Entering edit mode
8.2 years ago
mschmid
▴
180
I have a 20 nucleotide pattern. Now I want to find ALL of its occurences in a fasta file with about 200 sequences.
Then I want to ouput the positions either to a gff or into a sam file to be able to load into IGV. What is the most efficient way to do that?
It can have about 1-2 indels and about 2-4 SNPs. It is just important to find where the approximate pattern occurs often...