# HG changeset patch
# User hyungrolee
# Date 1402787335 14400
# Node ID 493e3b73c15bebeb9f5cb88b1939c42299448df9
# Parent  2fd354a78c5609b4fbeb9d950181cb845d8b21b9
Uploaded

diff -r 2fd354a78c56 -r 493e3b73c15b nonltr.xml
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/nonltr.xml	Sat Jun 14 19:08:55 2014 -0400
@@ -0,0 +1,61 @@
+<?xml version="1.0"?>
+
+<tool name="MGEScan-nonLTR" id="mgescan-nonltr" version="0.0.1" workflow_compatible="false">
+	<description>
+		computational identification and classification of non-LTR retroelements
+	</description>
+	<!--
+	<action module="galaxy.tools.actions.nonltr" class="nonltrToolAction"/>
+	<requirements>
+		<requirement type="package">HMMER</requirement>
+		<requirement type="package">EMBOSS</requirement>
+	</requirements>
+	-->
+	<command interpreter="bash">
+		<!--	mgescan.sh $input $input.name $hmmver None N $clade $qvalue_en $qvalue_rt None $nonltr_gff3 -->
+			mgescan.sh $input $input.name 3 None N $clade $qvalue_en $qvalue_rt None $nonltr_gff3
+	</command>
+	<inputs>
+		<!--
+		<param name="genome" type="text" label="directory where input genome data exists" />
+		<param name="data" type="text" label="directory of the output" />
+		-->
+		<param format="fasta" name="input" type="data" label="From"/>
+		<!--param name="hmmver" type="select" label="Hmmsearch version">
+			<option selected="selected" value="3">3</option>
+			<option value="2">2</option>
+		</param-->
+	</inputs>
+	<outputs>
+		<data format="fasta" name="clade" />
+		<data format="qfile" name="qvalue_en" />
+		<data format="qfile" name="qvalue_rt" />
+		<data format="gff3" name="nonltr_gff3" />
+	</outputs>
+	<help>
+
+Running the program
+===================
+
+To run MGEScan-nonLTR, follow the steps below:
+
+1. Select genome files a select box. You can upload your genome files through 'Get Data' at Tools menu bar.
+
+2. Click 'Execute' button. This tool reads your genome files and runs the whole process. 
+
+Output
+======
+
+Upon completion, MGEScan-nonLTR generates output, "info" in the data directory you specified. In this "info" directory, two sub-directories ("full" and "validation") are generated.
+
+ - The "full" directory is for storing sequences of elements. Each subdirectory in "full" is the name of clade. In each directory of clade, the DNA sequences of nonLTRs identified are listed. Each sequence is in fasta format. The header contains the position information of TEs identified, [genome_file_name]_[start position in the sequence]
+
+ - For example, >chr1_333 means that this element start at 333bp in the "chr1" file. - The "validation" directory is for storing Q values. In the files "en" and "rt", the first column corresponds to the element name and the last column Q value. 
+
+License
+============
+Copyright 2014 Mina Rho, Haixu Tang.
+You may redistribute this software under the terms of the GNU General Public License.
+
+	</help>
+</tool>