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1 <tool id="snippy" name="snippy" version="3.2">
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2 <requirements>
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3 <requirement type="package" version="3.2">snippy</requirement>
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4 </requirements>
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5 <stdio>
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6 <exit_code range="1:" />
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7 </stdio>
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8
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9 <command>
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10 <![CDATA[
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11 snippy
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12 --outdir out
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13 --cpus "\${GALAXY_SLOTS:-1}"
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14 --ref $ref
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15 $cleanup
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16 #if str( $advanced.is_advanced ) == "advanced"
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17 --mapqual $advanced.mapqual
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18 --mincov $advanced.mincov
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19 --minfrac $advanced.minfrac
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20 #if $advanced.rgid
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21 --rgid $advanced.rgid
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22 #end if
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23 #if $advanced.bwaopt
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24 --bwaopt $advanced.bwaopt
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25 #end if
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26 #end if
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27 --ctgs $input
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28
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29 &&
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30
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31 gunzip out/snps.depth.gz
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32
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33 &&
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34
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35 tar -czf out.tgz out
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36
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37
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38 ]]>
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39 </command>
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40 <inputs>
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41
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42 <param name="ref" type="data" format="fasta" label="Reference Fasta" />
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43 <param name="input" type="data" format="fasta" label="assembled contigs"/>
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44 <param name="cleanup" type="boolean" checked="true" truevalue="--cleanup" falsevalue="" label="Cleanup the non-snp output files" help="Remove all non-SNP files: BAMs, indices etc" />
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45 <conditional name="advanced">
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46 <param name="is_advanced" type="select" label="Advanced parameters" help="unhide advanced parameter settings">
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47 <option value="advanced">Show advanced settings</option>
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48 <option value="simple" selected="true">Hide advanced settings</option>
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49 </param>
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50 <when value="advanced">
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51 <param name="mapqual" type="float" value="60" label="Minimum mapping quality" help="Minimum mapping quality to allow" />
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52 <param name="mincov" type="float" value="10" label="Minimum coverage" help="Minimum coverage to call a snp" />
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53 <param name="minfrac" type="float" value="0.9" label="Minumum proportion for variant evidence" help="Minumum proportion for variant evidence" />
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54 <param name="rgid" type="text" value="" label="Bam header @RG ID" help="Use this @RG ID: in the BAM header" />
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55 <param name="bwaopt" type="text" value="" label="Extra BWA MEM options" help="Extra BWA MEM options, eg. -x pacbio" />
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56 </when>
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57 <when value="simple">
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58
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59 </when>
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60 </conditional>
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61 </inputs>
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62 <outputs>
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63 <data format="vcf" name="snpvcf" label="${tool.name} on ${on_string} snps vcf file" from_work_dir="out/snps.vcf"/>
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64 <data format="gff3" name="snpgff" label="${tool.name} on ${on_string} snps gff file" from_work_dir="out/snps.gff"/>
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65 <data format="tabular" name="snptab" label="${tool.name} on ${on_string} snps table" from_work_dir="out/snps.tab"/>
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66 <data format="tabular" name="snpsum" label="${tool.name} on ${on_string} snps summary" from_work_dir="out/snps.txt"/>
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67 <data format="txt" name="snplog" label="${tool.name} on ${on_string} log file" from_work_dir="out/snps.log"/>
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68 <data format="fasta" name="snpalign" label="${tool.name} on ${on_string} aligned fasta" from_work_dir="out/snps.aligned.fa"/>
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69 <data format="fasta" name="snpconsensus" label="${tool.name} on ${on_string} consensus fasta" from_work_dir="out/snps.consensus.fa"/>
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70 <data format="tabular" name="snpsdepth" label="${tool.name} on ${on_string} mapping depth" from_work_dir="out/snps.depth"/>
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71 <data format="bam" name="snpsbam" label="${tool.name} on ${on_string} mapped reads (bam)" from_work_dir="out/snps.bam">
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72 <filter>cleanup is False</filter>
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73 </data>
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74 <data format="zip" name="outdir" label="${tool.name} on ${on_string} out dir" from_work_dir="out.tgz" />
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75 </outputs>
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76
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77 <tests>
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78 <test>
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79 <param name="ref_type_selector" value="fasta" />
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80 <param name="ref" value="Ecoli.fna" ftype="fasta" />
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81 <param name="fastq_input_selector" value="paired" />
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82 <param name="fastq_input1" ftype="fastq" value="reads_1.fq" />
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83 <param name="fastq_input2" ftype="fastq" value="reads_2.fq" />
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84 <output name="snpsum" ftype="tabular" file="test/snps.txt" lines-diff="5" />
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85 </test>
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86 </tests>
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87
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88
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89 <help>
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90 <![CDATA[
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91 Synopsis:
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92 snippy 3.0 - fast bacterial variant calling from NGS reads
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93
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94 Author:
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95 Torsten Seemann <torsten.seemann@gmail.com>
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96
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97 Usage:
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98 snippy [options] --outdir <dir> --ref <ref> --pe1 <R1.fq.gz> --pe2 <R2.fq.gz>
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99
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100 snippy [options] --outdir <dir> --ref <ref> --se <454.fastq>
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101
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102 snippy [options] --outdir <dir> --ref <ref> --peil <velvet.fa.gz>
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103
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104 Options:
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105 --help This help
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106
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107 --version Print version and exit
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108
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109 --citation Print citation for referencing snippy
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110
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111 --quiet No screen output (default OFF)
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112
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113 --cpus [N] Maximum number of CPU cores to use (default '8')
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114
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115 --reference [X] Reference genome. Supports FASTA, GenBank, EMBL (not GFF) (default '')
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116
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117 --outdir [X] Output folder (default '')
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118
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119 --prefix [X] Prefix for output files (default 'snps')
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120
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121 --force Force overwrite of existing output folder (default OFF)
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122
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123 --pe1|R1|left [X] Reads, paired-end R1 (left) (default '')
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124
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125 --pe2|R2|right [X] Reads, paired-end R2 (right) (default '')
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126
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127 --se|single [X] Single-end reads (default '')
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128
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129 --peil [X] Reads, paired-end R1/R2 interleaved (default '')
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130
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131 --mapqual [n.n] Minimum mapping quality to allow (default '60')
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132
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133 --mincov [N] Minimum coverage of variant site (default '10')
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134
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135 --minfrac [n.n] Minumum proportion for variant evidence (default '0.9')
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136
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137 --report Produce long report with visual alignment (slow) (default OFF)
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138
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139 --cleanup Remove all non-SNP files: BAMs, indices etc (default OFF)
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140
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141 --rgid [X] Use this @RG ID: in the BAM header (default '')
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142
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143 --bwaopt [X] Extra BWA MEM options, eg. -x pacbio (default '')
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144
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145 ]]>
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146 </help>
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147 <citations>
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148 <citation type="bibtex">
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149 @UNPUBLISHED{Seemann2013,
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150 author = "Seemann T",
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151 title = "snippy: fast bacterial variant calling from NGS reads",
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152 year = "2015",
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153 note = "https://github.com/tseemann/snippy"}
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154 </citation>
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155 </citations>
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156
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157
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158 </tool> |
