Deck 5: Mapping and Identifying Genes for Monogenic Disorders
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Deck 5: Mapping and Identifying Genes for Monogenic Disorders
What supporting evidence can be used to decide whether variation in a gene is actually a mutation?
A) It is never found in people without the phenotype of interest
B) It must be in an exon
C) Additional variation is found in the same gene in other people with a similar phenotype
D) It is expressed only in a tissue relevant to the phenotype
E) All of the above
A) It is never found in people without the phenotype of interest
B) It must be in an exon
C) Additional variation is found in the same gene in other people with a similar phenotype
D) It is expressed only in a tissue relevant to the phenotype
E) All of the above
Additional variation is found in the same gene in other people with a similar phenotype
What is a contig?
A) A series of genetic markers across a genome
B) A series of markers across a chromosome
C) A series of clones with overlapping DNA that spans a particular genetic region
D) A series of clones from a variety of individuals that represent that same genetic region
E) A series of clones from a variety of organisms that represent syntenic regions
A) A series of genetic markers across a genome
B) A series of markers across a chromosome
C) A series of clones with overlapping DNA that spans a particular genetic region
D) A series of clones from a variety of individuals that represent that same genetic region
E) A series of clones from a variety of organisms that represent syntenic regions
A series of clones with overlapping DNA that spans a particular genetic region
The human genome contains approximately how many base pairs of DNA?
A) 3 x 10⁶
B) 3 x 10⁷
C) 3 x 10⁸
D) 3 x 10⁹
E) 3 x 10¹⁰
A) 3 x 10⁶
B) 3 x 10⁷
C) 3 x 10⁸
D) 3 x 10⁹
E) 3 x 10¹⁰
3 x 10⁹

