count_nmer | R Documentation |
This just calls PDict() and vcountPDict() on a sequence database given a pattern and number of mismatches. This may be used by divide_seq() normalization.
count_nmer(genome, pattern = "ATG", mismatch = 0)
genome |
Sequence database, genome in this case. |
pattern |
Count off this string. |
mismatch |
How many mismatches are acceptable? |
Set of counts by sequence.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.