Mercurial > repos > peterjc > mira4_assembler

annotate tools/mira4/mira4_mapping.xml @ 6:626d5cfd01aa draft

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Uploaded v0.0.1 preview 6, support for fragment length (using mira4_validator.py)
author peterjc
date Mon, 21 Oct 2013 12:01:47 -0400
parents ffefb87bd414
children 902f01c1084b
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1 <tool id="mira_4_0_mapping" name="MIRA v4.0 mapping" version="0.0.1">
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2 <description>Maps Sanger, Roche 454, Solexa/Illumina, Ion Torrent and PacBio reads</description>
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3 <requirements>
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4 <requirement type="binary">mira</requirement>
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5 <requirement type="package" version="4.0">MIRA</requirement>
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6 </requirements>
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7 <version_command interpreter="python">mira4.py --version</version_command>
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8 <command interpreter="python">
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9 mira4.py $manifest $out_maf $out_fasta $out_log
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10 </command>
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11 <inputs>
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12 <param name="job_type" type="select" label="Assembly type">
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13 <option value="genome">Genome</option>
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14 <option value="est">EST (transcriptome)</option>
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15 </param>
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16 <param name="job_quality" type="select" label="Assembly quality grade">
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17 <option value="accurate">Accurate</option>
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18 <option value="draft">Draft</option>
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19 </param>
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20 <!-- TODO? Allow technology type for references? -->
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21 <!-- TODO? Allow strain settings for reference(s) and reads? -->
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22 <!-- TODO? Use a repeat to allow for multi-strain references? -->
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23 <!-- TODO? Add strain to the mapping read groups? -->
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24 <param name="references" type="data" format="fasta,fastq,mira" multiple="true" required="true" label="Backbone reference file(s)"
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25 help="Multiple files allowed, for example one FASTA file per chromosome or plasmid." />
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26 <param name="strain_setup" type="select" label="Strain configuration (reference vs reads)">
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27 <option value="default">Different strains - mapping reads onto a related reference ('StrainX' vs 'ReferenceStrain')</option>
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28 <option value="same">Same strain - mapping reads from same reference (all 'StrainX')</option>
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29 </param>
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30 <repeat name="read_group" title="Read Group" min="1">
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31 <param name="technology" type="select" label="Read technology">
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32 <option value="solexa">Solexa/Illumina</option>
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33 <option value="sanger">Sanger cappillary sequencing</option>
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34 <option value="454">Roche 454</option>
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35 <option value="iontor">Ion Torrent</option>
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36 <option value="pcbiolq">PacBio low quality (raw)</option>
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37 <option value="pcbiohq">PacBio high quality (corrected)</option>
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38 <option value="text">Synthetic reads (database entries, consensus sequences, artifical reads, etc)</option>
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39 </param>
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40 <conditional name="segments">
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41 <param name="type" type="select" label="Are these paired reads?">
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42 <option value="paired">Paired reads</option>
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43 <option value="none">Single reads or not relevant (e.g. primer walking with Sanger capillary sequencing)</option>
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44 </param>
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45 <when value="paired">
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46 <param name="placement" type="select" label="Pairing type (segment placing)">
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47 <option value="FR">---&gt; &lt;--- (e.g. Sanger capillary or Solexa/Illumina paired-end library)</option>
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48 <option value="RF">&lt;--- ---&gt; (e.g. Solexa/Illumina mate-pair library)</option>
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49 <option value="SB">2---&gt; 1---&gt; (e.g. Roche 454 paired-end libraries or IonTorrent long-mate; see note)</option>
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50 </param>
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51 <param name="naming" type="select" label="Pair naming convention">
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52 <option value="solexa">Solexa/Illumina (using '/1' and '/2' suffixes)</option>
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53 <option value="FR">Forward/Reverse scheme (using '.f*' and '.r*' suffixes)</option>
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54 <option value="tigr">TIGR scheme (using 'TF*' and 'TR*' suffixes)</option>
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55 <option value="sanger">Sanger scheme (see notes)</option>
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56 <option value="stlouis">St. Louis scheme (see notes)</option>
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57 </param>
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58 </when>
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59 <when value="none" /><!-- no further questions -->
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60 </conditional>
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61 <param name="filenames" type="data" format="fastq,mira" multiple="true" required="true" label="Read file(s)"
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62 help="Multiple files allowed, for example paired reads can be given as two files (MIRA looks at read names to identify pairs)." />
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63 </repeat>
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64 </inputs>
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65 <outputs>
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66 <data name="out_fasta" format="fasta" label="MIRA #if str($strain_setup)=='same' then 'same strain' else 'reference' # mapping contigs (FASTA)" />
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67 <data name="out_maf" format="mira" label="MIRA #if str($strain_setup)=='same' then 'same strain' else 'reference' # mapping assembly" />
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68 <data name="out_log" format="txt" label="MIRA #if str($strain_setup)=='same' then 'same strain' else 'reference' # mapping log" />
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69 </outputs>
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70 <configfiles>
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71 <configfile name="manifest">
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72 project = MIRA
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73 job = mapping,${job_type},${job_quality}
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74 parameters = -GE:not=1 -NW:cmrnl -DI:trt=/tmp
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75 ## -GE:not is short for -GENERAL:number_of_threads and using one (1)
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76 ## can be useful for repeatability of assemblies and bug hunting.
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77 ##
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78 ## -NW:cmrnl is short for -NAG_AND_WARN:check_maxreadnamelength
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79 ## and without this MIRA aborts with read names over 40 characters
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80 ## due to limitations of some downstream tools.
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81 ##
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82 ## -DI:trt is short for -DIRECTORY:tmp_redirected_to and should
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83 ## point to a local hard drive (not something like NFS on network).
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84
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85 ##This bar goes into the manifest as a comment line
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86 #------------------------------------------------------------------------------
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87
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88 readgroup
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89 is_reference
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90 #if str($strain_setup)=="same"
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91 strain = StrainX
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92 #end if
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93 #for $f in $references
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94 ##Must now map Galaxy datatypes to MIRA file types...
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95 #if $f.ext.startswith("fastq")
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96 ##MIRA doesn't like fastqsanger etc, just plain old fastq:
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97 data = fastq::$f
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98 #elif $f.ext == "mira"
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99 ##We're calling *.maf the "mira" format in Galaxy (name space collision)
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100 data = maf::$f
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101 #elif $f.ext == "fasta"
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102 ##We're calling MIRA with the file type as "fna" as otherwise it wants quals
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103 data = fna::$f
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104 #else
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105 ##Currently don't expect anything else...
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106 data = ${f.ext}::$f
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107 #end if
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108 #end for
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109 #for $rg in $read_group
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110
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111 ##This bar goes into the manifest as a comment line
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112 #------------------------------------------------------------------------------
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113
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114 readgroup
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115 technology = ${rg.technology}
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116 #if str($strain_setup)=="same"
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117 ##This is perhaps redundant as MIRA defaults to StrainX for the reads:
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118 strain = StrainX
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119 #end if
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120 ##Record the segment placement (if any)
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121 #if str($rg.segments.type) == "paired"
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122 segmentplacement = ${rg.segments.placement}
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123 segmentnaming = ${rg.segments.naming}
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124 #end if
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125 #if str($rg.segments.type) == "none"
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126 segmentplacement = ?
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127 #end if
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128 ##MIRA will accept multiple filenames on one data line, or multiple data lines
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129 #for $f in $rg.filenames
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130 ##Must now map Galaxy datatypes to MIRA file types...
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131 #if $f.ext.startswith("fastq")
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132 ##MIRA doesn't like fastqsanger etc, just plain old fastq:
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133 data = fastq::$f
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134 #elif $f.ext == "mira"
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135 ##We're calling *.maf the "mira" format in Galaxy (name space collision)
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136 data = maf::$f
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137 #else
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138 ##Currently don't expect anything else...
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139 data = ${f.ext}::$f
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140 #end if
0
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141 #end for
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142 #end for
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143 </configfile>
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144 </configfiles>
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145 <tests>
4
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146 <!-- Deliberately using default read_group.technology value "solexa"
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147 as then Galaxy's broken <repeat> handling in tests should work... -->
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148 <!-- Tests currently failing,
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149 TwillException: more than one form; you must select one (use 'fv') before submitting
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150 <test>
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151 <param name="job_type" value="genome" />
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152 <param name="job_quality" value="accurate" />
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153 <param name="references" value="tvc_contigs.fasta" ftype="fasta" />
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154 <param name="strain_setup" value="default" />
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155 <param name="filenames" value="tvc_mini.fastq" ftype="fastqsanger" />
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156 <output name="out_fasta" file="tvc_map_same_strain.fasta" ftype="fasta" />
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157 </test>
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158 <test>
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159 <param name="job_type" value="genome" />
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160 <param name="job_quality" value="accurate" />
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161 <param name="references" value="tvc_contigs.fasta" ftype="fasta" />
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162 <param name="strain_setup" value="same" />
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163 <param name="filenames" value="tvc_mini.fastq" ftype="fastqsanger" />
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164 <output name="out_fasta" file="tvc_map_ref_strain.fasta" ftype="fasta" />
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165 </test>
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166 -->
0
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167 </tests>
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168 <help>
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169
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170 **What it does**
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171
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172 Runs MIRA v4.0 in mapping mode, collects the output, and throws away all the temporary files.
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173
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174 MIRA is an open source assembly tool capable of handling sequence data from
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175 a range of platforms (Sanger capillary, Solexa/Illumina, Roche 454, Ion Torrent
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176 and also PacBio).
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177
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178 It is particularly suited to small genomes such as bacteria.
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179
6
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180
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181 **Notes on paired reads**
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182
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183 .. class:: warningmark
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184
6
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185 MIRA uses read naming conventions to identify paired read partners
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186 (and does not care about their order in the input files). In most cases,
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187 the Solexa/Illumina setting is fine. For Sanger capillary sequencing,
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188 you may need to rename your reads to match one of the standard conventions
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189 supported by MIRA. For Roche 454 or Ion Torrent the appropriate settings
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190 depend on how the FASTQ file was produced:
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191
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192 * If using Roche's ``sffinfo`` or older versions of ``sff_extract``
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193 to convert SFF files to FASTQ, your reads will probably have the
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194 ``---&gt; &lt;---`` orientation and use the ``.f`` and ``.r``
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195 suffixes (FR naming).
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196
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197 * If using a recent version of ``sff_extract``, then the ``/1`` and ``/2``
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198 suffixes are used (Solexa/Illumina style naming) and the original
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199 ``2---&gt; 1---&gt;`` orientation is preserved.
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200
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201 The reason for this is the raw data for Roche 454 and Ion Torrent paired-end
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202 libraries sequences a circularised fragment such that the raw data begins
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203 with the end of the fragment, a linker, then the start of the fragment.
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204 This means both the start and end are sequenced from the same strand, and
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205 have the orientation ``2---&gt; 1---&gt;``. However, in order to use the data
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206 with traditional tools expecting Sanger capillary style ``---&gt; &lt;---``
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207 orientation it was common to reverse complement one of the pair to mimic this.
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208
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209
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210 **Citation**
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211
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212 If you use this Galaxy tool in work leading to a scientific publication please
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213 cite the following papers:
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214
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215 Peter J.A. Cock, Björn A. Grüning, Konrad Paszkiewicz and Leighton Pritchard (2013).
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216 Galaxy tools and workflows for sequence analysis with applications
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217 in molecular plant pathology. PeerJ 1:e167
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218 http://dx.doi.org/10.7717/peerj.167
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219
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220 Bastien Chevreux, Thomas Wetter and Sándor Suhai (1999).
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221 Genome Sequence Assembly Using Trace Signals and Additional Sequence Information.
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222 Computer Science and Biology: Proceedings of the German Conference on Bioinformatics (GCB) 99, pp. 45-56.
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223 http://www.bioinfo.de/isb/gcb99/talks/chevreux/main.html
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224
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225 This wrapper is available to install into other Galaxy Instances via the Galaxy
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226 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/mira4_assembler
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227 </help>
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228 </tool>