annotate tools/protein_analysis/psortb.xml @ 19:4cd848c5590b draft

Uploaded v0.2.5 preview 3, use $NSLOTS in the PSORT wrappers.
author peterjc
date Thu, 23 May 2013 12:49:18 -0400
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1 <tool id="Psortb" name="psortb" version="0.0.3">
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2 <description>Determines sub-cellular localisation of bacterial/archaeal protein sequences</description>
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3 <!-- If job splitting is enabled, break up the query file into parts -->
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4 <!-- Using 2000 chunks meaning 4 threads doing 500 each is ideal -->
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5 <parallelism method="basic" split_inputs="fasta_file" split_mode="to_size" split_size="2000" merge_outputs="tabular_file"></parallelism>
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6 <version_command interpreter="python">psortb.py --version</version_command>
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7 <command interpreter="python">
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8 psortb.py "\$NSLOTS" "$type" "$long" "$cutoff" "$divergent" "$sequence" "$outfile"
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9 ##I want the number of threads to be a Galaxy config option...
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10 ##Set the number of threads in the runner entry in universe_wsgi.ini
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11 ##which (on SGE at least) will set the $NSLOTS environment variable.
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12 ##If the environment variable isn't set, get "", and python wrapper
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13 ##defaults to four threads.
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14 </command>
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15 <stdio>
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16 <!-- Anything other than zero is an error -->
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17 <exit_code range="1:" />
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18 <exit_code range=":-1" />
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19 </stdio>
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20 <inputs>
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21 <param format="fasta" name="sequence" type="data"
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22 label="Input sequences for which to predict localisation (protein FASTA format)" />
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23 <param name="type" type="select"
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24 label="Organism type (N.B. all sequences in the above file must be of the same type)" >
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25 <option value="-p">Gram positive bacteria</option>
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26 <option value="-n">Gram negative bacteria</option>
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27 <option value="-a">Archaea</option>
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28 </param>
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29 <param name="long" type="select" label="Output type">
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30 <option value="terse">Short (terse, tabular with 3 columns)</option>
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31 <!-- The normal output is text, not tabular - worth offering?
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32 <option value="normal">Normal</option>
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33 -->
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34 <option value="long">Long (verbose, tabular with about 30 columns, depending on organism type)</option>
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35 </param>
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36 <param name="cutoff" size="10" type="float" optional="true" value=""
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37 label="Sets a cutoff value for reported results (e.g. 7.5)"
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38 help="Leave blank or use zero for no cutoff." />
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39 <param name="divergent" size="10" type="float" optional="true" value=""
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40 label="Sets a cutoff value for the multiple localization flag (e.g. 4.5)"
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41 help="Leave blank or use zero for no cutoff." />
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42 </inputs>
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43 <outputs>
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44 <data format="tabular" name="outfile" />
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45 </outputs>
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46 <requirements>
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47 <requirement type="binary">psort</requirement>
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48 </requirements>
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49 <tests>
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50 <test>
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51 <param name="sequence" value="empty.fasta" ftype="fasta"/>
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52 <param name="long" value="terse"/>
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53 <output name="outfile" file="empty_psortb_terse.tabular" ftype="tabular"/>
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54 </test>
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55 <test>
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56 <param name="sequence" value="k12_ten_proteins.fasta" ftype="fasta"/>
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57 <param name="long" value="terse"/>
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58 <output name="outfile" file="k12_ten_proteins_psortb_p_terse.tabular" ftype="tabular"/>
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59 </test>
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60 </tests>
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61 <help>
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62
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63 **What it does**
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64
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65 This calls the command line tool PSORTb v3.0 for prediction of prokaryotic
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66 localization sites. The input dataset needs to be protein FASTA sequences.
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67 The default output is a simple tabular file with three columns, one row
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68 per query sequence:
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69
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70 ====== ==============================
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71 Column Description
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72 ------ ------------------------------
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73 1 Sequence identifier
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74 2 Localisation, e.g. Cytoplasmic
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75 3 Score
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76 ====== ==============================
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77
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78 The long output is also tabular with one row per query sequence, but has
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79 lots more columns (a different set for each supported organism type). In
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80 both cases, a simple header line is included (starting with a hash, #,
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81 so that Galaxy treats it as a comment) giving the column names.
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82
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83
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84 **References**
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85
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86 N.Y. Yu, J.R. Wagner, M.R. Laird, G. Melli, S. Rey, R. Lo, P. Dao,
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87 S.C. Sahinalp, M. Ester, L.J. Foster, F.S.L. Brinkman (2010)
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88 PSORTb 3.0: Improved protein subcellular localization prediction with
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89 refined localization subcategories and predictive capabilities for all
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90 prokaryotes, Bioinformatics 26(13):1608-1615
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91 http://dx.doi.org/10.1093/bioinformatics/btq249
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92
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93 http://www.psort.org/documentation/index.html
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94
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95 This wrapper is available to install into other Galaxy Instances via the Galaxy
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96 Tool Shed at http://toolshed.g2.bx.psu.edu/view/peterjc/tmhmm_and_signalp
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97 </help>
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98 </tool>