--- a/arriba.xml	Wed Jul 27 11:24:44 2022 +0000
+++ b/arriba.xml	Fri Sep 23 13:50:25 2022 +0000
@@ -55,7 +55,7 @@
         -c '$chimeric'
     #end if
     -a '$genome_assembly'
-    -g '$genome_annotation'
+    -g 'genome.gtf'
     #if $blacklist
         -b '$blacklist_file'
     #end if
@@ -71,17 +71,17 @@
     #if $tags
         -t '$tags_file'
     #end if
-    #if str($wgs.use_wgs) == "yes"
-        -d '$wgs.wgs'
-        #if str($wgs.max_genomic_breakpoint_distance)
-            -D $wgs.max_genomic_breakpoint_distance
+    #if str($wgs_cond.use_wgs) == "yes"
+        -d '$wgs_cond.wgs'
+        #if str($wg_cond.max_genomic_breakpoint_distance)
+            -D $wgs_cond.max_genomic_breakpoint_distance
         #end if
     #end if
     -o fusions.tsv
-#if $output_fusions_discarded
+    #if $output_fusions_discarded
     -O fusions.discarded.tsv 
-#end if
-## Arriba options
+    #end if
+    ## Arriba options
     #if $options.gtf_features
         -G '$options.gtf_features'
     #end if
@@ -186,13 +186,13 @@
         </param>
         <param name="tags" argument="-t" type="data" format="tabular" optional="true" label="File containing tag names for a fusion."
                help="This can be the known fusions if that input has a third column with a name"/>
-        <conditional name="wgs">
+        <conditional name="wgs_cond">
             <param name="use_wgs" type="select" label="Use whole-genome sequencing data">
                 <option value="no">no</option>
                 <option value="yes">Yes</option>
             </param>
             <when value="yes">
-                <param name="wgs" argument="-d" type="data" format="tabular" label="whole-genome sequencing structural variant data"
+                <param name="wgs" argument="-d" type="data" format="tabular,vcf" label="whole-genome sequencing structural variant data"
                        help="These coordinates serve to increase sensitivity towards weakly expressed fusions and to eliminate fusions with low evidence."/>
                 <param name="max_genomic_breakpoint_distance" argument="-D" type="integer" value="100000" min="0" label="Max genomic breakpoint distance"
                        help="determines how far a genomic breakpoint may be away from a transcriptomic breakpoint to consider it as a related event."/>