Mercurial > repos > devteam > bwa
diff bwa-mem.xml @ 11:546ada4a9f43 draft
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bwa commit 610045611b00099e0a24183c8cf33aebfa9635cf
author | devteam |
---|---|
date | Tue, 19 Jan 2016 11:20:59 -0500 |
parents | 6069ffa8b240 |
children | bd3a1e0de84c |
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--- a/bwa-mem.xml Fri Jan 08 17:02:09 2016 -0500 +++ b/bwa-mem.xml Tue Jan 19 11:20:59 2016 -0500 @@ -1,5 +1,5 @@ <?xml version="1.0"?> -<tool id="bwa_mem" name="Map with BWA-MEM" version="0.7.12"> +<tool id="bwa_mem" name="Map with BWA-MEM" version="@VERSION@.1"> <description>- map medium and long reads (> 100 bp) against reference genome</description> <macros> <import>read_group_macros.xml</import> @@ -9,28 +9,7 @@ <expand macro="stdio" /> <command> <![CDATA[ - #set $reference_fasta_filename = "localref.fa" - - #if str( $reference_source.reference_source_selector ) == "history": - ln -s "${reference_source.ref_file}" "${reference_fasta_filename}" && - - ## The following shell commands decide which of the BWA indexing algorithms (IS or BWTSW) will be run - ## depending on the size of the input FASTA dataset - ( size=`stat -c %s "${reference_source.ref_file}" 2>/dev/null`; ## Linux - if [ $? -ne 0 ]; then - size=\$(stat -f %z "${reference_source.ref_file}"); ## OSX - fi && - if [ "\$size" -lt 2000000000 ]; then - echo "Reference genome size is \$size bytes, generating BWA index with is algorithm"; - bwa index -a is "${reference_fasta_filename}"; - else - echo "Reference genome size is \$size bytes, generating BWA index with bwtsw algorithm"; - bwa index -a bwtsw "${reference_fasta_filename}"; - fi - ) && - #else: - #set $reference_fasta_filename = str( $reference_source.ref_file.fields.path ) - #end if + @set_reference_fasta_filename@ ## Begin BWA-MEM command line @@ -124,25 +103,7 @@ </command> <inputs> - - <conditional name="reference_source"> - <param name="reference_source_selector" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options. See `Indexes` section of help below"> - <option value="cached">Use a built-in genome index</option> - <option value="history">Use a genome from history and build index</option> - </param> - <when value="cached"> - <param name="ref_file" type="select" label="Using reference genome" help="Select genome from the list"> - <options from_data_table="bwa_mem_indexes"> - <filter type="sort_by" column="2" /> - <validator type="no_options" message="No indexes are available" /> - </options> - <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/> - </param> - </when> - <when value="history"> - <param name="ref_file" type="data" format="fasta" label="Use the following dataset as the reference sequence" help="You can upload a FASTA sequence to the history and use it as reference" /> - </when> - </conditional> + <expand macro="reference_source_conditional" /> <conditional name="fastq_input"> <param name="fastq_input_selector" type="select" label="Single or Paired-end reads" help="Select between paired and single end data"> <option value="paired">Paired</option> @@ -290,6 +251,7 @@ <test> <param name="reference_source_selector" value="history" /> <param name="ref_file" ftype="fasta" value="bwa-mem-mt-genome.fa"/> + <param name="index_a" value="is"/> <param name="fastq_input_selector" value="paired"/> <param name="fastq_input1" ftype="fastqsanger" value="bwa-mem-fastq1.fq"/> <param name="fastq_input2" ftype="fastqsanger" value="bwa-mem-fastq2.fq"/>