Mercurial > repos > sanbi-uwc > shapeit_phase
view shapeit_phase.xml @ 15:201d098d6d67 draft
planemo upload for repository https://github.com/CPGRZA/cpgr_ancestry commit 72b6cb6029a3979b51e796a8c210fcf903cf7b23-dirty
author | sanbi-uwc |
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date | Tue, 18 Sep 2018 06:39:22 -0400 |
parents | f92f1cc9e382 |
children | 1a00583b6b2c |
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<tool id="shapeit_phase" name="shapeit_phase" version="0.14.0"> <description>genomic data with or without reference panel</description> <requirements> <requirement type="package" version="2.r837">shapeit</requirement> </requirements> <stdio> <exit_code range="1:" /> </stdio> <command><![CDATA[ #if str($input_files.input_type_select) == 'plink_bed_bim_fam_list': ln -s '${input_files.plink_bed_etc_list[0]}' input.plink_bed && ln -s '${input_files.plink_bed_etc_list[1]}' input.plink_bim && ln -s '${input_files.plink_bed_etc_list[2]}' input.plink_fam && echo "BED file" && ls -l input.plink_bed && echo "BIM file" && head -2 input.plink_bim && echo "FAM file" && head -2 input.plink_fam && PART=`head -1 input.plink_bim | cut -f1` && echo "Working on PART: \$PART" && #else PART='' #end if #if str($use_ref_panel.use_ref_panel_select) == "use_ref_panel_yes" and str($use_ref_panel.ref_panel_from_table.ref_panel_from_table_select) == "ref_panel_from_table_yes": REF_DIR='${use_ref_panel.ref_panel_from_table.ref_from_table.fields.path}' && REF_PREFIX='${use_ref_panel.ref_panel_from_table.ref_from_table.fields.reference_prefix}' && SAMPLE_PREFIX="\$REF_DIR/${use_ref_panel.ref_panel_from_table.ref_from_table.fields.sample_prefix}" && SAMPLE=`ls \$SAMPLE_PREFIX*.sample` && if [ ! -f "\$SAMPLE" ] ; then echo "Failed to find valid sample file at \$SAMPLE" >&2 && exit 1 ; fi && HAP="\${REF_DIR}/\${REF_PREFIX}\${PART}.hap.gz" && if [ ! -f "\$HAP" ] ; then echo "Failed to find valid .hap file at \$HAP" >&2 && exit 1 ; fi && LEGEND="\${REF_DIR}/\${REF_PREFIX}\${PART}.legend.gz" && if [ ! -f "\$LEGEND" ] ; then echo "Failed to find valid .legend file at \$LEGEND" >&2 && exit 1 ; fi && #end if #if $use_genetic_map.use_genetic_map_select == "use_genetic_map_yes" and $use_genetic_map.genetic_map_from_table.genetic_map_from_table_select == "genetic_map_from_table_yes": MAP_DIR='${use_genetic_map.genetic_map_from_table.map_from_table.fields.path}' && MAP_PREFIX='${use_genetic_map.genetic_map_from_table.map_from_table.fields.map_prefix}' && MAP=`ls \${MAP_DIR}/\${MAP_PREFIX}\${PART}_*` && if [ ! -f "\${MAP}" ] ; then echo "Failed to find valid map file at \${MAP}" >&2 && exit 1 ; fi && #end if #if $input_files.input_type_select == "plink_bed_bim_fam_list": echo "COLLECTION NAME:" ${input_files.plink_bed_etc_list.name} && #for $dat in $input_files.plink_bed_etc_list: echo Processing NAME '${dat.name}' && #end for #end if shapeit #if $input_files.input_type_select == "vcf": --input-vcf ${input_files.vcf_file} #else if $input_files.input_type_select == "plink_ped_map": --input-ped ${input_files.plink_ped} ${input_files.plink_map} #if $input_files.plink_missing_code != "0": --missing_code $input_files.plink_missing_code #end if #else if $input_files.input_type_select == "plink_bed_bim_fam": --input-bed ${input_files.plink_bed} ${input_files.plink_bim} ${input_files.plink_fam} #else if $input_files.input_type_select == "plink_bed_bim_fam_list": --input-bed input.plink_bed input.plink_bim input.plink_fam #else if $input_files.inputy_type_select == "oxford_gen_sample": --input-gen ${input_files.oxford_gen} ${input_files.oxford_sample} #if $input_files.oxford_threshold != "0.9": --input-thr $input_files.oxford_threshold #end if #end if #if $use_genetic_map.use_genetic_map_select == "use_genetic_map_yes": #if $use_genetic_map.genetic_map_from_table.genetic_map_from_table_select == "genetic_map_from_table_yes": --input-map \$MAP #else: --input-map $use_genetic_map.genetic_map #end if #else if $use_genetic_map.rho != "0.0004": --rho $use_genetic_map.rho #end if #if $use_ref_panel.use_ref_panel_select == "use_ref_panel_yes": #if $use_ref_panel.ref_panel_from_table.ref_panel_from_table_select == "ref_panel_from_table_yes": --input-ref \$HAP \$LEGEND \$SAMPLE #else --input-ref $use_ref_panel.ref_panel_from_table.ref_panel_haps $use_ref_panel.ref_panel_from_table.ref_panel_legend $use_ref_panel.ref_panel_from_table.ref_panel_sample #end if #if $use_ref_panel.disable_mcmc_iterations == "disable_mcmc_iterations_yes": --no-mcmc #end if #if $use_ref_panel.filter_groups == "exclude_groups": --exclude-grp $use_ref_panel.filter_groups.exclude_groups_file #else if $use_ref_panel.filter_groups == "include_groups": --include-grp $use_ref_panel.filter_groups.include_groups_file #end if #end if #if $use_filters.use_filters_select == "use_filters_yes": #if $use_filters.use_input_from == "use_input_from_yes": --input-from $input_from #end if #if $use_filters.use_input_to == "use_input_to_yes": --input-to $input_to #end if #if $use_filters.use_output_from == "use_output_from_yes": --output-from $output_from #end if #if $use_filters.use_output_to == "use_output_to_yes": --output-to $output_to #end if #if $use_filters.filter_individuals == "exclude_individuals": --exclude-ind $use_filters.exclude_inviduals_file #else if $use_filters.filter_individuals == "include_individuals": --include-ind $use_filters.include_inviduals_file #end if #if $use_filters.filter_individuals == "exclude_SNPs": --exclude-snp $use_filters.exclude_SNPs_file #else if $use_filters.filter_SNPs == "include_SNPs": --include-snp $use_filters.include_SNPs_file #end if #end if #if $use_advanced_parameters.use_advanced_parameters_select == "use_advanced_parameters_yes": #if $use_advanced_parameters.chrX == "chrX_yes": --chrX #end if #if $use_advanced_parameters.noped == "noped_yes": --noped #end if #if $use_advanced_parameters.states != "100": --states $use_advanced_parameters.states #end if #if $use_advanced_parameters.window != "2.0": --window $use_advanced_parameters.window #end if #if $use_advanced_parameters.model_version1 == "use_v1_yes": --model-version1 #end if #if $use_advanced_parameters.eff_size.eff_size_select == "eff_size_european": --effective-size 11418 #else if $use_advanced_parameters.eff_size.eff_size_select == "eff_size_african": --effective-size 17469 #else if $use_advanced_parameters.eff_size.eff_size_select == "eff_size_asian": --effective-size 14269 #else if $use_advanced_parameters.eff_size.eff_size_select == "eff_size_mixedpop": --effective-size $use_advanced_parameters.eff_size.eff_size_mixed #end if #if $use_advanced_parameters.burn != "7": --burn $use_advanced_parameters.burn #end if #if $use_advanced_parameters.prune != "8": --prune $use_advanced_parameters.prune #end if #if $use_advanced_parameters.main != "20": --main $use_advanced_parameters.main #end if #if $use_advanced_parameters.threads != "1": --threads $use_advanced_parameters.threads #end if #if $use_advanced_parameters.set_rng_seed.set_rng_seed_select == "set_rng_seed_yes": --seed $use_advanced_parameters.rng_seed #end if #end if --output-max $out_haps $out_sample --output-graph $out_graph --output-log $out_log ]]></command> <inputs> <conditional name="input_files"> <param name="input_type_select" type="select" label="Please specify your input files."> <option value="vcf" selected="True">VCF Variant Call Format</option> <option value="plink_ped_map">Plink PED/MAP format</option> <option value="plink_bed_bim_fam">Plink BED/BIM/FAM format</option> <option value="plink_bed_bim_fam_list">Plink BED/BIM/FAM format list</option> <option value="oxford_gen_sample">Oxford GEN/SAMPLE format</option> </param> <when value="plink_ped_map"> <param name="plink_ped" type="data" format="txt" label="Specify text genotype file (.ped)"/> <param name="plink_map" type="data" format="txt" label="Specify SNP map file (.map)"/> <param name="plink_missing_code" type="text" label="Missing data labeled as" value="0"/> </when> <when value="plink_bed_bim_fam"> <param name="plink_bed" type="data" format="binary" label="Specify binary genotype file (.bed)"/> <param name="plink_bim" type="data" format="txt" label="Specify SNP map file (.bim)"/> <param name="plink_fam" type="data" format="txt" label="Specify individual information file (.fam)"/> </when> <when value="plink_bed_bim_fam_list"> <param name="plink_bed_etc_list" type="data_collection" collection_type="list" label="BED/BIM/FAM files as a collection (list)" /> </when> <when value="oxford_gen_sample"> <param name="oxford_gen" type="data" format="txt" label="Specify text genotype file (.gen)"/> <param name="oxford_sample" type="data" format="txt" label="Specify individual information file (.sample)"/> <param name="oxford_threshold" type="float" label="SNP Probability threshold" value="0.9"/> </when> <when value="vcf"> <param name="vcf_file" type="data" format="vcf" label="Specify Variant Call Format file (.vcf)"/> </when> </conditional> <conditional name="use_genetic_map"> <param name="use_genetic_map_select" type="select" label="Do you want to use a genetic map?"> <option value="use_genetic_map_yes" selected="True">Yes</option> <option value="use_genetic_map_no">No</option> </param> <when value="use_genetic_map_yes"> <conditional name="genetic_map_from_table"> <param name="genetic_map_from_table_select" type="select" label="Use built in data?"> <option value="genetic_map_from_table_yes" selected="True">Yes</option> <option value="genetic_map_from_table_no">No</option> </param> <when value="genetic_map_from_table_yes"> <param name="map_from_table" type="select" label="Select reference map"> <options from_data_table="shapeit2_ref" /> </param> </when> <when value="genetic_map_from_table_no"> <param name="genetic_map" type="data" format="txt" label="Genetic map file (.gmap)" /> </when> </conditional> </when> <when value="use_genetic_map_no"> <param name="rho" type="float" value="0.0004" label="Adjust recombination rate (--rho) for human data (0.001)"/> </when> </conditional> <conditional name="use_ref_panel"> <param name="use_ref_panel_select" type="select" label="Do you want to use a reference panel?"> <option value="use_ref_panel_yes">Use a reference panel</option> <option value="use_ref_panel_no" selected="True">Do not use reference panel</option> </param> <when value="use_ref_panel_yes"> <conditional name="ref_panel_from_table"> <param name="ref_panel_from_table_select" type="select" label="Use built in data?"> <option value="ref_panel_from_table_yes" selected="True">Yes</option> <option value="ref_panel_from_table_no">No</option> </param> <when value="ref_panel_from_table_yes"> <param name="ref_from_table" type="select" label="Select reference panel"> <options from_data_table="shapeit2_ref" /> </param> </when> <when value="ref_panel_from_table_no"> <param name="ref_panel_haps" type="data" format="data" label="Specify reference haplotypes file (.haps)" /> <param name="ref_panel_legend" type="data" format="data" label="Specify SNP map file (.legend)" /> <param name="ref_panel_sample" type="data" format="data" label="Specify individual information file (.sample)" /> </when> </conditional> <conditional name="disable_mcmc_iterations"> <param name="disable_mcmc_iterations_select" type="select" label="Disable MCMC iterations"> <option value="disable_mcmc_iterations_yes">Yes</option> <option value="disable_mcmc_iterations_no" selected="True">No</option> </param> <when value="disable_mcmc_iterations_yes"></when> <when value="disable_mcmc_iterations_no"></when> </conditional> <conditional name="filter_groups"> <param name="filter_groups_select" type="select" label="Do you want to filter groups?"> <option value="no_individual_filter" selected="True">No filtering</option> <option value="exclude_groups">Exclude list of groups</option> <option value="include_groups">Limit list of groups</option> </param> <when value="no_individual_filter"></when> <when value="exclude_groups"> <param name="exclude_inviduals_file" type="data" format="txt" label="Specify file with excluded groups (.exc)"/> </when> <when value="include_groups"> <param name="include_inviduals_file" type="data" format="txt" label="Specify file with limited groups (.inc)"/> </when> </conditional> </when> <when value="use_ref_panel_no"> </when> </conditional> <conditional name="use_advanced_parameters"> <param name="use_advanced_parameters_select" type="select" label="Set parameters"> <option value="use_advanced_parameters_yes">Use advanced parameters</option> <option value="use_advanced_parameters_no" selected="True">Use standard parameters</option> </param> <when value="use_advanced_parameters_yes"> <param name="chrX" type="select" label="Use X chromosomal genotypes?"> <option value="chrX_yes">Yes</option> <option value="chrX_no" selected="True">No</option> </param> <param name="noped" type="select" label="Discard pedigree/family information?"> <option value="noped_yes">Yes</option> <option value="noped_no" selected="True">No</option> </param> <param name="states" type="integer" label="Number of conditioning haplotypes used during phasing (--states)" value="100"/> <param name="window" type="float" label="Window size [Mb] in which conditioning haplotypes are defined" value="2.0"/> <param name="model_version1" type="select" label="Use SHAPEIT v1 graphical model"> <option value="use_v1_yes">Yes</option> <option value="use_v1_no" selected="True">No</option> </param> <conditional name="eff_size"> <param name="eff_size_select" type="select" label="Effective population size for phasing"> <option value="eff_size_european">European population (11418)</option> <option value="eff_size_african">African population (17469)</option> <option value="eff_size_asian">Asian population (14269)</option> <option value="eff_size_mixed_option" selected="True">Mixed population</option> </param> <when value="eff_size_european"></when> <when value="eff_size_african"></when> <when value="eff_size_asian"></when> <when value="eff_size_mixed_option"> <param name="eff_size_mixed" type="integer" label="Specify effective population size, depending on proportions [11418,17469]" value="14443"/> </when> </conditional> <param name="burn" type="integer" value="7" label="Number of burn-in iterations to find good starting point"/> <param name="prune" type="integer" value="8" label="Number of pruning iterations to find parsimonious graphs"/> <param name="main" type="integer" value="20" label="Number of iterations to compute transition probabilities"/> <param name="threads" type="integer" value="1" label="Specify number of threads"/> <conditional name="set_rng_seed"> <param name="set_rng_seed_select" type="select" label="Set seed for random number generator (RNG)"> <option value="set_rng_seed_yes">Yes</option> <option value="set_rng_seed_no" selected="True">No</option> </param> <when value="set_rng_seed_yes"> <param name="rng_seed" type="integer" value="18011981" label="RNG seed" /> </when> <when value="set_rng_seed_no"></when> </conditional> </when> <when value="use_advanced_parameters_no"></when> </conditional> <conditional name="use_filters"> <param name="use_filters_select" type="select" label="Apply filtering"> <option value="use_filters_yes">Yes</option> <option value="use_filters_no" selected="True">No</option> </param> <when value="use_filters_yes"> <conditional name="use_input_from"> <param name="use_input_from_select" type="select" label="Only consider genotypes above a position?"> <option value="use_input_from_yes">Yes</option> <option value="use_input_from_no" selected="True">No</option> </param> <when value="use_input_from_yes"> <param name="input_from" type="integer" value="1" label="Set position:"/> </when> <when value="use_input_from_no"></when> </conditional> <conditional name="use_input_to"> <param name="use_input_to_select" type="select" label="Only consider genotypes above a position?"> <option value="use_input_to_yes">Yes</option> <option value="use_input_to_no" selected="True">No</option> </param> <when value="use_input_to_yes"> <param name="input_to" type="integer" value="1" label="Set position:"/> </when> <when value="use_input_to_no"></when> </conditional> <conditional name="use_output_from"> <param name="use_output_from_select" type="select" label="Only output genotypes above a position?"> <option value="use_output_from_yes">Yes</option> <option value="use_output_from_no" selected="True">No</option> </param> <when value="use_output_from_yes"> <param name="output_from" type="integer" value="1" label="Set position:"/> </when> <when value="use_output_from_no"></when> </conditional> <conditional name="use_output_to"> <param name="use_output_to_select" type="select" label="Only output genotypes above a position?"> <option value="use_output_to_yes">Yes</option> <option value="use_output_to_no" selected="True">No</option> </param> <when value="use_output_to_yes"> <param name="output_to" type="integer" value="1" label="Set position:"/> </when> <when value="use_output_to_no"></when> </conditional> <conditional name="filter_individuals"> <param name="filter_individuals_select" type="select" label="Do you want to filter individuals?"> <option value="no_individual_filter" selected="True">No filtering</option> <option value="exclude_individuals">Exclude list of individuals</option> <option value="include_individuals">Limit list of individuals</option> </param> <when value="no_individual_filter"></when> <when value="exclude_individuals"> <param name="exclude_inviduals_file" type="data" format="txt" label="Specify file with excluded individuals (.exc)"/> </when> <when value="include_individuals"> <param name="include_inviduals_file" type="data" format="txt" label="Specify file with limited individuals (.inc)"/> </when> </conditional> <conditional name="filter_SNPs"> <param name="filter_SNPs_select" type="select" label="Do you want to filter SNPs?"> <option value="no_individual_filter" selected="True">No filtering</option> <option value="exclude_SNPs">Exclude list of SNPs</option> <option value="include_SNPs">Limit list of SNPs</option> </param> <when value="no_individual_filter"></when> <when value="exclude_SNPs"> <param name="exclude_inviduals_file" type="data" format="txt" label="Specify file with excluded SNPs (.exc)"/> </when> <when value="include_SNPs"> <param name="include_inviduals_file" type="data" format="txt" label="Specify file with limited SNPs (.inc)"/> </when> </conditional> </when> <when value="use_filters_no"></when> </conditional> </inputs> <outputs> <data name="out_haps" format="tabular" label="${tool.name} on ${on_string} haplotypes (.haps)"/> <data name="out_sample" format="tabular" label="${tool.name} on ${on_string} additional information (.sample)"/> <data name="out_graph" format="txt" label="${tool.name} on ${on_string} haplotype graphs (.hgraph)"/> <data name="out_log" format="txt" label="${tool.name} on ${on_string} logfile (.log)"/> </outputs> <help><![CDATA[ TODO: Fill in help. ]]></help> <citations> <citation type="doi">10.1038/nmeth.1785</citation> </citations> </tool>