(a) We can see here that to write out the consensus sequence of the nontemplate strand, we identify the base occurring most often at each position in the set of sequences. If the base cannot be determined at a certain position, we put a dash.
What is consensus sequence?
It provides a straightforward representation of the most frequent bases at each position, giving a single sequence that is representative of the majority.
(a) To write out the consensus sequence of the nontemplate strand, we identify the base occurring most often at each position in the set of sequences. If the base cannot be determined at a certain position, we put a dash.
For example, let's say we have a set of DNA sequences:
Sequence 1: ATGCCG
Sequence 2: ATGACG
Sequence 3: ATGGCG
Sequence 4: ATGTTG
To determine the consensus sequence, we compare the bases at each position and choose the most frequent base. In this case, the consensus sequence would be:
Consensus Sequence: ATGGCG
The base "A" occurs most frequently at the first position, "T" at the second position, "G" at the third and fourth positions, "C" at the fifth position, and "G" again at the sixth position.
(b) The sequence logo provides more information than the consensus sequence. In a sequence logo, the height of each letter represents the frequency of occurrence of that base at a specific position, and the total height at each position represents the conservation level.