Mercurial > repos > iuc > polypolish
changeset 1:bd2a15dbcea1 draft
planemo upload for repository https://github.com/mesocentre-clermont-auvergne/galaxy-tools/tree/master/tools/polypolish commit afc3449a0b68d43fd1179543815dfe23b951e157
author | iuc |
---|---|
date | Fri, 20 Oct 2023 12:41:27 +0000 |
parents | aaa868913641 |
children | f355085dd2aa |
files | macro.xml polypolish.xml |
diffstat | 2 files changed, 58 insertions(+), 22 deletions(-) [+] |
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--- a/macro.xml Thu Sep 22 07:51:48 2022 +0000 +++ b/macro.xml Fri Oct 20 12:41:27 2023 +0000 @@ -1,7 +1,7 @@ <macros> <token name="@TOOL_VERSION@">0.5.0</token> - <token name="@VERSION_SUFFIX@">0</token> + <token name="@VERSION_SUFFIX@">1</token> <token name="@PROFILE@">21.05</token> <token name="@THREADS@">\${GALAXY_SLOTS:-7}</token> <xml name="version_command"> @@ -33,8 +33,8 @@ <option value="non_filter"> No filtering step</option> </param> <when value="filter"> - <param name="low" argument="--low" type="float" min="0" value="0.1" label="Low percentile threshold" help="Select the lower value to remove [default: 0.1]"/> - <param name="high" argument="--high" type="float" min="0" value="99.9" label="High percentile threshold" help="Select the lower value to remove [default: 99.9]"/> + <param argument="--low" type="float" min="0" value="0.1" label="Low percentile threshold" help="Select the lower value to remove [default: 0.1]"/> + <param argument="--high" type="float" min="0" value="99.9" label="High percentile threshold" help="Select the lower value to remove [default: 99.9]"/> </when> <when value="non_filter"> </when>
--- a/polypolish.xml Thu Sep 22 07:51:48 2022 +0000 +++ b/polypolish.xml Fri Oct 20 12:41:27 2023 +0000 @@ -14,25 +14,31 @@ For single SAM ======================================*# #if $input.sam_data_type.sam_selector == 'single' - #if $input.sam_data_type.single_sam.ext == 'unsorted.bam' + #if $input.sam_data_type.single_sam.is_of_type("unsorted.bam") samtools view -h $input.sam_data_type.single_sam > input_sam && #elif $input.sam_data_type.single_sam.ext == 'sam' ln -s $input.sam_data_type.single_sam input_sam && + #else + echo "${input.sam_data_type.single_sam} not a sam/bam file" #end if polypolish input_data input_sam > '$polished_fasta' #*====================================== For paired SAM ======================================*# #elif $input.sam_data_type.sam_selector == 'paired' - #if $input.sam_data_type.R1_sam.ext == 'unsorted.bam' + #if $input.sam_data_type.R1_sam.is_of_type("unsorted.bam") samtools view -h $input.sam_data_type.R1_sam > sample_R1.sam && #elif $input.sam_data_type.R1_sam.ext == 'sam' ln -s '$input.sam_data_type.R1_sam' sample_R1.sam && + #else + echo "${input.sam_data_type.single_sam} not a sam/bam file" #end if - #if $input.sam_data_type.R2_sam.ext == 'unsorted.bam' + #if $input.sam_data_type.R2_sam.is_of_type("unsorted.bam") samtools view -h $input.sam_data_type.R2_sam > sample_R2.sam && #elif $input.sam_data_type.R2_sam.ext == 'sam' ln -s '$input.sam_data_type.R2_sam' sample_R2.sam && + #else + echo "${input.sam_data_type.single_sam} not a sam/bam file" #end if #if $input.sam_data_type.insert_filter.filter_select == 'filter' polypolish_insert_filter.py --low '$input.sam_data_type.insert_filter.low' @@ -51,10 +57,12 @@ #elif $input.sam_data_type.sam_selector == 'multiple_single' mkdir single_collection && #for $value, $single_sam in enumerate($input.sam_data_type.single_collection): - #if $single_sam.ext == 'unsorted.bam' + #if $single_sam.is_of_type("unsorted.bam") samtools view -h $single_sam > 'single_collection/$(single_sam.element_identifier).sam' && #elif $single_sam.ext == 'sam' ln -s $single_sam 'single_collection/$(single_sam.element_identifier).$(single_sam.ext)' && + #else + echo "${single_sam} is not a sam/bam file" #end if #end for polypolish input_data single_collection/*.sam > '$polished_fasta' @@ -64,12 +72,12 @@ #elif $input.sam_data_type.sam_selector == "multiple_paired" mkdir paired_collection && #for $value, $paired_sam in enumerate($input.sam_data_type.paired_collection): - #if $paired_sam.forward.ext == 'unsorted.bam' + #if $paired_sam.forward.is_of_type("unsorted.bam") samtools view -h $paired_sam.forward > 'paired_collection/forward_input$(value)$(paired_sam.forward.element_identifier).sam' && #else ln -s '$paired_sam.forward' 'paired_collection/forward_input$(value)$(paired_sam.forward.element_identifier).sam' && #end if - #if $paired_sam.reverse.ext == 'unsorted.bam' + #if $paired_sam.reverse.is_of_type("unsorted.bam") samtools view -h $paired_sam.reverse > 'paired_collection/reverse_input$(value)$(paired_sam.reverse.element_identifier).sam' && #else ln -s '$paired_sam.reverse' 'paired_collection/reverse_input$(value)$(paired_sam.reverse.element_identifier).sam' && @@ -135,16 +143,16 @@ </conditional> </section> <section name="options" title="Options" expanded="False"> - <param name="min_depth" argument="--min_depth" type="integer" min="0" value="5" label="Minimal depth" + <param argument="--min_depth" type="integer" min="0" value="5" label="Minimal depth" help="A base must occur at least this many times in the pileup to be considered valid [default: 5]"/> - <param name="fraction_invalid" argument="--fraction_invalid" type="float" min="0" value="0.2" max="1" label="Minimal invalid fraction" + <param argument="--fraction_invalid" type="float" min="0" value="0.2" max="1" label="Minimal invalid fraction" help="A base must make up less than this fraction of the read depth to be considered invalid [default: 0.2]"/> - <param name="max_errors" argument="--max_errors" type="integer" min="0" value="10" label="Number of mismatch/indels to ignore alignments" + <param argument="--max_errors" type="integer" min="0" value="10" label="Number of mismatch/indels to ignore alignments" help="Ignore alignments with more than this many mismatches and indels [default: 10]"/> - <param name="fraction_valid" argument="--fraction_valid" type="float" min="0" value="0.5" max="1" label="Minimal valid fraction" + <param argument="--fraction_valid" type="float" min="0" value="0.5" max="1" label="Minimal valid fraction" help="A base must make up at least this fraction of the read depth to be considered valid [default: 0.5"/> <param name="keep_logfile" type="boolean" truevalue="true" falsevalue="false" label="Keep log file"/> - <param name="debug" argument="--debug" type="boolean" truevalue="true" falsevalue="false" label="Keep per base information file"/> + <param argument="--debug" type="boolean" truevalue="true" falsevalue="false" label="Keep per base information file"/> </section> </inputs> <outputs> @@ -343,9 +351,9 @@ <param name="sam_selector" value="multiple_single"/> <param name="single_collection"> <collection type="list"> - <element name="R1_sam" value="aligned_test_file/alignement_R1.bam" ftype="unsorted.bam"/> - <element name="R1_bis_sam" value="aligned_test_file/alignement_R1_bis.bam" ftype="unsorted.bam"/> - <element name="R1_ter_sam" value="aligned_test_file/alignement_R1_ter.bam" ftype="unsorted.bam"/> + <element name="R1_sam" value="aligned_test_file/alignement_R1.sam" ftype="sam"/> + <element name="R1_bis_sam" value="aligned_test_file/alignement_R1_bis.sam" ftype="sam"/> + <element name="R1_ter_sam" value="aligned_test_file/alignement_R1_ter.sam" ftype="sam"/> </collection> </param> </conditional> @@ -392,6 +400,34 @@ </section> <output name="polished_fasta" value="polished.fasta"/> </test> + <!-- Test_12 Test with bam files --> + <test expect_num_outputs="1"> + <section name="input"> + <param name="fasta_file" value="contigs.fa"/> + <conditional name="sam_data_type"> + <param name="sam_selector" value="single"/> + <param name="single_sam" value="aligned_test_file/alignement_R1.bam"/> + </conditional> + </section> + <output name="polished_fasta" value="polished.fasta"/> + </test> + <!-- Test_13 paired bam --> + <test expect_num_outputs="2"> + <section name="input"> + <param name="fasta_file" value="contigs.fa"/> + <conditional name="sam_data_type"> + <param name="sam_selector" value="paired"/> + <param name="R1_sam" value="aligned_test_file/alignement_R1.bam"/> + <param name="R2_sam" value="aligned_test_file/alignement_R2.bam"/> + </conditional> + </section> + <section name="options"> + <param name="debug" value="true"/> + <param name="keep_logfile" value="false"/> + </section> + <output name="polished_fasta" value="polished.fasta"/> + <output name="debug_file" value="debug_file_test_2.tsv"/> + </test> </tests> <help><![CDATA[ **What it does** @@ -401,10 +437,12 @@ **Polypolish pipeline steps** 1. [Optional] Filter aligned reads - - Exclude some alignments based on their insert size - - This should reduce the number of excessive alignments, particularly near the edges of repeat sequences, improving Polypolish's ability to fix errors in those regions. + Exclude some alignments based on their insert size + This should reduce the number of excessive alignments, + particularly near the edges of repeat sequences, improving Polypolish's ability to fix errors in those regions. 2. Clean assembly with filtered reads + **Inputs** Polypolish need SAM/BAM input format obtain from aligner with option to keep all possible location Polypolish take on or more assembly as input fasta. @@ -414,9 +452,7 @@ For example using bwa mem to align raw data before use, you need : 1. To align each read data independantly (also for paired data) 2. Set the option "Output all alignments for single-ends or unpaired paired-ends" in Select analysis mode>Set input/output options - - This allow multiple ailgnemnt output need to use polypolish - - + This allow multiple ailgnemnt output need to use polypolish ]]></help> <expand macro="citations"/> </tool>