Mercurial > repos > peterjc > mira_assembler
annotate tools/mira3/mira.xml @ 28:e28d6015fc56 draft default tip
planemo upload for repository https://github.com/peterjc/galaxy_mira/tree/master/tools/mira3/ commit 89578746a1c5b29c84a173d8b2709f086f69a7b6
author | peterjc |
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date | Mon, 03 Jun 2019 13:28:13 -0400 |
parents | 2e7e2bc0d718 |
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rev | line source |
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planemo upload for repository https://github.com/peterjc/galaxy_mira/tree/master/tools/mira3/ commit fd979d17340cde155de176604744831d9597c6b6
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1 <tool id="mira_assembler" name="Assemble with MIRA v3.4" version="0.0.12"> |
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2 <description>Takes Sanger, Roche, Illumina, and Ion Torrent data</description> |
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3 <requirements> |
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4 <requirement type="package" version="3.4.1.1">MIRA</requirement> |
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5 </requirements> |
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6 <version_command> |
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7 python $__tool_directory__/mira.py -v |
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8 </version_command> |
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9 <command detect_errors="aggressive"> |
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10 python $__tool_directory__/mira.py mira '$out_fasta' '$out_qual' '$out_ace' '$out_caf' '$out_wig' '$out_log' |
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11 ##Give the wrapper script list of output filenames, then the mira command... |
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12 mira --job=$job_method,$job_type,$job_quality |
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13 |
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14 ##Input files |
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15 #if $condBackbone.use == "true": |
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16 ## Can this be linked to job_method as well? If mapping we need the backbone... |
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17 -SB:lb=1:bft=fasta -FN:bbin=${condBackbone.filename} |
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18 #end if |
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19 #if $condSanger.use == "true": |
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20 SANGER_SETTINGS |
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21 ## Not easy in Galaxy to add sanger to --job, so use load_sequence_data(lsd) instead |
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22 ## I expect hard trimmed FASTQ files with no NCBI traceinfo XML file |
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23 -LR:lsd=1:mxti=0:ft=fastq -FN:fqi=${condSanger.filename} |
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24 #end if |
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25 #if $condRoche.use == "true": |
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26 454_SETTINGS |
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27 ## Not easy in Galaxy to add 454 to --job, so use load_sequence_data(lsd) instead |
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28 ## I expect hard trimmed FASTQ files with no NCBI traceinfo XML file |
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29 -LR:lsd=1:mxti=0:ft=fastq -FN:fqi=${condRoche.filename} |
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30 #end if |
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31 #if $condIllumina.use == "true": |
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32 SOLEXA_SETTINGS |
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33 ## Not easy in Galaxy to add solexa to --job, so use load_sequence_data(lsd) instead |
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34 -LR:lsd=1:ft=fastq -FN:fqi=${condIllumina.filename} |
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35 ##TODO - Look at -LR FASTQ qual offset (fqqo) |
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36 #end if |
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37 #if $condIonTorrent.use == "true": |
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38 IONTOR_SETTINGS |
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39 ## Not easy in Galaxy to add iontor to --job, so use load_sequence_data(lsd) instead |
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40 ## I expect hard trimmed FASTQ files with no NCBI traceinfo XML file |
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41 -LR:lsd=1:mxti=0:ft=fastq -FN:fqi=${condIonTorrent.filename} |
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42 #end if |
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43 |
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44 ##Output files |
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45 COMMON_SETTINGS |
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46 |
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47 ##ignore warnings about long read names |
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48 -MI:somrnl=0 |
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49 |
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50 ##Explicitly request the FASTA (+QUAL), CAF, ACE, WIG output |
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51 ##Explicitly disable formats we won't use like MAF (reduce IO) |
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52 -OUT:orf=1:orc=1:ora=1:orw=1:orm=0:org=0:ors=0 |
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53 |
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54 ##remove_rollover_tmps, remove_tmp_directory |
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55 -OUT:rrot=1:rtd=1 |
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56 |
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57 ##put mira temp directory on local storage |
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58 -DI:trt=/tmp |
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59 |
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60 </command> |
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61 <inputs> |
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62 <param name="job_method" type="select" label="Assembly method" help="Mapping mode requires backbone/reference sequence(s)"> |
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63 <option value="denovo">De novo</option> |
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64 <option value="mapping">Mapping</option> |
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65 </param> |
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66 <param name="job_type" type="select" label="Assembly type"> |
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67 <option value="genome">Genome</option> |
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68 <option value="est">EST (transcriptome)</option> |
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69 </param> |
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70 <param name="job_quality" type="select" label="Assembly quality grade"> |
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71 <option value="accurate">Accurate</option> |
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72 <option value="normal">Normal (deprecated)</option> |
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73 <option value="draft">Draft</option> |
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74 </param> |
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75 <!-- Backbone --> |
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76 <conditional name="condBackbone"> |
13 | 77 <param name="use" type="select" label="Backbones/reference chromosomes?" help="Required for mapping, optional for de novo assembly."> |
78 <option value="false">No</option> | |
79 <option value="true">Yes</option> | |
80 </param> | |
81 <when value="false" /> | |
82 <when value="true"> | |
83 <!-- MIRA also allows CAF and GenBank, but Galaxy doesn't define those (yet) --> | |
84 <param name="filename" type="data" format="fasta" label="Backbone/reference sequences" help="FASTA format" /> | |
85 </when> | |
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86 </conditional> |
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87 <!-- Sanger --> |
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88 <conditional name="condSanger"> |
13 | 89 <param name="use" type="select" label="Sanger/Capillary reads?"> |
90 <option value="false">No</option> | |
91 <option value="true">Yes</option> | |
92 </param> | |
93 <when value="false" /> | |
94 <when value="true"> | |
95 <param name="filename" type="data" format="fastq" label="Sanger/Capillary reads file" help="FASTQ format" /> | |
96 </when> | |
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97 </conditional> |
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98 <!-- Roche 454 --> |
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99 <conditional name="condRoche"> |
13 | 100 <param name="use" type="select" label="454 reads?"> |
101 <option value="false">No</option> | |
102 <option value="true">Yes</option> | |
103 </param> | |
104 <when value="false" /> | |
105 <when value="true"> | |
106 <!-- TODO? Support SFF files directly, e.g. with sff_extract, but will need linker sequences --> | |
107 <param name="filename" type="data" format="fastq" label="Roche 454 reads file" help="FASTQ format" /> | |
108 </when> | |
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109 </conditional> |
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110 <!-- Illumina --> |
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111 <conditional name="condIllumina"> |
13 | 112 <param name="use" type="select" label="Solexa/Illumina reads?"> |
113 <option value="false">No</option> | |
114 <option value="true">Yes</option> | |
115 </param> | |
116 <when value="false" /> | |
117 <when value="true"> | |
118 <param name="filename" type="data" format="fastq" label="Solexa/Illumina reads file" help="FASTQ format" /> | |
119 </when> | |
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120 </conditional> |
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121 <!-- Ion Torrent --> |
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122 <conditional name="condIonTorrent"> |
13 | 123 <param name="use" type="select" label="Ion Torrent reads?"> |
124 <option value="false">No</option> | |
125 <option value="true">Yes</option> | |
126 </param> | |
127 <when value="false" /> | |
128 <when value="true"> | |
129 <!-- TODO? Support SFF files directly, e.g. with sff_extract --> | |
130 <param name="filename" type="data" format="fastq" label="Ion Torrent reads file" help="FASTQ format" /> | |
131 </when> | |
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132 </conditional> |
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133 </inputs> |
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134 <outputs> |
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135 <data name="out_fasta" format="fasta" label="MIRA contigs (FASTA)" /> |
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136 <data name="out_qual" format="qual454" label="MIRA contigs (QUAL)" /> |
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137 <data name="out_caf" format="txt" label="MIRA contigs (CAF)" /> |
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138 <data name="out_ace" format="txt" label="MIRA contigs (ACE)" /> |
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139 <data name="out_wig" format="wig" label="MIRA coverage (Wiggle)" /> |
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140 <data name="out_log" format="txt" label="MIRA log" /> |
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141 </outputs> |
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142 <tests> |
13 | 143 <!-- Based on the MIRA v3.4.1.1 bundled minidemo/estdemo2 which uses |
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144 strain data and miraSearchESTSNPs. Here we just assemble it. --> |
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145 <test> |
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146 <param name="job_method" value="denovo" /> |
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147 <param name="job_type" value="est" /> |
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148 <param name="job_qual" value="accurate" /> |
13 | 149 <param name="condBackbone|use" value="false" /> |
150 <param name="condSanger|use" value="true" /> | |
151 <param name="condSanger|filename" value="tvc_mini.fastq" ftype="fastq" /> | |
152 <param name="condRoche|use" value="false" /> | |
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153 <param name="condIllumina|use" value="false" /> |
13 | 154 <param name="condIonTorrent|use" value="false" /> |
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155 <output name="out_fasta" file="tvc_contigs.fasta" ftype="fasta" /> |
13 | 156 <output name="out_qual" file="empty_file.dat" compare="contains" /> |
157 <output name="out_caf" file="empty_file.dat" compare="contains" /> | |
158 <output name="out_ace" file="empty_file.dat" compare="contains" /> | |
159 <output name="out_wig" file="empty_file.dat" compare="contains" /> | |
160 <output name="out_log" file="empty_file.dat" compare="contains" /> | |
161 </test> | |
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162 </tests> |
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163 <help> |
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164 |
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165 **What it does** |
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166 |
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167 Runs MIRA v3.4, collects the output, and throws away all the temporary files. |
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168 |
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169 MIRA is an open source assembly tool capable of handling sequence data from |
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170 a range of platforms (Sanger capillary, Solexa/Illumina, Roche 454 and also |
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171 Ion Torrent). |
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172 |
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173 It is particularly suited to small genomes such as bacteria. |
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174 |
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175 **Citation** |
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176 |
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177 If you use this Galaxy tool in work leading to a scientific publication please |
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178 cite the following papers: |
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179 |
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180 Peter J.A. Cock, Björn A. Grüning, Konrad Paszkiewicz and Leighton Pritchard (2013). |
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181 Galaxy tools and workflows for sequence analysis with applications |
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182 in molecular plant pathology. PeerJ 1:e167 |
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183 https://doi.org/10.7717/peerj.167 |
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184 |
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185 Bastien Chevreux, Thomas Wetter and Sándor Suhai (1999). |
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186 Genome Sequence Assembly Using Trace Signals and Additional Sequence Information. |
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187 Computer Science and Biology: Proceedings of the German Conference on Bioinformatics (GCB) 99, pp. 45-56. |
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188 http://www.bioinfo.de/isb/gcb99/talks/chevreux/main.html |
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189 |
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190 This wrapper is available to install into other Galaxy Instances via the Galaxy |
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191 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/mira_assembler |
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192 |
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193 </help> |
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194 <citations> |
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195 <citation type="doi">10.7717/peerj.167</citation> |
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196 <citation type="bibtex">@ARTICLE{Chevreux1999-mira3, |
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197 author = {B. Chevreux and T. Wetter and S. Suhai}, |
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198 year = {1999}, |
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199 title = {Genome Sequence Assembly Using Trace Signals and Additional Sequence Information}, |
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200 journal = {Computer Science and Biology: Proceedings of the German Conference on Bioinformatics (GCB)} |
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201 volume = {99}, |
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202 pages = {45-56}, |
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203 url = {http://www.bioinfo.de/isb/gcb99/talks/chevreux/main.html} |
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204 }</citation> |
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205 </citations> |
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206 </tool> |