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genomic-medicine-sweden / tomte

A nextflow pipeline for analysing expression and splicing in RNA seq data from rare disease patient
MIT License
12 stars 3 forks source link

Add tag in vcf #126

Closed jemten closed 6 months ago

jemten commented 6 months ago

Description of feature

It would be useful to have information regarding which variant caller that was used to make the call inspiration can be found here https://github.com/nf-core/raredisease/blob/master/subworkflows/local/variant_calling/call_snv_deepvariant.nf