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Hi
I am interested in comparing the signals for short (20-40 nt) modified oligos.
resquiggle runs error-free and produces the index file, yet it says:
Final unsuccessful reads summary (100.0% reads unsuccessfully processed; 7836 total reads):
100.0% (7836 reads): Alignment not produced
I wonder If the sequence is just too short, to give an alignment with sufficient quality? I can find the reference sequence in the fastq files by text search, so it is definitely there.
Does anyone know about some kind of threshold that prevents the alignment of short sequences?
Thanks for your help!
The text was updated successfully, but these errors were encountered:
Hi
I am interested in comparing the signals for short (20-40 nt) modified oligos.
resquiggle runs error-free and produces the index file, yet it says:
Final unsuccessful reads summary (100.0% reads unsuccessfully processed; 7836 total reads):
100.0% (7836 reads): Alignment not produced
I wonder If the sequence is just too short, to give an alignment with sufficient quality? I can find the reference sequence in the fastq files by text search, so it is definitely there.
Does anyone know about some kind of threshold that prevents the alignment of short sequences?
Thanks for your help!
The text was updated successfully, but these errors were encountered: