Open Jokendo-collab opened 9 months ago
Maybe you can provide a dummy empty VCF file for now to trick the pipeline?
Not sure if that can work but I will give it a try
It should work since that VCF will be used to substract the SNPs/indels only. So x - 0 = x meaning that you will get out back what goes in. Need to test to see how that will work though.
Description of feature
I am working with zebrafish genome and it lacks "known indels" and "dbsnp" databases and I see it is a mandatory requirement in this pipeline. How can one call variants from an organism lacking the above mentioned files?