comparison bamCoverage.xml @ 1:66947f20a9a8 draft

planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit 4fc171a2e9d37ef865695a04ff1b12068d8fe427
author bgruening
date Fri, 18 Dec 2015 08:00:06 -0500
parents af2607db5c89
children 8c6f450d266c
comparison
equal deleted inserted replaced
0:af2607db5c89 1:66947f20a9a8
39 #if $advancedOpt.smoothLength: 39 #if $advancedOpt.smoothLength:
40 --smoothLength '$advancedOpt.smoothLength' 40 --smoothLength '$advancedOpt.smoothLength'
41 #end if 41 #end if
42 42
43 @ADVANCED_OPTS_READ_PROCESSING@ 43 @ADVANCED_OPTS_READ_PROCESSING@
44 $advancedOpt.keepNAs 44 $advancedOpt.skipNAs
45 45
46 if str($advancedOpt.ignoreForNormalization).strip() != '': 46 if str($advancedOpt.ignoreForNormalization).strip() != '':
47 --ignoreForNormalization $advancedOpt.ignoreForNormalization 47 --ignoreForNormalization $advancedOpt.ignoreForNormalization
48 end if 48 end if
49 #end if 49 #end if
96 containing those chromosomes that should be excluded 96 containing those chromosomes that should be excluded
97 for computing the normalization. This is useful when 97 for computing the normalization. This is useful when
98 considering samples with unequal coverage across 98 considering samples with unequal coverage across
99 chromosomes like male samples. Example: chrX chrM" /> 99 chromosomes like male samples. Example: chrX chrM" />
100 100
101 <expand macro="keepNAs" /> 101 <expand macro="skipNAs" />
102 <expand macro="read_processing_options" /> 102 <expand macro="read_processing_options" />
103 103
104 <param argument="--MNase" type="boolean" truevalue="--MNase" falsevalue="" 104 <param argument="--MNase" type="boolean" truevalue="--MNase" falsevalue=""
105 label="Determine nucleosome positions from MNase-seq data" 105 label="Determine nucleosome positions from MNase-seq data"
106 help="Only 3 nucleotides at the center of each fragment are counted. The fragment ends are defined by the two mate reads. *NOTE*: Requires paired-end data." /> 106 help="Only 3 nucleotides at the center of each fragment are counted. The fragment ends are defined by the two mate reads. *NOTE*: Requires paired-end data." />