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annotate racon.xml @ 7:bd59160b6d88 draft

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"planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/racon commit 315fa3071141484b055db128f7d116a774cc5beb"
author bgruening
date Wed, 13 Apr 2022 15:38:24 +0000
parents ab52646465ad
children 24089304f9c4
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1 <tool id="racon" name="Racon" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@">
0
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2 <description>Consensus module for raw de novo DNA assembly of long uncorrected reads.</description>
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3 <macros>
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4 <import>macros.xml</import>
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5 </macros>
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6 <expand macro="requirements" />
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7 <version_command>racon --version</version_command>
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8 <command detect_errors="exit_code"><![CDATA[
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9 #if $reads.ext.startswith("fasta")
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10 #set ext="fasta"
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11 #else
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12 #set ext="fastq"
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13 #end if
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14 #if $reads.ext.endswith(".gz")
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15 #set ext=ext+".gz"
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16 #end if
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17
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18 ln -s '$reads' reads.$ext &&
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19 #if $overlaps.ext == 'sam':
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20 ln -s '$overlaps' overlaps.${overlaps.ext} &&
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21 #else:
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22 ln -s '$overlaps' overlaps.paf &&
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23 #end if
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25 #if $corrected_reads.ext.startswith("fasta")
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26 #set cext="fasta"
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27 #else
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28 #set cext="fastq"
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29 #end if
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30 #if $corrected_reads.ext.endswith(".gz")
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31 #set cext=cext+".gz"
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32 #end if
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33 ln -s '$corrected_reads' corrected_reads.$cext &&
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34
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35 racon
4
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36 reads.$ext
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37 #if $overlaps.ext == 'sam':
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38 overlaps.${overlaps.ext}
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39 #else:
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40 overlaps.paf
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41 #end if
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42 corrected_reads.$cext
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43 -t \${GALAXY_SLOTS:-4}
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44 $u
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45 $f
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46 -w $w
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47 -q $q
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48 -e $e
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49 -m $m
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50 -x $x
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51 -g $g
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52 > racon_polished_consensus.fa
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53 ]]></command>
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54 <inputs>
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55 <param type="data" name="reads" format="fasta,fasta.gz,fastq,fastq.gz" label="Sequences"/>
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56 <param type="data" name="overlaps" format="paf,sam,tabular" label="Overlaps"/>
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57 <param type="data" name="corrected_reads" format="fasta,fasta.gz,fastq,fastq.gz" label="Target sequences"/>
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58
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59 <param argument="-u" type="boolean" truevalue="-u" falsevalue="" label="output unpolished target sequences" />
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60 <param argument="-f" type="boolean" truevalue="-f" falsevalue="" label="perform fragment correction instead of contig polishing" />
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61 <param argument="-w" type="integer" value="500" label="Size of window on which POA is performed" />
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62 <param argument="-q" type="float" value="10.0" label="Threshold for average base quality of windows used in poa" />
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63 <param argument="-e" type="float" value="0.3" label="Maximum allowed error rate used for filtering overlaps" />
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64 <param argument="-m" type="integer" value="5" label="Score for matching bases" />
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65 <param argument="-x" type="integer" value="-4" label="Score for mismatching bases" />
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66 <param argument="-g" type="integer" value="-8" max="0" label="Gap penalty" />
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67
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68 </inputs>
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69 <outputs>
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70 <data name="consensus" format="fasta" from_work_dir="racon_polished_consensus.fa" />
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71 </outputs>
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72 <tests>
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73 <test>
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74 <param name="reads" ftype="fasta" value="sample_reads.fasta"/>
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75 <param name="overlaps" ftype="sam" value="sample_overlaps.sam"/>
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76 <param name="corrected_reads" ftype="fasta" value="sample_layout.fasta"/>
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77 <param name="u" value="true"/>
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78 <param name="f" value="true"/>
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79 <param name="w" value="800"/>
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80 <param name="e" value="0.2"/>
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81 <output name="consensus" ftype="fasta" file="consensus_result2.fasta"/>
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82 </test>
1
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83 <test>
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84 <param name="reads" ftype="fasta" value="sample_reads.fasta"/>
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85 <param name="overlaps" ftype="interval" value="sample_overlaps.paf"/>
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86 <param name="corrected_reads" ftype="fasta" value="sample_layout.fasta"/>
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87 <output name="consensus" ftype="fasta" file="consensus_result3.fasta"/>
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88 </test>
0
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89 </tests>
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90 <help><![CDATA[
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91
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92 **What it does**
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93
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94 Consensus module for raw de novo DNA assembly of long uncorrected reads.
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95
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96 Racon is intended as a standalone consensus module to correct raw contigs generated by rapid assembly methods
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97 which do not include a consensus step. The goal of Racon is to generate genomic consensus which is of similar
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98 or better quality compared to the output generated by assembly methods which employ both error correction
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99 and consensus steps, while providing a speedup of several times compared to those methods.
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100 It supports data produced by both Pacific Biosciences and Oxford Nanopore Technologies.
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101
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102 Racon can be used as a polishing tool after the assembly with either Illumina data or data
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103 produced by third generation of sequencing. The type of data inputed is automatically detected.
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104
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105 Racon takes as input only three files: contigs in FASTA/FASTQ format, reads in FASTA/FASTQ
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106 format and overlaps/alignments between the reads and the contigs in SAM format. Output is a set of polished contigs in FASTA format printed to stdout.
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107
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108 Racon can also be used as a read error-correction tool. In this scenario, the SAM file needs
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109 to contain pairwise overlaps between reads including dual overlaps.
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110
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111 ]]></help>
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112 <expand macro="citations" />
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113 </tool>