Mercurial > repos > bgruening > deeptools_bam_coverage
annotate bamCoverage.xml @ 12:a270ab018d9e draft
planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit 0a9265a12a303b54cdaa974e82e87c2ac60962ee-dirty
author | bgruening |
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date | Mon, 25 Jan 2016 19:47:29 -0500 |
parents | 300e98d37770 |
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af2607db5c89
planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit e1fd513c18e0d5b53071d99f539ac3509ced01aa-dirty
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1 <tool id="deeptools_bam_coverage" name="bamCoverage" version="@WRAPPER_VERSION@.0"> |
af2607db5c89
planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit e1fd513c18e0d5b53071d99f539ac3509ced01aa-dirty
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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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planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit e1fd513c18e0d5b53071d99f539ac3509ced01aa-dirty
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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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12 |
af2607db5c89
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13 @BINARY@ |
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14 @THREADS@ |
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15 |
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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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21 |
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22 #if $scaling.type=='rpkm': |
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23 --normalizeUsingRPKM |
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24 #elif $scaling.type=='1x': |
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25 #if $scaling.effectiveGenomeSize.effectiveGenomeSize_opt == "specific": |
af2607db5c89
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26 --normalizeTo1x $scaling.effectiveGenomeSize.effectiveGenomeSize |
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27 #else: |
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28 --normalizeTo1x $scaling.effectiveGenomeSize.effectiveGenomeSize_opt |
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29 #end if |
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30 #elif $scaling.type=='own': |
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31 --scaleFactor $scaling.scaleFactor |
af2607db5c89
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32 #end if |
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33 |
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34 #if str($region).strip() != '': |
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35 --region '$region' |
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36 #end if |
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37 |
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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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42 |
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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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49 #end if |
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50 ]]> |
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51 </command> |
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52 |
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53 <inputs> |
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54 <param name="bamInput" format="bam" type="data" label="BAM file" |
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55 help="The BAM file must be sorted."/> |
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56 |
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57 <param name="binSize" type="integer" value="50" min="1" |
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58 label="Bin size in bases" |
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59 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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60 |
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61 <conditional name="scaling"> |
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62 <param name="type" type="select" label="Scaling/Normalization method" > |
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63 <option value="1x">Normalize coverage to 1x</option> |
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64 <option value="rpkm">Normalize to fragments (reads) per kilobase per million (RPKM)</option> |
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65 <option value="no">Do not normalize or scale</option> |
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66 </param> |
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67 <when value="rpkm"> |
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68 <expand macro="scaleFactor" /> |
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69 </when> |
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70 <when value="no"/> |
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71 <when value="1x"> |
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72 <expand macro="effectiveGenomeSize" /> |
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73 <expand macro="scaleFactor" /> |
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74 </when> |
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75 </conditional> |
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76 |
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77 <param name="outFileFormat" type="select" label="Coverage file format"> |
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78 <option value="bigwig" selected="true">bigwig</option> |
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79 <option value="bedgraph">bedgraph</option> |
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80 </param> |
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81 |
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82 <expand macro="region_limit_operation" /> |
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83 |
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84 <conditional name="advancedOpt"> |
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85 <param name="showAdvancedOpt" type="select" label="Show advanced options" > |
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86 <option value="no" selected="true">no</option> |
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87 <option value="yes">yes</option> |
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88 </param> |
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89 <when value="no" /> |
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90 <when value="yes"> |
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91 <expand macro="smoothLength" /> |
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92 |
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93 <param argument="ignoreForNormalization" type="text" value="" |
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94 label="Regions that should be excluded for normalization" |
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95 help="A list of chromosome names separated by spaces |
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96 containing those chromosomes that should be excluded |
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97 during normalization. This is useful when |
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98 considering samples with unequal coverage across |
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99 chromosomes, like male and female samples. Example: chrX chrM" /> |
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100 |
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101 <expand macro="skipNAs" /> |
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102 <expand macro="read_processing_options" /> |
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103 |
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104 <param argument="--MNase" type="boolean" truevalue="--MNase" falsevalue="" |
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105 label="Determine nucleosome positions from MNase-seq data" |
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106 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." /> |
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107 |
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108 </when> |
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109 </conditional> |
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110 </inputs> |
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111 <outputs> |
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112 <data format="bigwig" name="outFileName"> |
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113 <change_format> |
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114 <when input="outFileFormat" value="bigwig" format="bigwig" /> |
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115 <when input="outFileFormat" value="bedgraph" format="bedgraph" /> |
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116 </change_format> |
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117 </data> |
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118 </outputs> |
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119 <tests> |
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120 <test> |
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121 <param name="bamInput" value="bowtie2-test1.bam" ftype="bam" /> |
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122 <param name="outFileFormat" value="bigwig" /> |
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123 <param name="showAdvancedOpt" value="no" /> |
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124 <param name="binSize" value="10" /> |
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125 <param name="type" value="no" /> |
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126 <output name="outFileName" file="bamCoverage_result1.bw" ftype="bigwig" /> |
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127 </test> |
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128 <test> |
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129 <param name="bamInput" value="bowtie2-test1.bam" ftype="bam" /> |
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130 <param name="outFileFormat" value="bigwig" /> |
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131 <param name="showAdvancedOpt" value="no" /> |
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132 <param name="binSize" value="10" /> |
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133 <output name="outFileName" file="bamCoverage_result2.bw" ftype="bigwig" /> |
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134 </test> |
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135 <test> |
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136 <param name="bamInput" value="bowtie2-test1.bam" ftype="bam" /> |
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137 <param name="outFileFormat" value="bedgraph" /> |
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138 <param name="showAdvancedOpt" value="no" /> |
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139 <param name="binSize" value="10" /> |
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140 <output name="outFileName" file="bamCoverage_result3.bg" ftype="bedgraph" /> |
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141 </test> |
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142 <test> |
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143 <param name="bamInput" value="phiX.bam" ftype="bam" /> |
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144 <param name="outFileFormat" value="bigwig" /> |
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145 <param name="showAdvancedOpt" value="no" /> |
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146 <param name="binSize" value="10" /> |
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147 <output name="outFileName" file="bamCoverage_result4.bw" ftype="bigwig" /> |
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148 </test> |
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149 <test> |
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150 <param name="bamInput" value="phiX.bam" ftype="bam" /> |
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151 <param name="outFileFormat" value="bedgraph" /> |
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152 <param name="showAdvancedOpt" value="yes" /> |
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153 <param name="binSize" value="10" /> |
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154 <output name="outFileName" file="bamCoverage_result4.bg" ftype="bedgraph" /> |
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155 </test> |
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156 </tests> |
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157 <help> |
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158 <![CDATA[ |
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159 **What it does** |
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160 |
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161 Given a BAM file, this tool generates a bigWig or bedGraph file of fragment or |
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162 read coverages. The way the method works is by first calculating all the |
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163 number of reads (either extended to match the fragment length or not) that |
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164 overlap each bin in the genome. The resulting read counts can be normalized |
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165 using either a given scaling factor, the RPKM formula or to get a 1x depth of |
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166 coverage (RPGC). In the case of paired-end mapping, each read mate is treated |
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167 independently to avoid a bias when a mixture of concordant and discordant |
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168 pairs is present. This means that *each end* will be extended to match the |
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169 fragment length. |
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170 |
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171 .. image:: $PATH_TO_IMAGES/norm_IGVsnapshot_indFiles.png |
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172 |
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173 |
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174 You can find more details on the bamCoverage doc page: https://deeptools.readthedocs.org/en/master/content/tools/bamCoverage.html |
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175 |
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176 |
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177 **Output files**: |
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178 |
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179 - coverage file either in bigWig or bedGraph format |
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180 |
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181 ----- |
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182 |
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183 @REFERENCES@ |
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184 ]]> |
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185 </help> |
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186 <expand macro="citations" /> |
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187 </tool> |