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.
Correct Answer
verified
Multiple Choice
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.
Correct Answer
verified
Multiple Choice
A) restriction fragment length polymorphisms.
B) shotgun sequencing.
C) sequenced-tagged sites.
D) clone by clone sequencing.
E) consensus sequencing.
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verified
Multiple Choice
A) inserted exon.
B) inserted intron.
C) inserted nucleosome.
D) inserted foreign gene.
E) inserted transcriptomE.
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verified
Multiple Choice
A) segmental duplications.
B) pseudogenes.
C) tandem clusters.
D) multigene families.
E) expressed sequences.
Correct Answer
verified
Multiple Choice
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.
Correct Answer
verified
Multiple Choice
A) 3.2 billion
B) 12.5 million
C) 12.8 million
D) 6.4 million
Correct Answer
verified
Multiple Choice
A) shotgun cloning.
B) the alignment of contigs.
C) the identification of open reading frames.
D) the construction of a genetic map.
Correct Answer
verified
Multiple Choice
A) haplotype map.
B) restriction map.
C) genomic map.
D) SNP map.
Correct Answer
verified
Multiple Choice
A) synteny.
B) exosymbiosis.
C) endosymbiosis.
D) draft sequencing of the proteomes of the mitochondria and chloroplasts by the nucleosome.
E) contiguous base pairing.
Correct Answer
verified
Multiple Choice
A) Nova Scotia
B) Iceland
C) Gibraltar
D) Portugal
E) Galapagos
Correct Answer
verified
Multiple Choice
A) proteome.
B) spliceosome.
C) nucleosome.
D) RNA motif.
E) transcriptomE.
Correct Answer
verified
Multiple Choice
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.
Correct Answer
verified
Multiple Choice
A) synteny.
B) homology.
C) analogous DNA.
D) a contig.
E) a comparative genomE.
Correct Answer
verified
Multiple Choice
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.
Correct Answer
verified
Multiple Choice
A) genetic map.
B) physical map.
C) restriction map.
D) haplotype map.
Correct Answer
verified
Multiple Choice
A) translation
B) splicing
C) mRNA modification
D) coupling
Correct Answer
verified
Multiple Choice
A) fragment
B) complex sequence
C) molecule of mRNA
D) simple sequence repeat
Correct Answer
verified
Multiple Choice
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.
Correct Answer
verified
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