Updated changelog

CHANGELOG.md

@@ -93,6 +93,7 @@ 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`
+- [#505](https://github.com/genomic-medicine-sweden/nallo/pull/505) - Updated TRGT to 1.2.0
 
 ### `Removed`
 
@@ -174,6 +175,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
 | samtools/merge | 1.2         | 1.21        |
 | stranger       | 0.9.1       | 0.9.2       |
 | multiqc        | 1.21        | 1.25.1      |
+| TRGT           | 0.4.0       | 1.2.0       |
 
 > [!NOTE]
 > Version has been updated if both old and new version information is present.