Merge branch 'dev' into fix-multiqc

CHANGELOG.md

@@ -98,6 +98,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
 - [#507](https://github.com/genomic-medicine-sweden/nallo/pull/507) - Changed the default value of `ch_hgnc_ids` to allow running without `--filter_variants_hgnc_ids` introduced in [#496](https://github.com/genomic-medicine-sweden/nallo/pull/443)
 - [#509](https://github.com/genomic-medicine-sweden/nallo/pull/509) - Updated documentation to fix mistakes
 - [#510](https://github.com/genomic-medicine-sweden/nallo/pull/510) - Changed the MultiQC methods description to update dynamically based on `ch_versions`
+- [#513](https://github.com/genomic-medicine-sweden/nallo/pull/513) - Updated CITATIONS.md link in README
 
 ### `Removed`
 

README.md

@@ -104,4 +104,4 @@ This pipeline uses code and infrastructure developed and maintained by the [nf-c
 >
 > _Nat Biotechnol._ 2020 Feb 13. doi: [10.1038/s41587-020-0439-x](https://dx.doi.org/10.1038/s41587-020-0439-x).
 
-An extensive list of references for the tools used by the pipeline can be found in the [`docs/CITATIONS.md`](CITATIONS.md) file.
+An extensive list of references for the tools used by the pipeline can be found in the [`docs/CITATIONS.md`](docs/CITATIONS.md) file.