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Clinical-Genomics · Mar 8, 2016 · 9547451 · 9547451
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diff --git a/CHANGELOG.md b/CHANGELOG.md
@@ -2,7 +2,11 @@
 All notable changes to this project will be documented in this file.
 This project adheres to [Semantic Versioning](http://semver.org/).
 
-## [3.3.4] - 2016-03-08
+## [3.4.1] - 2016-03-08
+### Changed
+- setup and tear down session in Flask app usage
+
+## [3.4.0] - 2016-03-08
 ### Added
 - All new transcript focused schema, generally activated by `--transcript` flag in CLI, this significantly reduces the database footprint and speeds up loading to only a few seconds for a full exome
 

diff --git a/setup.py b/setup.py
@@ -51,7 +51,7 @@ 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='3.4.0',
+    version='3.4.1',
 
     description='Coverage analysis tool for clinical sequencing',
     long_description=long_description,