Merge b5a7c6f into f580123

Clinical-Genomics · Nov 12, 2020 · a31dc0e · a31dc0e
2 parents f580123 + b5a7c6f
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diff --git a/CHANGELOG.md b/CHANGELOG.md
@@ -2,13 +2,15 @@
 All notable changes to this project will be documented in this file.
 This project adheres to [Semantic Versioning](http://semver.org/).
 
-## [4.4.0] - 2020-02-12
-
+## [4.5.0] - 2020-11-12
 ### Added
-- User can pass on file with row separated gene IDs for coverage calculation
 - Dockerfile
 - Added the Docker image build and push triggered by new releases
-- Added githib action running pytest and coveralls
+- Added github action running pytest and coveralls
+
+## [4.4.0] - 2020-02-12
+### Added
+- User can pass on file with row separated gene IDs for coverage calculation
 
 ## [4.3.0] - 2020-02-05
 

diff --git a/setup.py b/setup.py
@@ -58,7 +58,7 @@ def run_tests(self):
     # Versions should comply with PEP440. For a discussion on
     # single-sourcing the version across setup.py and the project code,
     # see http://packaging.python.org/en/latest/tutorial.html#version
-    version='4.4.0',
+    version='4.5.0',
 
     description='Coverage analysis tool for clinical sequencing',
     # What does your project relate to? Separate with spaces.