A user should be able to get a list of important "subsequences" for an input sequence for every genomic feature. These subsequences will be built based on the mutated base with the maximum score in a given position. The maximum score must also pass a certain threshold (e.g. 0.50), otherwise the base at that position will be N.
A user should be able to get a list of important "subsequences" for an input sequence for every genomic feature. These subsequences will be built based on the mutated base with the maximum score in a given position. The maximum score must also pass a certain threshold (e.g. 0.50), otherwise the base at that position will be N.