Mercurial > repos > simon-gladman > snippy
annotate snippy.xml @ 17:2fbf00cd46ca draft
Updated to new version of snippy with static binaries
| author | simon-gladman |
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| date | Wed, 08 Jun 2016 23:46:47 -0400 |
| parents | 29ad0319f14b |
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| rev | line source |
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1 <tool id="snippy" name="snippy" version="0.2.0"> |
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2 <requirements> |
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3 <requirement type="package" version="3.0">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><![CDATA[ |
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9
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10 #if str( $reftype.ref_type_selector ) == "fasta" |
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11 cp $reftype.ref foo.fna && |
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12 #end if |
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13 #if str( $reftype.ref_type_selector ) == "genbank" |
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14 cp $reftype.ref foo.gbk && |
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15 #end if |
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16 snippy |
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17 --outdir out |
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18 --cpus "\${GALAXY_SLOTS:-1}" |
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19 #if str( $reftype.ref_type_selector ) == "fasta" |
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20 --ref foo.fna |
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21 #end if |
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22 #if str( $reftype.ref_type_selector ) == "genbank" |
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23 --ref foo.gbk |
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24 #end if |
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25 $cleanup |
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26 #if str( $advanced.is_advanced ) == "advanced" |
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27 --mapqual $advanced.mapqual |
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28 --mincov $advanced.mincov |
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29 --minfrac $advanced.minfrac |
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30 #if $advanced.rgid |
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31 --rgid $advanced.rgid |
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32 #end if |
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33 #if $advanced.bwaopt |
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34 --bwaopt $advanced.bwaopt |
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35 #end if |
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36 #end if |
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37 #if str( $fastq_input.fastq_input_selector ) == "paired" |
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38 --pe1 $fastq_input.fastq_input1 |
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39 --pe2 $fastq_input.fastq_input2 |
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40 #end if |
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41 #if str( $fastq_input.fastq_input_selector ) == "paired_collection" |
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42 --pe1 $fastq_input.fastq_input1.forward |
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43 --pe2 $fastq_input.fastq_input1.reverse |
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44 #end if |
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45 #if str( $fastq_input.fastq_input_selector ) == "single" |
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46 --se $fastq_input.fastq_input1 |
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47 #end if |
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48 #if str( $fastq_input.fastq_input_selector ) == "paired_iv" |
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49 --peil $fastq_input.fastq_input1 |
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50 #end if |
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51 |
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52 && |
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53 |
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54 gunzip out/snps.depth.gz |
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55 |
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56 && |
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57 |
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58 tar -czf out.tgz out |
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59 |
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60 |
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61 ]]></command> |
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62 <inputs> |
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63 <conditional name="reftype"> |
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64 <param name="ref_type_selector" type="select" label="Reference type" help="File type of the reference file. (Fasta or Genbank)"> |
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65 <option value="genbank">Genbank</option> |
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66 <option value="fasta">Fasta</option> |
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67 </param> |
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68 <when value="fasta"> |
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69 <param name="ref" type="data" format="fasta" label="Reference Fasta" help="Fasta file to use as the reference" /> |
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70 </when> |
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71 <when value="genbank"> |
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72 <param name="ref" type="data" format="genbank" label="Reference Genbank" help="Genbank file to use as the reference" /> |
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73 </when> |
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74 </conditional> |
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75 <conditional name="fastq_input"> |
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76 <param name="fastq_input_selector" type="select" label="Single or Paired-end reads" help="Select between paired and single end data"> |
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77 <option value="paired">Paired</option> |
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78 <option value="single">Single</option> |
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79 <option value="paired_collection">Paired Collection</option> |
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80 <option value="paired_iv">Paired Interleaved</option> |
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81 </param> |
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82 <when value="paired"> |
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83 <param name="fastq_input1" type="data" format="fastqsanger,fasta" label="Select first set of reads" help="Specify dataset with forward reads"/> |
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84 <param name="fastq_input2" type="data" format="fastqsanger,fasta" label="Select second set of reads" help="Specify dataset with reverse reads"/> |
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85 </when> |
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86 <when value="single"> |
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87 <param name="fastq_input1" type="data" format="fastqsanger,fasta" label="Select fastq dataset" help="Specify dataset with single reads"/> |
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88 </when> |
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89 <when value="paired_collection"> |
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90 <param name="fastq_input1" format="fastqsanger,fasta" type="data_collection" collection_type="paired" label="Select a paired collection" help="See help section for an explanation of dataset collections"/> |
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91 </when> |
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92 <when value="paired_iv"> |
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93 <param name="fastq_input1" type="data" format="fastqsanger" label="Select fastq dataset" help="Specify dataset with interleaved reads"/> |
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94 </when> |
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95 </conditional> |
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96 <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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97 <conditional name="advanced"> |
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98 <param name="is_advanced" type="select" label="Advanced parameters" help="unhide advanced parameter settings"> |
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99 <option value="advanced">Show advanced settings</option> |
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100 <option value="simple" selected="true">Hide advanced settings</option> |
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101 </param> |
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102 <when value="advanced"> |
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103 <param name="mapqual" type="float" value="60" label="Minimum mapping quality" help="Minimum mapping quality to allow" /> |
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104 <param name="mincov" type="float" value="10" label="Minimum coverage" help="Minimum coverage to call a snp" /> |
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105 <param name="minfrac" type="float" value="0.9" label="Minumum proportion for variant evidence" help="Minumum proportion for variant evidence" /> |
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106 <param name="rgid" type="text" value="" label="Bam header @RG ID" help="Use this @RG ID: in the BAM header" /> |
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107 <param name="bwaopt" type="text" value="" label="Extra BWA MEM options" help="Extra BWA MEM options, eg. -x pacbio" /> |
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108 </when> |
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109 <when value="simple"> |
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110 |
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111 </when> |
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112 </conditional> |
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113 </inputs> |
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114 <outputs> |
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115 <data format="vcf" name="snpvcf" label="${tool.name} on ${on_string} snps vcf file" from_work_dir="out/snps.vcf"/> |
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116 <data format="gff3" name="snpgff" label="${tool.name} on ${on_string} snps gff file" from_work_dir="out/snps.gff"/> |
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117 <data format="tabular" name="snptab" label="${tool.name} on ${on_string} snps table" from_work_dir="out/snps.tab"/> |
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118 <data format="tabular" name="snpsum" label="${tool.name} on ${on_string} snps summary" from_work_dir="out/snps.txt"/> |
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119 <data format="txt" name="snplog" label="${tool.name} on ${on_string} log file" from_work_dir="out/snps.log"/> |
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120 <data format="fasta" name="snpalign" label="${tool.name} on ${on_string} aligned fasta" from_work_dir="out/snps.aligned.fa"/> |
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121 <data format="fasta" name="snpconsensus" label="${tool.name} on ${on_string} consensus fasta" from_work_dir="out/snps.consensus.fa"/> |
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122 <data format="tabular" name="snpsdepth" label="${tool.name} on ${on_string} mapping depth" from_work_dir="out/snps.depth"/> |
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123 <data format="bam" name="snpsbam" label="${tool.name} on ${on_string} mapped reads (bam)" from_work_dir="out/snps.bam"> |
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124 <filter>cleanup is False</filter> |
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125 </data> |
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126 <data format="zip" name="outdir" label="${tool.name} on ${on_string} out dir" from_work_dir="out.tgz" /> |
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127 </outputs> |
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128 |
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129 <tests> |
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130 <test> |
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131 <param name="ref_type_selector" value="fasta" /> |
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132 <param name="ref" value="Ecoli.fna" ftype="fasta" /> |
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133 <param name="fastq_input_selector" value="paired" /> |
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134 <param name="fastq_input1" ftype="fastq" value="reads_1.fq" /> |
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135 <param name="fastq_input2" ftype="fastq" value="reads_2.fq" /> |
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136 <output name="snpsum" ftype="tabular" file="test/snps.txt" lines-diff="5" /> |
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137 </test> |
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138 </tests> |
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139 |
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140 |
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141 <help><![CDATA[ |
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142 Synopsis: |
| 7 | 143 snippy 3.0 - fast bacterial variant calling from NGS reads |
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144 |
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145 Author: |
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146 Torsten Seemann <torsten.seemann@gmail.com> |
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147 |
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148 Usage: |
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149 snippy [options] --outdir <dir> --ref <ref> --pe1 <R1.fq.gz> --pe2 <R2.fq.gz> |
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150 |
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151 snippy [options] --outdir <dir> --ref <ref> --se <454.fastq> |
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152 |
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153 snippy [options] --outdir <dir> --ref <ref> --peil <velvet.fa.gz> |
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154 |
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155 Options: |
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156 --help This help |
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157 |
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158 --version Print version and exit |
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159 |
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160 --citation Print citation for referencing snippy |
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161 |
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162 --quiet No screen output (default OFF) |
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163 |
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164 --cpus [N] Maximum number of CPU cores to use (default '8') |
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165 |
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166 --reference [X] Reference genome. Supports FASTA, GenBank, EMBL (not GFF) (default '') |
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167 |
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168 --outdir [X] Output folder (default '') |
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169 |
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170 --prefix [X] Prefix for output files (default 'snps') |
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171 |
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172 --force Force overwrite of existing output folder (default OFF) |
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173 |
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174 --pe1|R1|left [X] Reads, paired-end R1 (left) (default '') |
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175 |
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176 --pe2|R2|right [X] Reads, paired-end R2 (right) (default '') |
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177 |
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178 --se|single [X] Single-end reads (default '') |
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179 |
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180 --peil [X] Reads, paired-end R1/R2 interleaved (default '') |
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181 |
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182 --mapqual [n.n] Minimum mapping quality to allow (default '60') |
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183 |
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184 --mincov [N] Minimum coverage of variant site (default '10') |
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185 |
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186 --minfrac [n.n] Minumum proportion for variant evidence (default '0.9') |
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187 |
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188 --report Produce long report with visual alignment (slow) (default OFF) |
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189 |
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190 --cleanup Remove all non-SNP files: BAMs, indices etc (default OFF) |
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191 |
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192 --rgid [X] Use this @RG ID: in the BAM header (default '') |
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193 |
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194 --bwaopt [X] Extra BWA MEM options, eg. -x pacbio (default '') |
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195 |
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196 ]]></help> |
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197 <citations> |
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198 <citation type="bibtex">@UNPUBLISHED{Seemann2013, |
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199 author = "Seemann T", |
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200 title = "snippy: fast bacterial variant calling from NGS reads", |
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201 year = "2015", |
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202 note = "https://github.com/tseemann/snippy"}</citation> |
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203 </citations> |
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204 |
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205 |
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206 </tool> |
