Mercurial > repos > miller-lab > genome_diversity
view select_snps.xml @ 10:9b92372de9f6
rename snp to gsSnp, sap to gdSap
author | Richard Burhans <burhans@bx.psu.edu> |
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date | Tue, 04 Sep 2012 12:49:53 -0400 |
parents | e29f4d801bb0 |
children |
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<tool id="gd_select_snps" name="Select" version="1.0.0"> <description>a specified number of SNPs</description> <command interpreter="python"> select_snps.py "--input=$input" "--output=$output" "--index_dir=$GALAXY_DATA_INDEX_DIR" "--num_snps=$num_snps" #if $override_metadata.choice == "0": "--ref_chrom_col=${input.metadata.ref}" "--ref_pos_col=${input.metadata.rPos}" "--ref_species=${input.metadata.dbkey}" #else "--ref_chrom_col=$ref_col" "--ref_pos_col=$rpos_col" "--ref_species=$ref_species" #end if </command> <inputs> <param format="tabular" name="input" type="data" label="Selected SNPS dataset"> <validator type="unspecified_build" message="This dataset does not have a reference species and cannot be used with this tool" /> </param> <param name="num_snps" type="integer" value="10" optional="false" min="1" label="Number of SNPs"/> <conditional name="override_metadata"> <param name="choice" type="select" format="integer" label="choose columns"> <option value="0" selected="true">No, get columns from metadata</option> <option value="1" >Yes, choose columns</option> </param> <when value="0" /> <when value="1"> <param name="ref_col" type="data_column" data_ref="input" numerical="false" label="Column with reference chromosome"/> <param name="rpos_col" type="data_column" data_ref="input" numerical="true" label="Column with reference position"/> <param name="ref_species" type="select" label="Choose reference species"> <options from_file="gd.ref_species.txt"> <column name="name" index="1"/> <column name="value" index="0"/> </options> </param> </when> </conditional> </inputs> <outputs> <data format="gdSnp" name="output" metadata_source="input"/> </outputs> <tests> <test> <param name="input" value="test_in/sample.gdSnp" ftype="gdSnp"/> <param name="num_snps" value="100"/> <param name="choice" value="0"/> <output name="output" file="test_out/select_snps/select_snps.gdSnp" /> </test> </tests> <help> **What it does** It attempts to select a specified number of SNPs from the dataset, making them approximately uniformly spaced relative to the reference genome. The number actually selected may be slightly more than the specified number. ----- **Example** - input file:: chr2_75111355_75112576 314 A C L F chr2 75111676 C F 15 4 53 2 9 48 Y 96 0.369 0.355 0.396 0 chr8_93901796_93905612 2471 A C A A chr8 93904264 A A 8 0 51 10 2 14 Y 961 0.016 0.534 0.114 2 chr10_7434473_7435447 524 T C S S chr10 7435005 T S 11 5 90 14 0 69 Y 626 0.066 0.406 0.727 0 chr14_80021455_80022064 138 G A H H chr14 80021593 G H 14 0 69 9 6 124 Y 377 0.118 0.997 0.195 1 chr15_64470252_64471048 89 G A Y Y chr15 64470341 G Y 5 6 109 14 0 69 Y 312 0.247 0.998 0.393 0 chr18_48070585_48071386 514 C T E K chr18 48071100 T K 7 7 46 14 0 69 Y 2 0.200 0.032 0.163 0 chr18_50154905_50155664 304 A G Y C chr18 50155208 A Y 4 2 17 5 1 22 Y 8 0.022 0.996 0.128 0 chr18_57379354_57380496 315 C T V V chr18 57379669 G V 11 0 60 9 6 62 Y 726 0.118 0.048 0.014 1 chr19_14240610_14242055 232 C T A V chr19 14240840 C A 18 8 56 15 5 42 Y 73 0.003 0.153 0.835 0 chr19_39866997_39874915 3117 C T P P chr19 39870110 C P 3 7 65 14 2 32 Y 6 0.321 0.911 0.462 4 etc. - output file:: chr2_75111355_75112576 314 A C L F chr2 75111676 C F 15 4 53 2 9 48 Y 96 0.369 0.355 0.396 0 chr8_93901796_93905612 2471 A C A A chr8 93904264 A A 8 0 51 10 2 14 Y 961 0.016 0.534 0.114 2 chr10_7434473_7435447 524 T C S S chr10 7435005 T S 11 5 90 14 0 69 Y 626 0.066 0.406 0.727 0 chr14_80021455_80022064 138 G A H H chr14 80021593 G H 14 0 69 9 6 124 Y 377 0.118 0.997 0.195 1 chr15_64470252_64471048 89 G A Y Y chr15 64470341 G Y 5 6 109 14 0 69 Y 312 0.247 0.998 0.393 0 chr18_48070585_48071386 514 C T E K chr18 48071100 T K 7 7 46 14 0 69 Y 2 0.200 0.032 0.163 0 chr19_14240610_14242055 232 C T A V chr19 14240840 C A 18 8 56 15 5 42 Y 73 0.003 0.153 0.835 0 etc. </help> </tool>