# HG changeset patch
# User blankenberg
# Date 1519851712 18000
# Node ID aff38ea879f1969fa1c514189323de8e494ca2e0
# Parent  5c852eca82e036e32cece1325d7ea2c0e68b1dcc
planemo upload for repository https://github.com/blankenberg/tools-blankenberg/tree/master/tools/naive_variant_caller commit dfca863a9a361877d6d98b92072f1ebc316c5767

diff -r 5c852eca82e0 -r aff38ea879f1 naive_variant_caller.xml
--- a/naive_variant_caller.xml	Wed Feb 28 15:54:57 2018 -0500
+++ b/naive_variant_caller.xml	Wed Feb 28 16:01:52 2018 -0500
@@ -1,4 +1,4 @@
-<tool id="naive_variant_caller" name="Naive Variant Caller" version="0.0.3">
+<tool id="naive_variant_caller" name="Naive Variant Caller (NVC)" version="0.0.3">
   <description> - tabulate variable sites from BAM datasets</description>
   <requirements>
     <requirement type="package" version="0.0.3">nvc</requirement>
@@ -147,6 +147,10 @@
       </test>
   </tests>
   <help>
+The **Naive Variant Caller** tool (NVC).
+
+------
+
 **What it does**
 
 This tool is a naive variant caller that processes aligned sequencing reads from the BAM format and produces a VCF file containing per position variant calls. This tool allows multiple BAM files to be provided as input and utilizes read group information to make calls for individual samples.