Hi, everyone!
I have several primer pairs and want to map them onto genome, then calculate the coverage.
My plan now is as follows:
using BSgenome to load the genome library;
using function matchPattern in BSgenome to get the start and end information of the primer pairs;
using function getseq to get sequences;
alignment these sequences with genome sequence and calculate the coverage.
I'm wondering is there a packages which can map the primer pair on genome and get the sequences directly?
Thanks in advance!
2 answers
Check this question: How to find a 28bp 'primer' sequence in a genome?
You could probably use Rsubread to map the primer pair as a paired-end dataset with only one pair in it. Make sure to set the appropriate options for multi-mapping and such.
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Hmmm. I've got a wrapper for invoking NCBI's e-pcr and importing a table of results...... What your after...?