Mercurial > repos > iuc > samtools_merge
view macros.xml @ 3:36677f429310 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/samtools/samtools_merge commit 5cb103832529f17e5c72e7f122758c13519fbe5e
author | iuc |
---|---|
date | Mon, 15 Aug 2022 09:18:27 +0000 |
parents | b40e2d865d52 |
children | 65a38e8c8e2a |
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<macros> <xml name="requirements"> <requirements> <requirement type="package" version="@TOOL_VERSION@">samtools</requirement> <yield/> </requirements> </xml> <token name="@TOOL_VERSION@">1.15.1</token> <token name="@PROFILE@">20.05</token> <token name="@FLAGS@"><![CDATA[ #set $flags = 0 #if $filter #set $flags = sum(map(int, str($filter).split(','))) #end if ]]></token> <token name="@PREPARE_IDX@"><![CDATA[ ##prepare input and indices ln -s '$input' infile && #if $input.is_of_type('bam'): #if str( $input.metadata.bam_index ) != "None": ln -s '${input.metadata.bam_index}' infile.bai && #else: samtools index infile infile.bai && #end if #elif $input.is_of_type('cram'): #if str( $input.metadata.cram_index ) != "None": ln -s '${input.metadata.cram_index}' infile.crai && #else: samtools index infile infile.crai && #end if #end if ]]></token> <token name="@PREPARE_IDX_MULTIPLE@"><![CDATA[ ##prepare input and indices #for $i, $bam in enumerate( $input_bams ): ln -s '$bam' '${i}' && #if $bam.is_of_type('bam'): #if str( $bam.metadata.bam_index ) != "None": ln -s '${bam.metadata.bam_index}' '${i}.bai' && #else: samtools index '${i}' '${i}.bai' && #end if #elif $bam.is_of_type('cram'): #if str( $bam.metadata.cram_index ) != "None": ln -s '${bam.metadata.cram_index}' '${i}.crai' && #else: samtools index '${i}' '${i}.crai' && #end if #end if #end for ]]></token> <token name="@PREPARE_FASTA_IDX@"><![CDATA[ ## Make the user-selected reference genome, if any, accessible through ## a shell variable $reffa, index the reference if necessary, and make ## the fai-index file available through a shell variable $reffai. ## For a cached genome simply sets the shell variables to point to the ## genome file and its precalculated index. ## For a genome from the user's history, if that genome is a plain ## fasta file, the code creates a symlink in the pwd, creates the fai ## index file next to it, then sets the shell variables to point to the ## symlink and its index. ## For a fasta.gz dataset from the user's history, it tries the same, ## but this will only succeed if the file got compressed with bgzip. ## For a regular gzipped file samtools faidx will fail, in which case ## the code falls back to decompressing to plain fasta before ## reattempting the indexing. ## Indexing of a bgzipped file produces a regular fai index file *and* ## a compressed gzi file. The former is identical to the fai index of ## the uncompressed fasta. ## If the user has not selected a reference (it's an optional parameter ## in some samtools wrappers), a cheetah boolean use_ref is set to ## False to encode that fact. #set use_ref=True #if $addref_cond.addref_select == "history": #if $addref_cond.ref.is_of_type('fasta'): reffa="reference.fa" && ln -s '${addref_cond.ref}' \$reffa && samtools faidx \$reffa && #else: reffa="reference.fa.gz" && ln -s '${addref_cond.ref}' \$reffa && { samtools faidx \$reffa || { echo "Failed to index compressed reference. Trying decompressed ..." 1>&2 && gzip -dc \$reffa > reference.fa && reffa="reference.fa" && samtools faidx \$reffa; } } && #end if reffai=\$reffa.fai && #elif $addref_cond.addref_select == "cached": ## in case of cached the absolute path is used which allows to read ## a cram file without specifying the reference reffa='${addref_cond.ref.fields.path}' && reffai=\$reffa.fai && #else #set use_ref=False #end if ]]></token> <xml name="optional_reference" token_help="" token_argument=""> <conditional name="addref_cond"> <param name="addref_select" type="select" label="Use a reference sequence"> <help>@HELP@</help> <option value="no">No</option> <option value="history">Use a genome/index from the history</option> <option value="cached">Use a built-in genome</option> </param> <when value="no"/> <when value="history"> <param name="ref" argument="@ARGUMENT@" type="data" format="fasta,fasta.gz" label="Reference"/> </when> <when value="cached"> <param name="ref" argument="@ARGUMENT@" type="select" label="Reference"> <options from_data_table="fasta_indexes"> <filter type="data_meta" ref="input" key="dbkey" column="dbkey"/> </options> <validator type="no_options" message="No reference genome is available for the build associated with the selected input dataset"/> </param> </when> </conditional> </xml> <xml name="mandatory_reference" token_help="" token_argument=""> <conditional name="addref_cond"> <param name="addref_select" type="select" label="Use a reference sequence"> <help>@HELP@</help> <option value="history">Use a genome/index from the history</option> <option value="cached">Use a built-in genome</option> </param> <when value="history"> <param name="ref" argument="@ARGUMENT@" type="data" format="fasta,fasta.gz" label="Reference"/> </when> <when value="cached"> <param name="ref" argument="@ARGUMENT@" type="select" label="Reference"> <options from_data_table="fasta_indexes"> <filter type="data_meta" ref="input" key="dbkey" column="dbkey"/> <validator message="No reference genome is available for the build associated with the selected input dataset" type="no_options" /> </options> </param> </when> </conditional> </xml> <token name="@ADDTHREADS@"><![CDATA[ ##compute the number of ADDITIONAL threads to be used by samtools (-@) addthreads=\${GALAXY_SLOTS:-1} && (( addthreads-- )) && ]]></token> <token name="@ADDMEMORY@"><![CDATA[ ##compute the number of memory available to samtools sort (-m) ##use only 75% of available: https://github.com/samtools/samtools/issues/831 addmemory=\${GALAXY_MEMORY_MB_PER_SLOT:-768} && ((addmemory=addmemory*75/100)) && ]]></token> <xml name="seed_input"> <param name="seed" type="integer" optional="True" label="Seed for random number generator" help="If empty a random seed is used." /> </xml> <xml name="flag_options" token_s1="false" token_s2="false" token_s4="false" token_s8="false" token_s16="false" token_s32="false" token_s64="false" token_s128="false" token_s256="false" token_s512="false" token_s1024="false" token_s2048="false"> <option value="1" selected="@S1@">Read is paired</option> <option value="2" selected="@S2@">Read is mapped in a proper pair</option> <option value="4" selected="@S4@">Read is unmapped</option> <option value="8" selected="@S8@">Mate is unmapped</option> <option value="16" selected="@S16@">Read is mapped to the reverse strand of the reference</option> <option value="32" selected="@S32@">Mate is mapped to the reverse strand of the reference</option> <option value="64" selected="@S64@">Read is the first in a pair</option> <option value="128" selected="@S128@">Read is the second in a pair</option> <option value="256" selected="@S256@">Alignment of the read is not primary</option> <option value="512" selected="@S512@">Read fails platform/vendor quality checks</option> <option value="1024" selected="@S1024@">Read is a PCR or optical duplicate</option> <option value="2048" selected="@S2048@">Alignment is supplementary</option> </xml> <!-- region specification macros and tokens for tools that allow the specification of region by bed file / space separated list of regions --> <token name="@REGIONS_FILE@"><![CDATA[ #if $cond_region.select_region == 'tab': -t '$cond_region.targetregions' #end if ]]></token> <token name="@REGIONS_MANUAL@"><![CDATA[ #if $cond_region.select_region == 'text': #for $i, $x in enumerate($cond_region.regions_repeat): '${x.region}' #end for #end if ]]></token> <xml name="regions_macro"> <conditional name="cond_region"> <param name="select_region" type="select" label="Filter by regions" help="restricts output to only those alignments which overlap the specified region(s)"> <option value="no" selected="True">No</option> <option value="text">Manualy specify regions</option> <option value="tab">Regions from tabular file</option> </param> <when value="no"/> <when value="text"> <repeat name="regions_repeat" min="1" default="1" title="Regions"> <param name="region" type="text" label="region" help="format chr:from-to"> <validator type="regex" message="Required format: CHR[:FROM[-TO]]; where CHR: string containing any character except quotes, whitespace and colon; FROM and TO: any integer">^[^\s'\":]+(:\d+(-\d+){0,1}){0,1}$</validator> </param> </repeat> </when> <when value="tab"> <param name="targetregions" argument="-t/--target-regions" type="data" format="tabular" label="Target regions file" help="Do stats in these regions only. Tab-delimited file chr,from,to (1-based, inclusive)" /> </when> </conditional> </xml> <xml name="citations"> <citations> <citation type="bibtex"> @misc{SAM_def, title={Definition of SAM/BAM format}, url = {https://samtools.github.io/hts-specs/},} </citation> <citation type="doi">10.1093/bioinformatics/btp352</citation> <citation type="doi">10.1093/bioinformatics/btr076</citation> <citation type="doi">10.1093/bioinformatics/btr509</citation> <citation type="bibtex"> @misc{Danecek_et_al, Author={Danecek, P., Schiffels, S., Durbin, R.}, title={Multiallelic calling model in bcftools (-m)}, url = {http://samtools.github.io/bcftools/call-m.pdf},} </citation> <citation type="bibtex"> @misc{Durbin_VCQC, Author={Durbin, R.}, title={Segregation based metric for variant call QC}, url = {http://samtools.github.io/bcftools/rd-SegBias.pdf},} </citation> <citation type="bibtex"> @misc{Li_SamMath, Author={Li, H.}, title={Mathematical Notes on SAMtools Algorithms}, url = {http://www.broadinstitute.org/gatk/media/docs/Samtools.pdf},} </citation> <citation type="bibtex"> @misc{SamTools_github, title={SAMTools GitHub page}, url = {https://github.com/samtools/samtools},} </citation> </citations> </xml> <xml name="version_command"> <version_command><![CDATA[samtools 2>&1 | grep Version]]></version_command> </xml> <xml name="stdio"> <stdio> <exit_code range="1:" level="fatal" description="Error" /> </stdio> </xml> </macros>