Entering edit mode
3.2 years ago
dreamfeathers08
▴
10
Hi,
I have an existing dataset from nanopore run in fast5 format. I'm using GALAXY to convert it into fastq format. The tools which I've trialled from the tools list are : 1) extract fastq in tabular format from a set of fast5 files and 2) extract read in fasta or fastq format from nanopore files.
I got either 1 line or 0 bytes from these runs,,,no output.
Does anyone has any idea why? or which step did i miss or input the wrong thing?
Thank you.
galaxy outputs the logs, for each job. Look at the logs.
Hi,
I'll have a look at it.
Thank you.
Galaxy related questions are best posted on their help forum: https://help.galaxyproject.org/
Hi,
Noted!
Thank you!