I have a VCF file with all the called variants. I want to keep just the SNPs. This is achievable in all sorts of ways outside of Galaxy, but I'm curious if (and how) this can be done within Galaxy.
Thanks!
I have a VCF file with all the called variants. I want to keep just the SNPs. This is achievable in all sorts of ways outside of Galaxy, but I'm curious if (and how) this can be done within Galaxy.
Thanks!
There is SnpSift varType, but it gives an error (it seems Galaxy only allows access to the "filter" tool from SnpSift). As for "all the ways", well, most tools don't exist in Galaxy (e.g., vcftools - Galaxy uses vcflib instead, which doesn't have that functionality, AFAIK).
That's pretty cool, I didn't know about the Tool Shed. Unfortunately, I need this in the "public" Galaxy (I'm OK with the command line tools, but I do want to find something more user-friendly for the other labmates). Though maybe it's worth it to have our own installation, with all the extra tools.
The Galaxy community makes hosting and running an own Galaxy instance really easy. Especially with Galaxy Docker flavours the ansible playbooks or VMs with Galaxy. Also consider using CloundMan, a Cloud Galaxy instance for Amazon.