diff bamCoverage.xml @ 29:3a2aab18a217 draft

Uploaded
author bgruening
date Tue, 16 Sep 2014 13:46:05 -0400
parents f7712a057440
children 5231f398d784
line wrap: on
line diff
--- a/bamCoverage.xml	Wed Apr 02 09:15:44 2014 -0400
+++ b/bamCoverage.xml	Tue Sep 16 13:46:05 2014 -0400
@@ -47,6 +47,8 @@
                 --minMappingQuality '$advancedOpt.minMappingQuality'
             #end if
 
+            --missingDataAsZero $advancedOpt.missingDataAsZero
+
             ##if str($advancedOpt.ignoreForNormalization).strip() != '':
             ##    --ignoreForNormalization $advancedOpt.ignoreForNormalization
             ##end if
@@ -114,6 +116,8 @@
                     label="Minimum mapping quality"
                     help= "If set, only reads that have a mapping quality score higher than the given value are considered. *Note* Bowtie's Mapping quality is related to uniqueness: the higher the score, the more unique is a read. A mapping quality defined by Bowtie of 10 or less indicates that there is at least a 1 in 10 chance that the read truly originated elsewhere."/>
 
+                <expand macro="missingDataAsZero" />
+
              <!--   <param name="ignoreForNormalization" type="text" value="" size="50"
                     label="regions that should be excluded for calculating the scaling factor"
                     help="Sometimes it makes sense to exclude certain regions when calculating the scaling factor. For example, if you know some regions that you suspect to be present more often in your sample's genome than in the reference genome that will therefore accumulate reads (CNV). Another typical example is the single X chromosome in male samples that should be scaled separately from the diploid autosomes. For example chrX,chrY,chr3. or chr10:12220-128932" />
@@ -158,4 +162,5 @@
 @REFERENCES@
 
     </help>
+    <expand macro="citations" />
 </tool>