Mercurial > repos > bgruening > deeptools_alignmentsieve

annotate alignmentSieve.xml @ 6:1c41728a2026 draft

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planemo upload for repository https://github.com/deeptools/deepTools/tree/master/galaxy/wrapper/ commit 6f68c67a609ee0ee720f7c6e197fe37ecd940b57
author bgruening
date Tue, 02 Apr 2019 07:14:57 -0400
parents 28b2aa3ac6a6
children 5e3816edfd1b
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1 <tool id="deeptools_alignmentsieve" name="alignmentsieve" version="@WRAPPER_VERSION@.0">
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2 <description>Filter BAM/CRAM files according to specified parameters</description>
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3 <macros>
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4 <token name="@BINARY@">alignmentSieve</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 #import re
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11 #set label = re.sub('[^\.\s\w\-]', '_', str($bamfile.element_identifier))
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12 ln -s '$bamfile' one.bam &&
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13 #if $bamfile.ext == 'bam':
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14 ln -s '${bamfile.metadata.bam_index}' one.bam.bai &&
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15 #else:
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16 ln -s '${bamfile.metadata.cram_index}' one.bam.crai &&
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17 #end if
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18
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19 @BINARY@
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20 @THREADS@
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21 -b one.bam
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22
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23 --label '$label'
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24
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25 #if str($filterRNAstrand) != 'no':
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26 --filterRNAstrand '$filterRNAstrand'
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27 #end if
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28
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29 $ignoreDuplicates
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30
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31 #if $minMappingQuality:
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32 --minMappingQuality '$minMappingQuality'
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33 #end if
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34
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35 #if $samFlagInclude:
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36 --samFlagInclude $samFlagInclude
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37 #end if
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38
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39 #if $samFlagExclude:
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40 --samFlagExclude $samFlagExclude
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41 #end if
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42
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43 #if $minFragmentLength:
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44 --minFragmentLength $minFragmentLength
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45 #end if
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46
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47 #if $maxFragmentLength:
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48 --maxFragmentLength $maxFragmentLength
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49 #end if
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50
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51 #if ' '.join( map(str, $blackListFileName) ) != 'None':
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52 #set blfiles=[]
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53 #for $f in $blackListFileName:
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54 #silent $blfiles.append("'%s'" % $f)
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55 #end for
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56 #if $blfiles != ["'None'"]:
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57 --blackListFileName #echo ' '.join($blfiles)#
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58 #end if
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59 #end if
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60
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61 #if $filterMetrics:
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62 --filterMetrics '$filterMetricsFile'
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63 #end if
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64
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65 #if $filteredOutReads:
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66 --filteredOutReads '$outFileFiltered'
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67 #end if
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68
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69 #if str($shift) != "":
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70 #set shifts = " ".join(["'{}'".format(x) for x in $shift.split(" ")])
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71 --shift $shifts
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72 #elif $ATACshift:
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73 --ATACshift
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74 #end if
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75 #if $BED:
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76 --BED
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77 -o '$outFile'
2
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78 #elif str($shift) != "" or $ATACshift:
0
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79 -o foo.bam &&
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80 samtools sort -o '$outFile' -T foo.tmp -@ "\${GALAXY_SLOTS:-4}" foo.bam &&
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81 rm foo.bam
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82 #else:
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83 -o '$outFile'
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84 #end if
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85 ]]>
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86 </command>
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87
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88 <inputs>
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89 <param name="bamfile" format="bam,cram" type="data" label="BAM file" />
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90 <param name="BED" argument="--BED" type="boolean" label="Output in BEDPE format?"
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91 help="Instead of producing BAM files, write output in BEDPE format (as defined by MACS2). Note that only reads/fragments passing filtering criterion are written in BEDPE format." />
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92 <param argument="--shift" type="text" label="Amount to shift fragments" value=""
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93 help="Shift the left and right end of a fragment. A positive
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94 value shift an end to the right (on the + strand) and
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95 a negative value shifts a fragment to the left. Either
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96 2 or 4 integers can be provided. For example, '2 -3'
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97 will shift the left-most fragment end two bases to the
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98 right and the right-most end 3 bases to the left. If 4
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99 integers are provided, then the first and last two
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100 refer to fragments whose read 1 is on the left or
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101 right, respectively. Consequently, it is possible to
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102 take strand into consideration for strand-specific
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103 protocols. Note that only properly paired reads are considered."/>
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104 <param argument="--ATACshift" type="boolean" label="Shift fragment ends as appropriate for ATAC-seq" />
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105 <param argument="filterRNAstrand" type="select" label="Only include reads originating from fragments from the forward or reverse strand."
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106 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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107 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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108 <option value="no" selected="true">no</option>
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109 <option value="forward">forward</option>
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110 <option value="reverse">reverse</option>
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111 </param>
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112
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113 <expand macro="ignoreDuplicates" />
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114 <expand macro="minMappingQuality" />
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115 <expand macro="samFlags" />
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116 <expand macro="fragLength" />
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117 <expand macro="blacklist" />
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118 <param argument="--filterMetrics" type="boolean" label="Save the total number of reads seen and remaining after filtering to a text file?" help="" />
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119 <param argument="--filteredOutReads" type="boolean" label="Save alignments NOT passing the filtering criteria?" help="" />
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120 </inputs>
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121 <outputs>
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122 <data format="tabular" name="filterMetricsFile" label="${tool.name} on ${on_string}: filtering metrics">
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123 <filter>filterMetrics is True</filter>
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124 </data>
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125 <data format="bam" name="outFileFiltered" label="${tool.name} on ${on_string}: Filtered Out Alignments">
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126 <filter>filteredOutReads is True</filter>
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127 </data>
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128 <data format="bam" name="outFile" label="${tool.name} on ${on_string}">
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129 <change_format>
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130 <when input="BED" value='true' format='bed'/>
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131 </change_format>
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132 </data>
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133 </outputs>
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134 <tests>
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135 <test>
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136 <param name="bamfile" value="paired_chr2L.bam" ftype="bam" />
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137 <param name="minMappingQuality" value="10" />
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138 <param name="filterMetrics" value="True" />
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139 <output name="outFile" file="alignmentSieve.bam" ftype="bam" />
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140 <output name="filterMetricsFile" file="alignmentSieve.txt" ftype="tabular" />
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141 </test>
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142 <test>
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143 <param name="bamfile" value="paired_chr2L.bam" ftype="bam" />
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144 <param name="minMappingQuality" value="10" />
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145 <param name="BED" value="yes" />
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146 <param name="shift" value="1 -2 3 -4" />
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147 <output name="outFile" file="alignmentSieve.bed" ftype="bed" />
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148 </test>
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149 <test>
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150 <param name="bamfile" value="paired_chr2L.bam" ftype="bam" />
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151 <param name="minMappingQuality" value="10" />
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152 <param name="shift" value="1 -2 3 -4" />
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153 <output name="outFile" file="alignmentSieve2.bam" ftype="bam" />
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154 </test>
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155 <test>
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156 <param name="bamfile" value="paired_chr2L.cram" ftype="cram" />
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157 <param name="minMappingQuality" value="10" />
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158 <param name="shift" value="1 -2 3 -4" />
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159 <output name="outFile" file="alignmentSieve3.bam" ftype="bam" />
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160 </test>
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161 </tests>
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162
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163 <help>
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164 <![CDATA[
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165
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166 What it does
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167 -------------
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168
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169 This tool is very much the counterpart of estimateReadFiltering, in that it can filter alignments based on a variety of desired criterion. While much of this can be done with samtools, this tool can additionally filter by fragment strand and length (e.g., for RNA-seq and ATAC-seq experiments, respectively). Finally, this program can produce BEDPE files, which can be used as input into MACS2 for peak calling, where the fragment ends have been optionally shifted.
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170
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171 Output
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172 --------
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173
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174 The primary output is a BAM file with all alignments passing the desired criteria. Note that all unmapped reads are removed. Additionally, an optional text file can be produced with the following entries:
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175
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176 * Number of reads passing the filtering criteria
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177 * Total number of initial reads
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178
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179 Instead of producing a filtered BAM file, a BEDPE file appropriate for use with MACS2 can be used, optionally with fragment ends shifted. This is useful in cases like ATAC-seq.
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180
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181 The ``--shift`` option can take either 2 or 4 integers. If two integers are given, then the first value shifts the left-most end of a fragment and the second the right-most end. Positive values shift to the right and negative values to the left. See below for how setting ``--shift`` to '-5 3' would shift a single fragment::
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182
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183 ----> read 1
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184 read 2 <----
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185
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186 ------------------------ fragment
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187
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188 -------------------------------- shifted fragment
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189
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190 The same results will be produced if read 1 and read 2 are swapped. If, instead, the protocol is strand-specific, then the first set of integers in a pair would be applied to fragments where read 1 precedes read 2, and the second set to cases where read 2 precedes read 1. In this case, the first value in each pair is applied to the end of read 1 and the second to the end of read 2. For example, suppose "-5 3 -1 4" were given as the option to ``--shift``. The ``-5 3`` set would produce the following::
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191
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192 ----> read 1
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193 read 2 <----
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194
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195 ------------------------ fragment
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196
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197 -------------------------------- shifted fragment
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198
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199 and the ``-1 4`` set would produce the following::
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200
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201 ----> read 2
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202 read 1 <----
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203
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204 ------------------------ fragment
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205
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206 --------------------- shifted fragment
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207
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208 As can be seen, such fragments are considered to be on the ``-`` strand, so negative values then shift to the left on its frame of reference (thus, to the right relative to the ``+`` strand).
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209
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210 -----
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211
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212 @REFERENCES@
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213 ]]>
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214 </help>
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215 <expand macro="citations" />
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216 </tool>