diff --git a/topics/sequence-analysis/tutorials/sars-with-galaxy-on-anvil/tutorial.md b/topics/sequence-analysis/tutorials/sars-with-galaxy-on-anvil/tutorial.md
index 388bc3da0bea18..9273b90052746c 100644
--- a/topics/sequence-analysis/tutorials/sars-with-galaxy-on-anvil/tutorial.md
+++ b/topics/sequence-analysis/tutorials/sars-with-galaxy-on-anvil/tutorial.md
@@ -314,7 +314,7 @@ We have aligned our data but it is currently a table of where the reads align. T
 
 > <hands-on-title>Visualize Reference Data</hands-on-title>
 >
-> 1. Scroll down in the Tools menu to STATISTICS AND VISUALIZATION. Under "Graph/Display Data", select {% tool [JBrowse](https://toolshed.g2.bx.psu.edu/view/iuc/jbrowse/a6e57ff585c0) %}.
+> 1. Scroll down in the Tools menu to STATISTICS AND VISUALIZATION. Under "Graph/Display Data", select {% tool [JBrowse](toolshed.g2.bx.psu.edu/repos/iuc/jbrowse/jbrowse/1.16.9+galaxy0) %}.
 >    - {% icon param-select %} *"Reference genome to display"*: `Use a genome from history` 
 >    - {% icon param-select %} *"Select the reference genome"*: `SARS-CoV-2_reference_genome.fasta`
 > 2. Click "Run Tool".