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Hi developers. I have tried to use bbmapskimmer.sh to map some primer sequences on my pacbio reads. It seems that a read gets different results depending on it being in a single fasta or in a multifasta.
Hi developers. I have tried to use bbmapskimmer.sh to map some primer sequences on my pacbio reads. It seems that a read gets different results depending on it being in a single fasta or in a multifasta.
The command I run:
bbmapskimmer.sh in=primer.fasta out=samout.sam ref=$STR idfilter=0.1 k=8 noheader=t threads=4 ambiguous=all nodisk
primer.fasta:
The sequence in question
Run the command on this sequence alone, I get:
Notice that "ssu_2" has a flag 0 and I am certain that except an insertion "T", ssu_2 maps to "problematic_seq".
However, if I add two others into the file:
I get:
So the "problematic_seq" is not having the ssu_2 hit as in my first attempt.
Please help! Thank you!
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