diff SMART/galaxy/plotCoverage.xml @ 15:440ceca58672

Uploaded
author m-zytnicki
date Mon, 22 Apr 2013 11:08:07 -0400
parents 769e306b7933
children 94ab73e8a190
line wrap: on
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--- a/SMART/galaxy/plotCoverage.xml	Fri Apr 19 10:13:11 2013 -0400
+++ b/SMART/galaxy/plotCoverage.xml	Mon Apr 22 11:08:07 2013 -0400
@@ -169,7 +169,7 @@
 		</conditional>
 
 		<conditional name="optiontitle">
-			<param name="title" type="select" label="title of the plots ">
+			<param name="title" type="select" label="title for the figure">
 					<option value="Yes">Yes</option>
 					<option value="No" selected="true">No</option>
 			</param>
@@ -260,6 +260,12 @@
 	</outputs> 
 	
     <help>
-        This script gives a .tar out file, if you want to take look at the results, you have to download it.
+Plot the coverage of the first set of genomic coordinates with respect to the second set of genomic coordinates. For each element of the second set (we will suppose that they are annotated genes), it computes the number of  elements of the first set (reads, for instance) which overlap it.
+
+Alternatively, if the first file is in GFF format, and contains the **Target** file, you can omit the second file. However, a fasta file corresponding to the second file should be given (to compute the size of the reference elements).
+
+The tool produces two plots per gene. The first plot gives the coverage: a point (*x*, *y*) $ means that *y* reads cover the *x*th nucleotide of the gene. The second figure displays the (possibly spliced) gene in black, and the overlapping reads (blue is colinear, red is anti-sense).
+
+This script gives a .tar out file, if you want to take look at the results, you have to download it.
     </help>		
 </tool>