prettier

Author: FriederikeHanssen

CHANGELOG.md

@@ -40,6 +40,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
 - [#1173](https://github.com/nf-core/sarek/pull/1173) - Fixed duplicated entries in joint germline recalibrated VCF ([#966](https://github.com/nf-core/sarek/pull/966), [#1102](https://github.com/nf-core/sarek/pull/1102)),
   fixed grouping joint germline recalibrated VCF ([#1137](https://github.com/nf-core/sarek/pull/1137))
 - [#1177](https://github.com/nf-core/sarek/pull/1177) - Fix status inference when using nf-validation plugin
+- [#1183](https://github.com/nf-core/sarek/pull/1183) - Add docs for concatentated germline variants
 
 ### Dependencies
 

docs/output.md

@@ -764,7 +764,6 @@ It requires a normal sample for each tumour to differentiate the somatic and ger
 
 Germline VCFs from `DeepVariant`, `FreeBayes`, `HaplotypeCaller`, `Haplotyper`, `Manta`, `bcftools mpileup`, `Strelka2`, or `Tiddit` are concatenated with `bcftools concat`. The field `SOURCE` is added to the VCF header to report the variant caller.
 
-
 <details markdown="1">
 <summary>Concatenated VCF-files for normal samples</summary>