Open pmenzel opened 3 years ago
Sorry, forgot to respond to this sooner. For the amplicon length, are you including the lengths of the primers in that? If not, I believe you should be. I think the amplicon length with the primer lengths you gave is having issues because there isn't enough overlap to analyze.
Hi,
I build the docker container and run it on 2x251bp MiSeq reads of the V3-V4 amplicon using the command
and get the following error:
The log file in the output-folder is empty.
I already filtered the fastq files to only include reads with length 251 to get past the length check.
Further, I needed to reduce the
AMPLICONLENGTH
option to 450, otherwise I would getbest, Peter