diff macros.xml @ 1:30584e80d61e draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/virheat commit 5ae40d4f44fc2716f3c37a9fad2077a0d0230a6d

--- a/macros.xml	Wed May 15 13:37:49 2024 +0000
+++ b/macros.xml	Mon Jun 03 09:37:09 2024 +0000
@@ -1,6 +1,6 @@
 <?xml version="1.0"?>
 <macros>
-    <token name="@TOOL_VERSION@">0.6</token>
+    <token name="@TOOL_VERSION@">0.7</token>
     <token name="@VERSION_SUFFIX@">0</token>
     <token name="@PROFILE@">21.01</token>
     <xml name="biotools">
@@ -22,12 +22,14 @@
 ============
 
 This tool generates multi-sample variant-frequency plots from SnpEff-annotated
-viral variant lists.  The tool provides a condensed look at variant frequencies after mapping  raw reads to a viral/bacterial reference genome and compares multiple vcf files at the same time. 
+viral variant lists. The tool provides a condensed look at variant frequencies after mapping raw reads to a viral/bacterial reference genome and compares multiple vcf files at the same time. 
 
 The tool expects either the length of a reference genome or the gff3 file if the sequence annotation is needed.
 
 Additionally, to analyze whether mutations are sufficiently covered and to display non-covered cells in grey, first create per-base coverage TSV files for each BAM file with Qualimap and provide them in the same folder as the VCF files. Give them the same name as your VCF files.
 
+Moreover, there is an option to include visualizations of additional scores (e.g., MAVE scores for binding affinity, expression level, antibody escape, etc.) mapped to mutations on the heatmap.
+
 The tool expects input variant lists in VCF format. VCF datasets as produced by standard variant callers with
 
    - variant allele frequencies encoded in an ``AF`` INFO field