instruct your group to begin sequence annotation,which involves

A)shotgun cloning.
B)the alignment of contigs.
C)the identification of open reading frames.
D)the construction of a genetic map.
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46
How is the study of genomics expected to influence future health care?

A)The study of genomics is expected to provide insight into the relationship between genes and the environment,and why certain people get sick while others remain healthy.It should enable us to learn more about the causes and effects of various diseases,illnesses,and infections.Such information will help us to identify ways to improve health care and prevent disease.
B)The study of genomics will allow us to treat,with the use of genetic engineering,various diseases of genetic origin.It is just a matter of time before we are able to treat all diseases of genetic origin with this technique.
C)The study of genomics will allow us to use bacteria and viruses to create vaccinations for virually all diseases of genetic origin.
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47
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
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48
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.
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49
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.
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50
In the early 1980s,a number of clones encoding highly-related forms of actin were isolated from a human cDNA library.Given the information that (i)the restriction enzyme maps of the coding regions were dissimilar,and (ii)each clone contained sufficient coding region to encode all or most of an entire actin gene,you would conclude that

A)multiple actin genes arose as a result of a segmental duplication.
B)the various forms of actin are a result of alternative splicing.
C)actin proteins are encoded by genes found in a tandem cluster.
D)actin proteins are encoded by a multigene family.
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51
Given an ideal sequencing reaction of approximately 500 successive nucleotides (excluding overlap),how many sequencing reactions would be needed to determine the complete human genome?

A)3.2 billion
B)12.5 million
C)12.8 million
D)6.4 million
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52
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.
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53
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.
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54
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.
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55
A catalog of common genetic variants that occur in humans is called a

A)haplotype map.
B)restriction map.
C)genomic map.
D)SNP map.
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56
Which of the following statements regarding pseudogenes is false?

A)Pseudogenes may have some gene-like features such as a promoter and splice sites.
B)Pseudogenes encode proteins,but the translated proteins are non-functional.
C)Pseudogenes can provide insight into the evolutionary history of the related functional gene.
D)Every pseudogene has a similar DNA sequence to some functional gene.
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57
Which of the following organisms has the largest genome?

A)rice
B)human
C)fruit fly
D)yeast
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58
Which of the following organisms has the greatest number of genes?

A)rice
B)human
C)fruit fly
D)yeast
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59
A pharmaceutical company is trying to develop a new drug to help combat a rare disease.To facilitate the identification of new drug targets,they could

A)search the sequenced human genome for mutations involved in the development of the disease,and design drugs that bind to the mutated proteins.
B)employ protein microarray technology to evaluate the binding of drugs to various proteins.
C)test new drugs in transgenic organisms that display disease characteristics.
D)use antibodies to screen a DNA microarray.
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