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planemo upload for repository https://github.com/qiime2/galaxy-tools/tree/main/tools/suite_qiime2__rescript commit 5f71b597c9495eae67a447744fded834f56ca1f7 |
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qiime2__rescript__get_bv_brc_genomes.xml test-data/.gitkeep |
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diff -r 000000000000 -r 9dd05f5c60b9 qiime2__rescript__get_bv_brc_genomes.xml --- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/qiime2__rescript__get_bv_brc_genomes.xml Wed Oct 30 19:55:18 2024 +0000 |
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b'@@ -0,0 +1,168 @@\n+<?xml version=\'1.0\' encoding=\'utf-8\'?>\n+<!--\n+Copyright (c) 2024, QIIME 2 development team.\n+\n+Distributed under the terms of the Modified BSD License. (SPDX: BSD-3-Clause)\n+-->\n+<!--\n+This tool was automatically generated by:\n+ q2galaxy (version: 2024.10.0)\n+for:\n+ qiime2 (version: 2024.10.1)\n+-->\n+<tool name="qiime2 rescript get-bv-brc-genomes" id="qiime2__rescript__get_bv_brc_genomes" version="2024.10.0+q2galaxy.2024.10.0" profile="22.05" license="BSD-3-Clause">\n+ <description>Get genome sequences from the BV-BRC database.</description>\n+ <xrefs>\n+ <xref type="bio.tools">qiime2</xref>\n+ </xrefs>\n+ <requirements>\n+ <container type="docker">quay.io/qiime2/amplicon:2024.10</container>\n+ </requirements>\n+ <version_command>q2galaxy version rescript</version_command>\n+ <command detect_errors="exit_code">q2galaxy run rescript get_bv_brc_genomes \'$inputs\'</command>\n+ <configfiles>\n+ <inputs name="inputs" data_style="staging_path_and_source_path"/>\n+ </configfiles>\n+ <inputs>\n+ <section name="__q2galaxy__GUI__section__extra_opts__" title="Click here for additional options">\n+ <conditional name="ids_metadata">\n+ <param name="type" type="select" label="ids_metadata: MetadataColumn[Numeric | Categorical]" help="[optional] A metadata column obtained with the action get-bv-brc-metadata that can be used as a query.">\n+ <option value="none" selected="true">None (default)</option>\n+ <option value="tsv">Metadata from TSV</option>\n+ <option value="qza">Metadata from Artifact</option>\n+ </param>\n+ <when value="none"/>\n+ <when value="tsv">\n+ <param name="source" type="data" format="tabular,qiime2.tabular" label="Metadata Source"/>\n+ <param name="column" type="data_column" label="Column Name" data_ref="source" use_header_names="true">\n+ <validator type="expression" message="The first column cannot be selected (they are IDs).">value != "1"</validator>\n+ </param>\n+ </when>\n+ <when value="qza">\n+ <param name="source" type="data" format="qza" label="Metadata Source"/>\n+ <param name="column" type="text" label="Column Name">\n+ <validator type="empty_field"/>\n+ </param>\n+ </when>\n+ </conditional>\n+ <conditional name="__q2galaxy__GUI__conditional__rql_query__" label="rql_query: Str">\n+ <param name="__q2galaxy__GUI__select__" type="select" label="rql_query: Str" help="[optional] Query in RQL format. To download all data for genome_ids "224308.43" and "2030927.4755", the RQL query looks like this: "in(genome_id,(224308.43,2030927.4755))". While "in" is an RQL operator, "genome_id" is a data field and "224308.43,2030927.4755" are the values. It is important to percent encode values if they contain illegal characters like spaces. The values "Bacillus subtilis" and "Bacteroidales bacterium" have to be provided with percent encoded quotes (%22) and spaces (%20) like this: "in(species,(%22Bacillus%20subtilis%22,%22Bacteroidales%20bacterium%22))". Check https://www.bv-brc.org/api/doc/ for documentation on data types and corresponding data fields.">\n+ <option value="__q2galaxy__::control::default" selected="true">None (Use default behavior)</option>\n+ <option value="__q2galaxy__::control::provide">Provide a value</option>\n+ </param>\n+ <when value="__q2galaxy__::control::default">\n+ <param name="rql_query" type="hidden" value="__q2galaxy__::literal::None"/>\n+ </when>\n+ <when value="__q2galaxy__::control::provide"'..b' <option value="subclass">subclass</option>\n+ <option value="infraclass">infraclass</option>\n+ <option value="cohort">cohort</option>\n+ <option value="superorder">superorder</option>\n+ <option value="order">order</option>\n+ <option value="suborder">suborder</option>\n+ <option value="infraorder">infraorder</option>\n+ <option value="parvorder">parvorder</option>\n+ <option value="superfamily">superfamily</option>\n+ <option value="family">family</option>\n+ <option value="subfamily">subfamily</option>\n+ <option value="tribe">tribe</option>\n+ <option value="subtribe">subtribe</option>\n+ <option value="genus">genus</option>\n+ <option value="subgenus">subgenus</option>\n+ <option value="species group">species group</option>\n+ <option value="species subgroup">species subgroup</option>\n+ <option value="species">species</option>\n+ <option value="subspecies">subspecies</option>\n+ <option value="forma">forma</option>\n+ <validator type="expression" message="Please verify this parameter.">value != \'__q2galaxy__::literal::None\'</validator>\n+ </param>\n+ </repeat>\n+ <param name="rank_propagation" type="boolean" truevalue="__q2galaxy__::literal::True" falsevalue="__q2galaxy__::literal::False" checked="true" label="rank_propagation: Bool" help="[default: Yes] If a rank has no taxonomy associated with it, the taxonomy from the upper-level rank of that lineage, will be propagated downward. For example, if we are missing the genus label for \'f__Pasteurellaceae; g__\'then the \'f__\' rank will be propagated to become: \'f__Pasteurellaceae; g__Pasteurellaceae\'."/>\n+ </section>\n+ </inputs>\n+ <outputs>\n+ <data name="genomes" format="qza" label="${tool.name} on ${on_string}: genomes.qza" from_work_dir="genomes.qza"/>\n+ <data name="taxonomy" format="qza" label="${tool.name} on ${on_string}: taxonomy.qza" from_work_dir="taxonomy.qza"/>\n+ </outputs>\n+ <tests/>\n+ <help>\n+QIIME 2: rescript get-bv-brc-genomes\n+====================================\n+Get genome sequences from the BV-BRC database.\n+\n+\n+Outputs:\n+--------\n+:genomes.qza: Genome sequences for specified query.\n+:taxonomy.qza: Taxonomy data for all sequences.\n+\n+| \n+\n+Description:\n+------------\n+Fetch genome sequences from BV-BRC. BV-BRC (Bacterial and Viral Bioinformatics Resource Center) is a database for bacterial and viral genomes, annotations, and metadata. There are three ways to query data: You can use an RQL query to refine your search and get targeted genomes. By providing IDs/values and a corresponding data field, you can retrieve all genomes associated with those specific values in that data field. And as a third option a metadata column can be provided, to use metadata obtained with the action get-bv-brc-metadata as a new query. Check https://www.bv-brc.org/api/doc/ for documentation.\n+\n+\n+| \n+\n+</help>\n+ <citations>\n+ <citation type="bibtex">@article{cite1,\n+ author = {Olson, Robert D and Assaf, Rida and Brettin, Thomas and Conrad, Neal and Cucinell, Clark and Davis, James J and Dempsey, Donald M and Dickerman, Allan and Dietrich, Emily M and Kenyon, Ronald W and others},\n+ journal = {Nucleic acids research},\n+ number = {D1},\n+ pages = {D678--D689},\n+ publisher = {Oxford University Press},\n+ title = {Introducing the bacterial and viral bioinformatics resource center (BV-BRC): a resource combining PATRIC, IRD and ViPR},\n+ volume = {51},\n+ year = {2023}\n+}\n+</citation>\n+ <citation type="doi">10.1371/journal.pcbi.1009581</citation>\n+ <citation type="doi">10.1038/s41587-019-0209-9</citation>\n+ </citations>\n+</tool>\n' |