Mercurial > repos > peterjc > tmhmm_and_signalp
annotate tools/protein_analysis/psortb.xml @ 27:9e36a1b9302d draft
planemo upload for repository https://github.com/peterjc/pico_galaxy/tools/protein_analysis commit 3c6f0dca0e1318eecd1e07d177ffc5752b4f6c95
author | peterjc |
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date | Thu, 21 May 2015 10:57:40 -0400 |
parents | 20139cb4c844 |
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planemo upload for repository https://github.com/peterjc/pico_galaxy/tools/protein_analysis commit 221d4187992cbb993e02dc3ea0ef0150c7916a4a-dirty
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1 <tool id="Psortb" name="psortb" version="0.0.7"> |
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2 <description>Determines sub-cellular localisation of bacterial/archaeal protein sequences</description> |
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3 <!-- If job splitting is enabled, break up the query file into parts --> |
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4 <!-- Using 2000 chunks meaning 4 threads doing 500 each is ideal --> |
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5 <parallelism method="basic" split_inputs="fasta_file" split_mode="to_size" split_size="2000" merge_outputs="tabular_file"></parallelism> |
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6 <requirements> |
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7 <requirement type="binary">psort</requirement> |
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8 <requirement type="package">psort</requirement> |
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9 </requirements> |
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10 <stdio> |
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11 <!-- Anything other than zero is an error --> |
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12 <exit_code range="1:" /> |
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13 <exit_code range=":-1" /> |
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14 </stdio> |
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15 <version_command interpreter="python">psortb.py --version</version_command> |
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16 <command interpreter="python"> |
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17 psortb.py "\$GALAXY_SLOTS" "$type" "$long" "$cutoff" "$divergent" "$sequence" "$outfile" |
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18 ##If the environment variable isn't set, get "", and python wrapper |
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19 ##defaults to four threads. |
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20 </command> |
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21 <inputs> |
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22 <param format="fasta" name="sequence" type="data" |
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23 label="Input sequences for which to predict localisation (protein FASTA format)" /> |
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24 <param name="type" type="select" |
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25 label="Organism type (N.B. all sequences in the above file must be of the same type)" > |
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26 <option value="-p">Gram positive bacteria</option> |
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27 <option value="-n">Gram negative bacteria</option> |
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28 <option value="-a">Archaea</option> |
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29 </param> |
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30 <param name="long" type="select" label="Output type"> |
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31 <option value="terse">Short (terse, tabular with 3 columns)</option> |
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32 <!-- The normal output is text, not tabular - worth offering? |
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33 <option value="normal">Normal</option> |
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34 --> |
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35 <option value="long">Long (verbose, tabular with about 30 columns, depending on organism type)</option> |
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36 </param> |
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37 <param name="cutoff" size="10" type="float" optional="true" value="" |
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38 label="Sets a cutoff value for reported results (e.g. 7.5)" |
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39 help="Leave blank or use zero for no cutoff." /> |
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40 <param name="divergent" size="10" type="float" optional="true" value="" |
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41 label="Sets a cutoff value for the multiple localization flag (e.g. 4.5)" |
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42 help="Leave blank or use zero for no cutoff." /> |
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43 </inputs> |
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44 <outputs> |
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45 <data format="tabular" name="outfile" /> |
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46 </outputs> |
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47 <tests> |
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48 <test> |
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49 <param name="sequence" value="empty.fasta" ftype="fasta"/> |
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50 <param name="long" value="terse"/> |
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51 <output name="outfile" file="empty_psortb_terse.tabular" ftype="tabular"/> |
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52 </test> |
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53 <test> |
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54 <param name="sequence" value="k12_ten_proteins.fasta" ftype="fasta"/> |
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55 <param name="long" value="terse"/> |
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56 <output name="outfile" file="k12_ten_proteins_psortb_p_terse.tabular" ftype="tabular"/> |
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57 </test> |
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58 </tests> |
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59 <help> |
8 | 60 |
61 **What it does** | |
62 | |
63 This calls the command line tool PSORTb v3.0 for prediction of prokaryotic | |
64 localization sites. The input dataset needs to be protein FASTA sequences. | |
65 The default output is a simple tabular file with three columns, one row | |
66 per query sequence: | |
67 | |
68 ====== ============================== | |
69 Column Description | |
70 ------ ------------------------------ | |
71 1 Sequence identifier | |
72 2 Localisation, e.g. Cytoplasmic | |
73 3 Score | |
74 ====== ============================== | |
75 | |
76 The long output is also tabular with one row per query sequence, but has | |
77 lots more columns (a different set for each supported organism type). In | |
78 both cases, a simple header line is included (starting with a hash, #, | |
79 so that Galaxy treats it as a comment) giving the column names. | |
80 | |
81 | |
82 **References** | |
83 | |
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84 If you use this Galaxy tool in work leading to a scientific publication please |
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85 cite the following papers: |
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86 |
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87 Peter J.A. Cock, Björn A. Grüning, Konrad Paszkiewicz and Leighton Pritchard (2013). |
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88 Galaxy tools and workflows for sequence analysis with applications |
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89 in molecular plant pathology. PeerJ 1:e167 |
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90 http://dx.doi.org/10.7717/peerj.167 |
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91 |
8 | 92 N.Y. Yu, J.R. Wagner, M.R. Laird, G. Melli, S. Rey, R. Lo, P. Dao, |
93 S.C. Sahinalp, M. Ester, L.J. Foster, F.S.L. Brinkman (2010) | |
94 PSORTb 3.0: Improved protein subcellular localization prediction with | |
95 refined localization subcategories and predictive capabilities for all | |
96 prokaryotes, Bioinformatics 26(13):1608-1615 | |
97 http://dx.doi.org/10.1093/bioinformatics/btq249 | |
98 | |
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99 See also http://www.psort.org/documentation/index.html |
8 | 100 |
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101 This wrapper is available to install into other Galaxy Instances via the Galaxy |
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102 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/tmhmm_and_signalp |
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103 </help> |
25 | 104 <citations> |
105 <citation type="doi">10.7717/peerj.167</citation> | |
106 <citation type="doi">10.1093/bioinformatics/btq249</citation> | |
107 </citations> | |
8 | 108 </tool> |