Mercurial > repos > bebatut > metaphlan2
comparison metaphlan2.xml @ 0:d2448d2bf1f8 draft
planemo upload for repository https://github.com/ASaiM/galaxytools/tree/master/tools/metaphlan2/ commit 450bf3326f301c344103272b0d761e8625ce0c44-dirty
author | bebatut |
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date | Wed, 01 Jun 2016 10:45:26 -0400 |
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children | 8991e05c44e4 |
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1 <tool id="metaphlan2" name="MetaPhlAn2" version="2.5.0"> | |
2 | |
3 <description>to profile the composition of microbial communities</description> | |
4 | |
5 <macros> | |
6 <import>metaphlan2_macros.xml</import> | |
7 </macros> | |
8 | |
9 <expand macro="requirements"/> | |
10 <expand macro="stdio"/> | |
11 | |
12 <version_command> | |
13 <![CDATA[ | |
14 metaphlan2.py -v | |
15 ]]> | |
16 </version_command> | |
17 | |
18 <command> | |
19 <![CDATA[ | |
20 (which bowtie2 || exit 200) | |
21 | |
22 && | |
23 | |
24 #if $db.db_selector == "history" | |
25 mkdir ref_db | |
26 && | |
27 bowtie2-build $db.db_sequences ref_db/ref_db | |
28 && | |
29 python $__tool_directory__/transform_json_to_pkl.py | |
30 --json_input $db_metadata | |
31 --pkl_output ref_db/metadata.pkl | |
32 && | |
33 #end if | |
34 | |
35 metaphlan2.py | |
36 $input_file | |
37 -o $output_file | |
38 --input_type ${input_file.datatype.file_ext} | |
39 | |
40 --bowtie2_exe `which bowtie2` | |
41 | |
42 #if $db.db_selector == "cached" | |
43 #set $table = dict([(_[0], _[2]) for _ in $db.cached_db.input.options.tool_data_table.data]) | |
44 #set $db_choice = $db.cached_db.value | |
45 --bowtie2db $table[$db_choice] | |
46 --mpa_pkl $table[$db_choice]".pkl" | |
47 #else | |
48 --bowtie2db ref_db/ref_db | |
49 --mpa_pkl ref_db/metadata.pkl | |
50 #end if | |
51 | |
52 --no_map | |
53 | |
54 -t $analysis_type.analysis_type_select | |
55 #if $analysis_type.analysis_type_select == "rel_ab" | |
56 --tax_lev $analysis_type.taxonomic_level | |
57 #else if $analysis_type.analysis_type_select == "marker_ab_table" | |
58 --nreads $analysis_type.nreads | |
59 #else if $analysis_type.analysis_type_select == "marker_pres_table" | |
60 --pres_th $analysis_type.pres_th | |
61 #end if | |
62 | |
63 --min_cu_len $min_cu_len | |
64 --min_alignment_len $min_alignment_len | |
65 | |
66 $ignore_viruses | |
67 $ignore_eukaryotes | |
68 $ignore_bacteria | |
69 $ignore_archaea | |
70 | |
71 --stat_q $stat_q | |
72 -s $sam_output_file | |
73 ]]> | |
74 </command> | |
75 | |
76 <inputs> | |
77 <param name="input_file" type="data" format="fastq,fasta,sam" label="Input file" help=""/> | |
78 | |
79 <conditional name="db"> | |
80 <param name="db_selector" type="select" label="Database with clade-specific marker genes" help=""> | |
81 <option value="cached" selected="true">Locally cached</option> | |
82 <option value="history">From history</option> | |
83 </param> | |
84 | |
85 <when value="cached"> | |
86 <param name="cached_db" label="Cached database with clade-specific marker genes" type="select" > | |
87 <options from_data_table="metaphlan2_db" /> | |
88 </param> | |
89 </when> | |
90 <when value="history"> | |
91 <param name="db_sequences" type="data" format="fasta" label="Database with clade-specific marker genes from history" help="(--bowtie2db)"/> | |
92 <param name="db_metadata" type="data" format="json" label="Metadata associate to the database with clade-specific marker genes from history" help="(--mpa_pkl)"/> | |
93 </when> | |
94 </conditional> | |
95 | |
96 <conditional name="analysis_type"> | |
97 <param name="analysis_type_select" type="select" label="Type of analysis to perform" help="(-t)"> | |
98 <option value="rel_ab" selected="true">Profiling a metagenomes in terms of relative abundances</option> | |
99 <option value="reads_map">Mapping from reads to clades (only reads hitting a marker)</option> | |
100 <option value="clade_profiles">Normalized marker counts for clades with at least a non-null marker</option> | |
101 <option value="marker_ab_table">Normalized marker counts (only when > 0.0 and normalized by metagenome size if --nreads is specified)</option> | |
102 <option value="marker_counts">Non-normalized marker counts (use with extreme caution)</option> | |
103 <option value="marker_pres_table">List of markers present in the sample (threshold at 1.0 if not differently specified with --pres_th</option> | |
104 </param> | |
105 | |
106 <when value="rel_ab"> | |
107 <param name="taxonomic_level" type="select" label="Taxonomic level for the relative abundance output" help="(--tax_lev)"> | |
108 <option value="a" selected="true">All taxonomic levels</option> | |
109 <option value="k">Kingdoms (Bacteria and Archaea) only</option> | |
110 <option value="p">Phyla only</option> | |
111 <option value="c">Classes only</option> | |
112 <option value="o">Orders only</option> | |
113 <option value="f">Families only</option> | |
114 <option value="g">Genera only</option> | |
115 <option value="s">Species only</option> | |
116 </param> | |
117 </when> | |
118 | |
119 <when value="reads_map"/> | |
120 <when value="clade_profiles"/> | |
121 | |
122 <when value="marker_ab_table"> | |
123 <param name="nreads" type="integer" value="0" label="Total number of reads in the original metagenome" help="It is used for normalizing the length-normalized counts with the metagenome size as well. No normalization applied if the value is not specified"/> | |
124 </when> | |
125 | |
126 <when value="marker_counts"/> | |
127 | |
128 <when value="marker_pres_table"> | |
129 <param name="pres_th" type="integer" value="0" label=" Threshold for calling a marker present" help=""/> | |
130 </when> | |
131 </conditional> | |
132 | |
133 <param name="min_cu_len" type="integer" value="2000" label="Minimum total nucleotide length for the markers in a clade for estimating the abundance without considering sub-clade abundances" help=""/> | |
134 | |
135 <param name="min_alignment_len" type="integer" value="0" label="Sam records for aligned reads with the longest subalignment length smaller than this threshold will be discarded." help=""/> | |
136 | |
137 <param name="ignore_viruses" type='boolean' checked="true" truevalue='' falsevalue='--ignore_viruses' label="Profile viral organisms?" help="" /> | |
138 <param name="ignore_eukaryotes" type='boolean' checked="true" truevalue='' falsevalue='--ignore_eukaryotes' label="Profile eukaryotic organisms?" help="" /> | |
139 | |
140 <param name="ignore_bacteria" type='boolean' checked="true" truevalue='' falsevalue='--ignore_bacteria' label="Profile bacteria organisms?" help="" /> | |
141 | |
142 <param name="ignore_archaea" type='boolean' checked="true" truevalue='' falsevalue='--ignore_archaea' label="Profile archea organisms?" help="" /> | |
143 | |
144 <param name="stat_q" type="float" value="0.1" label="Quantile value for the robust average" help=""/> | |
145 </inputs> | |
146 | |
147 <outputs> | |
148 <data format="tabular" name="output_file" label="${tool.name} on ${on_string}: Community profile" /> | |
149 <data format="sam" name="sam_output_file" label="${tool.name} on ${on_string}: Sam file" /> | |
150 </outputs> | |
151 | |
152 <tests> | |
153 <test> | |
154 <param name="input_file" value="input_sequences.fasta"/> | |
155 <param name="db_selector" value="history" /> | |
156 <param name="db_metadata" value="marker_metadata.json" /> | |
157 <param name="db_sequences" value="marker_sequences.fasta" /> | |
158 <param name="analysis_type_select" value="rel_ab" /> | |
159 <param name="taxonomic_level" value="a" /> | |
160 <param name="min_cu_len" value="2000" /> | |
161 <param name="min_alignment_len" value="0" /> | |
162 <param name="ignore_viruses" value="" /> | |
163 <param name="ignore_eukaryotes" value="" /> | |
164 <param name="ignore_bacteria" value="" /> | |
165 <param name="ignore_archaea" value="" /> | |
166 <param name="stat_q" value="0.1" /> | |
167 <output name="output_file" file="community_profile.tabular"/> | |
168 </test> | |
169 </tests> | |
170 | |
171 <help><![CDATA[ | |
172 **What it does** | |
173 | |
174 MetaPhlAn is a computational tool for profiling the composition of microbial communities (Bacteria, Archaea, Eukaryotes and Viruses) from metagenomic shotgun sequencing data with species level resolution. For more information, check the `user manual <https://bitbucket.org/biobakery/metaphlan2/>`_. | |
175 | |
176 **Inputs** | |
177 | |
178 Metaphlan2 takes as input a sequence file in fasta, fastq, a BowTie2 produced SAM file. | |
179 | |
180 It is also possible to use a custom database with clade-specific marker genes. In this case, a fasta file with marker gene sequences is required and also a file containing metadata. This file is a json file with: | |
181 | |
182 :: | |
183 | |
184 { | |
185 "taxonomy": { | |
186 "taxonomy of genome1": genome1_length, | |
187 "taxonomy of genome2": genome2_length, | |
188 ... | |
189 } | |
190 "markers": { | |
191 "marker1_name": { | |
192 "clade": the clade that the marker belongs to, | |
193 "ext": [list of external genomes where the marker appears], | |
194 "len": length of the marker, | |
195 "score": score of the marker, | |
196 "taxon": the taxon of the marker | |
197 } | |
198 ... | |
199 } | |
200 } | |
201 | |
202 The marker names correspond to sequence name in corresponding fasta file with marker gene sequences. | |
203 | |
204 **Outputs** | |
205 | |
206 The main output file is a tab-separated output file of the predicted taxon relative abundances. | |
207 | |
208 ]]></help> | |
209 | |
210 <citations> | |
211 <citation type="doi">10.1038/nmeth.3589</citation> | |
212 </citations> | |
213 </tool> |