# HG changeset patch
# User geert-vandeweyer
# Date 1392284806 18000
# Node ID 26a5b8623597614936e740e8916f0e65da32a9f5
# Parent  2799221681dda4ae00db3651d5551d4c2840141f
Uploaded

diff -r 2799221681dd -r 26a5b8623597 tool_dependencies.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_dependencies.xml	Thu Feb 13 04:46:46 2014 -0500
@@ -0,0 +1,28 @@
+<?xml version="1.0"?>
+<tool_dependency>
+    <package name="R" version="2.11.0">
+        <repository changeset_revision="8d0a55bf7aaf" name="package_r_2_11_0" owner="devteam" toolshed="http://toolshed.g2.bx.psu.edu" />
+    </package>
+    <package name="bedtools" version="2.18.2">
+	<install version="1.0">
+		<actions>
+			<action type="download_by_url" target_filename="bedtools-2.18.2.tar.gz" >https://github.com/arq5x/bedtools2/releases/download/v2.18.2/bedtools-2.18.2.tar.gz</action>
+			<action type="shell_command">make</action>
+			<action type="move_file">
+				<source>bin/</source>	
+				<destination>$INSTALL_DIR/bin</destination>
+			</action>
+			<action type="set_environment">
+				<environment_variable name="PATH" action="prepend_to">$INSTALL_DIR/bin</environment_variable>
+               		</action>
+            	</actions>
+        </install>
+        <readme>
+		Collectively, the bedtools utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks. The most widely-used tools enable genome arithmetic: that is, set theory on the genome. For example, bedtools allows one to intersect, merge, count, complement, and shuffle genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF.
+     	</readme>
+   </package>
+   <package name="samtools" version="0.1.18">
+	<repository changeset_revision="171cd8bc208d" name="package_samtools_0_1_18" owner="devteam" toolshed="http://toolshed.g2.bx.psu.edu" />
+   </package>
+</tool_dependency>				
+