Mercurial > repos > devteam > pgsnp2gd_snp
diff pgSnp2gd_snp.xml @ 0:d189d06d23cf draft
Imported from capsule None
author | devteam |
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date | Mon, 28 Jul 2014 11:30:09 -0400 |
parents | |
children | 57c5ac41f22c |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/pgSnp2gd_snp.xml Mon Jul 28 11:30:09 2014 -0400 @@ -0,0 +1,97 @@ +<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"> + #if $snptab.tab2 == "yes" + #if $snptab.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=${ref} -chr=${input1.metadata.chromCol} > $out_file1 + #end if + #else #pgSnp2gd_snp.pl $input1 -name=$indName -build=${input1.metadata.dbkey} -ref=${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"> <!-- do nothing --> + </when> + </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" size="20" 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' /> + <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>