diff --git a/CHANGELOG.md b/CHANGELOG.md index 53150492a6..9de8cb7b22 100644 --- a/CHANGELOG.md +++ b/CHANGELOG.md @@ -24,6 +24,8 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0 ### Fixed +- [#342](https://github.com/nf-core/sarek/pull/342) - Update `README.md` + ### Deprecated ### Removed diff --git a/README.md b/README.md index 243b3ee239..4dd8539702 100644 --- a/README.md +++ b/README.md @@ -23,7 +23,7 @@ Sarek is a workflow designed to detect variants on whole genome or targeted sequ Initially designed for Human, and Mouse, it can work on any species with a reference genome. Sarek can also handle tumour / normal pairs and could include additional relapses. -The pipeline is built using [`Nextflow`](https://www.nextflow.io), a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It comes with `Docker` containers making installation trivial and results highly reproducible. +The pipeline is built using [`Nextflow`](https://www.nextflow.io), a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It uses containers from [`BioContainers`](https://biocontainers.pro/) making installation trivial and results highly reproducible.