annotate tool_dependencies.xml @ 1:ccf97ee7a024 draft default tip

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/packages/package_pathoscope_2_0_6 commit bd736b6361ba659a1251dd1a1a05f7e3b633bdf5
author iuc
date Tue, 22 Dec 2015 19:26:46 -0500
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1 <?xml version="1.0"?>
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2 <tool_dependency>
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3 <package name="python" version="2.7.10">
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4 <repository changeset_revision="a28e3c30828d" name="package_python_2_7_10" owner="iuc" prior_installation_required="True" toolshed="https://testtoolshed.g2.bx.psu.edu" />
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5 </package>
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6 <package name="pathoscope" version="2.0.6">
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7 <install version="1.0">
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8 <actions>
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9 <action type="setup_python_environment">
1
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10 <repository changeset_revision="a28e3c30828d" name="package_python_2_7_10" owner="iuc" toolshed="https://testtoolshed.g2.bx.psu.edu">
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11 <package name="python" version="2.7.10" />
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12 </repository>
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13 <package>https://github.com/PathoScope/PathoScope/archive/v2.0.6.zip</package>
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14 </action>
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15 <action type="set_environment">
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16 <environment_variable action="set_to" name="PYTHONPATH_PATHOSCOPE">$INSTALL_DIR</environment_variable>
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17 </action>
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18 </actions>
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19 </install>
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20 <readme>
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21 Pathoscope 2.0 consists of four core and two optional analysis modules
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22 for sequencing-based metagenomic profiling. The PathoLib module
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23 extracts genome reference libraries (target or host/filter) from all
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24 available sequences in the NCBI Nucleotide database that belong to a
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25 user-defined taxonomic clade. The PathoMap module aligns the reads to
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26 the target reference library and removes any reads that have sequence
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27 similarity with the host or filter genomes. PathoID resolves read
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28 ambiguity, identifies which of the target genomes are present in the
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29 sample and estimates the proportions of reads originating from each
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30 genome. PathoReport provides two report files: 1) a summary report
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31 (.tsv) that contains the numbers and proportions of reads aligned to
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32 each genome identified in the sample, and 2) detailed report (.xml)
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33 including read coverage, read assignments, and contiguous sequences
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34 generated by combining the reads. The PathoDB is an optional module
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35 that provides additional annotation (organism taxonomic lineage, gene
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36 loci, protein products) for all sequences identified in the sample.
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37 The PathoQC module can be used to preprocess the reads prior to
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38 alignment with PathoMap.
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39 </readme>
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40 </package>
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41 </tool_dependency>