Exam 10: Human Genetic Mapping, Genome Wide Association Studies, and Complex Traits
Exam 1: Darwins Finches: Evolution, Genomes, and Genes18 Questions
Exam 2: The Central Dogma of Molecular Biology30 Questions
Exam 3: Genome Structure, Organization, and Variation27 Questions
Exam 4: Descent With Modification: Dna Replication and Mutation28 Questions
Exam 5: The Inheritance of Single Gene Traits28 Questions
Exam 6: The Cellular Basis for Mendelian Genetics31 Questions
Exam 7: X-Linked Genes and Sex Chromosomes31 Questions
Exam 8: The Inheritance of Multiple Genes28 Questions
Exam 9: The Locations of Genes on Chromosomes: Linkage and Genetic Maps25 Questions
Exam 10: Human Genetic Mapping, Genome Wide Association Studies, and Complex Traits28 Questions
Exam 11: Exchange and Evolution31 Questions
Exam 12: Transcription: Reading and Expressing Genes37 Questions
Exam 13: Translation: From Nucleic Acids to Amino Acids33 Questions
Exam 14: Networks of Gene Regulation33 Questions
Exam 15: Genetic Analysis of Cellular Processes28 Questions
Exam 16: The Genetics of Populations25 Questions
Exam 17: Metagenomes: Genome Analysis of Communities32 Questions
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Which of the following can a genome-wide association study not do?
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(Multiple Choice)
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Correct Answer:
D
Which of the following pieces of evidence suggest that genetic factors have an influence on height? Please select all that apply.
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(Multiple Choice)
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Correct Answer:
A, B, D
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.
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(Multiple Choice)
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Correct Answer:
B, C
For a locus to be classed as polymorphic, the second most common polymorphism must be found at least 10% of the time.
(True/False)
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Why are regions between genes (intergenic regions) often chosen as mapping markers in genome-wide association studies? Please select all that apply.
(Multiple Choice)
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Match the type of DNA sequence variation with its name
-Additions or deletions of pieces of DNA
(Multiple Choice)
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People with a genetic disease that is common in one population but uncommon in other populations usually have the same haplotype.
(True/False)
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Match the type of DNA sequence variation with its name
-Changes at one nucleotide
(Multiple Choice)
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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.
(Multiple Choice)
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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.
(Multiple Choice)
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What term is used for the fraction of phenotypic variation that can be attributed to genetic differences among individuals?
(Multiple Choice)
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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?
(Multiple Choice)
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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
(Short Answer)
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Match the type of DNA sequence variation with its name
-Changes in the number of copies of a small sequence
(Multiple Choice)
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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?
(Multiple Choice)
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Match the type of DNA sequence variation with its name
-Changes occurring only in a small number of related individuals
(Multiple Choice)
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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.
(Short Answer)
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Which if the following statements about human evolution and diversity is true?
(Multiple Choice)
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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?
(Multiple Choice)
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