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planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/mapping_to_ucsc commit a1517c9d22029095120643bbe2c8fa53754dd2b7
author | devteam |
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date | Wed, 11 Nov 2015 12:20:00 -0500 |
parents | 601abbd22cea |
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<tool id="mapToUCSC" name="Format mapping data" version="1.0.0"> <description> as UCSC custom track</description> <command interpreter="python"> mapping_to_ucsc.py $out_file1 $input $chr_col $coord_col $track.track_type #if $track.track_type == "coverage" or $track.track_type == "both" $track.coverage_col "${track.cname}" "${track.cdescription}" "${track.ccolor}" "${track.cvisibility}" #end if #if $track.track_type == "snp" or $track.track_type == "both" "${track.sdescription}" "${track.svisibility}" $track.col2 #end if </command> <inputs> <param format="tabular" name="input" type="data" label="Select mapping data"/> <param name="chr_col" type="data_column" data_ref="input" label="Column for reference chromosome" /> <param name="coord_col" type="data_column" data_ref="input" numerical="True" label="Numerical column for reference co-ordinate" /> <conditional name="track"> <param name="track_type" type="select" label="Display"> <option value="snp" selected="true">SNPs</option> <option value="coverage">Read coverage</option> <option value="both">Both</option> </param> <when value = "coverage"> <param name="coverage_col" type="data_column" data_ref="input" numerical="True" label="Numerical column for read coverage" /> <param name="cname" type="text" value="User Track" label="Coverage track name"> <validator type="length" max="15"/> </param> <param name="cdescription" type="text" value="User Supplied Coverage Track (from Galaxy)" label="Coverage track description"> <validator type="length" max="60"/> </param> <param label="Coverage track Color" name="ccolor" type="select"> <option selected="yes" value="0-0-0">Black</option> <option value="255-0-0">Red</option> <option value="0-255-0">Green</option> <option value="0-0-255">Blue</option> <option value="255-0-255">Magenta</option> <option value="0-255-255">Cyan</option> <option value="255-215-0">Gold</option> <option value="160-32-240">Purple</option> <option value="255-140-0">Orange</option> <option value="255-20-147">Pink</option> <option value="92-51-23">Dark Chocolate</option> <option value="85-107-47">Olive green</option> </param> <param label="Coverage track Visibility" name="cvisibility" type="select"> <option selected="yes" value="1">Dense</option> <option value="2">Full</option> <option value="3">Pack</option> <option value="4">Squish</option> <option value="0">Hide</option> </param> </when> <when value = "snp"> <!-- <param name="col1" type="data_column" data_ref="input" label="Column containing the reference nucleotide" /> --> <param name="col2" type="data_column" data_ref="input" label="Column containing the read nucleotide" /> <!-- <param name="sname" type="text" value="User Track-2" label="SNP track name"> <validator type="length" max="15"/> </param> --> <param name="sdescription" type="text" value="User Supplied Track (from Galaxy)" label="SNP track description"> <validator type="length" max="60"/> </param> <param label="SNP track Visibility" name="svisibility" type="select"> <option selected="yes" value="1">Dense</option> <option value="2">Full</option> <option value="3">Pack</option> <option value="4">Squish</option> <option value="0">Hide</option> </param> </when> <when value = "both"> <param name="coverage_col" type="data_column" data_ref="input" numerical="True" label="Numerical column for read coverage" /> <param name="cname" type="text" value="User Track" label="Coverage track name"> <validator type="length" max="15"/> </param> <param name="cdescription" type="text" value="User Supplied Track (from Galaxy)" label="Coverage track description"> <validator type="length" max="60"/> </param> <param label="Coverage track Color" name="ccolor" type="select"> <option selected="yes" value="0-0-0">Black</option> <option value="255-0-0">Red</option> <option value="0-255-0">Green</option> <option value="0-0-255">Blue</option> <option value="255-0-255">Magenta</option> <option value="0-255-255">Cyan</option> <option value="255-215-0">Gold</option> <option value="160-32-240">Purple</option> <option value="255-140-0">Orange</option> <option value="255-20-147">Pink</option> <option value="92-51-23">Dark Chocolate</option> <option value="85-107-47">Olive green</option> </param> <param label="Coverage track Visibility" name="cvisibility" type="select"> <option selected="yes" value="1">Dense</option> <option value="2">Full</option> <option value="3">Pack</option> <option value="4">Squish</option> <option value="0">Hide</option> </param> <!-- <param name="col1" type="data_column" data_ref="input" label="Column containing the reference nucleotide" /> --> <param name="col2" type="data_column" data_ref="input" label="Column containing the read nucleotide" /> <!-- <param name="sname" type="text" value="User Track-2" label="SNP track name"> <validator type="length" max="15"/> </param> --> <param name="sdescription" type="text" value="User Supplied Track (from Galaxy)" label="SNP track description"> <validator type="length" max="60"/> </param> <param label="SNP track Visibility" name="svisibility" type="select"> <option selected="yes" value="1">Dense</option> <option value="2">Full</option> <option value="3">Pack</option> <option value="4">Squish</option> <option value="0">Hide</option> </param> </when> </conditional> </inputs> <outputs> <data format="customtrack" name="out_file1"/> </outputs> <help> .. class:: infomark **What it does** This tool turns mapping data generated by short read mappers into a format that can be displayed in the UCSC genome browser as a custom track. ----- .. class:: warningmark **Note** This tool requires the mapping data to contain at least the following information: chromosome, genome coordinate, read nucleotide (if option to display is SNPs), read coverage (if option to display is Read coverage). ----- **Example** For the following Mapping data:: #chr g_start read_id read_coord g_nt read_nt qual read_coverage chrM 1 1:29:1672:1127/1 11 G G 40 134 chrM 1 1:32:93:933/1 4 G A 40 134 chrM 1 1:34:116:2032/1 11 G A 40 134 chrM 1 1:39:207:964/1 1 G G 40 134 chrM 2 1:3:359:848/1 1 G C 40 234 chrM 2 1:40:1435:1013/1 1 G G 40 234 chrM 3 1:40:730:972/1 9 G G 40 334 chrM 4 1:42:1712:921/2 31 G T 35 434 chrM 4 1:44:1649:493/1 4 G G 40 434 running this tool to display both SNPs and Read coverage will return the following tracks, containing aggregated data per genome co-ordinate:: track type=wiggle_0 name="Coverage Track" description="User Supplied Track (from Galaxy)" color=0,0,0 visibility=1 variableStep chrom=chrM 1 134 2 234 3 334 4 434 track type=wiggle_0 name="Track A" description="User Supplied SNP Track (from Galaxy)" color=255,0,0 visibility=1 variableStep chrom=chrM 1 2 track type=wiggle_0 name="Track T" description="User Supplied SNP Track (from Galaxy)" color=0,255,0 visibility=1 variableStep chrom=chrM 4 1 track type=wiggle_0 name="Track G" description="User Supplied SNP Track (from Galaxy)" color=0,0,255 visibility=1 variableStep chrom=chrM 1 2 2 1 3 1 4 1 track type=wiggle_0 name="Track C" description="User Supplied SNP Track (from Galaxy)" color=255,0,255 visibility=1 variableStep chrom=chrM 2 1 </help> </tool>