Mercurial > repos > iuc > plink
diff plink.xml @ 10:2c0ac05fe240 draft default tip
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/plink commit 6d29c051fe8a6564805da7a13668d067c31f0e86
author | iuc |
---|---|
date | Tue, 14 Nov 2023 17:51:25 +0000 |
parents | 272aca44b3dd |
children |
line wrap: on
line diff
--- a/plink.xml Sun Dec 19 15:53:35 2021 +0000 +++ b/plink.xml Tue Nov 14 17:51:25 2023 +0000 @@ -1,7 +1,8 @@ <tool id='plink' name='plink' version='@TOOL_VERSION@+galaxy@VERSION_SUFFIX@'> + <description>genome association analysis toolset</description> <macros> <token name='@TOOL_VERSION@'>1.90b6.21</token> - <token name='@VERSION_SUFFIX@'>0</token> + <token name='@VERSION_SUFFIX@'>1</token> <xml name='template_sanitizer'> <sanitizer> <valid initial='default'> @@ -50,6 +51,7 @@ </xrefs> <requirements> <requirement type='package' version='@TOOL_VERSION@'>plink</requirement> + <requirement type='package' version='5.3.0'>gawk</requirement> </requirements> <command detect_errors='exit_code'><![CDATA[ @@ -62,17 +64,17 @@ #if $functions.func == 'data_manage': #if $functions.bmerge.set == 'Yes': && mkdir bmerge_files - && ln -s '$functions.bmerge.bed.extra_files_path'/RgeneticsData.bed bmerge_files/bmerge_input.bed - && ln -s '$functions.bmerge.bed.extra_files_path'/RgeneticsData.bim bmerge_files/bmerge_input.bim - && ln -s '$functions.bmerge.bed.extra_files_path'/RgeneticsData.fam bmerge_files/bmerge_input.fam + && ln -s '$functions.bmerge.bed.extra_files_path/RgeneticsData.bed' 'bmerge_files/bmerge_input.bed' + && ln -s '$functions.bmerge.bed.extra_files_path/RgeneticsData.bim' 'bmerge_files/bmerge_input.bim' + && ln -s '$functions.bmerge.bed.extra_files_path/RgeneticsData.fam' 'bmerge_files/bmerge_input.fam' #end if #end if #if $inputs.inputs.filetype == 'bfile': - && ln -s '$inputs.inputs.bed.extra_files_path'/RgeneticsData.bed plink_input/plink_input.bed - && ln -s '$inputs.inputs.bed.extra_files_path'/RgeneticsData.bim plink_input/plink_input.bim - && ln -s '$inputs.inputs.bed.extra_files_path'/RgeneticsData.fam plink_input/plink_input.fam + && ln -s '$inputs.inputs.bed.extra_files_path/RgeneticsData.bed' 'plink_input/plink_input.bed' + && ln -s '$inputs.inputs.bed.extra_files_path/RgeneticsData.bim' 'plink_input/plink_input.bim' + && ln -s '$inputs.inputs.bed.extra_files_path/RgeneticsData.fam' 'plink_input/plink_input.fam' && plink --bfile plink_input/plink_input #elif $inputs.inputs.filetype == 'vcf': #if $inputs.inputs.input.is_of_type('bcf'): @@ -84,7 +86,7 @@ ## Plink commands by section #if $inputs.covar_input: - --covar '$inputs.covar_input' + --covar '$inputs.covar_input' #end if #if $inputs.set_pheno.set_pheno == 'Yes': --pheno $inputs.set_pheno.pheno $inputs.set_pheno.all_pheno @@ -232,7 +234,6 @@ #end if #elif $functions.func == 'data_manage': - #if $functions.bmerge.set == 'Yes': --bmerge bmerge_files/bmerge_input #end if @@ -285,8 +286,6 @@ #end if #end if #end if - - #elif $functions.func == 'link': #if $functions.set_indep.choice == 'Yes': --indep-pairwise $functions.set_indep.window $functions.set_indep.step $functions.set_indep.r2 @@ -382,8 +381,8 @@ #end if #end if -## #elif $functions.func == 'scoring': -## + #elif $functions.func == 'scoring': + --score '$functions.score_file' $functions.variant_id_i $functions.allel_codes_j $functions.scores_k $functions.header $functions.sum ## #else: ## --rerun $functions.logfile ## @@ -410,9 +409,12 @@ #end if #end if && mkdir '$plink_out.extra_files_path' - && cp plink_output/plink_output.bed '$plink_out.extra_files_path'/RgeneticsData.bed - && cp plink_output/plink_output.bim '$plink_out.extra_files_path'/RgeneticsData.bim - && cp plink_output/plink_output.fam '$plink_out.extra_files_path'/RgeneticsData.fam + && cp plink_output/plink_output.bed '$plink_out.extra_files_path/RgeneticsData.bed' + && cp plink_output/plink_output.bim '$plink_out.extra_files_path/RgeneticsData.bim' + && cp plink_output/plink_output.fam '$plink_out.extra_files_path/RgeneticsData.fam' + #if $functions.func == 'scoring': + && awk -v OFS="\t" '{$1=$1; print}' plink_output/plink_output.profile > plink_output/plink_output.profile.tab + #end if ]]></command> <inputs> <section name='inputs' title='Data inputs' expanded='true'> @@ -450,6 +452,7 @@ <option value='stratification'>Population stratification</option> <option value='association'>Association analysis</option> <option value='ibd'>Identity-by-descent</option> + <option value='scoring'>Apply a linear scoring system (--score)</option> <!-- <option value='rerun'>Rerun</option> --> </param> <when value='filtering'> @@ -970,8 +973,20 @@ </conditional> <param name='lambda' type='float' label='Lambda value' optional='true'/> </when> - <!-- <when value='scoring'> - </when> --> + <when value='scoring'> + <!-- this implements a part of the -\-score parameter --> + <param name='score_file' format='tabular' type='data' label='Scoring system which should be applied to all samples'/> + <param name="variant_id_i" type="data_column" data_ref="score_file" label="Variant ID column"/> + <param name="allel_codes_j" type="data_column" data_ref="score_file" label="Allel column"/> + <param name="scores_k" type="data_column" data_ref="score_file" label="Score column"/> + <param name='header' type='boolean' truevalue='header' falsevalue='' checked='false' label='Is a header line present in the scores file?'/> + + <param name="sum" type="select" label="How to combine the valid per-variant scores?" help="Average is the default, but it can be changed to sum."> + <option value="">Final scores are averages of the valid per-variant scores</option> + <option value="sum">Report sums (sum; can not be used with 'no-mean-imputation'; is automatically on with dosage data)</option> + <option value="no-sum">Disable sum (no-sum)</option> + </param> + </when> <when value='ibd'> <conditional name='genome'> <param name='output_genome' type='select' help='Perform and return results of IBS/IBD computation'> @@ -1060,6 +1075,11 @@ <filter>functions['func'] == 'ibd' and functions['genome']['output_genome']</filter> </data> + <!--scores--> + <data name='scores' format='tabular' from_work_dir='plink_output/plink_output.profile.tab' label='${tool.name}: Scores'> + <filter>functions['func'] == 'scoring'</filter> + </data> + <!--Stratifiction--> <data name='mds' format='txt' from_work_dir='plink_output/plink_output.mds' label='${tool.name}: MDS'> <filter>functions['func'] == 'stratification' and functions['cluster']['cluster'] == 'Yes' and functions['cluster']['mds']['mds_scaling'] == 'Yes'</filter> @@ -1203,6 +1223,7 @@ <expand macro="log_out_assert"/> </test> + <test expect_num_outputs='8'> <section name='inputs'> <conditional name='inputs'> @@ -1393,6 +1414,30 @@ <expand macro="log_out_assert"/> <output name='genome' file='out.genome'/> </test> + <!-- scoring function test--> + <test expect_num_outputs='3'> + <section name='inputs'> + <conditional name='inputs'> + <param name='filetype' value='bfile'/> + <param name='bed' value='' ftype="pbed"> + <composite_data value="plink.bim"/> + <composite_data value="plink.bed"/> + <composite_data value="plink.fam"/> + </param> + </conditional> + </section> + <conditional name='functions'> + <param name='func' value='scoring'/> + <param name='score_file' value='scores_file.tab'/> + <param name='variant_id_i' value='1'/> + <param name='allel_codes_j' value='2'/> + <param name='scores_k' value='3'/> + <param name='header' value='true'/> + <param name='sum' value='sum'/> + </conditional> + <expand macro="log_out_assert"/> + <output name='scores' file='scores_results.tab'/> + </test> </tests> <help><![CDATA[ PLINK is a free, open-source whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner.