--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/HGVS2VCF.xml	Wed Mar 25 13:38:09 2015 -0600
@@ -0,0 +1,19 @@
+<?xml version="1.0"?>
+
+<tool id="hgvs2vcf_1" name="Convert a variant table with HGVS syntax into a VCF">
+  <version_string>echo 1.0.0</version_string>
+  <command interpreter="perl">hgvs_to_vcf $in_hgvs_table $output_vcf $sample_name hg19
+  </command>
+  <inputs>
+    <param name="in_hgvs_table" format="achri_snp_table" type="data" label="SNP table with HGVS calls"/>
+    <param type="text" name="sample_name" value="ANON" label="Name for the sample in the output VCF file's header"/>
+  </inputs>
+  <outputs>
+    <data format="vcf" name="output_vcf" type="data" label="Sequence variant calls"/>
+  </outputs>
+
+  <tests>
+  </tests>
+
+  <help>This tools converts the tabular format used to describe variants and associate annotation at ACHRI into a standard Variant Calls Format (VCF) version 4.1 file, which is accepted by many genetic analysis programs.</help>
+</tool>