Closed simonharnqvist closed 6 months ago
Hi,
sorry for the late reply. What exactly are the names of your RNA-seq libraries? For paired-end RNA-Seq reads, the naming convention for BRAKER is either 'ID[1,2].fastq' or 'ID[R1,R2].fastq' (with an underscore and not a dot between ID and 1/2).
Best, Lars
This issue may be similar to Issue #777 .
Haven't tried this as I'm trying to get the Singularity container working instead of a local install. Closing for now.
Thanks!
Hi,
I'm having an issue probably related to #621, but with FASTQ files instead. I'm trying to run BRAKER on local FASTQ files, but BRAKER seems to insist on downloading SRA files.
The stderr gives me:
This is the command I tried to run:
I've tried changing the names of my samples, but the files names definitely correspond to the given sample names and follow the ID.[12].fastq rule.
Any advice on what I can do to get this to work would be great. Thanks!