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Is your feature request related to a problem? Please describe.
While currently not used in the field (AFAIK) might be worth including bcftools stats for getting statistics on VCF files from genotyping. This would help for genotyping assessiment when not using MultiVCFAnalyzer (which is only really used in aDNA pathogen work).
It would be a simple process, with input channel being VCFs and
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I'm getting an error when trying to pull with singularity (version 3.5.2-1.el7)
singularity pull --name nf-core-deepvariant.simg shub://nf-core/deepvariant
FATAL: While pulling shub image: failed to get manifest for: shub://nf-core/deepvariant: the requested manifest was not found in singularity hub
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Hi,
The time for fastqc is not enough...
I'm getting the following error: