Mercurial > repos > bgruening > deeptools_compute_gc_bias
diff computeGCBias.xml @ 8:1c9d626635b4 draft
planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit 2c5f94de9ddf6798e49b7e9c340c841ca2bfbcfe
author | bgruening |
---|---|
date | Tue, 20 Sep 2016 02:59:47 -0400 |
parents | 12a3082cf023 |
children | 4c03a58a512e |
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--- a/computeGCBias.xml Fri May 13 14:16:53 2016 -0400 +++ b/computeGCBias.xml Tue Sep 20 02:59:47 2016 -0400 @@ -32,13 +32,11 @@ --sampleSize '$advancedOpt.sampleSize' --regionSize '$advancedOpt.regionSize' - #if $advancedOpt.filterOut: - --filterOut $advancedOpt.filterOut - #end if - #if $advancedOpt.extraSampling: --extraSampling $advancedOpt.extraSampling #end if + + @blacklist@ #end if #if str($image_format) != 'none': @@ -72,15 +70,10 @@ is set to 300 bases, which is close to the standard fragment size of many sequencing applications. However, if the depth of sequencing is low, a larger bin size will be required, otherwise many bins will not overlap with any read. (--regionSize)"/> - <param name="filterOut" type="data" format="bed" optional="true" - label="BED file containing genomic regions to be excluded from the estimation of the correction" - help="Such regions usually contain repetitive regions and peaks that, if included, would - bias the correction. It is recommended to filter out known repetitive regions if multi-reads - (reads that map to more than one genomic position) were excluded. In the case of ChIP-seq data, - it is recommended to first use a peak caller to identify and filter out the identified peaks. (--filterOut)" /> <param name="extraSampling" type="data" format="bed" optional="true" label="BED file containing genomic regions for which extra sampling is required because they are underrepresented in the genome" help="(--extraSampling)" /> + <expand macro="blacklist" /> </when> </conditional> <param name="image_format" type="select"