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@@ -94,6 +94,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
-[#502](https://github.com/genomic-medicine-sweden/nallo/pull/502) - Changed to annotating and ranking SNVs per family instead of per project
-[#502](https://github.com/genomic-medicine-sweden/nallo/pull/502) - Changed output documentation and structure to match `sample` and `family` for all variants
-[#502](https://github.com/genomic-medicine-sweden/nallo/pull/502) - Changed the way of validating the samplesheet to remove outputing false errors with `ifEmpty`
