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view pgSnp2gd_snp.xml @ 1:57c5ac41f22c draft default tip
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author | devteam |
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date | Tue, 13 Oct 2015 12:27:32 -0400 |
parents | d189d06d23cf |
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<tool id="pgSnp2gd_snp" name="pgSnp to gd_snp" hidden="false" version="1.0.0"> <description>Convert from pgSnp to gd_snp</description> <command interpreter="perl"> <![CDATA[ #if $snptab.tab2 == "yes" #if $snptab.needRef.colsOnly == "addColsOnly" pgSnp2gd_snp.pl '$input1' -tab=${snptab.input2} -name=$indName -build=${input1.metadata.dbkey} -addColsOnly -chr=${input1.metadata.chromCol} > '$out_file1' #else pgSnp2gd_snp.pl '$input1' -tab=${snptab.input2} -name=$indName -build=${input1.metadata.dbkey} -ref=${snptab.needRef.ref} -chr=${input1.metadata.chromCol} > '$out_file1' #end if #else pgSnp2gd_snp.pl '$input1' -name=$indName -build=${input1.metadata.dbkey} -ref=${snptab.ref} -chr=${input1.metadata.chromCol} > '$out_file1' #end if ]]> </command> <inputs> <param format="tab" name="input1" type="data" label="pgSnp dataset" /> <conditional name="snptab"> <param name="tab2" type="select" label="Append to gd_snp dataset in history"> <option value="yes">yes</option> <option value="no" selected="true">no</option> </param> <when value="yes"> <param format="gd_snp" name="input2" type="data" label="gd_snp dataset" /> <conditional name="needRef"> <param name="colsOnly" type="select" label="Skip new SNPs"> <option value="no" selected="true">no</option> <option value="addColsOnly">yes</option> </param> <when value="no"> <param name="ref" type="data_column" data_ref="input1" label="Column with reference allele" /> </when> <when value="addColsOnly" /> </conditional> </when> <when value="no"> <param name="ref" type="data_column" data_ref="input1" label="Column with reference allele" /> </when> </conditional> <param name="indName" type="text" label="Label for new individual/group" value="na" /> </inputs> <outputs> <data format="gd_snp" name="out_file1" /> </outputs> <tests> <test> <param name="input1" value="pgSnpTest.ref.txt" ftype="interval" dbkey="hg19" /> <param name="tab2" value="no" /> <param name="ref" value="8" /> <param name="indName" value="na" /> <output name="output" file="pgSnp2snp_output.txt" /> </test> </tests> <help> **Dataset formats** The input dataset is of Galaxy datatype interval_, with the additional columns required for pgSnp_ format. Any further columns beyond those defined for pgSnp will be ignored. The output dataset is a gd_snp_ table. (`Dataset missing?`_) .. _interval: ./static/formatHelp.html#interval .. _pgSnp: ./static/formatHelp.html#pgSnp .. _gd_snp: ./static/formatHelp.html#gd_snp .. _Dataset missing?: ./static/formatHelp.html ----- **What it does** This tool converts a pgSnp dataset to gd_snp format, either starting a new dataset or appending to an old one. When appending, if any new SNPs appear only in the pgSnp file they can either be skipped entirely, or backfilled with "-1" (meaning "unknown") for previous individuals/groups in the input gd_snp dataset. If any new SNPs are being added (either by creating a new table or by backfilling), then an extra column with the reference allele must be supplied in the pgSnp dataset, as shown in the example below. ----- **Example** - input pgSnp file, with reference allele added:: chr1 1888681 1888682 C/T 2 4,3 0.8893,0.8453 T chr1 3118325 3118326 T 1 8 0.8796 C chr1 3211457 3211458 A/C 2 17,10 0.8610,0.8576 A etc. - gd_snp output:: chr1 1888681 T C -1 3 4 1 0.8893 chr1 3118325 C T -1 0 8 0 0.8796 chr1 3211457 A C -1 17 10 1 0.8576 etc. </help> </tool>