From b83a355982b178ee026d167aacf7c77276b84eec Mon Sep 17 00:00:00 2001
From: Graham McVicker <gmcvicker@salk.edu>
Date: Tue, 3 Jul 2018 14:00:36 -0700
Subject: [PATCH] update CHANGELOG in preparation for v0.3.0 release

---
 CHANGELOG.md | 12 ++++++++++++
 1 file changed, 12 insertions(+)

diff --git a/CHANGELOG.md b/CHANGELOG.md
index 645c9e4..75ab045 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -1,3 +1,15 @@
+Version 0.3.0 - July 3, 2018
+-----------
+This release moves the codebase from Python2 to Python3 and includes several additional improvements.
+
+Changes include:
+* Switch to Python3 from Python2
+* Switch to PyTables version 3
+* General cleanup of code to conform to PEP8 style
+* Better matching of VCF files to chromosomes in snp2h5 (uses name of chromosome within VCF, rather than relying on filename)
+* add --txt_counts option to bam2h5.py as a simple way to obtain a file with allele-specific counts. The bam2h5.py should now be used instead of the get_as_counts.py script (which double counts reads that overlap multiple SNPs).
+
+
 Version 0.2.2 - November 15, 2017
 -----------