Mercurial > repos > bgruening > deeptools_bam_coverage

annotate bamCoverage.xml @ 9:e22b1110529c draft

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planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit 2f53e1ab939f99201f72ef1a900cb9c542e3f484
author bgruening
date Tue, 25 Oct 2016 19:12:11 -0400
parents 028fcce954f1
children aa33302db115
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1 <tool id="deeptools_bam_coverage" name="bamCoverage" version="@WRAPPER_VERSION@.0">
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2 <description>generates a coverage bigWig file from a given BAM file</description>
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3 <macros>
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4 <token name="@BINARY@">bamCoverage</token>
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5 <import>deepTools_macros.xml</import>
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6 </macros>
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7 <expand macro="requirements" />
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8 <command>
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9 <![CDATA[
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10 ln -s '$bamInput' one.bam &&
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11 ln -s '${bamInput.metadata.bam_index}' one.bam.bai &&
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13 @BINARY@
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14 @THREADS@
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16 --bam one.bam
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17 --outFileName '$outFileName'
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18 --outFileFormat '$outFileFormat'
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19
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20 --binSize $binSize
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22 #if $scaling.type=='rpkm':
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23 --normalizeUsingRPKM
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24 --scaleFactor $scaling.scaleFactor
0
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25 #elif $scaling.type=='1x':
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26 #if $scaling.effectiveGenomeSize.effectiveGenomeSize_opt == "specific":
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27 --normalizeTo1x $scaling.effectiveGenomeSize.effectiveGenomeSize
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28 #else:
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29 --normalizeTo1x $scaling.effectiveGenomeSize.effectiveGenomeSize_opt
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30 #end if
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31 --scaleFactor $scaling.scaleFactor
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32 #end if
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33
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34 #if str($region).strip() != '':
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35 --region '$region'
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36 #end if
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38 #if $advancedOpt.showAdvancedOpt == "yes":
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39 #if $advancedOpt.smoothLength:
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40 --smoothLength '$advancedOpt.smoothLength'
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41 #end if
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43 @ADVANCED_OPTS_READ_PROCESSING@
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44 $advancedOpt.skipNAs
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45
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46 #if str($advancedOpt.ignoreForNormalization).strip() != '':
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47 --ignoreForNormalization $advancedOpt.ignoreForNormalization
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48 #end if
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50 #if str($advancedOpt.filterRNAstrand) != 'no':
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51 --filterRNAstrand '$advancedOpt.filterRNAstrand'
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52 #end if
8
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53
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54 #if $advancedOpt.Offset:
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55 --Offset '$advancedOpt.Offset'
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56 #end if
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57
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58 @blacklist@
0
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59 #end if
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60 ]]>
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61 </command>
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62
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63 <inputs>
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64 <param name="bamInput" format="bam" type="data" label="BAM file"
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65 help=""/>
0
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66
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67 <param name="binSize" type="integer" value="50" min="1"
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68 label="Bin size in bases"
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69 help="The genome will be divided into bins of the specified size. For each bin, the overlaping number of fragments (or reads) will be reported. If only half a fragment overlaps, this fraction will be reported. "/>
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70
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71 <conditional name="scaling">
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72 <param name="type" type="select" label="Scaling/Normalization method" >
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73 <option value="1x">Normalize coverage to 1x</option>
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74 <option value="rpkm">Normalize to fragments (reads) per kilobase per million (RPKM)</option>
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75 <option value="no">Do not normalize or scale</option>
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76 </param>
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77 <when value="rpkm">
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78 <expand macro="scaleFactor" />
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79 </when>
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80 <when value="no"/>
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81 <when value="1x">
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82 <expand macro="effectiveGenomeSize" />
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83 <expand macro="scaleFactor" />
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84 </when>
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85 </conditional>
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86
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87 <param name="outFileFormat" type="select" label="Coverage file format">
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88 <option value="bigwig" selected="true">bigwig</option>
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89 <option value="bedgraph">bedgraph</option>
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90 </param>
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91
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92 <expand macro="region_limit_operation" />
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93
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94 <conditional name="advancedOpt">
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95 <param name="showAdvancedOpt" type="select" label="Show advanced options" >
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96 <option value="no" selected="true">no</option>
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97 <option value="yes">yes</option>
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98 </param>
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99 <when value="no" />
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100 <when value="yes">
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101 <expand macro="smoothLength" />
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102
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103 <param argument="ignoreForNormalization" type="text" value=""
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104 label="Regions that should be excluded for normalization"
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105 help="A list of chromosome names separated by spaces
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106 containing those chromosomes that should be excluded
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107 during normalization. This is useful when
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108 considering samples with unequal coverage across
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109 chromosomes, like male and female samples. Example: chrX chrM" />
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110
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111 <expand macro="skipNAs" />
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112 <expand macro="read_processing_options" />
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113
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114 <param argument="--MNase" type="boolean" truevalue="--MNase" falsevalue=""
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115 label="Determine nucleosome positions from MNase-seq data"
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116 help="Only the 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. By default, only fragments between 130 and 200 bases will be used, though this can be changed with the --minFragmentLength and --maxFragmentLength options." />
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117
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118 <param argument="--Offset" type="integer" value="" optional="True"
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119 label="Offset inside each alignment to use for the signal location."
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120 help="Uses this offset inside of each read as the signal. This is useful in
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121 cases like RiboSeq or GROseq, where only the 12th, 15th or 1st base aligned
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122 should be used to denote where the signal is (rather than the span of the
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123 whole alignment). This can be paired with the --filterRNAstrand option. Note
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124 that negative values indicate offsets from the end of each read. A value of
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125 1 indicates the first base of the alignment (taking alignment orientation
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126 into account). Likewise, a value of -1 is the last base of the alignment. An
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127 offset of 0 is not permitted. By default, the entire alignment is used to
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128 denote where the signal is located." />
0
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129
3
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130 <param argument="filterRNAstrand" type="select" label="Only include reads originating from fragments from the forward or reverse strand."
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131 help="By default (the no option), all reads are processed, regardless of the strand they originated from. For RNAseq, it can be useful to separately create bigWig files for the forward or reverse strands.
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132 Note that this tools assumes that a dUTP-based method was used, so fragments will be assigned to the reverse strand if the second read in a pair is reverse complemented.">
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133 <option value="no" selected="true">no</option>
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134 <option value="forward">forward</option>
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135 <option value="reverse">reverse</option>
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136 </param>
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137 <expand macro="blacklist" />
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138
0
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139 </when>
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140 </conditional>
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141 </inputs>
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142 <outputs>
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143 <data format="bigwig" name="outFileName">
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144 <change_format>
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145 <when input="outFileFormat" value="bigwig" format="bigwig" />
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146 <when input="outFileFormat" value="bedgraph" format="bedgraph" />
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147 </change_format>
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148 </data>
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149 </outputs>
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150 <tests>
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151 <test>
6
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152 <param name="bamInput" value="bowtie2 test1.bam" ftype="bam" />
0
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153 <param name="outFileFormat" value="bigwig" />
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154 <param name="showAdvancedOpt" value="no" />
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155 <param name="binSize" value="10" />
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156 <param name="type" value="no" />
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157 <output name="outFileName" file="bamCoverage_result1.bw" ftype="bigwig" />
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158 </test>
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159 <test>
6
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160 <param name="bamInput" value="bowtie2 test1.bam" ftype="bam" />
0
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161 <param name="outFileFormat" value="bigwig" />
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162 <param name="showAdvancedOpt" value="no" />
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163 <param name="binSize" value="10" />
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164 <output name="outFileName" file="bamCoverage_result2.bw" ftype="bigwig" />
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165 </test>
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166 <test>
6
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167 <param name="bamInput" value="bowtie2 test1.bam" ftype="bam" />
0
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168 <param name="outFileFormat" value="bedgraph" />
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169 <param name="showAdvancedOpt" value="no" />
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170 <param name="binSize" value="10" />
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171 <output name="outFileName" file="bamCoverage_result3.bg" ftype="bedgraph" />
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172 </test>
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173 <test>
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174 <param name="bamInput" value="phiX.bam" ftype="bam" />
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175 <param name="outFileFormat" value="bigwig" />
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176 <param name="showAdvancedOpt" value="no" />
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177 <param name="binSize" value="10" />
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178 <output name="outFileName" file="bamCoverage_result4.bw" ftype="bigwig" />
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179 </test>
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180 <test>
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181 <param name="bamInput" value="phiX.bam" ftype="bam" />
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182 <param name="outFileFormat" value="bedgraph" />
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183 <param name="showAdvancedOpt" value="yes" />
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184 <param name="binSize" value="10" />
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185 <output name="outFileName" file="bamCoverage_result4.bg" ftype="bedgraph" />
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186 </test>
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187 <test>
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188 <param name="bamInput" value="phiX.bam" ftype="bam" />
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189 <param name="outFileFormat" value="bigwig" />
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190 <param name="showAdvancedOpt" value="yes" />
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191 <param name="filterRNAstrand" value="reverse" />
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192 <param name="binSize" value="10" />
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193 <output name="outFileName" file="bamCoverage_result5.bw" ftype="bigwig" />
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194 </test>
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195 </tests>
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196 <help>
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197 <![CDATA[
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198
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199 What it does
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200 --------------
0
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201
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202 Given a BAM file, this tool generates a bigWig or bedGraph file of fragment or
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203 read coverages. The way the method works is by first calculating all the
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204 number of reads (either extended to match the fragment length or not) that
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205 overlap each bin in the genome. The resulting read counts can be normalized
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206 using either a given scaling factor, the RPKM formula or to get a 1x depth of
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207 coverage (RPGC). In the case of paired-end mapping, each read mate is treated
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208 independently to avoid a bias when a mixture of concordant and discordant
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209 pairs is present. This means that *each end* will be extended to match the
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210 fragment length.
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211
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212 See the usage hints below.
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213
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214 .. image:: $PATH_TO_IMAGES/norm_IGVsnapshot_indFiles.png
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215 :width: 600
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216 :height: 336
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217
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218 Output
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219 -------------
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220
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221 ``bamCoverage`` produces a coverage file, either in bigWig or bedGraph format, where for each bin the number of overlapping reads (possibly normalized) is noted.
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222
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223 Like BAM files, bigWig files are compressed, binary files. If you would like to see the coverage values, choose the bedGraph output. For more information on typical NGS file formats, see our `Glossary <http://deeptools.readthedocs.org/en/latest/content/help_glossary.html#file-formats>`_
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224
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225 .. image:: $PATH_TO_IMAGES/bamCoverage_output.png
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226 :width: 600
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227 :height: 450
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228
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229 Usage hints
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230 ------------
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231
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232 * A smaller ``bin size`` value will result in a higher resolution of the coverage track but also in a larger file size.
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233 * The ``1x normalization`` (RPGC) requires the input of a value for the **effective genome size**, which is the mappable part of the reference genome. Of course, this value is species-specific.
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234 * It might be useful for some studies to exclude certain chromosomes in order to avoid biases, e.g. chromosome X for many mammals where the males contain a pair of each autosome, but often only a single X chromosome.
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235 * By default, the read length is **NOT** extended! This is the preferred setting for **spliced-read** data like RNA-seq, where one usually wants to rely on the detected read locations only. A read extension would neglect potential splice sites in the unmapped part of the fragment.
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236 Other data, e.g. ChIP-seq, where fragments are known to map contiuously, should be processed with read extension (``--extendReads [INT]``).
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237 * For paired-end data, the fragment length is generally defined by the two read mates. The user-provided fragment length is only used as a fallback for singletons or mate reads that map too far apart (with a distance greater than four times the fragment length or if the mates are located on different chromosomes).
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238
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239 WARNING: If you already normalized for GC bias using ``correctGCbias``, you should absolutely **NOT** set the parameter ``--ignoreDuplicates``!
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240
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241
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242 -----
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243
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244 @REFERENCES@
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245 ]]>
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246 </help>
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247 <expand macro="citations" />
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248 </tool>