Mercurial > repos > matthias > stacks2_gstacks
view stacks_gstacks.xml @ 1:192f1d5f301e draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit 8b047549e9e8791a5ca9424b1ef391e8980aba79-dirty
author | matthias |
---|---|
date | Fri, 30 Nov 2018 07:38:39 -0500 |
parents | ce90584be117 |
children | 4301ded2ea50 |
line wrap: on
line source
<tool id="stacks2_gstacks" name="Stacks2: gstacks" version="@STACKS_VERSION@+galaxy@WRAPPER_VERSION@"> <description>match stacks to a catalog</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"/> <expand macro="stdio"/> <command><![CDATA[ @CLEAN_EXT@ mkdir bam_inputs stacks_outputs && #if $mode_cond.mode_select == "denovo" and not $popmap: #if $input_type.input_type_selector == 'manual': #set count = len($input_type.input_bam) #else #set count = len($input_type.input_bam.keys()) #end if #if count == 1: #for $bam in $input_bam: ln -s '$bam' bam_inputs/catalog.bam && #end for #else >&2 echo "exactly one (merged) bam file is needed in denovo mode if no population map is given" && exit 1 && #end if #else @BAM_INPUT@ #end if gstacks #if $mode_cond.mode_select == "denovo": -P bam_inputs $mode_cond.ignore_pe_reads #if $mode_cond.advanced_cond.advanced_select == "yes": --kmer-length $mode_cond.advanced_cond.kmer_length --max-debruijn-reads $mode_cond.advanced_cond.max_debruijn_reads --min-kmer-cov $mode_cond.advanced_cond.min_kmer_cov #end if #else: #if $popmap -I bam_inputs #else $bamlist #end if #if $mode_cond.paired_cond.paired_select == '' $mode_cond.paired_cond.rm_unpaired_reads $mode_cond.paired_cond.rm_pcr_duplicates #else: $mode_cond.paired_cond.paired_select #end if #if $mode_cond.advanced_cond.advanced_select == "yes": --min-mapq $mode_cond.advanced_cond.min_mapq --max-clipped $mode_cond.advanced_cond.max_clipped --max-insert-len $mode_cond.advanced_cond.max_insert_len $mode_cond.advanced_cond.details --phasing-cooccurrences-thr-range $mode_cond.advanced_cond.phasing_cooccurrences_thr_min,$mode_cond.advanced_cond.phasing_cooccurrences_thr_max $mode_cond.advanced_cond.phasing_dont_prune_hets #end if #end if #if $popmap -M '$popmap' #end if -O stacks_outputs -t \${GALAXY_SLOTS:-1} ##Model options: --model $model_cond.model #if $model_cond.model != "snp": --var-alpha $model_cond.var_alpha #end if --gt-alpha $model_cond.gt_alpha ## annoyingly gstacks creates stacks_output/population.log ## instead of just writing to stderr as the other tools ## hence we do not use the tokens and return populations.log as log file and take the stderr && mv stacks_outputs/gstacks.log $output_log ## the catalog.calls output is a gzip-ed vcf extract it ## to make it usable in Galaxy (with the downside that we ## need to gzip it again for downstream calls like populations) && gunzip -c stacks_outputs/catalog.calls > stacks_outputs/catalog.calls.vcf ## TODO extract individual distributions from stacks_outputs/gstacks.log.distribs ## alternative extra tool ## for i in \$(stacks-dist-extract stacks_outputs/gstacks.log.distribs) ## do ## stacks-dist-extract stacks_outputs/gstacks.log.distribs $i > stacks_outputs/gstacks.log.\$i.tsv ## done ## TODO make optional output collection ]]></command> <inputs> <expand macro="bam_input_macro"/> <param name="popmap" type="data" format="tabular,txt" label="Population map" help="If set, matching will be done only for samples listed in this file" optional="true" argument="-M" /> <conditional name="mode_cond"> <param name="mode_select" type="select" label="Mode"> <option value="denovo" selected="true">De novo mode</option> <option value="refbased">Reference-based</option> </param> <when value="denovo"> <param argument="--ignore-pe-reads" name="ignore_pe_reads" type="boolean" checked="false" truevalue="--ignore-pe-reads" falsevalue="" label="ignore paired-end reads" help="ignore paired-end reads even if present in the input" /> <conditional name="advanced_cond"> <param name="advanced_select" type="select" label="Advanced options"> <option value="no">No</option> <option value="yes">Yes</option> </param> <when value="yes"> <param argument="--kmer-length" name="kmer_length" type="integer" value="31" min="2" max="31" label="kmer length for the de Bruijn graph" /> <param argument="--max-debruijn-reads" name="max_debruijn_reads" type="integer" value="1000" min="1" label="maximum number of reads to use in the de Bruijn graph" /> <param argument="--min-kmer-cov" name="min_kmer_cov" type="integer" value="2" label="minimum coverage to consider a kmer" /> </when> <when value="no"/> </conditional> </when> <when value="refbased"> <conditional name="paired_cond"> <param name="paired_select" type="select" label="paired end options" help="select single/paired for single end data or to select advanced paired end options, --unpaired: treat reverse reads as if they were forward reads; --ignore-pe-reads: ignore paired-end reads even if present in the input"> <option value="" selected="true">single/paired</option> <option value="--unpaired" selected="true">ignore read pairing (--unpaired)</option> <option value="--ignore-pe-reads" selected="true">ignore paired-end reads (--ignore-pe-reads)</option> </param> <when value=""> <param argument="--rm-unpaired-reads" name="rm_unpaired_reads" type="boolean" checked="false" truevalue="--rm-unpaired-reads" falsevalue="" label="discard unpaired reads" /> <param argument="--rm-pcr-duplicates" name="rm_pcr_duplicates" type="boolean" checked="false" truevalue="--rm-pcr-duplicates" falsevalue="" label="remove read pairs of the same sample that have the same insert length" help="implies --rm-unpaired-reads" /> </when> <when value="--unpaired"/> <when value="--ignore-pe-reads"/> </conditional> <conditional name="advanced_cond"> <param name="advanced_select" type="select" label="Advanced options"> <option value="no">No</option> <option value="yes">Yes</option> </param> <when value="yes"> <param argument="--min-mapq" name="min_mapq" type="integer" value="10" min="0" max="255" label="minimum PHRED-scaled mapping quality to consider a read" /> <param argument="--max-clipped" name="max_clipped" type="float" value="0.2" min="0.0" max="1.1" label="maximum soft-clipping level" help="in fraction of read length" /> <param argument="--max-insert-len" name="max_insert_len" type="integer" value="1000" min="0" label="maximum allowed sequencing insert length" /> <param argument="--details" type="boolean" checked="false" truevalue="--details" falsevalue="" label="write a heaview output" /> <param name="phasing_cooccurrences_thr_min" type="integer" value="1" min="0" label="edge coverage min" help="(--phasing-cooccurrences-thr-range)" /> <param name="phasing_cooccurrences_thr_max" type="integer" value="2" min="0" label="edge coverage max" help="range of edge coverage thresholds to iterate over when building the graph of allele cooccurrences for SNP phasing (--phasing-cooccurrences-thr-range)"/> <param argument="--phasing-dont-prune-hets" name="phasing_dont_prune_hets" type="boolean" checked="false" truevalue="--phasing-dont-prune-hets" falsevalue="" label="don't try to ignore dubious heterozygote genotypes during phasing" /> </when> <when value="no"/> </conditional> </when> </conditional> <conditional name="model_cond"> <param argument="--model" type="select" label="model to use to call variants and genotypes"> <option value="marukilow" selected="true">marukilow</option> <option value="marukihigh">marukihigh</option> <option value="snp">snp</option> </param> <when value="marukilow"> <expand macro="variant_calling_options_vg"/> </when> <when value="marukihigh"> <expand macro="variant_calling_options_vg"/> </when> <when value="snp"> <expand macro="variant_calling_options_g"/> </when> </conditional> <expand macro="in_log"/> </inputs> <outputs> <expand macro="out_log"/> <data format="txt" name="distribs" label="${tool.name} on ${on_string} distribs" from_work_dir="gstacks.log.distribs" /> <expand macro="gstacks_outputs_macro"/> </outputs> <tests> <!-- denovomode, w popmap --> <test> <param name="input_bam"> <collection type="list"> <element name="PopA_01.matches" ftype="bam" value="tsv2bam/PopA_01.matches.bam" /> <element name="PopA_02.matches" ftype="bam" value="tsv2bam/PopA_02.matches.bam" /> </collection> </param> <param name="popmap" ftype="tabular" value="denovo_map/popmap_cstacks.tsv" /> <conditional name="mode_cond"> <param name="mode_select" value="denovo"/> </conditional> <param name="add_log" value="yes" /> <output name="output_log" ftype="txt" file="gstacks/gstacks.log" lines_diff="8"/> <output_collection name="gstacks_out" type="list" count="2"> <element name="catalog.calls.vcf" file="gstacks/catalog.calls.tsv" ftype="vcf" lines_diff="2"/> <element name="catalog.fa.gz" file="gstacks/catalog.fa.gz" ftype="fasta.gz" compare="sim_size"/> </output_collection> </test> <!-- denovomode, wo popmap (allows for only one input), ignore PE, advanced, alt model --> <test> <param name="input_bam" value="tsv2bam/PopA_01.matches.bam" ftype="bam"/> <conditional name="mode_cond"> <param name="mode_select" value="denovo" /> <param name="ignore_pe_reads" value="--ignore-pe-reads" /> <conditional name="advanced_cond"> <param name="advanced_select" value="yes"/> <param name="kmer_length" value="23" /> <param name="max_debruijn_reads" value="666"/> <param name="min_kmer_cov" value="3" /> </conditional> </conditional> <conditional name="model_cond"> <param name="model" value="marukihigh"/> <param name="var_alpha" value="0.1" /> <param name="gt_alpha" value="0.1" /> </conditional> <param name="add_log" value="yes" /> <assert_command> <has_text text="--ignore-pe-reads" /> <has_text text="--rm-pcr-duplicates" /> <has_text text="--kmer-length 23" /> <has_text text="--max-debruijn-reads 666" /> <has_text text="--min-kmer-cov 3" /> <has_text text="--model marukihigh" /> <has_text text="--var-alpha 0.1" /> <has_text text="--gt-alpha 0.1" /> </assert_command> <output name="output_log"><assert_contents><has_text text="gstacks is done." /></assert_contents></output> <output_collection name="gstacks_out" type="list" count="2"/> </test> <!-- refbased wo popmap, paired options, removing all unpaired reads results in an error --> <test expect_failure="true" expect_exit_code="1"> <param name="input_bam" value="tsv2bam/PopA_01.matches.bam,tsv2bam/PopA_02.matches.bam"/> <conditional name="mode_cond"> <param name="mode_select" value="refbased"/> <conditional name="paired_cond"> <param name="paired_select" value=""/> <!--<param name="rm_unpaired_reads" value="\-\-rm-unpaired-reads" /> removes to much of the test data and gstacks fails--> <param name="rm_pcr_duplicates" value="--rm-pcr-duplicates" /> </conditional> </conditional> <param name="add_log" value="yes" /> <assert_command> <has_text text="-I bam_inputs" /> <not_has_text text="-B " /> <has_text text="--rm-unpaired-reads" /> <has_text text="--rm-pcr-duplicates" /> </assert_command> </test> <!-- refbased w popmap (here bam names need to be equal to sample names in popmap), \-\-unpaired, advanced, snp model --> <test> <param name="input_bam"> <collection type="list"> <element name="PopA_01" ftype="bam" value="tsv2bam/PopA_01.matches.bam" /> <element name="PopA_02" ftype="bam" value="tsv2bam/PopA_02.matches.bam" /> </collection> </param> <param name="popmap" ftype="tabular" value="denovo_map/popmap_cstacks.tsv" /> <conditional name="mode_cond"> <param name="mode_select" value="refbased"/> <conditional name="paired_cond"> <param name="paired_select" value="--unpaired"/> </conditional> <conditional name="advanced_cond"> <param name="advanced_select" value="yes" /> <param name="min_mapq" value="23" /> <param name="max_clipped" value="0.23" /> <param name="max_insert_len" value="666" /> <param name="details" value="--detailed"/> <param name="phasing_cooccurrences_thr_min" value="2"/> <param name="phasing_cooccurrences_thr_max" value="3"/> <param name="phasing_dont_prune_hets" value="--phasing-dont-prune-hets" /> </conditional> </conditional> <param name="model_cond|model" value="snp"/> <param name="model_cond|gt_alpha" value="0.1" /> <param name="add_log" value="yes" /> <assert_command> <not_has_text text="-I bam_inputs" /> <has_text text="-B " /> <has_text text="--unpaired" /> <has_text text="--min-mapq 23" /> <has_text text="--max-clipped 0.23" /> <has_text text="--max-insert-len 666" /> <has_text text="--detailed" /> <has_text text="--phasing-cooccurrences-thr-range 2,3" /> <has_text text="--phasing-dont-prune-hets" /> <has_text text="--model snp" /> <has_text text="--gt-alpha 0.1" /> </assert_command> <output name="output_log"><assert_contents><has_text text="gstacks is done." /></assert_contents></output> <output_collection name="gstacks_out" type="list" count="2"/> </test> <!-- refbased wo popmap (here bam names don't matter), \-\-ignorepe --> <test> <param name="input_bam"> <collection type="list"> <element name="PopA_01.matches" ftype="bam" value="tsv2bam/PopA_01.matches.bam" /> <element name="PopA_02.matches" ftype="bam" value="tsv2bam/PopA_02.matches.bam" /> </collection> </param> <conditional name="mode_cond"> <param name="mode_select" value="refbased"/> <conditional name="paired_cond"> <param name="paired_select" value="--ignore-pe-reads"/> </conditional> </conditional> <param name="add_log" value="yes" /> <assert_command> <has_text text="-I bam_inputs" /> <not_has_text text="-B " /> <has_text text="--ignore-pe-reads" /> </assert_command> <output name="output_log"><assert_contents><has_text text="gstacks is done." /></assert_contents></output> <output_collection name="gstacks_out" type="list" count="2"> <element name="catalog.calls.vcf" file="gstacks/catalog.calls.tsv" ftype="vcf" lines_diff="2"/> <element name="catalog.fa.gz" file="gstacks/catalog.fa.gz" ftype="fasta.gz" compare="sim_size"/> </output_collection> </test> </tests> <help> <![CDATA[ .. class:: infomark **What it does** For de novo analyses, this program will pull in paired-end reads, if available, assemble the paired-end contig and merge it with the single-end locus, align reads to the locus, and call SNPs. For reference-aligned analyses, this program will build loci from the single and/or paired-end reads before calling SNPs. The single- and paired-end reads must be aligned and stored together in the intput BAM or SAM files and the reads must be sorted. The gstacks program will detect if single- or paired-end reads are present. In either mode, gstacks is able to remove PCR duplicates if requested. -------- **Input files** If a population map is given BAM records must be assigned to samples using BAM "reads groups" (gstacks uses the ID/identifier and SM/sample name fields). Read groups must be consistent if repeated different files. Otherwise read groups are unneeded and ignored. **Output files** TODO @STACKS_INFOS@ ]]> </help> <expand macro="citation" /> </tool>