annotate sailfish.xml @ 2:20eab032389f draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit b9ccc98180d52233931768511b909ccd6142f158
author bgruening
date Mon, 21 Dec 2015 14:00:53 -0500
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children 03c74355227f
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1 <tool id="sailfish" name="Sailfish" version="0.7.6.0">
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2 <description>transcript quantification from RNA-seq data</description>
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3 <requirements>
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4 <requirement type="package" version="0.7.6">sailfish</requirement>
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5 </requirements>
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6 <macros>
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7 <xml name="strandedness">
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8 <param name="strandedness" type="select" label="Specify the strandedness of the reads">
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9 <option value="U" selected="True">Not stranded (U)</option>
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10 <option value="SF">read 1 (or single-end read) comes from the forward strand (SF)</option>
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11 <option value="SR">read 1 (or single-end read) comes from the reverse strand (SR)</option>
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12 </param>
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13 </xml>
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14 </macros>
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15 <stdio>
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16 <exit_code range="1:" />
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17 <exit_code range=":-1" />
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18 <regex match="Error:" />
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19 <regex match="Exception:" />
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20 <regex match="Exception :" />
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21 </stdio>
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22 <version_command>sailfish -version</version_command>
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23 <command>
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24 <![CDATA[
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25
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26 #if $refTranscriptSource.TranscriptSource == "history":
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27 sailfish index
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28 --transcripts $refTranscriptSource.ownFile
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29 --kmerSize $refTranscriptSource.kmerSize
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30 --out ./index_dir
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31 --threads "\${GALAXY_SLOTS:-4}"
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32 #set $index_path = './index_dir'
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33 #else:
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34 #set $index_path = $refTranscriptSource.index.fields.path
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35 #end if
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36
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37 &&
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39 #if $single_or_paired.single_or_paired_opts == 'single':
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41 #if $single_or_paired.input_singles.ext == 'fasta':
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42 #set $ext = 'fasta'
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43 #else:
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44 #set $ext = 'fastq'
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45 #end if
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46
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47 ln -s $single_or_paired.input_singles ./single.$ext &&
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48 #else:
1
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49
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50 #if $single_or_paired.input_mate1.ext == 'fasta':
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51 #set $ext = 'fasta'
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52 #else:
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53 #set $ext = 'fastq'
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54 #end if
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55
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56 ln -s $single_or_paired.input_mate1 ./mate1.$ext &&
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57 ln -s $single_or_paired.input_mate2 ./mate2.$ext &&
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58 #end if
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59
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61 #if $geneMap:
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62 ln -s "$geneMap" ./geneMap.$geneMap.ext &&
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63 #end if
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64
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65 sailfish quant
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66 --index $index_path
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67 #if $single_or_paired.single_or_paired_opts == 'single':
1
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68 --libType ${single_or_paired.strandedness}
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69 --unmatedReads ./single.$ext
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70 #else:
1
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71 --mates1 ./mate1.$ext
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72 --mates2 ./mate2.$ext
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73 --libType "${single_or_paired.orientation}${single_or_paired.strandedness}"
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74 #end if
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75 --output ./
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76 $biasCorrect
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77 --threads "\${GALAXY_SLOTS:-4}"
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78
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79 #if $fldMean:
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80 --fldMean $fldMean
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81 #end if
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82
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83 #if $fldSD:
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84 --fldSD $fldSD
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85 #end if
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86
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87 #if $maxReadOcc:
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88 --maxReadOcc $maxReadOcc
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89 #end if
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90
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91 #if $geneMap:
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92 --geneMap ./geneMap.${geneMap.ext}
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93 #end if
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94
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95 $noEffectiveLengthCorrection
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96 $useVBOpt
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97 $allowOrphans
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98
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99 $unsmoothedFLD
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100 --maxFragLen ${maxFragLen}
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101 --txpAggregationKey "${txpAggregationKey}"
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102
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103 ]]>
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104 </command>
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105 <inputs>
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106 <conditional name="refTranscriptSource">
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107 <param name="TranscriptSource" type="select" label="Select a reference transcriptome from your history or use a built-in index?" help="Built-ins were indexed using default options">
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108 <option value="indexed">Use a built-in index</option>
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109 <option value="history" selected="True">Use one from the history</option>
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110 </param>
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111 <when value="indexed">
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112 <param name="index" type="select" label="Select a reference transcriptome" help="If your transcriptome of interest is not listed, contact your Galaxy admin">
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113 <options from_data_table="sailfish_indexes">
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114 <filter type="sort_by" column="2"/>
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115 <validator type="no_options" message="No indexes are available for the selected input dataset"/>
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116 </options>
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117 </param>
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118 </when> <!-- build-in -->
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119 <when value="history">
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120 <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select the reference transcriptome" />
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121 <param argument="kmerSize" type="integer" value="21" max="32" label="The size of the k-mer on which the index is built"
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122 help="There is a tradeoff here between the distinctiveness of the k-mers and their robustness to errors.
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123 The shorter the k-mers, the more robust they will be to errors in the reads, but the longer the k-mers,
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124 the more distinct they will be. We generally recommend using a k-mer size of at least 20."/>
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125 </when> <!-- history -->
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126 </conditional> <!-- refTranscriptSource -->
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127
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128 <conditional name="single_or_paired">
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129 <param name="single_or_paired_opts" type="select" label="Is this library mate-paired?">
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130 <option value="single">Single-end</option>
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131 <option value="paired">Paired-end</option>
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132 </param>
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133 <when value="single">
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134 <param name="input_singles" type="data" format="fastq,fasta" label="FASTQ/FASTA file" help="FASTQ file." />
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135 <expand macro="strandedness" />
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136 </when>
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137 <when value="paired">
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138 <param name="input_mate1" type="data" format="fastq,fasta" label="Mate pair 1" help="FASTQ file." />
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139 <param name="input_mate2" type="data" format="fastq,fasta" label="Mate pair 2" help="FASTQ file." />
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140 <param name="orientation" type="select" label="Relative orientation of reads within a pair">
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141 <option value="M">Mates are oriented in the same direction (M = matching)</option>
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142 <option value="O">Mates are oriented away from each other (O = outward)</option>
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143 <option value="I" selected="True">Mates are oriented toward each other (I = inward)</option>
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144 </param>
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145 <expand macro="strandedness" />
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146 </when>
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147 </conditional>
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148
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149 <param argument="--geneMap" type="data" format="tabular,gff,gtf" optional="True" label="File containing a mapping of transcripts to genes"
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150 help="Calculates the aggregated gene-level abundance estimations. This file should be eiher a GTF file or tab-delimited format
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151 where each line contains the name of a transcript and the gene to which it belongs separated by a tab." />
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152
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153 <param argument="--biasCorrect" type="boolean" truevalue="--biasCorrect" falsevalue="" checked="False"
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154 label="Perform bias correction" help=""/>
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155
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156 <param argument="--fldMean" type="integer" value="200" optional="True" label="Calculate effective lengths"
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157 help="If single end reads are being used for quantification, or there are an insufficient number of uniquely mapping reads when performing paired-end quantification
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158 to estimate the empirical fragment length distribution, then use this value to calculate effective lengths."/>
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159
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160 <param argument="--fldSD" type="integer" value="80" optional="True" label="Standard deviation"
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161 help="The standard deviation used in the fragment length distribution for single-end quantification or when an empirical distribution cannot be learned."/>
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162
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163 <param argument="--maxReadOcc" type="integer" value="200" optional="True" label="Maximal read mapping occurence"
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164 help="Reads mapping to more than this many places won't be considered."/>
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165
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166 <param argument="--noEffectiveLengthCorrection" type="boolean" truevalue="--noEffectiveLengthCorrection" falsevalue="" checked="False"
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167 label="Disable effective length correction" help="Disables effective length correction when computing the probability that a fragment was generated from a transcript.
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168 If this flag is passed in, the fragment length distribution is not taken into account when computing this probability."/>
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169
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170 <param argument="--useVBOpt" type="boolean" truevalue="--useVBOpt" falsevalue="" checked="False"
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171 label="Use Variational Bayesian EM algorithm for optimization" help=""/>
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172
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173 <param argument="--allowOrphans" type="boolean" truevalue="--allowOrphans" falsevalue="" checked="False"
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174 label="Consider orphaned reads as valid hits when performing lightweight-alignment"
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175 help="This option will increase sensitivity (allow more reads to map and more transcripts to be detected), but may decrease specificity as orphaned alignments are more likely to be spurious."/>
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176
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177 <param argument="--unsmoothedFLD" type="boolean" truevalue="--unsmoothedFLD" falsevalue="" checked="False"
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178 label="Use the un-smoothed approach to effective length correction" help="This traditional approach works by convolving the FLD with the characteristic function over each transcript."/>
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179
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180 <param argument="--maxFragLen" type="integer" value="1000" optional="True"
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181 label="The maximum length of a fragment to consider when building the empirical fragment length distribution"
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182 help=""/>
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183
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184 <param argument="--txpAggregationKey" value="gene_id" type="text" label="The key for aggregating transcripts during gene-level estimates"
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185 help="The default is the gene_id field, but other fields (e.g. gene_name) might be useful depending on the specifics of the annotation being used." />
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186
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187 </inputs>
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188 <outputs>
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189 <data name="output_quant" format="tabular" from_work_dir="quant.sf" label="${tool.name} on ${on_string} (Quantification)" />
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190 <data name="output_bias_corrected_quant" format="tabular" from_work_dir="quant_bias_corrected.sf" label="${tool.name} on ${on_string} (Bias corrected Quantification)">
1
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191 <filter>biasCorrect is True</filter>
0
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192 </data>
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193 <data name="output_gene_quant" format="tabular" from_work_dir="quant.genes.sf" label="${tool.name} on ${on_string} (Gene Quantification)">
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194 <filter>geneMap is True</filter>
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195 </data>
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196 </outputs>
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197 <tests>
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198 <test>
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199 <param name="single_or_paired_opts" value="paired" />
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200 <param name="input_mate1" value="reads_1.fastq" />
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201 <param name="input_mate2" value="reads_2.fastq" />
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202 <param name="biasCorrect" value="True" />
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203 <param name="TranscriptSource" value="history" />
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204 <param name="ownFile" value="transcripts.fasta" ftype="fasta" />
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205 <output file="sailfish_quant_result1.tab" ftype="tabular" name="output_quant" />
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206 <output file="sailfish_bias_result1.tab" ftype="tabular" name="output_bias_corrected_quant" />
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207 </test>
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208 </tests>
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209 <help>
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210 <![CDATA[
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211 **What it does**
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212
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213 Sailfish is a tool for transcript quantification from RNA-seq data. It
2
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214 requires a set of target transcripts (either from a reference or de-novo
0
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215 assembly) to quantify. All you need to run Sailfish is a fasta file containing
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216 your reference transcripts and a (set of) fasta/fastq file(s) containing your
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217 reads. Sailfish runs in two phases; indexing and quantification. The indexing
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218 step is independent of the reads, and only need to be run one for a particular
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219 set of reference transcripts and choice of k (the k-mer size). The
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220 quantification step, obviously, is specific to the set of RNA-seq reads and is
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221 thus run more frequently.
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222
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223 When the quantification output contains a number of columns:
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224 (1) Transcript ID,
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225 (2) Transcript Length,
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226 (3) Transcripts per Million (TPM) and
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227 (4) Estimated number of reads (an estimate of the number of reads drawn from this transcript given the transcript’s relative abundance and length).
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228
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229 The first two columns are self-explanatory, the next four are measures of transcript abundance and the final is a commonly used input for differential expression tools.
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230 The Transcripts per Million quantification number is computed as described in [1], and is meant as an estimate of the number of transcripts, per million observed transcripts,
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231 originating from each isoform. Its benefit over the F/RPKM measure is that it is independent of the mean expressed transcript length
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232 (i.e. if the mean expressed transcript length varies between samples, for example, this alone can affect differential analysis based on the K/RPKM.).
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233
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234
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235
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236 Fragment Library Types
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237 ======================
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238
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239 There are numerous library preparation protocols for RNA-seq that result in
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240 sequencing reads with different characteristics. For example, reads can be
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241 single end (only one side of a fragment is recorded as a read) or paired-end
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242 (reads are generated from both ends of a fragment). Further, the sequencing
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243 reads themselves may be unstraned or strand-specific. Finally, paired-end
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244 protocols will have a specified relative orientation. To characterize the
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245 various different typs of sequencing libraries, we've created a miniature
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246 "language" that allows for the succinct description of the many different types
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247 of possible fragment libraries. For paired-end reads, the possible
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248 orientations, along with a graphical description of what they mean, are
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249 illustrated below:
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250
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251 .. image:: ReadLibraryIllustration.png
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252
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253 The library type string consists of three parts: the relative orientation of
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254 the reads, the strandedness of the library, and the directionality of the
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255 reads.
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256
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257 The first part of the library string (relative orientation) is only provided if
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258 the library is paired-end. The possible options are:
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259
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260 ::
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261
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262 I = inward
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263 O = outward
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264 M = matching
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265
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266 The second part of the read library string specifies whether the protocol is
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267 stranded or unstranded; the options are:
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268
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269 ::
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270
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271 S = stranded
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272 U = unstranded
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273
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274 If the protocol is unstranded, then we're done. The final part of the library
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275 string specifies the strand from which the read originates in a strand-specific
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276 protocol — it is only provided if the library is stranded (i.e. if the
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277 library format string is of the form S). The possible values are:
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278
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279 ::
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280
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281 F = read 1 (or single-end read) comes from the forward strand
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282 R = read 1 (or single-end read) comes from the reverse strand
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283
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284 So, for example, if you wanted to specify a fragment library of strand-specific
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285 paired-end reads, oriented toward each other, where read 1 comes from the
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286 forward strand and read 2 comes from the reverse strand, you would specify ``-l
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287 ISF`` on the command line. This designates that the library being processed has
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288 the type "ISF" meaning, **I**\ nward (the relative orientation), **S**\ tranted
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289 (the protocol is strand-specific), **F**\ orward (read 1 comes from the forward
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290 strand).
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291
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292 The single end library strings are a bit simpler than their pair-end counter
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293 parts, since there is no relative orientation of which to speak. Thus, the
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294 only possible library format types for single-end reads are ``U`` (for
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295 unstranded), ``SF`` (for strand-specific reads coming from the forward strand)
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296 and ``SR`` (for strand-specific reads coming from the reverse strand).
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297
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298 A few more examples of some library format strings and their interpretations are:
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299
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300 ::
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301
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302 IU (an unstranded paired-end library where the reads face each other)
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303
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304 ::
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305
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306 SF (a stranded single-end protocol where the reads come from the forward strand)
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307
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308 ::
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309
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310 OSR (a stranded paired-end protocol where the reads face away from each other,
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311 read1 comes from reverse strand and read2 comes from the forward strand)
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312
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313 .. note:: Correspondence to TopHat library types
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314
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315 The popular `TopHat <http://ccb.jhu.edu/software/tophat/index.shtml>`_ RNA-seq
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316 read aligner has a different convention for specifying the format of the library.
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317 Below is a table that provides the corresponding sailfish/salmon library format
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318 string for each of the potential TopHat library types:
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319
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320
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321 +---------------------+-------------------------+
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322 | TopHat | Salmon (and Sailfish) |
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323 +=====================+============+============+
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324 | | Paired-end | Single-end |
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325 +---------------------+------------+------------+
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326 |``-fr-unstranded`` |``-l IU`` |``-l U`` |
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327 +---------------------+------------+------------+
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328 |``-fr-firststrand`` |``-l ISR`` |``-l SR`` |
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329 +---------------------+------------+------------+
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330 |``-fr-secondstrand`` |``-l ISF`` |``-l SF`` |
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331 +---------------------+------------+------------+
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332
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333 The remaining salmon library format strings are not directly expressible in terms
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334 of the TopHat library types, and so there is no direct mapping for them.
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335
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337 ]]>
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338 </help>
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339 </tool>