Mercurial > repos > bgruening > hicexplorer_hiccorrectmatrix

annotate hicCorrectMatrix.xml @ 4:b55d7936cbe0 draft

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planemo upload for repository https://github.com/maxplanck-ie/HiCExplorer/tree/master/galaxy/wrapper/ commit dfa5a68cb20842407941c7ffda9ef956a0e86a04
author iuc
date Sat, 16 Dec 2017 16:35:10 -0500
parents ecf11dda45f7
children 44919af9194b
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d5bf8c60d661 planemo upload for repository https://github.com/maxplanck-ie/HiCExplorer/tree/master/galaxy/wrapper/ commit 2f347b0756d720114f037ed1ff9ba4836e1b3b04
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1 <tool id="hicexplorer_hiccorrectmatrix" name="@BINARY@" version="@WRAPPER_VERSION@.0">
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2 <description>Runs Dekker's iterative correction over a hic matrix.</description>
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3 <macros>
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4 <token name="@BINARY@">hicCorrectMatrix</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 <command detect_errors="exit_code"><![CDATA[
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9
0
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10 ln -s '$matrix' temp_matrix.npz.h5 &&
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11
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12 hicCorrectMatrix
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13 $mode.mode_selector
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14 --matrix temp_matrix.npz.h5
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15
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16 ## special: --chromosomes is optional, but if given needs at least one argument
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17 #set chroms = '" "'.join([ str($var.chromosome) for $var in $chromosomes ])
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18 #if chroms
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19 --chromosomes "$chroms"
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20 #end if
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22 #if $mode.mode_selector == 'correct':
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23
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24 --iterNum $mode.iterNum
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25 --outFileName corrected_matrix.npz.h5
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26
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27 #if $mode.filterThreshold_low and $mode.filterThreshold_large:
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28 --filterThreshold $mode.filterThreshold_low $mode.filterThreshold_large
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29 #end if
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30
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31 #if $mode.inflationCutoff:
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32 --inflationCutoff $mode.inflationCutoff
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33 #end if
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34
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35 #if $mode.transCutoff:
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36 --transCutoff $mode.transCutoff
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37 #end if
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38
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39 #if $mode.sequencedCountCutoff:
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40 --sequencedCountCutoff $mode.sequencedCountCutoff
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41 #end if
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42
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43 $mode.skipDiagonal
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44 $mode.perchr
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45
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46 #elif $mode.mode_selector == 'merge_failed':
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47 --plotName diagnostic_plot.png
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48 --outMatrixFile corrected_matrix.npz.h5
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49 #if $mode.xMax:
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50 --xMax $mode.xMax
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51 #end if
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52 #if $mode.filterThreshold_low and $mode.filterThreshold_large:
2
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53 --filterThreshold '$mode.filterThreshold_low' '$mode.filterThreshold_large'
0
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54 #end if
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55 #else:
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56 --plotName diagnostic_plot.png
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57 #if $mode.xMax:
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58 --xMax $mode.xMax
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59 #end if
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60 #end if
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61
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62 ]]>
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63 </command>
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64 <inputs>
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65 <param argument="--matrix" name="matrix" type="data" format="h5"
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66 label="Hi-C matrix" />
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67
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68 <conditional name="mode">
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69 <param name="mode_selector" type="select" label="Range restriction (in bp)" argument="--range">
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70 <option value="diagnostic_plot">Diagnostic plot</option>
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71 <option value="correct">Correct matrix</option>
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72 </param>
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73 <when value="diagnostic_plot">
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74 <expand macro="xMax" />
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75 </when>
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76 <when value="correct">
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77 <param argument="--iterNum" name="iterNum" type="integer" optional="true" value="500"
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78 label="Number of iterations" />
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79
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80 <param argument="--inflationCutoff" name="inflationCutoff" type="float" optional="true"
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81 label="Inflation cutoff" value=""
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82 help="Value corresponding to the maximum number of times a bin can be scaled up during the iterative correction.
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83 For example, a inflationCutoff of 3 will filter out all bins that were expanded 3 times or more during the iterative correction."/>
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84
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85 <param argument="--transCutoff" name="transCutoff" type="float" optional="true"
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86 label="Trans region cutoff" value=""
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87 help="Clip high counts in the top -transcut trans regions (i.e. between chromosomes). A usual value is 0.05."/>
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88
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89 <param argument="--sequencedCountCutoff" name="sequencedCountCutoff" optional="true" type="float"
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90 label="Sequenced count cutoff"
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91 help="Each bin receives a value indicating the fraction that is covered by reads.
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92 A cutoff of 0.5 will discard all those bins that have less than half of the bin covered."/>
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93
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94 <param argument="--skipDiagonal" name="skipDiagonal" type="boolean" truevalue="--skipDiagonal" falsevalue="" checked="false"
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95 label="Skip diagonal counts"/>
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96
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97 <param argument="--perchr" name="perchr" type="boolean" truevalue="--perchr" falsevalue="" checked="false"
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98 label="Normalize each chromosome separately" />
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99 <expand macro="filterThreshold" />
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100
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101 </when>
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102 </conditional>
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103
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104 <repeat name="chromosomes" min="0"
0
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105 title="Include chromosomes" help="List of chromosomes to be included in the iterative correction.
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106 The order of the given chromosomes will be kept for the resulting corrected matrix">
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107 <param name="chromosome" type="text" value="" >
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108 <validator type="empty_field" />
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109 </param>
0
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110 </repeat>
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111
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112 </inputs>
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113 <outputs>
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114 <data name="outFileName" from_work_dir="corrected_matrix.npz.h5" format="h5">
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115 <filter>mode['mode_selector'] == "correct"</filter>
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116 </data>
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117 <data name="diagnostic_plot" from_work_dir="diagnostic_plot.png" format="png">
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118 <filter>mode['mode_selector'] == "diagnostic_plot"</filter>
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119 </data>
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120 </outputs>
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121 <tests>
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122 <test>
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123 <param name="matrix" value="small_test_matrix.h5" ftype="h5"/>
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124 <param name="mode_selector" value="correct"/>
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125 <repeat name="chromosomes">
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126 <param name="chromosome" value="chrUextra"/>
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127 </repeat>
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128 <repeat name="chromosomes">
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129 <param name="chromosome" value="chr3LHet"/>
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130 </repeat>
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131 <output name="outFileName" file="hicCorrectMatrix_result1.npz.h5" ftype="h5" compare="sim_size"/>
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132 </test>
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133 <test>
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134 <param name="matrix" ftype="h5" value="small_test_matrix.h5"/>
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135 <param name="mode_selector" value="diagnostic_plot"/>
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136 <repeat name="chromosomes">
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137 <param name="chromosome" value="chrUextra"/>
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138 </repeat>
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139 <repeat name="chromosomes">
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140 <param name="chromosome" value="chr3LHet"/>
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141 </repeat>
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142 <output name="diagnostic_plot" file="diagnostic_plot.png" ftype="png" compare="sim_size"/>
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143 </test>
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144 </tests>
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145 <help><![CDATA[
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146
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147 Matrix correction
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148 ==================
0
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149
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150 | ``hicCorrectMatrix`` runs Dekker's iterative correction over a Hi-C matrix (`Imakaev 2012`_.). For correcting the matrix,
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151 | it is important to remove the unassembled scaffolds (e.g. `NT_`), mitochondrial DNA and Y chromosome and keep only
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152 | chromosomes, as scaffolds create problems with matrix correction. Therefore
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153 | we use the chromosome names (1-19, X, Y) here.
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154 |
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155 | **Important**: Use ‘chr1 chr2 chr3 etc.’ if your genome index uses chromosome names with the ‘chr’ prefix.
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156
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157 Matrix correction works in two steps: first a histogram containing the sum of contact per bin (row sum) is produced. This plot needs to be inspected to decide the best threshold for removing bins with lower number of reads. The second steps removes the low scoring bins and does the correction.
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158
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159 Input
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160 -----
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161
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162
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163 Diagnostic plot
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164 ~~~~~~~~~~~~~~~~
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165 Plots a histogram of the coverage per bin together with the
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166 modified z-score based on the median absolute deviation
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167 method.
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168
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169 See Boris Iglewicz and David Hoaglin 1993, Volume 16:
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170 How to Detect and Handle Outliers The ASQC Basic References in Quality Control: Statistical Techniques,
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171 Edward F. Mykytka, Ph.D., Editor.
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172
4
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173 Parameters
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174 __________
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175 - the contact matrix
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176 - Max value for the x-axis in counts per bin
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177 - include chromosomes
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178
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179
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180 Correct
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181 ~~~~~~~
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182
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183 Run the iterative correction.
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184
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185 Parameters
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186 __________
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187 - number of iterations
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188 - inflation cutoff
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189 - trans region cutoff
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190 - sequenced count cutoff
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191 - skip diagonal counts
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192 - normalize each chromosome separately
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193 - remove bins of low coverage
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194 - remove bins of large coverage
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195 - include chromosomes
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196
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197 Output
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198 ------
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199
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200 Diagnostic plot:
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201
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202 .. image:: $PATH_TO_IMAGES/diagnostic_plot.png
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203 :width: 70%
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204
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205 Correct:
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206 - the corrected contact matrix
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207
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208 | For more information about HiCExplorer please consider our documentation on readthedocs.io_
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209
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210 .. _readthedocs.io: http://hicexplorer.readthedocs.io/en/latest/index.html
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211
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212 .. _`Imakaev 2012`: http://doi.org/doi:10.1038/nmeth.2148
0
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213 ]]></help>
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214 <expand macro="citations" />
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215 </tool>
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216