The basis of Sanger DNA sequencing is to
A) identify ESTs and place them in order based on their function to derive the overall sequence.
B) collect all of the mRNAs of a given cell type, make cDNAs from them, align the cDNAs, and derive the overall sequence.
C) break several copies of a genome into 3-base codons, and align them to derive the overall sequence.
D) generate a series of fragments from an overall DNA sequence that differ by the end base of each. Overlap the pieces and read off the overhangs to derive the sequence.
E) tag each of the four DNA bases with a fluorescent marker molecule and align them by the intensity of the fluorescence to derive the overall sequence.
Correct Answer:
Verified
Q17: If an insufficient number of genomes are
Q18: Two technologies that sped progress of the
Q19: The term genomics means
A) the study of
Q20: The strategy that was ultimately the most
Q21: According to the genomic analysis of Mycoplasma
Q23: The following sequence is part of
Q24: Genes that are highly conserved are
A) found
Q25: Genome sequencing shows that humans share the
Q26: Sequencing of the first three human genomes
Q27: Once people began to have their genomes
Unlock this Answer For Free Now!
View this answer and more for free by performing one of the following actions
Scan the QR code to install the App and get 2 free unlocks
Unlock quizzes for free by uploading documents