Mercurial > repos > galaxytrakr > mitokmer
annotate mitokmer.xml @ 8:2b1f3db24c25 draft default tip
planemo upload commit 41caf97a4a9a7928318af8b24601f84a380fe2db
| author | galaxytrakr |
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| date | Fri, 18 Sep 2026 12:26:54 +0000 |
| parents | 56b71adcaba7 |
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| rev | line source |
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1 <tool id="mitokmer" name="mitoKmer" version="2.0+galaxy0.24" profile="21.05"> |
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2 <description>Identify metagenomic mitochondrial reads by k-mer database matching</description> |
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3 <requirements> |
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4 <container type="docker">quay.io/galaxytrakr/mitokmer:e57a559</container> |
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5 </requirements> |
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6 |
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7 <command detect_errors="exit_code"><![CDATA[ |
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8 #import re |
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9 #def fix_ext($ext): |
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10 #set ext = $ext.replace('fastqsanger', 'fastq') |
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11 #set ext = $ext.replace('fastqillumina', 'fastq') |
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12 #return $ext |
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13 #end def |
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14 |
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15 mkdir -p ./mitochondria7 ./jobs7m && |
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16 |
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17 ## ── Link database files into working directory ──────────────────────── |
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18 ln -sf '${probe_db.fields.path}'/* ./mitochondria7/ && |
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19 |
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20 ## ── Symlink kmerread7 binary into working directory ─────────────────── |
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21 ln -sf /usr/local/bin/kmerread7 ./kmerread7 && |
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22 |
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23 ## ── Stage input reads and build jobs file ──────────────────────────── |
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24 #if $reads.reads_type == "single_file" |
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25 mkdir -p ./reads && |
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26 #set sample_name = re.sub('[^\w\-_.]', '_', $reads.input.name) |
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27 #set ext = $fix_ext($reads.input.ext) |
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28 #set fname = re.sub('[^\w\-_.]', '_', $reads.input.element_identifier) + '.' + $ext |
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29 ln -sf '$reads.input' './reads/${fname}' && |
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30 printf '%s\t1\n' '${sample_name}' > ./jobs7m/jobs7m.txt && |
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31 printf '%s\n' './reads/${fname}' >> ./jobs7m/jobs7m.txt && |
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32 #else if $reads.reads_type == "single" |
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33 mkdir -p ./reads && |
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34 #set sample_name = re.sub('[^\w\-_.]', '_', $reads.input.name) |
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35 #set read_count = 0 |
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36 #for $read in $reads.input |
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37 #set ext = $fix_ext($read.ext) |
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38 #set fname = re.sub('[^\w\-_.]', '_', $read.element_identifier) + '.' + $ext |
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39 ln -sf '$read' './reads/${fname}' && |
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40 #set read_count = $read_count + 1 |
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41 #end for |
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42 printf '%s\t%d\n' '${sample_name}' ${read_count} > ./jobs7m/jobs7m.txt && |
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43 #for $read in $reads.input |
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44 #set ext = $fix_ext($read.ext) |
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45 #set fname = re.sub('[^\w\-_.]', '_', $read.element_identifier) + '.' + $ext |
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46 printf '%s\n' './reads/${fname}' >> ./jobs7m/jobs7m.txt && |
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47 #end for |
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48 #else |
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49 ## paired collection: forward + reverse |
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50 mkdir -p ./reads && |
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51 #set sample_name = re.sub('[^\w\-_.]', '_', $reads.input.name) |
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52 #set fwd_ext = $fix_ext($reads.input.forward.ext) |
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53 #set rev_ext = $fix_ext($reads.input.reverse.ext) |
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54 #set base = re.sub('[^\w\-_.]', '_', $reads.input.element_identifier) |
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55 #set fwd_fname = $base + '_1.' + $fwd_ext |
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56 #set rev_fname = $base + '_2.' + $rev_ext |
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57 ln -sf '$reads.input.forward' './reads/${fwd_fname}' && |
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58 ln -sf '$reads.input.reverse' './reads/${rev_fname}' && |
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59 printf '%s\t2\n' '${sample_name}' > ./jobs7m/jobs7m.txt && |
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60 printf '%s\n' './reads/${fwd_fname}' >> ./jobs7m/jobs7m.txt && |
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61 printf '%s\n' './reads/${rev_fname}' >> ./jobs7m/jobs7m.txt && |
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62 #end if |
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63 |
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64 ## ── Run the Python orchestrator ─────────────────────────────────────── |
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65 python3 /opt/mitokmer2/kmer_read_m7.py && |
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66 |
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67 ## ── Copy output CSV to Galaxy output path ───────────────────────────── |
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68 cp ./jobs7m/jobs7m.csv '${results_csv}' |
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69 ]]></command> |
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70 |
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71 <inputs> |
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72 <param name="probe_db" type="select" label="Mitochondrial k-mer probe database" |
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73 help="Select a pre-installed mitochondrial k-mer probe database. |
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74 Databases are managed by your Galaxy administrator via the |
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75 mitokmer_probe_db data table."> |
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76 <options from_data_table="mitokmer_probe_db"> |
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77 <filter type="sort_by" column="1" /> |
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78 <validator type="no_options" message="No mitochondrial k-mer probe databases are |
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79 currently installed. Please contact your Galaxy administrator." /> |
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80 </options> |
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81 </param> |
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82 |
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83 <conditional name="reads"> |
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84 <param name="reads_type" type="select" label="Input read type"> |
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85 <option value="single_file">Single FASTA or FASTQ dataset</option> |
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86 <option value="single">Single-end or unpaired reads / FASTA (list collection)</option> |
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87 <option value="paired">Paired-end reads (paired collection)</option> |
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88 </param> |
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89 <when value="single_file"> |
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90 <param name="input" type="data" |
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91 format="fastqsanger,fastqsanger.gz,fastqillumina,fastqillumina.gz,fasta,fasta.gz" |
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92 label="Input FASTA or FASTQ dataset" |
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93 help="Provide a single FASTA or FASTQ file from your history." /> |
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94 </when> |
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95 <when value="single"> |
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96 <param name="input" type="data_collection" collection_type="list" |
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97 format="fastqsanger,fastqsanger.gz,fastqillumina,fastqillumina.gz,fasta,fasta.gz" |
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98 label="Input reads (FASTQ or FASTA, gzipped or plain)" |
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99 help="Provide one or more single-end or unpaired read files as a Galaxy |
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100 list collection. For paired-end data, use the 'Paired-end reads' |
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101 option instead." /> |
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102 </when> |
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103 <when value="paired"> |
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104 <param name="input" type="data_collection" collection_type="paired" |
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105 format="fastqsanger,fastqsanger.gz,fastqillumina,fastqillumina.gz" |
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106 label="Paired-end reads (paired collection)" |
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107 help="Provide a Galaxy paired collection containing forward (R1) and |
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108 reverse (R2) reads. Light quality trimming of read ends is |
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109 performed internally; pre-trimming is optional." /> |
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110 </when> |
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111 </conditional> |
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112 </inputs> |
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113 |
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114 <outputs> |
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115 <data name="results_csv" format="csv" label="mitoKmer results for ${on_string}" /> |
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116 </outputs> |
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117 |
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118 <tests> |
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119 <!-- Test 1: single FASTA dataset --> |
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120 <test> |
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121 <param name="probe_db" value="mitoch_probes_sample" /> |
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122 <conditional name="reads"> |
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123 <param name="reads_type" value="single_file" /> |
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124 <param name="input" value="test/Plodia_assembly.fasta" ftype="fasta" /> |
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125 </conditional> |
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126 <output name="results_csv"> |
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127 <assert_contents> |
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128 <has_text text="Plodia" /> |
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129 </assert_contents> |
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130 </output> |
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131 </test> |
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132 <!-- Test 2: paired-end FASTQ via paired collection --> |
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133 <test> |
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134 <param name="probe_db" value="mitoch_probes_sample" /> |
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135 <conditional name="reads"> |
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136 <param name="reads_type" value="paired" /> |
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137 <param name="input"> |
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138 <collection type="paired"> |
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139 <element name="forward" value="test/Plodia_R1.fastq.gz" ftype="fastqsanger.gz" /> |
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140 <element name="reverse" value="test/Plodia_R2.fastq.gz" ftype="fastqsanger.gz" /> |
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141 </collection> |
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142 </param> |
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143 </conditional> |
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144 <output name="results_csv"> |
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145 <assert_contents> |
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146 <has_text text="Plodia" /> |
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147 </assert_contents> |
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148 </output> |
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149 </test> |
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150 <!-- Test 3: single-end FASTQ via list collection --> |
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151 <test> |
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152 <param name="probe_db" value="mitoch_probes_sample" /> |
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153 <conditional name="reads"> |
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154 <param name="reads_type" value="single" /> |
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155 <param name="input"> |
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156 <collection type="list"> |
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157 <element name="Plodia_R1" value="test/Plodia_R1.fastq.gz" ftype="fastqsanger.gz" /> |
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158 </collection> |
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159 </param> |
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160 </conditional> |
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161 <output name="results_csv"> |
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162 <assert_contents> |
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163 <has_text text="Plodia" /> |
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164 </assert_contents> |
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165 </output> |
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166 </test> |
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167 <!-- Test 4: FASTA list collection --> |
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168 <test> |
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169 <param name="probe_db" value="mitoch_probes_sample" /> |
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170 <conditional name="reads"> |
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171 <param name="reads_type" value="single" /> |
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172 <param name="input"> |
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173 <collection type="list"> |
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174 <element name="Plodia_assembly" value="test/Plodia_assembly.fasta" ftype="fasta" /> |
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175 </collection> |
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176 </param> |
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177 </conditional> |
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178 <output name="results_csv"> |
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179 <assert_contents> |
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180 <has_text text="Plodia" /> |
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181 </assert_contents> |
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182 </output> |
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183 </test> |
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184 </tests> |
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185 |
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186 <help><![CDATA[ |
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187 **mitoKmer** — Metagenomic Mitochondrial Read Identification by K-mer Database |
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188 =============================================================================== |
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189 |
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190 Overview |
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191 -------- |
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192 mitoKmer identifies the taxonomic origin of short-read shotgun sequencing data |
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193 by matching reads against a database of species-specific mitochondrial k-mer |
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194 probes. It reports the relative abundance of taxa at multiple taxonomic ranks |
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195 (e.g. order, species) along with the number of matching reads and supporting |
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196 unique k-mers. |
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197 |
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198 Inputs |
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199 ------ |
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200 **Mitochondrial k-mer probe database** |
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201 Select a pre-installed probe database from the dropdown. Databases are |
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202 managed by your Galaxy administrator and registered in the |
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203 ``mitokmer_probe_db`` data table. The database consists of a directory |
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204 of ``.txt`` files. |
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205 |
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206 **Input read type** |
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207 Choose the input mode that matches your data: |
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208 |
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209 *Single FASTA or FASTQ dataset* |
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210 Provide a single FASTA or FASTQ file directly from your history. |
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211 This is the simplest option for a single assembled sequence or |
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212 single-end read file. |
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213 |
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214 *Single-end or unpaired reads / FASTA (list collection)* |
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215 Provide a Galaxy **list** collection containing one or more FASTQ |
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216 (``fastqsanger``, ``fastqsanger.gz``) or FASTA (``fasta``, |
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217 ``fasta.gz``) files. Use this for single-end sequencing data or |
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218 multiple assembled FASTA sequences processed together. |
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219 |
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220 *Paired-end reads (paired collection)* |
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221 Provide a Galaxy **paired** collection where the forward (R1) and |
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222 reverse (R2) reads are paired together. Both files must be FASTQ |
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223 format (``fastqsanger`` or ``fastqsanger.gz``). |
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224 |
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225 In all cases, light window-based quality trimming of read ends is |
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226 performed internally; pre-trimming is optional. |
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227 |
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228 Output |
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229 ------ |
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230 **Results CSV** |
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231 A comma-separated file with one row per taxon detected. Columns: |
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232 |
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233 ========= ============================================================ |
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234 Column Description |
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235 ========= ============================================================ |
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236 Rank Taxonomic rank (e.g. Order, Species) |
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237 Taxon Taxon name |
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238 Reads Number of reads matching this taxon |
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239 Rel_Abund Relative abundance (%) |
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240 Unique_kmers Number of unique k-mers supporting the match |
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241 ========= ============================================================ |
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242 |
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243 Only taxa with non-zero relative abundance are reported. |
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244 |
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245 Example output for the "Plodia" test sample:: |
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246 |
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247 Rank Taxon Reads Rel_Abund(%) Unique_kmers |
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248 Order Lepidoptera 10 0.1 329 |
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249 Species Plodia interpunctella 462 99.9 466 |
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250 |
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251 Citation |
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252 -------- |
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253 Please cite the mitoKmer GitHub repository if you use this tool in published work. |
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254 ]]></help> |
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255 |
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256 <citations> |
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257 <citation type="bibtex"> |
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258 @misc{githubmitokmer2, |
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259 author = {Mammel, Mark}, |
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260 title = {mitoKmer2}, |
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261 year = {2024}, |
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262 publisher = {GitHub}, |
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263 journal = {GitHub repository}, |
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264 url = {https://github.com/mmammel8/mitokmer2}, |
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265 } |
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266 </citation> |
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267 </citations> |
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268 </tool> |
