Mercurial > repos > iuc > mash
view mash_screen.xml @ 4:86dec4abcea8 draft default tip
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/mash commit 57309b08e7a08b6f72982f0d78cb5574616c7b67"
author | iuc |
---|---|
date | Sat, 24 Apr 2021 11:29:35 +0000 |
parents | f8e51626fc56 |
children |
line wrap: on
line source
<tool id="mash_screen" name="mash screen" version="@TOOL_VERSION@+galaxy3" profile="19.01"> <description>determines how well query sequences are contained within a pool of sequences</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements" /> <expand macro="version_command" /> <command detect_errors="exit_code"><![CDATA[ #if str( $queries_input_source.queries_input_source_selector ) == "tool_data_table": ln -s '$queries_input_source.queries.fields.path' queries.msh && #elif str( $queries_input_source.queries_input_source_selector ) == 'history': ln -s '$queries_input_source.queries' queries.msh && #end if mash screen $winner_takes_all -i $minimum_identity_to_report -v $maximum_p_value_to_report queries.msh #if str( $pool_input.pool_input_selector ) == "paired" '$pool_input.pool_1' '$pool_input.pool_2' #end if #if str( $pool_input.pool_input_selector ) == "paired_collection" '$pool_input.pool.forward' '$pool_input.pool.reverse' #end if #if str( $pool_input.pool_input_selector ) == "single" '$pool_input.pool' #end if > '$output' ]]></command> <inputs> <conditional name="pool_input"> <param name="pool_input_selector" type="select" label="Single or Paired-end reads" help="Select between paired and single end data"> <option value="paired">Paired</option> <option value="single">Single</option> <option value="paired_collection">Paired Collection</option> </param> <when value="paired"> <param name="pool_1" type="data" format="@INTYPES@" label="Select first set of reads" help="Specify dataset with forward reads"/> <param name="pool_2" type="data" format="@INTYPES@" label="Select second set of reads" help="Specify dataset with reverse reads"/> </when> <when value="single"> <param name="pool" type="data" format="@INTYPES@" label="Select fastq dataset" help="Specify dataset with single reads"/> </when> <when value="paired_collection"> <param name="pool" format="@INTYPES@" type="data_collection" collection_type="paired" label="Select a paired collection" help="See help section for an explanation of dataset collections"/> </when> </conditional> <conditional name="queries_input_source"> <param name="queries_input_source_selector" type="select" label="Select queries from your history or use one from a tool data table?" help=""> <option value="tool_data_table">Queries from tool data table</option> <option selected="True" value="history">Queries from history</option> </param> <when value="tool_data_table"> <param name="queries" type="select" label="Queries (Mash Sketch)"> <options from_data_table="mash_sketches"/> </param> </when> <when value="history"> <param name="queries" type="data" format="msh" /> </when> </conditional> <param name="winner_takes_all" argument="-w" type="boolean" checked="true" truevalue="-w" falsevalue="" label="'Winner takes all' to remove redundancy in the result" help="If this option is not enabled, every matching strain from the same species of the reference database is reported in the result."/> <param type="float" name="minimum_identity_to_report" argument="-i" value="0." min="-1." max="1." label="Minimum identity to report" /> <param type="float" name="maximum_p_value_to_report" argument="-v" value="1." min="0." max="1." label="Maximum p-value to report" /> </inputs> <outputs> <data name="output" format="tabular" /> </outputs> <tests> <test> <param name="queries_input_source_selector" value="history"/> <param name="queries" value="NZ_MYON01000010.1.msh"/> <param name="pool_input_selector" value="single"/> <param name="pool" value="ERR024951_seqtk_sample_1000_1.fastq"/> <output name="output" file="mash_screen_NZ_MYON01000010.1_ERR024951_seqtk_sample_1000_1.tsv"/> </test> <test> <param name="queries_input_source_selector" value="tool_data_table"/> <param name="queries" value="test_sketch"/> <param name="pool_input_selector" value="single"/> <param name="pool" value="ERR024951_seqtk_sample_1000_2.fastq"/> <output name="output" file="mash_screen_NZ_MYON01000010.1_ERR024951_seqtk_sample_1000_2.tsv"/> </test> <test> <param name="queries_input_source_selector" value="history"/> <param name="queries" value="NZ_MYON01000010.1.msh"/> <param name="pool_input_selector" value="paired"/> <param name="pool_1" value="ERR024951_seqtk_sample_1000_1.fastq"/> <param name="pool_2" value="ERR024951_seqtk_sample_1000_2.fastq"/> <output name="output" file="mash_screen_NZ_MYON01000010.1_ERR024951_seqtk_sample_1000_1and2.tsv"/> </test> </tests> <help><![CDATA[ **What it does** Determine how well query sequences are contained within a pool of sequences. The queries must be formatted as a single Mash sketch file (.msh), created with the `mash sketch` command. The <pool> files can be contigs or reads, in fasta or fastq, gzipped or not, and "-" can be given for <pool> to read from standard input. The <pool> sequences are assumed to be nucleotides, and will be 6-frame translated if the <queries> are amino acids. The output fields are [identity, shared-hashes, median-multiplicity, p-value, query-ID, query-comment], where median-multiplicity is computed for shared hashes, based on the number of observations of those hashes within the pool. ]]></help> <expand macro="citations"/> </tool>