annotate hicBuildMatrix.xml @ 6:30d427846764 draft

planemo upload for repository https://github.com/maxplanck-ie/HiCExplorer/tree/master/galaxy/wrapper/ commit 8def073a083b0619e366436a067a614555190058
author iuc
date Tue, 02 Jan 2018 10:14:52 -0500
parents 3bc1425f9000
children be42758f532e
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1 <tool id="hicexplorer_hicbuildmatrix" name="@BINARY@" version="@WRAPPER_VERSION@.1">
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2 <description>creates a contact matrix</description>
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3 <macros>
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4 <token name="@BINARY@">hicBuildMatrix</token>
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5 <import>macros.xml</import>
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6 </macros>
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7 <expand macro="requirements" >
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8 <requirement type="package" version="1.6">samtools</requirement>
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9 </expand>
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10 <command detect_errors="exit_code"><![CDATA[
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12 mkdir ./QCfolder &&
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13 mkdir $qc.files_path &&
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14 hicBuildMatrix
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16 --samFiles
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17 #for $repeat in $samFiles:
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18 '${repeat.samFile}'
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19 #end for
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20
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21 #if $restrictionCutFileBinSize_conditional.restrictionCutFileBinSize_selector == "optionRestrictionCutFile":
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22 --restrictionCutFile '$restrictionCutFileBinSize_conditional.restrictionCutFile'
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23 --minDistance $restrictionCutFileBinSize_conditional.minDistance
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24 --maxLibraryInsertSize $restrictionCutFileBinSize_conditional.maxLibraryInsertSize
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25 #end if
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27 #if $restrictionCutFileBinSize_conditional.restrictionCutFileBinSize_selector == "optionBinSize":
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28 --binSize $restrictionCutFileBinSize_conditional.binSize
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29 #end if
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32 #if $restrictionSequence:
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33 --restrictionSequence '$restrictionSequence'
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34 #end if
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36 #if $region:
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37 --region '$region'
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38 #end if
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39
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40 #if $outputFormat == 'h5'
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41 --outFileName matrix.h5
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42 #elif $outputFormat == 'cool'
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43 --outFileName matrix.cool
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44 #end if
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45 --outBam ./unsorted.bam
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46
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47 $keepSelfCircles
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49 #if $minMappingQuality and $minMappingQuality is not None:
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50 --minMappingQuality $minMappingQuality
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51 #end if
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52
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53 #if $danglingSequence:
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54 --danglingSequence '$danglingSequence'
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55 #end if
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56
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57 --threads @THREADS@
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58
0
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59 --QCfolder ./QCfolder
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60 &&
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61 mv ./QCfolder/* $qc.files_path/
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62 &&
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63 mv $qc.files_path/hicQC.html $qc
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64 && mv $qc.files_path/*.log raw_qc
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65 && samtools sort ./unsorted.bam -o sorted.bam
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66
0
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67 ]]>
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68 </command>
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69 <inputs>
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70 <repeat max="2" min="2" name="samFiles" title="Sam/Bam files to process">
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71 <param name="samFile" type="data" format="sam,bam"/>
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72 </repeat>
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73 <conditional name="restrictionCutFileBinSize_conditional">
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74 <param name="restrictionCutFileBinSize_selector" type="select" label="Choose to use a restriction cut file or a bin size">
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75 <option value="optionRestrictionCutFile">Restriction cut file</option>
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76 <option value="optionBinSize" selected="True">Bin size</option>
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77 </param>
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78 <when value="optionRestrictionCutFile">
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79 <param argument="--restrictionCutFile" type="data" format="bed" optional="true" label="BED file with all restriction cut places"
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80 help="Should contaion only mappable restriction sites. If given, the bins are set to match the restriction fragments
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81 (i.e. the region between one restriction site and the next)." />
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82 <param argument="--minDistance" type="integer" value="" optional="true" label="Minimum distance between restriction sites"
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83 help="Restriction sites that are closer that this distance are merged into one.
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84 This option only applies if --restrictionCutFile is given."/>
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85 <param argument="--maxLibraryInsertSize" type="integer" value="" optional="true"
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86 label="Maximum library insert size defines different cut offs based on the maximum expected library size"
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87 help="*This is not the average fragment size* but the higher end of the fragment size distribution (obtained using for example Fragment Analyzer)
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88 which usually is between 800 to 1500 bp. If this value if not known use the default of 1000. The insert value is used to decide if two mates
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89 belong to the same fragment (by checking if they are within this max insert size) and to decide if a mate
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90 is too far away from the nearest restriction site." />
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91 </when>
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92 <when value="optionBinSize">
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93 <param argument="--binSize" type="integer" value="" optional="true" label="Bin size in bp"
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94 help="If used, the restriction cut places (if given) are used to only consider reads that are in the vicinity of the resctriction sites.
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95 Otherwise all reads in the interval are considered. "/>
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96 </when>
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97 </conditional>
0
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98
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99 <param argument="--restrictionSequence" type="text" optional="true" label="Sequence of the restriction site"
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100 help="This is used to discard reads that end/start with such sequence and that are considered un-ligated fragments or
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101 &quot;dangling-ends&quot;. If not given, such statistics will not be available." />
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102
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103 <expand macro="region" />
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104
2
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105 <param argument="--keepSelfCircles" type="boolean" truevalue="--keepSelfCircles" falsevalue=""
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106 label="Keep self circles"
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107 help="If set, outward facing reads without any restriction fragment (self circles) are kept. They will be counted and shown in the QC plots." />
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108
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109 <expand macro="minMappingQuality" />
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110
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111 <param argument="--danglingSequence" type="text" optional="true" label="The dangling sequence"
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112 help="Dangling end sequence left by the restriction enzyme. For DpnII for example,
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113 the dangling end is the same restriction sequence. This is used
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114 to discard reads that end/start with such sequence
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115 and that are considered un-ligated fragments or
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116 'dangling-ends'. If not given, such statistics will
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117 not be available."/>
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118 <param name='outputFormat' type='select' label="Output file format">
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119 <option value='h5'>HiCExplorer format</option>
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120 <option value="cool">cool</option>
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121 </param>
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122 </inputs>
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123 <outputs>
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124 <data name="outBam" from_work_dir="sorted.bam" format="bam" label="${tool.name} BAM file on ${on_string}"/>
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125 <data name="outFileName_h5" from_work_dir="matrix.h5" format="h5" label="${tool.name} MATRIX on ${on_string}">
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126 <filter>outputFormat == 'h5'</filter>
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127 </data>
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128 <data name="outFileName_cool" from_work_dir="matrix.cool" format="cool" label="${tool.name} MATRIX on ${on_string}">
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129 <filter>outputFormat == 'cool'</filter>
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130 </data>
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131 <data name="qc" format="html" label="${tool.name} QC"/>
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132 <data name="raw_qc" from_work_dir='raw_qc' label="${tool.name} raw QC" />
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133 </outputs>
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134 <tests>
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135 <test>
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136 <repeat name="samFiles">
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137 <param name="samFile" value="small_test_R1_unsorted.sam"/>
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138 </repeat>
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139 <repeat name="samFiles">
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140 <param name="samFile" value="small_test_R2_unsorted.sam"/>
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141 </repeat>
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142 <conditional name="restrictionCutFileBinSize_conditional">
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143 <param name="restrictionCutFileBinSize_selector" value="optionBinSize"/>
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144 <param name="binSize" value="5000"/>
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145 </conditional>
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146 <param name='outputFormat' value='h5'/>
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147
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148 <output name="outBam" file="small_test_matrix_result_sorted.bam" ftype="bam"/>
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149 <output name="outFileName_h5" file="small_test_matrix_2.h5" ftype="h5" compare="sim_size"/>
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150 <output name="raw_qc" file='raw_qc_report' compare='diff' lines_diff='2'/>
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151 </test>
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152 </tests>
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153 <help><![CDATA[
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154
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155 Creation of the contact matrix
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156 ===============================
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157
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158 ``hicBuildMatrix`` creates a contact matrix based on Hi-C read pairs. It requires two sam or bam files
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159 corresponding to the first and second mates of the paired-end H-C reads. The sam and bam files should
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160 not be sorted by position. There are two main options to create the Hi-C contact matrix, either by
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161 fixed bin size (eg. 10.000 bp) or by bins of variable restriction fragment size length.
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162 ``hicBuildMatrix`` generates a quality control output that can be used to analyze the quality of the Hi-C reads.
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163
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164 Input
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165 -----
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166
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167 `hicBuildMatrix` is having the following parameters:
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168
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169 Parameters
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170 __________
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171
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172
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173 - two input BAM/SAM files
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174 - a bin size
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175 - a restriction cut file as an alternative to the bin size
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176 - restriction sequence: e.g. HindIII: GATC
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177
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178
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179
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180 Output
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181 ------
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182
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183 `hicBuildMatrix` creates as an output:
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184 - the contact matrix
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185 - a bam file with the accepted alignments
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186 - a quality report.
0
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187
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188 Example plot
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189 -----------------------------------------------------------------
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190 .. image:: $PATH_TO_IMAGES/SRR027956.svg
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191 :width: 70%
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192
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193 Contact matrix created with `hicPlotMatrix`.
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194
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195 Quality report
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196 --------------
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197
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198 The quality report gives you information about:
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199
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200 - how many pairs were used to build the contact matrix
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201 - dangling end pairs: These are reads that start with the restriction site and constitute reads that were digested but no ligated.
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202 - same fragment pairs: These are read mates, facing inward, separated by up to 800 bp that do not have a restriction enzyme in between. These read pairs are not valid Hi-C pairs.
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203 - self circles: Self circles are defined as pairs within 25kb with 'outward' read orientation
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204 - self ligations: These are read pairs with a restriction site in between that are within 800 bp.
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205
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206 Contact distance:
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207 _________________
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208 - inter chromosomal
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209 - short range < 20 kb
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210 - long range
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211
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212 Read orientation:
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213 _________________
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214 - inward pairs
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215 - outward pairs
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216 - left pairs
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217 - right pairs
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218
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219 .. image:: $PATH_TO_IMAGES/hicQC.png
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220 :width: 70 %
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221
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222
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223 | For more information about HiCExplorer please consider our documentation on readthedocs.io_.
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224
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225 .. _readthedocs.io: http://hicexplorer.readthedocs.io/en/latest/index.html
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226
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227
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228 ]]></help>
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229 <expand macro="citations" />
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230 </tool>