-
Notifications
You must be signed in to change notification settings - Fork 446
New issue
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
Make guppyplex input handling more flexible #4353
Conversation
This allows the user to specify which sequence input files guppyplex should collapse into a single output, and which ones it should keep separate. Also makes the tool work with fastq and fastq.gz data alike and exposes the --quality threshold parameter. The changeset also contains a fix for the artic minion pipeline, which should make it handle input data with spaces in its name.
Currently I cannot fully test this locally because my conda fails to resolve the bioconda artic package's dependencies. |
The artic bioconda package is rather huge, and best installed with mamba. (We have actually switched to using Singularity in Galaxy to a large extent because of this package!) |
I'm impressed: conda chewed on this for hours without success before I killed it. mamba resolved things in under 30 secs! |
Since the wrapper has to symlink each input file separately it could generate a very long command line when there are lots of files to concatenate.
This allows the user to specify which sequence input files guppyplex
should collapse into a single output, and which ones it should keep
separate. Also makes the tool work with fastq and fastq.gz data alike
and exposes the --quality threshold parameter.
The changeset also contains a fix for the artic minion pipeline, which
should make it handle input data with spaces in its name.
FOR CONTRIBUTOR: