# HG changeset patch
# User sanbi-uwc
# Date 1539758151 14400
# Node ID 4f3f7d3903829435a1e83f18a7ee93853b665e2f
# Parent  f58178c0f00d72c687de3f24b0a22a747bb6c73f
planemo upload for repository https://github.com/sanbi-sa/tools-sanbi-uwc commit 3e5c71977e50ec920d4f45be809d2528e55bff76-dirty

diff -r f58178c0f00d -r 4f3f7d390382 vcf_to_alignment.xml
--- a/vcf_to_alignment.xml	Mon Oct 15 00:34:44 2018 -0400
+++ b/vcf_to_alignment.xml	Wed Oct 17 02:35:51 2018 -0400
@@ -1,5 +1,5 @@
 <?xml version="1.0" encoding="utf-8" ?>
-<tool id="vcf_to_alignment" name="Generate FASTA alignment from VCF collection" version="0.4">
+<tool id="vcf_to_alignment" name="Generate FASTA alignment from VCF collection" version="0.5">
   <description>Generate a multiple sequence alignment given a collection of variants and a reference sequence</description>
   <requirements>
       <requirement type="package" version="1.67">biopython</requirement>
@@ -47,7 +47,7 @@
       </when>
     </conditional>
     <conditional name="exclude_list">
-      <param name="do_exclude" type="select">
+      <param name="do_exclude" type="select" label="Exclude SNPs from specified regions">
         <option value="yes">Yes</option>
         <option value="no" selected="true">No</option>
       </param>