diff --git a/CHANGELOG.md b/CHANGELOG.md
index ffe57e81e9..6f2711708f 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -19,6 +19,7 @@ The format is based on [Keep a Changelog](http://keepachangelog.com/en/1.0.0/) a
 - [#85](https://github.com/nf-core/sarek/pull/85) - Use new merged vcf files for known indels to simplify setting up channel
 - [#104](https://github.com/nf-core/sarek/pull/104) - Update Figure 1
 - [#107](https://github.com/nf-core/sarek/pull/107) - Switch params to snake_case
+- [#109](https://github.com/nf-core/sarek/pull/109) - Update publication with F1000Research preprint
 
 ### `Fixed`
 
diff --git a/README.md b/README.md
index 83b42c68ff..00bbc0efc8 100644
--- a/README.md
+++ b/README.md
@@ -97,7 +97,7 @@ For further information or help, don't hesitate to get in touch on [Slack](https
 ## Citation
 
 If you use `nf-core/sarek` for your analysis, please cite the `Sarek` pre-print as follows:
-> Garcia MU, Juhos S, Larsson M, Olason PI, Martin M, Eisfeldt J, DiLorenzo S, Sandgren J, de Ståhl TD, Wirta V, Nistér M, Nystedt B, Käller M. **Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants**. *bioRxiv*. 2018. p. 316976. [doi: 10.1101/316976](https://www.biorxiv.org/content/10.1101/316976v1).
+> Garcia MU, Juhos S, Larsson M, Olason PI, Martin M, Eisfeldt J, DiLorenzo S, Sandgren J, Díaz De Ståhl TD, Ewels P, Wirta V, Nistér M, Käller M, Nystedt B. **Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants**. *F1000Research*. 2020. 9:63. [doi: 10.12688/f1000research.16665.1](https://doi.org/10.12688/f1000research.16665.1).
 
 You can cite the sarek zenodo record for a specific version using the following [doi: 10.5281/zenodo.3476426](https://zenodo.org/badge/latestdoi/184289291)