diff --git a/CHANGELOG.md b/CHANGELOG.md
index c60b36ee..bc5b6a4c 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -3,30 +3,19 @@
 The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/)
 and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).
 
-## v1.0dev - [date]
+## v0.1.0 - [date]
 
 Initial release of genomic-medicine-sweden/skierfe, created with the [nf-core](https://nf-co.re/) template.
 
 ### `Added`
 
-- Added a switch to choose phasing software [#83](https://github.com/genomic-medicine-sweden/skierfe/pull/83)
-- Added SNV annotation subworkflow to test profile [#75](https://github.com/genomic-medicine-sweden/skierfe/pull/75)
-- Refactored conditionally required parameters validation [#69](https://github.com/genomic-medicine-sweden/skierfe/pull/69)
-- Added CNV workflow to test profile [#68](https://github.com/genomic-medicine-sweden/skierfe/pull/68)
-- Updated and rename output directories [#65](https://github.com/genomic-medicine-sweden/skierfe/pull/65)
-- Updated GLNexus version [#58](https://github.com/genomic-medicine-sweden/skierfe/pull/58)
-- Added uBAM support and multisample test [#51](https://github.com/genomic-medicine-sweden/skierfe/pull/51)
-- Added Revio BAM test data [#50](https://github.com/genomic-medicine-sweden/skierfe/pull/50)
-- Updated template to 2.13.1 [#38](https://github.com/genomic-medicine-sweden/skierfe/pull/38)
-- Updated pipeline to run with a small test dataset [#35](https://github.com/genomic-medicine-sweden/skierfe/pull/35)
-- Added test data and test profile [#33](https://github.com/genomic-medicine-sweden/skierfe/pull/33)
-
-### `Fixed`
-
-- Fix input file validation [#67](https://github.com/genomic-medicine-sweden/skierfe/pull/67)
-- Fix BCFTools merge module inputs [#43](https://github.com/genomic-medicine-sweden/skierfe/pull/43)
-- Fix Mosdepth input channel when run without a bed file [#66](https://github.com/genomic-medicine-sweden/skierfe/pull/66)
-
-### `Dependencies`
-
-### `Deprecated`
+- Raw read QC with FastQC and FQCRS
+- Align reads to reference with minimap2
+- Aligned read QC with cramino and mosdepth
+- Call SNVs with DeepVariant and merge with GLNexus
+- Annotate SNVs with echtvar and VEP
+- Call SVs with Sniffles, tandem repeats with TRGT and CNVs with HiFiCNV
+- Phase variants and haplotag reads with whatshap or HiPhase
+- Create methylation pileups with modkit
+- Assemble genomes with hifiasm
+- Align assemly to reference and call variants with dipcall
diff --git a/assets/multiqc_config.yml b/assets/multiqc_config.yml
index 63ae759e..cb0bb247 100644
--- a/assets/multiqc_config.yml
+++ b/assets/multiqc_config.yml
@@ -1,5 +1,5 @@
 report_comment: >
-  This report has been generated by the <a href="https://github.com/genomic-medicine-sweden/skierfe/tree/dev" target="_blank">genomic-medicine-sweden/skierfe</a>
+  This report has been generated by the <a href="https://github.com/genomic-medicine-sweden/skierfe/releases/tag/0.1.0" target="_blank">genomic-medicine-sweden/skierfe</a>
   analysis pipeline.
 report_section_order:
   "genomic-medicine-sweden-skierfe-methods-description":
diff --git a/nextflow.config b/nextflow.config
index a41453fa..3b5c7d35 100644
--- a/nextflow.config
+++ b/nextflow.config
@@ -266,7 +266,7 @@ manifest {
     description     = """Long-read variant calling pipeline"""
     mainScript      = 'main.nf'
     nextflowVersion = '!>=23.04.0'
-    version         = ''
+    version         = '0.1.0'
     doi             = ''
 }