Hello,
I have a sgRNA pattern CACC+G+20 nucleotides+GTT. When I am running this data.extract line, I get 0% aligned reads. Could anyone help solving this?
The sgRNAs in the FASTA files are G+20 nucleotides.
My code is:
data.extract(scriptpath = scriptpath, datapath = datapath,
fastqfile = fastqfile[1], referencefile = "human_epi", pattern = "CACC(.*(21))GTT", mapping = TRUE, createindex = TRUE)
My output is:
4235022 reads; of these:
4235022 (100.00%) were unpaired; of these:
4235022 (100.00%) aligned 0 times
0 (0.00%) aligned exactly 1 time
0 (0.00%) aligned >1 times
0.00% overall alignment rate
Thanks,
Alex