Mercurial > repos > matthias > dada2_filterandtrim

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planemo upload for repository https://github.com/bernt-matthias/mb-galaxy-tools/tree/topic/dada2/tools/dada2 commit df2dfeb75f88b326f567cab8df4e6c4a7f2e548c
author matthias
date Tue, 15 Oct 2019 07:26:30 -0400
parents fafeee96dead
children
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1 <tool id="dada2_filterAndTrim" name="dada2: filterAndTrim" version="@DADA2_VERSION@+galaxy@WRAPPER_VERSION@" profile="19.09">
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2 <description>Filters and trims an short read data</description>
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3 <macros>
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4 <import>macros.xml</import>
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5 </macros>
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6 <expand macro="requirements"/>
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7 <expand macro="stdio"/>
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8 <expand macro="version_command"/>
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9 <command detect_errors="exit_code"><![CDATA[
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10 Rscript '$dada2_script'
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11 ## && sed -i '1!b;s/^/#dataset/' $outtab
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12 ]]></command>
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13 <configfiles>
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14 <configfile name="dada2_script"><![CDATA[
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15 truncQ <- c($trim.truncQ)
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16 truncLen <- c($trim.truncLen)
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17 trimLeft <- c($trim.trimLeft)
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18 trimRight <- c($trim.trimRight)
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19 #if str($filter.maxLen) == ""
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20 maxLen <- c(Inf)
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21 #else:
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22 maxLen <- c($filter.maxLen)
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23 #end if
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24 minLen <- c($filter.minLen)
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25 maxN <- c($filter.maxN)
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26 minQ <- c($filter.minQ)
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27 #if str($filter.maxEE) == ""
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28 maxEE <- c(Inf)
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29 #else:
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30 maxEE <- c($filter.maxEE)
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31 #end if
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32 #if $paired_cond.paired_select != "single" and $seprev_cond.seprev_select == "yes"
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33 truncQ <- c(truncQ,$seprev_cond.trim.truncQ)
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34 truncLen <- c(truncLen,$seprev_cond.trim.truncLen)
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35 trimLeft <- c(trimLeft,$seprev_cond.trim.trimLeft)
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36 trimRight <- c(trimRight,$seprev_cond.trim.trimRight)
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37 #if str($seprev_cond.filter.maxLen) == ""
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38 maxLen <- c(maxLen,Inf)
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39 #else:
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40 maxLen <- c(maxLen,$seprev_cond.filter.maxLen)
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41 #end if
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42 minLen <- c(minLen,$seprev_cond.filter.minLen)
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43 maxN <- c(maxN,$seprev_cond.filter.maxN)
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44 minQ <- c(minQ,$seprev_cond.filter.minQ)
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45 #if str($seprev_cond.filter.maxEE) == ""
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46 maxEE <- c(maxEE,Inf)
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47 #else:
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48 maxEE <- c(maxEE,$seprev_cond.filter.maxEE)
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49 #end if
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50 #end if
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51
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52 fwd <- NULL
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53 rev <- NULL
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54 filt.fwd <- NULL
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55 filt.rev <- NULL
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56 #if $paired_cond.paired_select == "paired"
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57 fwd <- c(fwd, '$paired_cond.reads.forward')
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58 rev <- c(rev, '$paired_cond.reads.reverse')
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59 filt.fwd <- c(filt.fwd, '$paired_output.forward')
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60 filt.rev <- c(filt.rev, '$paired_output.reverse')
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61 #else if $paired_cond.paired_select == "separate"
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62 fwd <- c(fwd, '$paired_cond.reads')
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63 rev <- c(rev, '$paired_cond.sdaer')
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64 filt.fwd <- c(filt.fwd, '$output_fwd')
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65 filt.rev <- c(filt.rev, '$output_rev')
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66 #else
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67 fwd <- c(fwd, '$paired_cond.reads')
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68 filt.fwd <- c(filt.fwd, '$output_single')
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69 #end if
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70
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71 library(dada2, quietly=T)
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72
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73 ftout <- filterAndTrim(fwd, filt.fwd, rev = rev, filt.rev, compress = TRUE,
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74 truncQ = truncQ, truncLen = truncLen, trimLeft = trimLeft, trimRight = trimRight, maxLen = maxLen,
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75 minLen = minLen, maxN = maxN, minQ = minQ, maxEE = maxEE, rm.phix = $rmPhiX, orient.fwd = '$orientFwd')
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76
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77 rownames(ftout) <- c( '$paired_cond.reads.element_identifier' )
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78 write.table(ftout, "$outtab", quote=F, sep="\t", col.names=NA)
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79 ]]></configfile>
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80 </configfiles>
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81 <inputs>
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82 <expand macro="fastq_input" multiple="False" collection_type="paired" argument_fwd="fwd" argument_rev="rev"/>
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83 <expand macro="trimmers"/>
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84 <expand macro="filters"/>
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85 <conditional name="seprev_cond">
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86 <param name="seprev_select" type="select" label="Separate filters and trimmers for reverse reads" help="only applies to paired end data">
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87 <option value="no">no</option>
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88 <option value="yes">yes</option>
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89 </param>
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90 <when value="no"/>
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91 <when value="yes">
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92 <expand macro="trimmers"/>
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93 <expand macro="filters"/>
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94 </when>
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95 </conditional>
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96 <param argument="rmPhiX" truevalue="TRUE" falsevalue="FALSE" type="boolean" checked="true" label="Discard reads matching the PhiX genome" />
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97 <param name="orientFwd" argument="orient.fwd" type="text" value="" optional="true" label="String present at the start of valid reads" help="see below"/>
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98 <param name="output_statistics" truevalue="TRUE" falsevalue="FALSE" type="boolean" checked="true" label="Output statistics" help="Create extra table with the number of reads pre and post filtering" />
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99 </inputs>
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100 <outputs>
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101 <collection name="paired_output" type="paired" format_source="reads['forward']">
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102 <filter>paired_cond['paired_select'] == "paired"</filter>
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103 </collection>
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104 <data name="output_single" format_source="reads" >
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105 <filter>paired_cond['paired_select'] == "single"</filter>
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106 </data>
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107 <data name="output_fwd" format_source="reads" label="${tool.name} on ${on_string}: Forward reads" >
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108 <filter>paired_cond['paired_select'] == "separate"</filter>
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109 </data>
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110 <data name="output_rev" format_source="sdaer" label="${tool.name} on ${on_string}: Reverse reads" >
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111 <filter>paired_cond['paired_select'] == "separate"</filter>
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112 </data>
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113 <data name="outtab" format="tabular" label="${tool.name} on ${on_string}: Statistics">
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114 <filter>output_statistics</filter>
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115 </data>
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116 </outputs>
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117 <tests>
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118 <!-- paired data
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119 currently removed `expect_num_outputs="2"` because of https://github.com/galaxyproject/galaxy/pull/7894-->
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120 <test expect_num_outputs="4">
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121 <conditional name="paired_cond">
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122 <param name="paired_select" value="paired"/>
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123 <param name="reads">
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124 <collection type="paired">
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125 <element name="forward" value="F3D0_S188_L001_R1_001.fastq.gz" ftype="fastqsanger.gz"/>
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126 <element name="reverse" value="F3D0_S188_L001_R2_001.fastq.gz" ftype="fastqsanger.gz"/>
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127 </collection>
2
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128 </param>
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129 </conditional>
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130 <output_collection name="paired_output" type="paired" count="2">
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131 <element name="forward" value="filterAndTrim_F3D0_R1.fq.gz" ftype="fastqsanger.gz" />
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132 <element name="reverse" value="filterAndTrim_F3D0_R2.fq.gz" ftype="fastqsanger.gz" />
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133 </output_collection>
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134 <output name="outtab" value="filterAndTrim_F3D0.tab" ftype="tabular"/>
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135 </test>
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136 <!-- separate paired data -->
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137 <test expect_num_outputs="3">
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138 <conditional name="paired_cond">
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139 <param name="paired_select" value="separate"/>
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140 <param name="reads" value="F3D0_S188_L001_R1_001.fastq.gz" ftype="fastqsanger.gz"/>
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141 <param name="sdaer" value="F3D0_S188_L001_R2_001.fastq.gz" ftype="fastqsanger.gz"/>
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142 </conditional>
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143 <output name="output_fwd" value="filterAndTrim_F3D0_R1.fq.gz" ftype="fastqsanger.gz" />
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144 <output name="output_rev" value="filterAndTrim_F3D0_R2.fq.gz" ftype="fastqsanger.gz" />
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145 <output name="outtab" value="filterAndTrim_F3D0.tab" ftype="tabular" compare="sim_size"/>
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146 </test>
2
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147 <!-- single end data -->
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148 <test expect_num_outputs="1">
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149 <conditional name="paired_cond">
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150 <param name="paired_select" value="single"/>
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151 <param name="reads" value="F3D0_S188_L001_R1_001.fastq.gz" ftype="fastqsanger.gz"/>
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152 </conditional>
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153 <param name="output_statistics" value="FALSE" />
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154 <output name="output_fwd" value="filterAndTrim_single_F3D0_R1.fq.gz" ftype="fastqsanger.gz" />
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155 </test>
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156 <!-- single end data trimming -->
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157 <test expect_num_outputs="1">
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158 <conditional name="paired_cond">
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159 <param name="paired_select" value="single"/>
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160 <param name="reads" value="F3D0_S188_L001_R1_001.fastq.gz" ftype="fastqsanger.gz"/>
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161 </conditional>
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162 <param name="trim|truncQ" value="30" />
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163 <param name="trim|trimLeft" value="150" />
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164 <param name="trim|trimRight" value="2" />
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165 <param name="trim|truncLen" value="2" />
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166 <param name="output_statistics" value="FALSE" />
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167 <output name="output_fwd" value="filterAndTrim_single_trimmers_F3D0_R1.fq.gz" ftype="fastqsanger.gz" />
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168 </test>
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169 <!-- single end data filtering -->
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170 <test expect_num_outputs="1">
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171 <conditional name="paired_cond">
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172 <param name="paired_select" value="single"/>
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173 <param name="reads" value="F3D0_S188_L001_R1_001.fastq.gz" ftype="fastqsanger.gz"/>
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174 </conditional>
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175 <param name="filter|maxLen" value="255" />
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176 <param name="filter|minLen" value="60" />
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177 <param name="filter|maxN" value="100" />
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178 <param name="filter|minQ" value="13" />
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179 <param name="filter|maxEE" value="1" />
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180 <param name="output_statistics" value="FALSE" />
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181 <output name="output_fwd" value="filterAndTrim_single_filters_F3D0_R1.fq.gz" ftype="fastqsanger.gz" />
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182 </test>
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183 <!-- paired data w separate filters and trimmers for reverse
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184 currently removed `expect_num_outputs="1"` because of https://github.com/galaxyproject/galaxy/pull/7894-->
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185 <test expect_num_outputs="3">
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186 <conditional name="paired_cond" >
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187 <param name="paired_select" value="paired"/>
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188 <param name="reads">
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189 <collection type="paired">
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190 <element name="forward" value="F3D0_S188_L001_R1_001.fastq.gz" ftype="fastqsanger.gz"/>
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191 <element name="reverse" value="F3D0_S188_L001_R2_001.fastq.gz" ftype="fastqsanger.gz"/>
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192 </collection>
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193 </param>
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194 </conditional>
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195 <param name="seprev_cond|seprev_select" value="yes"/>
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196 <param name="seprev_cond|trim|truncQ" value="30" />
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197 <param name="seprev_cond|trim|trimLeft" value="150" />
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198 <param name="seprev_cond|trim|trimRight" value="2" />
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199 <param name="seprev_cond|trim|truncLen" value="2" />
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200 <param name="seprev_cond|filter|maxLen" value="255" />
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201 <param name="seprev_cond|filter|minLen" value="60" />
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202 <param name="seprev_cond|filter|maxN" value="100" />
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203 <param name="seprev_cond|filter|minQ" value="13" />
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204 <param name="seprev_cond|filter|maxEE" value="1" />
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205 <param name="output_statistics" value="FALSE" />
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206 <output_collection name="paired_output" type="paired" count="2"/>
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207 </test>
0
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208 </tests>
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209
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210 <help><![CDATA[
2
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211 Description
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212 ...........
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213
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214 Filters and trims a FASTQ dataset (can be compressed) based on several user-definable criteria, and outputs a compressed FASTQ data set containing those trimmed reads which passed the filters. For paired end data forward and reverse FASTQ datasets can be provided as pair of FASTQ datasets (or two separate data sets), in which case filtering is performed on the forward and reverse reads independently, and both reads must pass for the read pair to be in the output.
2
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215
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216 Usage
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217 .....
2
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218
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219 **Input** is a FASTQ dataset (or a pair in case of paired end data) containing all reads of a sample. It is suggested to organize them in a (paired) collection (in particular if you have multiple samples).
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220
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221 **Output** is a (paired) collection of filtered and trimmed paired FASTQ datasets (again one data set or pair per sample).
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222
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223 Upstream dada2 tools are *dada2: derepFastq* and *dada2: learnErrorRates*. Note that these tools do not work on paired end data. So, if you have paired end data you need to split the generated paired collection into one containing the forward reads and one containing the reverse reads. This can be done by the *unzip collection* tool.
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224
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225 An additional tabular output gives the number of reads before and after trimming. This can data set can be used as input for *dada2: sequence counts* to track the sequence counts for each sample through all dada2 pipeline step.
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226
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227 Details
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228 .......
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230 *Trimming and filtering*:
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232 - Truncation of the read length is enforced after trimming of the right end.
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233 - The long read filter is applied before trimming and the short read filter after trimming.
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234 - For details on the calculation of the number of expected errors see also https://doi.org/10.1093/bioinformatics/btv401
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237 *String present at the start of valid reads*:
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239 This string is compared to the start of each read, and the reverse complement of each read. If it exactly matches the start of the read, the read is kept. If it exactly matches the start of the reverse complement read, the read is reverse-complemented and kept. Otherwise the read if filtered out. For paired reads, the string is compared to the start of the forward and reverse reads, and if it matches the start of the reverse read the reads are swapped and kept. The primary use of this parameter is to unify the orientation of amplicon sequencing libraries that are a mixture of forward and reverse orientations, and that include the forward primer on the reads.
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241 Notes
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242 .....
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243
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244 This step may be replaced by alternative tools to filter and trim short read data if the following is ensured:
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245
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246 - For paired end data unpaired reads must be removed.
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247 - There must not be a read containing a non-canonical nucleotide (N).
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249 @HELP_OVERVIEW@
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250 ]]></help>
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251 <expand macro="citations"/>
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252 </tool>