release

mikessh · Dec 20, 2016 · 5bb2461 · 5bb2461
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diff --git a/README.md b/README.md
@@ -9,3 +9,5 @@ MAGERI implements consensus assembly, alignment and variant calling and allows t
 datasets into ready SAM and VCF files in a single command. Its main purpose is to analyze targeted region genome re-sequencing data for tumor heterogeneity and circulating tumor DNA studies, however it can be also applied to other tasks that require accurate rare variant detection.
 
 See [mageri-paper repository](https://github.com/mikessh/mageri-paper) for examples and supplementary data.
+
+Software binaries can be found in the [releases section](https://github.com/mikessh/mageri/releases/latest), the documentation is available [here](http://mageri.readthedocs.io/en/latest/).
diff --git a/pom.xml b/pom.xml
@@ -4,7 +4,7 @@
 
     <groupId>com.antigenomics</groupId>
     <artifactId>mageri</artifactId>
-    <version>1.1.1-SNAPSHOT</version>
+    <version>1.1.1</version>
     <packaging>jar</packaging>
     <name>MAGERI</name>
Original file line number	Diff line number	Diff line change
Expand Up		@@ -9,3 +9,5 @@ MAGERI implements consensus assembly, alignment and variant calling and allows t
		datasets into ready SAM and VCF files in a single command. Its main purpose is to analyze targeted region genome re-sequencing data for tumor heterogeneity and circulating tumor DNA studies, however it can be also applied to other tasks that require accurate rare variant detection.

		See [mageri-paper repository](https://github.com/mikessh/mageri-paper) for examples and supplementary data.

		Software binaries can be found in the [releases section](https://github.com/mikessh/mageri/releases/latest), the documentation is available [here](http://mageri.readthedocs.io/en/latest/).