diff --git a/CHANGELOG.md b/CHANGELOG.md
index cd99af18d7..7c8bf46d19 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -22,6 +22,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
 - [#1143](https://github.com/nf-core/sarek/pull/1143) - `snpeff_db` is now a string
 - [#1145](https://github.com/nf-core/sarek/pull/1145) - Fixed Zenodo links in `README.md` and in `WorkflowMain.groovy`
 - [#1149](https://github.com/nf-core/sarek/pull/1149) - Update `Manta` modules and fix usage of `--exome` flag
+- [#1155](https://github.com/nf-core/sarek/pull/1155) - Restore proper rendering in `usage.md`
 
 ## [3.2.3](https://github.com/nf-core/sarek/releases/tag/3.2.3) - Gällivare
 
diff --git a/docs/usage.md b/docs/usage.md
index b0f7b080f9..b807523ba1 100644
--- a/docs/usage.md
+++ b/docs/usage.md
@@ -2,6 +2,8 @@
 
 ## :warning: Please read this documentation on the nf-core website: [https://nf-co.re/sarek/usage](https://nf-co.re/sarek/usage)
 
+> _Documentation of pipeline parameters is generated automatically from the pipeline schema and can no longer be found in markdown files._
+
 # Introduction
 
 Sarek is a workflow designed to detect germline and somatic variants on whole genome, whole exome, or targeted sequencing data.