Deck 10: Human Genetic Mapping, Genome Wide Association Studies, and Complex Traits

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Question
What molecular genetics term is used for making a connection between the gene as it relates to a phenotype and the gene in terms of its DNA sequence?

A) Linkage
B) Mapping
C) Genome-wide association
D) Positional cloning
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Question
The On-line Mendelian Inheritance in Man (OMIM) database is an important resource for human genetics. Most of the content in OMIM relates to monogenic diseases. Which of the following conditions are not generally thought to be monogenic? Please select all that apply.

A) Hypertension
B) Cystic fibrosis
C) Type 2 diabetes
D) Huntington disease
Question
Genetic analysis in model organisms such as Drosophila cannot easily be replicated in humans. Which of the following factors are true of Drosophila but not humans? Please select all that apply.

A) Short generation times
B) Crossovers between homologous chromosomes
C) Large numbers of offspring
D) Haploid gametes
Question
Match the missing words in the following phrase. In [A]-Wide Association Studies, researchers identify lots of [B] with ([C]) and without ([D]) a [E]. Genomes are compared and any [F] that are consistently associated with the trait are identified.
Question
What does linkage disequilibrium refer to?

A) Genes on different chromosomes
B) Genes on the same chromosome
C) Association of phenotypes
D) Sex-linked phenotypes
Question
Match the type of DNA sequence variation with its name

-Changes in the number of copies of a small sequence

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Question
Match the type of DNA sequence variation with its name

-Changes at one nucleotide

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Question
Match the type of DNA sequence variation with its name

-Changes occurring only in a small number of related individuals

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Question
Match the type of DNA sequence variation with its name

-Additions or deletions of pieces of DNA

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Question
For a locus to be classed as polymorphic, the second most common polymorphism must be found at least 10% of the time.
Question
Why are regions between genes (intergenic regions) often chosen as mapping markers in genome-wide association studies? Please select all that apply.

A) Intergenic regions are usually not under positive or negative selection
B) Polymorphism frequency in intergenic regions is usually unaffected by the health of the individuals
C) Intergenic regions are less likely to contain crossovers during meiosis
D) Variation in intergenic regions is more strongly linked to ethnicity than is variation in genic regions
Question
Consider two genes, A and B, with alleles A & a, and B & b. In a population, 60% of gametes have A and 40% have a; 90% of gametes have B and 10% have b. In an experiment, 625 gametes are AB, 408 are aB, 72 are Ab, and 45 ab. Which of the following statements are true about genes A and B in this population? Please select all that apply.

A) Linkage disequilibrium is present
B) Linkage disequilibrium is not present
C) Alleles A and B are linked
D) Alleles A and B are not linked
Question
Exome sequencing is powerful technique that has been used to identify genes linked to a number of rare genetic conditions. Which of the following is a disadvantage of exome sequencing?

A) Exome sequencing only identifies conditions associated with recessive alleles.
B) Exome sequencing does not directly identify the gene, but identifies only the region of the genome containing the gene.
C) Exome sequences are more difficult to analyze than whole genome sequences
D) Exome sequencing does not identify conditions linked to regulatory regions.
Question
Microarrays can be used to examine gene expression and also to conduct genome-wide association studies (GWAS). Which of the following are true about these microarrays? Please select all that apply.

A) Both expression microarrays and GWAS arrays are hybridized with genomic DNA
B) Both expression microarrays and GWAS arrays are made of printed DNA features
C) Expression microarrays contain features from genes, GWAS arrays contain features from the whole genome
D) Both expression microarrays and GWAS arrays are made of printed RNA features
Question
Nine features of a GWAS array are shown, as well as the hybridization results from an experiment (hybridized = red, not hybridized = white). What is the genotype of the person being investigated?
..GCTAGTCCG.. ..AAATATCAGT.. ..CCTGGGCTAG.. ..GCTACTCCG.. ..AAATTTCAGT.. ..CCTGGCCTAG.. ..GCTAATCCG.. ..CCTGGACTAG.. ..CCTGGTCTAG.. \begin{array} { | l | l | l | } \hline \text {..GCTAGTCCG.. } & \text {..AAATATCAGT.. } & \text {..CCTGGGCTAG.. } \\\hline \text {..GCTACTCCG.. } & \text {..AAATTTCAGT.. } & \text {..CCTGGCCTAG.. } \\\hline \text {..GCTAATCCG.. } & \text {..CCTGGACTAG.. } & \text {..CCTGGTCTAG.. } \\\hline\end{array}

 <strong>Nine features of a GWAS array are shown, as well as the hybridization results from an experiment (hybridized = red, not hybridized = white). What is the genotype of the person being investigated?  \begin{array} { | l | l | l | } \hline \text {..GCTAGTCCG.. } & \text {..AAATATCAGT.. } & \text {..CCTGGGCTAG.. } \\ \hline \text {..GCTACTCCG.. } & \text {..AAATTTCAGT.. } & \text {..CCTGGCCTAG.. } \\ \hline \text {..GCTAATCCG.. } & \text {..CCTGGACTAG.. } & \text {..CCTGGTCTAG.. } \\ \hline \end{array}    </strong> A) G/A, T/C, T/T B) G/G, T/T, G/G C) A/C, A/A, G/A D) G/G, A/T, C/T <div style=padding-top: 35px>

A) G/A, T/C, T/T
B) G/G, T/T, G/G
C) A/C, A/A, G/A
D) G/G, A/T, C/T
Question
What term is used for a block of alleles that is inherited together?

A) Genome
B) Marker
C) Polymorphism
D) Haplotype
Question
Which if the following statements about human evolution and diversity is true?

A) Humans first evolved in the Middle East
B) Human populations are a subset of the genetic diversity found in the Middle East
C) Most of the genetic diversity in humans is found outside of Africa
D) Genetic diversity is greater in Africa than in other regions of the world
Question
Fill in the blank. Migrating humans often lived in small groups, and by chance the genetic diversity in these groups may have been different to the diversity in the wider population. This phenomenon is known as the ____ ___
Question
Cystic fibrosis (CF) is a common disease in European populations. Most individuals with the disease have the same mutation in the CF gene. What does this suggest about the evolution of CF?

A) The CF mutation first arose in Africa
B) The CF mutation is more common in homozygotes than in heterozygotes
C) Carriers of the European CF mutation are descended from the same person
D) There is a common variant for CF
Question
People with a genetic disease that is common in one population but uncommon in other populations usually have the same haplotype.
Question
Which of the following pieces of evidence suggest that genetic factors have an influence on height? Please select all that apply.

A) Japanese Americans tend to be shorter than Swedish Americans
B) Adopted children are closer in height to their birth parents than their adopted parents
C) Identical twins are not always the same height
D) Sibling heights are often more similar to each other than to heights of others in the same environment.
Question
What term is used for genes that affect the phenotype of a complex trait?

A) Polymorphic genes
B) Polygenic traits
C) Multifactorial traits
D) Quantitative trait loci
Question
Match the missing words in the following phrase. Analysis of complex traits requires [A] analysis to determine how much of the [B] in a trait is attributable to genetics. When measurements are taken of a [C] in a population, e. g., height, the results form a [D]. Many of these follow [E] shapes but this is not always the case - for example, flies with red or white eyes fall into two [F] categories.
Question
Complex traits are affected by multiple genes. Individuals with the same phenotype for a complex trait will also share the same genotype.
Question
Fill in the blank. If all individuals in a population carry the same allele for a particular gene, then the allele is said to be ____ in that population
Question
Which of the following can a genome-wide association study not do?

A) Identify different haplotypes in different populations
B) Identify haplotypes associated with a trait
C) Identify multiple regions of the genome that influence a trait
D) Identify causative genes underlying a trait
Question
What term is used for the fraction of phenotypic variation that can be attributed to genetic differences among individuals?

A) quantitative traits
B) variance
C) mean
D) heritability
Question
What does a Manhattan plot show?

A) The inheritance pattern of a particular trait.
B) Associations of phenotypes with locations on the chromosomes
C) The genes associated with a particular trait
D) The distribution of phenotypes in a population
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Deck 10: Human Genetic Mapping, Genome Wide Association Studies, and Complex Traits
1
What molecular genetics term is used for making a connection between the gene as it relates to a phenotype and the gene in terms of its DNA sequence?

A) Linkage
B) Mapping
C) Genome-wide association
D) Positional cloning
Positional cloning
2
The On-line Mendelian Inheritance in Man (OMIM) database is an important resource for human genetics. Most of the content in OMIM relates to monogenic diseases. Which of the following conditions are not generally thought to be monogenic? Please select all that apply.

A) Hypertension
B) Cystic fibrosis
C) Type 2 diabetes
D) Huntington disease
Hypertension
Type 2 diabetes
3
Genetic analysis in model organisms such as Drosophila cannot easily be replicated in humans. Which of the following factors are true of Drosophila but not humans? Please select all that apply.

A) Short generation times
B) Crossovers between homologous chromosomes
C) Large numbers of offspring
D) Haploid gametes
Short generation times
Large numbers of offspring
4
Match the missing words in the following phrase. In [A]-Wide Association Studies, researchers identify lots of [B] with ([C]) and without ([D]) a [E]. Genomes are compared and any [F] that are consistently associated with the trait are identified.
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5
What does linkage disequilibrium refer to?

A) Genes on different chromosomes
B) Genes on the same chromosome
C) Association of phenotypes
D) Sex-linked phenotypes
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Unlock Deck
k this deck
6
Match the type of DNA sequence variation with its name

-Changes in the number of copies of a small sequence

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
7
Match the type of DNA sequence variation with its name

-Changes at one nucleotide

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
8
Match the type of DNA sequence variation with its name

-Changes occurring only in a small number of related individuals

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
9
Match the type of DNA sequence variation with its name

-Additions or deletions of pieces of DNA

A) CNV
B) SNP
C) Private polymorphism
D) Indel
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
10
For a locus to be classed as polymorphic, the second most common polymorphism must be found at least 10% of the time.
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k this deck
11
Why are regions between genes (intergenic regions) often chosen as mapping markers in genome-wide association studies? Please select all that apply.

A) Intergenic regions are usually not under positive or negative selection
B) Polymorphism frequency in intergenic regions is usually unaffected by the health of the individuals
C) Intergenic regions are less likely to contain crossovers during meiosis
D) Variation in intergenic regions is more strongly linked to ethnicity than is variation in genic regions
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
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12
Consider two genes, A and B, with alleles A & a, and B & b. In a population, 60% of gametes have A and 40% have a; 90% of gametes have B and 10% have b. In an experiment, 625 gametes are AB, 408 are aB, 72 are Ab, and 45 ab. Which of the following statements are true about genes A and B in this population? Please select all that apply.

A) Linkage disequilibrium is present
B) Linkage disequilibrium is not present
C) Alleles A and B are linked
D) Alleles A and B are not linked
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Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
13
Exome sequencing is powerful technique that has been used to identify genes linked to a number of rare genetic conditions. Which of the following is a disadvantage of exome sequencing?

A) Exome sequencing only identifies conditions associated with recessive alleles.
B) Exome sequencing does not directly identify the gene, but identifies only the region of the genome containing the gene.
C) Exome sequences are more difficult to analyze than whole genome sequences
D) Exome sequencing does not identify conditions linked to regulatory regions.
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
14
Microarrays can be used to examine gene expression and also to conduct genome-wide association studies (GWAS). Which of the following are true about these microarrays? Please select all that apply.

A) Both expression microarrays and GWAS arrays are hybridized with genomic DNA
B) Both expression microarrays and GWAS arrays are made of printed DNA features
C) Expression microarrays contain features from genes, GWAS arrays contain features from the whole genome
D) Both expression microarrays and GWAS arrays are made of printed RNA features
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
15
Nine features of a GWAS array are shown, as well as the hybridization results from an experiment (hybridized = red, not hybridized = white). What is the genotype of the person being investigated?
..GCTAGTCCG.. ..AAATATCAGT.. ..CCTGGGCTAG.. ..GCTACTCCG.. ..AAATTTCAGT.. ..CCTGGCCTAG.. ..GCTAATCCG.. ..CCTGGACTAG.. ..CCTGGTCTAG.. \begin{array} { | l | l | l | } \hline \text {..GCTAGTCCG.. } & \text {..AAATATCAGT.. } & \text {..CCTGGGCTAG.. } \\\hline \text {..GCTACTCCG.. } & \text {..AAATTTCAGT.. } & \text {..CCTGGCCTAG.. } \\\hline \text {..GCTAATCCG.. } & \text {..CCTGGACTAG.. } & \text {..CCTGGTCTAG.. } \\\hline\end{array}

 <strong>Nine features of a GWAS array are shown, as well as the hybridization results from an experiment (hybridized = red, not hybridized = white). What is the genotype of the person being investigated?  \begin{array} { | l | l | l | } \hline \text {..GCTAGTCCG.. } & \text {..AAATATCAGT.. } & \text {..CCTGGGCTAG.. } \\ \hline \text {..GCTACTCCG.. } & \text {..AAATTTCAGT.. } & \text {..CCTGGCCTAG.. } \\ \hline \text {..GCTAATCCG.. } & \text {..CCTGGACTAG.. } & \text {..CCTGGTCTAG.. } \\ \hline \end{array}    </strong> A) G/A, T/C, T/T B) G/G, T/T, G/G C) A/C, A/A, G/A D) G/G, A/T, C/T

A) G/A, T/C, T/T
B) G/G, T/T, G/G
C) A/C, A/A, G/A
D) G/G, A/T, C/T
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16
What term is used for a block of alleles that is inherited together?

A) Genome
B) Marker
C) Polymorphism
D) Haplotype
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
17
Which if the following statements about human evolution and diversity is true?

A) Humans first evolved in the Middle East
B) Human populations are a subset of the genetic diversity found in the Middle East
C) Most of the genetic diversity in humans is found outside of Africa
D) Genetic diversity is greater in Africa than in other regions of the world
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
18
Fill in the blank. Migrating humans often lived in small groups, and by chance the genetic diversity in these groups may have been different to the diversity in the wider population. This phenomenon is known as the ____ ___
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
19
Cystic fibrosis (CF) is a common disease in European populations. Most individuals with the disease have the same mutation in the CF gene. What does this suggest about the evolution of CF?

A) The CF mutation first arose in Africa
B) The CF mutation is more common in homozygotes than in heterozygotes
C) Carriers of the European CF mutation are descended from the same person
D) There is a common variant for CF
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
20
People with a genetic disease that is common in one population but uncommon in other populations usually have the same haplotype.
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
21
Which of the following pieces of evidence suggest that genetic factors have an influence on height? Please select all that apply.

A) Japanese Americans tend to be shorter than Swedish Americans
B) Adopted children are closer in height to their birth parents than their adopted parents
C) Identical twins are not always the same height
D) Sibling heights are often more similar to each other than to heights of others in the same environment.
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
22
What term is used for genes that affect the phenotype of a complex trait?

A) Polymorphic genes
B) Polygenic traits
C) Multifactorial traits
D) Quantitative trait loci
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
23
Match the missing words in the following phrase. Analysis of complex traits requires [A] analysis to determine how much of the [B] in a trait is attributable to genetics. When measurements are taken of a [C] in a population, e. g., height, the results form a [D]. Many of these follow [E] shapes but this is not always the case - for example, flies with red or white eyes fall into two [F] categories.
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Unlock for access to all 28 flashcards in this deck.
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24
Complex traits are affected by multiple genes. Individuals with the same phenotype for a complex trait will also share the same genotype.
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25
Fill in the blank. If all individuals in a population carry the same allele for a particular gene, then the allele is said to be ____ in that population
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Unlock for access to all 28 flashcards in this deck.
Unlock Deck
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26
Which of the following can a genome-wide association study not do?

A) Identify different haplotypes in different populations
B) Identify haplotypes associated with a trait
C) Identify multiple regions of the genome that influence a trait
D) Identify causative genes underlying a trait
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
27
What term is used for the fraction of phenotypic variation that can be attributed to genetic differences among individuals?

A) quantitative traits
B) variance
C) mean
D) heritability
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
28
What does a Manhattan plot show?

A) The inheritance pattern of a particular trait.
B) Associations of phenotypes with locations on the chromosomes
C) The genes associated with a particular trait
D) The distribution of phenotypes in a population
Unlock Deck
Unlock for access to all 28 flashcards in this deck.
Unlock Deck
k this deck
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Unlock Deck
Unlock for access to all 28 flashcards in this deck.