diff SMART/galaxy/getDifference.xml @ 31:0ab839023fe4

Uploaded

--- a/SMART/galaxy/getDifference.xml	Mon Apr 29 03:45:52 2013 -0400
+++ b/SMART/galaxy/getDifference.xml	Tue Apr 30 14:33:21 2013 -0400
@@ -1,8 +1,5 @@
-<tool id="getDifference" name="get difference">
-	<description>Gets all the regions of the genome, except the one given in an annotation file. Alternatively, it may also give all the elements from the first set which does not ovelap with the second set (at the nucleotide level).</description>
-	<requirements>
-		<requirement type="set_environment">PYTHONPATH</requirement>
-	</requirements>
+<tool id="getDifference" name="get Difference">
+	<description>Gets all the regions of the genome, except the one given or get all the elements from the first set which does not ovelap with the second set (at the nucleotide level).</description>
 	<command interpreter="python">
 		../Java/Python/getDifference.py -i $formatType.inputFileName1
 		#if $formatType.FormatInputFileName1 == 'bed':
@@ -34,6 +31,7 @@
 			-g gtf
 		#end if
 
+
 		$split
 		
 		#if $OptionSequence.option == "Yes":
@@ -104,7 +102,8 @@
 			</when>
 		</conditional>
 
-		<param name="split" type="boolean" truevalue="-p" falsevalue="" checked="false" label="When comparing to a set of genomic coordinates, do not join into exons."/>
+		<param name="split" type="boolean" truevalue="-p" falsevalue="" checked="false" label="split option" help="When comparing to a set of genomic coordinates, do not join."/>
+
 		
 		<conditional name="OptionSequence">
 			<param name="option" type="select" label="Compare with a reference fasta file.">
@@ -122,12 +121,7 @@
 
 
 	<outputs>
-		<data name="outputFileGff" format="gff3" label="[get difference] output file."/>
+		<data name="outputFileGff" format="gff3" label="[getDifference]output File."/>
 	</outputs> 
 
-	<help>
-This tools has two different (but similar) uses. When given two sets of transcripts, it trims the elements of the set so that they do not overlap with the second set.
-
-When only one set of transcripts is given, together with a reference genome, it produces a list of transcripts which complements the first set.
-	</help>
 </tool>