diff --git a/CHANGELOG.md b/CHANGELOG.md
index 00b6e2a..3b70d98 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -1,5 +1,18 @@
 # Changelog
 
+## [0.2.0](https://github.com/genomic-medicine-sweden/poppy/compare/v0.1.0...v0.2.0) (2024-06-27)
+
+
+### Features
+
+* add background to reference pipeline and annotation to snvs vcfs ([#70](https://github.com/genomic-medicine-sweden/poppy/issues/70)) ([f5c1903](https://github.com/genomic-medicine-sweden/poppy/commit/f5c1903686952f99439683850004391935ae6222))
+* update hydra genetics version to include software version into multiqc ([#63](https://github.com/genomic-medicine-sweden/poppy/issues/63)) ([19b33d3](https://github.com/genomic-medicine-sweden/poppy/commit/19b33d37d1bdf583f01d5663a61183a25b526cca))
+
+
+### Bug Fixes
+
+* remove default string for all col when loading samples.tsv ([#67](https://github.com/genomic-medicine-sweden/poppy/issues/67)) ([9efae47](https://github.com/genomic-medicine-sweden/poppy/commit/9efae473e1cb1c9319e010f3ffe6aecd970cd4f8))
+
 ## 0.1.0 (2024-03-08)
 
 
diff --git a/version.txt b/version.txt
index 6e8bf73..0ea3a94 100644
--- a/version.txt
+++ b/version.txt
@@ -1 +1 @@
-0.1.0
+0.2.0