Repository 'varscan_somatic'
hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/varscan_somatic

Changeset 10:a57606054bd7 (2020-01-18)
Previous changeset 9:4e97191a1ff7 (2019-08-16) Next changeset 11:cf8ffc79db67 (2021-12-04)
Commit message:
"planemo upload for repository https://github.com/galaxyproject/iuc/tree/master/tools/varscan commit 46018cbdd8b4ca124d5c6230862012b9081d56e4"
modified:
varscan_somatic.xml
b
diff -r 4e97191a1ff7 -r a57606054bd7 varscan_somatic.xml
--- a/varscan_somatic.xml Fri Aug 16 15:49:54 2019 -0400
+++ b/varscan_somatic.xml Sat Jan 18 03:19:29 2020 -0500
b
@@ -1,4 +1,4 @@
-<tool id="varscan_somatic" name="VarScan somatic" version="@VERSION@.5">
+<tool id="varscan_somatic" name="VarScan somatic" version="@VERSION@.6">
     <description>Call germline/somatic and LOH variants from tumor-normal sample pairs</description>
     <macros>
         <import>macros.xml</import>
@@ -410,7 +410,7 @@
             </conditional>
             <assert_stderr>
                 <has_line_matching
-                expression=" Min coverage:&#09;2x for Normal, 2x for Tumor" />
+                expression=" *Min coverage:&#09;2x for Normal, 2x for Tumor" />
                 <has_line_matching
                 expression="Min reads2:&#09;1" />
                 <has_line_matching