Mercurial > repos > peterjc > mira4_assembler
annotate tools/mira4/mira4_de_novo.xml @ 18:381aa262c8cb draft
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author | peterjc |
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date | Tue, 25 Mar 2014 07:37:50 -0400 |
parents | 5bbaa930d7fa |
children | 8487d70e82aa |
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9 | 1 <tool id="mira_4_0_de_novo" name="MIRA v4.0 de novo assember" version="0.0.2"> |
4 | 2 <description>Takes 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> |
9 | 5 <requirement type="binary">miraconvert</requirement> |
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6 <requirement type="package" version="4.0">MIRA</requirement> |
9 | 7 <requirement type="binary">samtools</requirement> |
8 <requirement type="package" version="0.1.19">samtools</requirement> | |
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9 </requirements> |
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10 <version_command interpreter="python">mira4.py --version</version_command> |
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11 <command interpreter="python"> |
9 | 12 mira4.py "$manifest" "$out_maf" "$out_bam" "$out_fasta" "$out_log" |
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13 </command> |
9 | 14 <stdio> |
15 <!-- Assume anything other than zero is an error --> | |
16 <exit_code range="1:" /> | |
17 <exit_code range=":-1" /> | |
18 </stdio> | |
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19 <inputs> |
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20 <param name="job_type" type="select" label="Assembly type"> |
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21 <option value="genome">Genome</option> |
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22 <option value="est">EST (transcriptome)</option> |
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23 </param> |
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24 <param name="job_quality" type="select" label="Assembly quality grade"> |
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25 <option value="accurate">Accurate</option> |
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26 <option value="draft">Draft</option> |
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27 </param> |
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28 <repeat name="read_group" title="Read Group" min="1"> |
4 | 29 <param name="technology" type="select" label="Read technology"> |
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30 <option value="solexa">Solexa/Illumina</option> |
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31 <option value="sanger">Sanger cappillary sequencing</option> |
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32 <option value="454">Roche 454</option> |
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33 <option value="iontor">Ion Torrent</option> |
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34 <option value="pcbiolq">PacBio low quality (raw)</option> |
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35 <option value="pcbiohq">PacBio high quality (corrected)</option> |
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36 <option value="text">Synthetic reads (database entries, consensus sequences, artifical reads, etc)</option> |
15 | 37 <!-- TODO reference/backbone as an entry here? --> |
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38 </param> |
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39 <conditional name="segments"> |
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40 <param name="type" type="select" label="Are these paired reads?"> |
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41 <option value="paired">Paired reads</option> |
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42 <option value="none">Single reads or not relevant (e.g. primer walking with Sanger capillary sequencing)</option> |
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43 </param> |
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44 <when value="paired"> |
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45 <param name="placement" type="select" label="Pairing type (segment placing)"> |
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46 <option value="FR">---> <--- (e.g. Sanger capillary or Solexa/Illumina paired-end library)</option> |
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47 <option value="RF"><--- ---> (e.g. Solexa/Illumina mate-pair library)</option> |
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48 <option value="SB">2---> 1---> (e.g. Roche 454 paired-end libraries or IonTorrent long-mate; see note)</option> |
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49 </param> |
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50 <!-- min/max validation is done via the <code> tag --> |
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51 <param name="min_size" type="integer" optional="true" min="0" value="" |
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52 label="Minimum size of 'good' DNA templates in the library preparation" |
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53 help="Optional, but if used you must also supply a maximum value." /> |
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54 <param name="max_size" type="integer" optional="true" min="0" value="" |
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55 label="Maximum size of 'good' DNA templates in the library preparation" |
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56 help="Optional, but if used you must also supply a minimum value." /> |
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57 <param name="naming" type="select" label="Pair naming convention"> |
7 | 58 <option value="solexa">Solexa/Illumina (using '/1' and '/2' suffixes, or later Illumina colon system)</option> |
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59 <option value="FR">Forward/Reverse scheme (using '.f*' and '.r*' suffixes)</option> |
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60 <option value="tigr">TIGR scheme (using 'TF*' and 'TR*' suffixes)</option> |
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61 <option value="sanger">Sanger scheme (see notes)</option> |
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62 <option value="stlouis">St. Louis scheme (see notes)</option> |
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63 </param> |
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64 </when> |
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65 <when value="none" /><!-- no further questions --> |
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66 </conditional> |
15 | 67 <param name="filenames" type="data" format="fastq,mira" multiple="true" required="true" label="Read file(s)" |
68 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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69 </repeat> |
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70 </inputs> |
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71 <code file="mira4_validator.py" /> |
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72 <outputs> |
4 | 73 <data name="out_fasta" format="fasta" label="MIRA de novo contigs (FASTA)" /> |
9 | 74 <data name="out_bam" format="bam" label="MIRA de novo assembly (BAM)" /> |
4 | 75 <data name="out_maf" format="mira" label="MIRA de novo assembly" /> |
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76 <!-- TODO? |
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77 <data name="out_contigstats" format="tabular" label="MIRA contig stats" /> |
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78 --> |
4 | 79 <data name="out_log" format="txt" label="MIRA de novo log" /> |
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80 </outputs> |
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81 <configfiles> |
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82 <configfile name="manifest"> |
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83 project = MIRA |
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84 job = denovo,${job_type},${job_quality} |
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85 parameters = -NW:cmrnl=no -DI:trt=/tmp |
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86 ## -GE:not is short for -GENERAL:number_of_threads and using one (1) |
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87 ## can be useful for repeatability of assemblies and bug hunting. |
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88 ## This is overriden by the command line -t switch which is easier |
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89 ## to set from within Galaxy. |
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90 ## |
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91 ## -NW:cmrnl is short for -NAG_AND_WARN:check_maxreadnamelength |
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92 ## and without this MIRA aborts with read names over 40 characters |
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93 ## due to limitations of some downstream tools. |
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94 ## |
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95 ## -DI:trt is short for -DIRECTORY:tmp_redirected_to and should |
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96 ## point to a local hard drive (not something like NFS on network). |
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97 ## We replace /tmp with an environment variable via mira4.py |
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98 |
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99 #for $rg in $read_group |
4 | 100 |
101 ##This bar goes into the manifest as a comment line | |
102 #------------------------------------------------------------------------------ | |
103 | |
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104 readgroup |
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105 technology = ${rg.technology} |
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106 ##Record the segment placement (if any) |
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107 #if str($rg.segments.type) == "paired" |
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108 segment_placement = ${rg.segments.placement} |
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109 segment_naming = ${rg.segments.naming} |
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110 #if str($rg.segments.min_size) != "" or str($rg.segments.max_size) != "" |
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111 ##If our min/max validation failed I trust MIRA to give an error message... |
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112 template_size = $rg.segments.min_size $rg.segments.max_size |
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113 #end if |
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114 #end if |
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115 ##if str($rg.segments.type) == "none" |
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116 ##MIRA4 manual says use segment_placement = unknown or ? for unpaired data |
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117 ##but this stopped working in MIRA 4.0 RC5 and 4.0 (final). See: |
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118 ##http://www.freelists.org/post/mira_talk/Unpaired-reads-and-segment-placement--or-unknown |
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119 ##segment_placement = ? |
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120 ##end if |
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121 ##MIRA will accept multiple filenames on one data line, or multiple data lines |
4 | 122 #for $f in $rg.filenames |
123 ##Must now map Galaxy datatypes to MIRA file types... | |
124 #if $f.ext.startswith("fastq") | |
125 ##MIRA doesn't like fastqsanger etc, just plain old fastq: | |
126 data = fastq::$f | |
127 #elif $f.ext == "mira" | |
128 ##We're calling *.maf the "mira" format in Galaxy (name space collision) | |
129 data = maf::$f | |
130 #else | |
131 ##MIRA is happy with fasta as name, | |
132 data = ${f.ext}::$f | |
133 #end if | |
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134 #end for |
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135 #end for |
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136 </configfile> |
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137 </configfiles> |
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138 <tests> |
9 | 139 <!-- Tiger mitochondria, selected paired end Illumina reads from SRR639755 |
140 Note we're using just one repeat group, and only the filenames parameter | |
141 within it, so this should work with current test framework limitations: | |
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142 TODO: Revise example and/or -NW:cac=warn and -NW:acv=80 settings |
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143 MIRA 4.0 complains as coverage is about x93 which is over 80 limit. |
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144 Also MIRA 4.0 gives three contigs as output. |
9 | 145 <test> |
146 <param name="job_type" value="genome" /> | |
147 <param name="job_quality" value="accurate" /> | |
148 <param name="filenames" value="SRR639755_mito_pairs.fastq.gz" ftype="fastqsanger" /> | |
149 <output name="out_fasta" file="SRR639755_mito_pairs.mira4_de_novo.fasta" ftype="fasta" /> | |
150 </test> | |
151 --> | |
152 <!-- Simple assembly based on MIRA's minidemo/demo4 example | |
153 Note we're using just one repeat group, | |
154 but several parameters with the repeat | |
17 | 155 --> |
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156 <test> |
9 | 157 <param name="job_type" value="genome" /> |
158 <param name="job_quality" value="accurate" /> | |
159 <param name="technology" value="sanger" /> | |
160 <param name="type" value="none" /> | |
161 <param name="filenames" value="U13small_m.fastq" ftype="fastqsanger" /> | |
162 <output name="out_fasta" file="U13small_m.mira4_de_novo.fasta" ftype="fasta" /> | |
17 | 163 <output name="out_bam" file="empty_file.dat" compare="contains" /> |
164 <output name="out_maf" file="empty_file.dat" compare="contains" /> | |
165 <output name="out_log" file="empty_file.dat" compare="contains" /> | |
9 | 166 </test> |
17 | 167 <!-- Simple assembly based on MIRA's minidemo/solexa1 example |
9 | 168 Note we're using just one repeat group, |
169 but two parameters within the repeat (filename, no pairing) | |
15 | 170 --> |
9 | 171 <test> |
172 <param name="job_type" value="genome" /> | |
173 <param name="job_quality" value="accurate" /> | |
174 <param name="type" value="none" /> | |
175 <param name="filenames" value="ecoli.fastq" ftype="fastqsanger" /> | |
176 <output name="out_fasta" file="ecoli.mira4_de_novo.fasta" ftype="fasta" /> | |
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177 <output name="out_bam" file="empty_file.dat" compare="contains" /> |
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178 <output name="out_maf" file="empty_file.dat" compare="contains" /> |
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179 <output name="out_log" file="empty_file.dat" compare="contains" /> |
9 | 180 </test> |
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181 </tests> |
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182 <help> |
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183 |
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184 **What it does** |
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185 |
9 | 186 Runs MIRA v4.0 in de novo mode, collects the output, generates a sorted BAM |
187 file, and then throws away all the temporary files. | |
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188 |
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189 MIRA is an open source assembly tool capable of handling sequence data from |
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190 a range of platforms (Sanger capillary, Solexa/Illumina, Roche 454, Ion Torrent |
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191 and also PacBio). |
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192 |
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193 It is particularly suited to small genomes such as bacteria. |
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194 |
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195 |
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196 **Notes on paired reads** |
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197 |
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198 .. class:: warningmark |
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199 |
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200 MIRA uses read naming conventions to identify paired read partners |
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201 (and does not care about their order in the input files). In most cases, |
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202 the Solexa/Illumina setting is fine. For Sanger capillary sequencing, |
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203 you may need to rename your reads to match one of the standard conventions |
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204 supported by MIRA. For Roche 454 or Ion Torrent the appropriate settings |
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205 depend on how the FASTQ file was produced: |
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206 |
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207 * If using Roche's ``sffinfo`` or older versions of ``sff_extract`` |
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208 to convert SFF files to FASTQ, your reads will probably have the |
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209 ``---> <---`` orientation and use the ``.f`` and ``.r`` |
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210 suffixes (FR naming). |
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211 |
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212 * If using a recent version of ``sff_extract``, then the ``/1`` and ``/2`` |
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213 suffixes are used (Solexa/Illumina style naming) and the original |
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214 ``2---> 1--->`` orientation is preserved. |
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215 |
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216 The reason for this is the raw data for Roche 454 and Ion Torrent paired-end |
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217 libraries sequences a circularised fragment such that the raw data begins |
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218 with the end of the fragment, a linker, then the start of the fragment. |
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219 This means both the start and end are sequenced from the same strand, and |
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220 have the orientation ``2---> 1--->``. However, in order to use the data |
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221 with traditional tools expecting Sanger capillary style ``---> <---`` |
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222 orientation it was common to reverse complement one of the pair to mimic this. |
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223 |
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224 |
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225 **Citation** |
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226 |
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227 If you use this Galaxy tool in work leading to a scientific publication please |
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228 cite the following papers: |
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229 |
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230 Peter J.A. Cock, Björn A. Grüning, Konrad Paszkiewicz and Leighton Pritchard (2013). |
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231 Galaxy tools and workflows for sequence analysis with applications |
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232 in molecular plant pathology. PeerJ 1:e167 |
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233 http://dx.doi.org/10.7717/peerj.167 |
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234 |
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235 Bastien Chevreux, Thomas Wetter and Sándor Suhai (1999). |
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236 Genome Sequence Assembly Using Trace Signals and Additional Sequence Information. |
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237 Computer Science and Biology: Proceedings of the German Conference on Bioinformatics (GCB) 99, pp. 45-56. |
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238 http://www.bioinfo.de/isb/gcb99/talks/chevreux/main.html |
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239 |
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240 This wrapper is available to install into other Galaxy Instances via the Galaxy |
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241 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/mira4_assembler |
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242 </help> |
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243 </tool> |