Mercurial > repos > iuc > stacks_denovomap
changeset 8:39d2b6c1c030 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks commit dc23703c260d004a28fe24a2a7c00cb4371bc32e
author | iuc |
---|---|
date | Thu, 27 Apr 2017 04:17:51 -0400 |
parents | 2505774ded94 |
children | 2b1dd7ab69f7 |
files | macros.xml stacks_denovomap.xml test-data/demultiplexed/PopA_01.1.fq.gzip test-data/denovo_map/popmap_cstacks.tsv test-data/procrad/R1.fq.gzip test-data/ustacks/ustacks.out |
diffstat | 6 files changed, 234 insertions(+), 81 deletions(-) [+] |
line wrap: on
line diff
--- a/macros.xml Fri Apr 07 11:47:48 2017 -0400 +++ b/macros.xml Thu Apr 27 04:17:51 2017 -0400 @@ -2,14 +2,14 @@ <macros> <xml name="requirements"> <requirements> - <requirement type="package" version="1.42">stacks</requirement> + <requirement type="package" version="1.46">stacks</requirement> <requirement type="package" version="1.2.10">velvet</requirement> - <container type="docker">quay.io/biocontainers/stacks:1.42--2</container> + <requirement type="package" version="1.1">stacks_summary</requirement> <yield/> </requirements> </xml> - <token name="@WRAPPER_VERSION@">1.42</token> + <token name="@WRAPPER_VERSION@">1.46</token> <xml name="stdio"> <stdio> @@ -90,6 +90,7 @@ <option value="bsaHI">bsaHI</option> <option value="hpaII">hpaII</option> <option value="ncoI">ncoI</option> + <option value="ApaLI">ApaLI</option> </xml> <xml name="cross_types"> @@ -100,6 +101,19 @@ <option value="GEN">GEN (generic, unspecific to any map type)</option> </xml> + <token name="@CLEAN_EXT@"> + <![CDATA[ + #from os.path import splitext + #import re + #def clean_ext($identifier) + #while $identifier.endswith(('.1', '.fa', '.fq', '.fasta', '.fastq', '.gz', '.gzip', '.sam', '.bam')) + #set $identifier = splitext($identifier)[0] + #end while +$identifier#slurp + #end def + ]]> + </token> + <token name="@NORM_GENOTYPES_OUTPUT_LIGHT@"> <![CDATA[ ## We need to do this as the output file names contains the value of an option (min progeny)
--- a/stacks_denovomap.xml Fri Apr 07 11:47:48 2017 -0400 +++ b/stacks_denovomap.xml Thu Apr 27 04:17:51 2017 -0400 @@ -6,54 +6,47 @@ <expand macro="requirements"/> <expand macro="stdio"/> <command><![CDATA[ - #from os.path import splitext - #import re - #if str( $options_usage.rad_analysis_type ) == "genetic": - #for $input_parent in $options_usage.parent_sequences: + @CLEAN_EXT@ - #if $input_parent.is_of_type('fastqsanger'): - #set $data_path = splitext($input_parent.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fq" - #else: - #set $data_path = splitext($input_parent.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fa" + #if str( $options_usage.rad_analysis_type ) == "genetic" + #for $input_parent in $options_usage.parent_sequences + #if $input_parent.is_of_type('fastqsanger') + #set $data_path = $clean_ext($input_parent.element_identifier) + ".fq" + #else if $input_parent.is_of_type('fastqsanger.gz') + #set $data_path = $clean_ext($input_parent.element_identifier) + ".fq.gz" + #else + #set $data_path = $clean_ext($input_parent.element_identifier) + ".fa" #end if - ln -s "${input_parent}" "${data_path}" && + ln -s '${input_parent}' '${data_path}' && #end for - #for $input_progeny in $options_usage.progeny_sequences: - #if $input_progeny: - #if $input_progeny.is_of_type('fastqsanger'): - #set $data_path = splitext($input_progeny.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fq" - #else: - #set $data_path = splitext($input_progeny.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fa" + #for $input_progeny in $options_usage.progeny_sequences + #if $input_progeny + #if $input_progeny.is_of_type('fastqsanger') + #set $data_path = $clean_ext($input_progeny.element_identifier) + ".fq" + #else if $input_progeny.is_of_type('fastqsanger.gz') + #set $data_path = $clean_ext($input_progeny.element_identifier) + ".fq.gz" + #else + #set $data_path = $clean_ext($input_progeny.element_identifier) + ".fa" #end if - ln -s "${input_progeny}" "${data_path}" && + ln -s '${input_progeny}' '${data_path}' && #end if #end for - #else: - #for $input_indiv in $options_usage.individual_sample: + #else + #for $input_indiv in $options_usage.individual_sample - #if $input_indiv.is_of_type('fastqsanger'): - #set $data_path = splitext($input_indiv.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fq" - #else: - #set $data_path = splitext($input_indiv.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fa" + #if $input_indiv.is_of_type('fastqsanger') + #set $data_path = $clean_ext($input_indiv.element_identifier) + ".fq" + #else if $input_indiv.is_of_type('fastqsanger.gz') + #set $data_path = $clean_ext($input_indiv.element_identifier) + ".fq.gz" + #else + #set $data_path = $clean_ext($input_indiv.element_identifier) + ".fa" #end if - ln -s "${input_indiv}" "${data_path}" && + ln -s '${input_indiv}' '${data_path}' && #end for #end if @@ -65,64 +58,58 @@ -T \${GALAXY_SLOTS:-1} - #if str( $options_usage.rad_analysis_type ) == "genetic": - #for $input_parent in $options_usage.parent_sequences: - #if $input_parent.is_of_type('fastqsanger'): - #set $data_path = splitext($input_parent.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fq" - #else: - #set $data_path = splitext($input_parent.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fa" + #if str( $options_usage.rad_analysis_type ) == "genetic" + #for $input_parent in $options_usage.parent_sequences + #if $input_parent.is_of_type('fastqsanger') + #set $data_path = $clean_ext($input_parent.element_identifier) + ".fq" + #else if $input_parent.is_of_type('fastqsanger.gz') + #set $data_path = $clean_ext($input_parent.element_identifier) + ".fq.gz" + #else + #set $data_path = $clean_ext($input_parent.element_identifier) + ".fa" #end if - -p "${data_path}" + -p '${data_path}' #end for -A $options_usage.cross_type - #for $input_progeny in $options_usage.progeny_sequences: - #if $input_progeny: - #if $input_progeny.is_of_type('fastqsanger'): - #set $data_path = splitext($input_progeny.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fq" - #else: - #set $data_path = splitext($input_progeny.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fa" + #for $input_progeny in $options_usage.progeny_sequences + #if $input_progeny + #if $input_progeny.is_of_type('fastqsanger') + #set $data_path = $clean_ext($input_progeny.element_identifier) + ".fq" + #else if $input_progeny.is_of_type('fastqsanger.gz') + #set $data_path = $clean_ext($input_progeny.element_identifier) + ".fq.gz" + #else + #set $data_path = $clean_ext($input_progeny.element_identifier) + ".fa" #end if - -r "${data_path}" + -r '${data_path}' #end if #end for - #if str($assembly_options.P): + #if str($assembly_options.P) -P $assembly_options.P #end if - #else: - #for $i_indiv, $input_indiv in enumerate($options_usage.individual_sample): + #else + #for $i_indiv, $input_indiv in enumerate($options_usage.individual_sample) - #if $input_indiv.is_of_type('fastqsanger'): - #set $data_path = splitext($input_indiv.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fq" - #else: - #set $data_path = splitext($input_indiv.element_identifier)[0] - #set $data_path = re.sub(r'\.1$', '', $data_path) - #set $data_path = $data_path + ".fa" + #if $input_indiv.is_of_type('fastqsanger') + #set $data_path = $clean_ext($input_indiv.element_identifier) + ".fq" + #else if $input_indiv.is_of_type('fastqsanger.gz') + #set $data_path = $clean_ext($input_indiv.element_identifier) + ".fq.gz" + #else + #set $data_path = $clean_ext($input_indiv.element_identifier) + ".fa" #end if - -s "${data_path}" + -s '${data_path}' #end for - -O "$options_usage.popmap" + -O '$options_usage.popmap' #end if - #if str($assembly_options.m): + #if str($assembly_options.m) -m $assembly_options.m #end if - #if str($assembly_options.N): + #if str($assembly_options.N) -N $assembly_options.N #end if -M $assembly_options.M @@ -137,19 +124,29 @@ -S ## snp_model - #if str( $snp_options.select_model.model_type) == "bounded": + #if str( $snp_options.select_model.model_type) == "bounded" --bound_low $snp_options.select_model.bound_low --bound_high $snp_options.select_model.bound_high --alpha $snp_options.select_model.alpha - #else if str( $snp_options.select_model.model_type) == "snp": + #else if str( $snp_options.select_model.model_type) == "snp" --alpha $snp_options.select_model.alpha #end if -o stacks_outputs - #if str( $options_usage.rad_analysis_type ) == "genetic": + #if str( $options_usage.rad_analysis_type ) == "genetic" @NORM_GENOTYPES_OUTPUT_LIGHT@ #end if + + ## If input is in gz format, stacks will output gzipped files (no option to control this) + && if ls stacks_outputs/*.gz > /dev/null 2>&1; then gunzip stacks_outputs/*.gz; fi + + && + + stacks_summary.py --stacks-prog denovo_map.pl --res-dir stacks_outputs --logfile stacks_outputs/denovo_map.log --summary stacks_outputs/summary.html + #if str( $options_usage.rad_analysis_type ) == "population" + --pop-map '$options_usage.popmap' + #end if ]]></command> <inputs> @@ -159,16 +156,16 @@ <option value="population">Population</option> </param> <when value="genetic"> - <param name="parent_sequences" argument="-p" format="fastqsanger,fasta" type="data" multiple="true" label="Files containing parent sequences" help="Files containing parent sequences from a mapping cross (only R1 reads). Dataset names will be used as sample name (no space allowed)." /> + <param name="parent_sequences" argument="-p" format="fastqsanger,fastqsanger.gz,fasta" type="data" multiple="true" label="Files containing parent sequences" help="Files containing parent sequences from a mapping cross (only R1 reads). Dataset names will be used as sample name (no space allowed)." /> - <param name="progeny_sequences" argument="-r" format="fastqsanger,fasta" type="data" multiple="true" optional="true" label="Files containing progeny sequences" help="files containing progeny sequences from a mapping cross (only R1 reads). Dataset names will be used as sample name (no space allowed)." /> + <param name="progeny_sequences" argument="-r" format="fastqsanger,fastqsanger.gz,fasta" type="data" multiple="true" optional="true" label="Files containing progeny sequences" help="files containing progeny sequences from a mapping cross (only R1 reads). Dataset names will be used as sample name (no space allowed)." /> <param name="cross_type" argument="-A" type="select" label="Cross type"> <expand macro="cross_types"/> </param> </when> <when value="population"> - <param name="individual_sample" argument="-s" format="fastqsanger,fasta" type="data" multiple="true" label="Files containing an individual sample from a population" help="files containing an individual sample from a population (only R1 reads). Dataset names will be used as sample name (no space allowed)." /> + <param name="individual_sample" argument="-s" format="fastqsanger,fastqsanger.gz,fasta" type="data" multiple="true" label="Files containing an individual sample from a population" help="files containing an individual sample from a population (only R1 reads). Dataset names will be used as sample name (no space allowed)." /> <param name="popmap" argument="-O" type="data" format="tabular,txt" label="Specify a population map" /> </when> </conditional> @@ -193,6 +190,8 @@ <outputs> <data format="txt" name="output_log" label="denovo_map.log with ${tool.name} on ${on_string}" from_work_dir="stacks_outputs/denovo_map.log" /> + <data format="html" name="output_summary" label="Summary from ${tool.name} on ${on_string}" from_work_dir="stacks_outputs/summary.html" /> + <data format="tabular" name="catalogtags" label="Catalog assembled loci (tags) with ${tool.name} on ${on_string}" from_work_dir="stacks_outputs/batch_1.catalog.tags.tsv" /> <data format="tabular" name="catalogsnps" label="Catalog model calls (snps) with ${tool.name} on ${on_string}" from_work_dir="stacks_outputs/batch_1.catalog.snps.tsv" /> <data format="tabular" name="catalogalleles" label="Catalog haplotypes (alleles) with ${tool.name} on ${on_string}" from_work_dir="stacks_outputs/batch_1.catalog.alleles.tsv" /> @@ -232,6 +231,11 @@ <has_text text="denovo_map.pl completed" /> </assert_contents> </output> + <output name="output_summary"> + <assert_contents> + <has_text text="Stacks Statistics" /> + </assert_contents> + </output> <!-- catalog --> <output name="catalogtags"> @@ -312,6 +316,11 @@ <has_text text="denovo_map.pl completed" /> </assert_contents> </output> + <output name="output_summary"> + <assert_contents> + <has_text text="Stacks Statistics" /> + </assert_contents> + </output> <!-- catalog --> <output name="catalogtags"> @@ -392,6 +401,11 @@ <has_text text="denovo_map.pl completed" /> </assert_contents> </output> + <output name="output_summary"> + <assert_contents> + <has_text text="Stacks Statistics" /> + </assert_contents> + </output> <!-- catalog --> <output name="catalogtags"> @@ -467,6 +481,89 @@ </element> </output_collection> </test> + <test> + <param name="options_usage|rad_analysis_type" value="genetic"/> + <param name="options_usage|parent_sequences" value="demultiplexed/PopA_01.1.fq.gzip" ftype="fastqsanger.gz" /> + <output name="output_log"> + <assert_contents> + <has_text text="denovo_map.pl completed" /> + </assert_contents> + </output> + <output name="output_summary"> + <assert_contents> + <has_text text="Stacks Statistics" /> + </assert_contents> + </output> + + <!-- catalog --> + <output name="catalogtags"> + <assert_contents> + <has_text text="catalog generated on" /> + </assert_contents> + </output> + <output name="catalogsnps"> + <assert_contents> + <has_text text="catalog generated on" /> + </assert_contents> + </output> + <output name="catalogalleles"> + <assert_contents> + <has_text text="catalog generated on" /> + </assert_contents> + </output> + + <!-- genotypes --> + <output name="out_generic_haplo"> + <assert_contents> + <has_text text="Catalog ID" /> + </assert_contents> + </output> + <output name="out_sql_markers"> + <assert_contents> + <has_text text="Total Genotypes" /> + </assert_contents> + </output> + <output name="out_joinmap"> + <assert_contents> + <has_text text="batch_1.genotypes_" /> + </assert_contents> + </output> + <output name="out_sql_genotypes"> + <assert_contents> + <has_text text="SQL ID" /> + </assert_contents> + </output> + + <!-- samples --> + <output_collection name="tags"> + <element name="PopA_01.tags"> + <assert_contents> + <has_text text="generated on " /> + </assert_contents> + </element> + </output_collection> + <output_collection name="snps"> + <element name="PopA_01.snps"> + <assert_contents> + <has_text text="generated on " /> + </assert_contents> + </element> + </output_collection> + <output_collection name="alleles"> + <element name="PopA_01.alleles"> + <assert_contents> + <has_text text="generated on " /> + </assert_contents> + </element> + </output_collection> + <output_collection name="matches"> + <element name="PopA_01.matches"> + <assert_contents> + <has_text text="generated on " /> + </assert_contents> + </element> + </output_collection> + </test> </tests> <help>
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/test-data/denovo_map/popmap_cstacks.tsv Thu Apr 27 04:17:51 2017 -0400 @@ -0,0 +1,1 @@ +PopA_01 myPopA
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/test-data/ustacks/ustacks.out Thu Apr 27 04:17:51 2017 -0400 @@ -0,0 +1,41 @@ +ustacks parameters selected: + Sample ID: 1 + Min depth of coverage to create a stack: 2 + Max distance allowed between stacks: 2 + Max distance allowed to align secondary reads: 4 + Max number of stacks allowed per de novo locus: 3 + Deleveraging algorithm: disabled + Removal algorithm: enabled + Model type: SNP + Alpha significance level for model: 0.05 + Gapped alignments: disabled +Parsing stacks_inputs/PopA_01.fq +Loading RAD-Tags...done +Loaded 66 RAD-Tags. + Inserted 7 elements into the RAD-Tags hash map. + 0 reads contained uncalled nucleotides that were modified. +4 initial stacks were populated; 3 stacks were set aside as secondary reads. +Initial coverage mean: 15.75; Std Dev: 7.46241; Max: 27 +Deleveraging trigger: 23; Removal trigger: 31 +Calculating distance for removing repetitive stacks. + Distance allowed between stacks: 1; searching with a k-mer length of 47 (48 k-mers per read); 1 k-mer hits required. +Removing repetitive stacks. + Removed 0 stacks. + 4 stacks remain for merging. +Post-Repeat Removal, coverage depth Mean: 15.75; Std Dev: 7.46241; Max: 27 +Calculating distance between stacks... + Distance allowed between stacks: 2; searching with a k-mer length of 31 (64 k-mers per read); 2 k-mer hits required. +Merging stacks, maximum allowed distance: 2 nucleotide(s) + 4 stacks merged into 3 loci; deleveraged 0 loci; blacklisted 0 loci. +After merging, coverage depth Mean: 21; Std Dev: 4.24264; Max: 27 +Merging remainder radtags + 3 remainder sequences left to merge. + Distance allowed between stacks: 4; searching with a k-mer length of 17 (78 k-mers per read); 10 k-mer hits required. + Matched 3 remainder reads; unable to match 0 remainder reads. +After remainders merged, coverage depth Mean: 22; Std Dev: 4.32049; Max: 28 +Calling final consensus sequences, invoking SNP-calling model... +Number of utilized reads: 66 +Writing loci, SNPs, and alleles to 'stacks_outputs/'... + Refetching sequencing IDs from stacks_inputs/PopA_01.fq... read 66 sequence IDs. +done. +ustacks is done.