diff --git a/CHANGELOG.md b/CHANGELOG.md
index 0e068f6cb3f5ee5b55f98bd40b0cc828a4cbb40d..02e02c7f13388f31d25d1e4f9c4f3dd112b084a9 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -1,4 +1,4 @@
-# v2.2.0-indev
+# v2.2.0
 **User Facing**
 * Add cellranger version 4.0.0
 * Add references version 2020-A (GRCh38, mm10, mix)
diff --git a/workflow/main.nf b/workflow/main.nf
index 1fb8fca096757974b9b7d1f285cf29fbecfdf2c5..c11872f4f19095b5dfa33897e033adaaacae37ce 100755
--- a/workflow/main.nf
+++ b/workflow/main.nf
@@ -64,7 +64,7 @@ if (params.astrocyte) {
 params.genomeLocationFull = params.genomeLocation+params.genome
 
 // Define variables from input
-pipelineVersion = "2.2.0-indev"
+pipelineVersion = "2.2.0"
 name = params.name
 designLocation = Channel
   .fromPath(params.designFile)
diff --git a/workflow/nextflow.config b/workflow/nextflow.config
index 1ab9a50bd365b61631b3df6441a59dd34480855b..779748f26f37199189e2fc2efc56a88549d3a328 100644
--- a/workflow/nextflow.config
+++ b/workflow/nextflow.config
@@ -48,6 +48,6 @@ manifest {
   homePage = 'https://git.biohpc.swmed.edu/BICF/Astrocyte/cellranger_count'
   description = 'This pipeline is a wrapper for the cellranger count tool from 10x Genomics. It takes fastq files from 10x Genomics Single Cell Gene Expression libraries, performs alignment, filtering, barcode counting, and UMI counting. It uses the Chromium cellular barcodes to generate gene-barcode matrices, determine clusters, and perform gene expression analysis.'
   mainScript = 'main.nf'
-  version = '2.2.0-indev'
+  version = '2.2.0'
   nextflowVersion = '>=0.31.0'
 }