Mercurial > repos > thanhlv > snippy
diff snippy.xml @ 2:4e478a5f2742 draft
planemo upload commit c9db1bf13e663b9e2122fc610007679a2f117aa6-dirty
| author | thanhlv |
|---|---|
| date | Sun, 08 Sep 2019 16:16:50 -0400 |
| parents | 8cdc3f9c2dc5 |
| children | e10e0c41a6f3 |
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--- a/snippy.xml Tue Jun 25 11:09:37 2019 -0400 +++ b/snippy.xml Sun Sep 08 16:16:50 2019 -0400 @@ -1,73 +1,89 @@ -<tool id="snippy" name="snippy_qib" version="@VERSION@+galaxy1"> - <description> +<tool id="snippy" name="snippy" version="@VERSION@+galaxy2"> + <description> Snippy finds SNPs between a haploid reference genome and your NGS sequence reads. - </description> - <macros> - <import>macros.xml</import> - </macros> - <expand macro="requirements" /> - <expand macro="version_command" /> + </description> + <macros> + <import>macros.xml</import> + </macros> + <expand macro="requirements" /> + <expand macro="version_command" /> <command detect_errors="exit_code"><![CDATA[ - - ln -f -s '$snippy_ref.fields.path' 'foo.fna' && - + #if $reference_source.reference_source_selector == 'history' + ln -sf '$reference_source.ref_file' 'ref' && + #elif $reference_source.reference_source_selector == 'cached' + ln -sf '$reference_source.ref_file.fields.path' 'ref' && + #end if snippy --outdir 'out' - --cpus "\${GALAXY_SLOTS:-1}" - --ref 'foo.fna' + --cpus \${GALAXY_SLOTS:-1} + --ram \$((\${GALAXY_MEMORY_MB:-4096}/1024)) + --ref 'ref' --mapqual $adv.mapqual --mincov $adv.mincov --minfrac $adv.minfrac + --minqual $adv.minqual #if $adv.rgid - --rgid '$advanced.rgid' + --rgid '$adv.rgid' #end if #if $adv.bwaopt - --bwaopt '$advanced.bwaopt' + --bwaopt '$adv.bwaopt' #end if #if str( $fastq_input.fastq_input_selector ) == "paired" - --pe1 '$fastq_input.fastq_input1' - --pe2 '$fastq_input.fastq_input2' - #end if - #if str( $fastq_input.fastq_input_selector ) == "paired_collection" - --pe1 '$fastq_input.fastq_input.forward' - --pe2 '$fastq_input.fastq_input.reverse' + --R1 '$fastq_input.fastq_input1' + --R2 '$fastq_input.fastq_input2' + #elif str( $fastq_input.fastq_input_selector ) == "paired_collection" + --R1 '$fastq_input.fastq_input.forward' + --R2 '$fastq_input.fastq_input.reverse' + #elif str( $fastq_input.fastq_input_selector ) == "single" + --se '$fastq_input.fastq_input_single' + #elif str( $fastq_input.fastq_input_selector ) == "paired_iv" + --peil '$fastq_input.fastq_input_interleaved' #end if - #if str( $fastq_input.fastq_input_selector ) == "single" - --se '$fastq_input.fastq_input' - #end if - #if str( $fastq_input.fastq_input_selector ) == "paired_iv" - --peil '$fastq_input.fastq_input' - #end if - - && - - gunzip out/snps.depth.gz && #import re #if str( $fastq_input.fastq_input_selector ) == "paired" #set $dir_name = re.sub('[^\w_]', '_', $fastq_input.fastq_input1.element_identifier) - #else - #set $dir_name = re.sub('[^\w_]', '_', $fastq_input.fastq_input.element_identifier) + #elif str( $fastq_input.fastq_input_selector ) == "paired_collection" + #set $dir_name = re.sub('[^\w_]', '_', $fastq_input.fastq_input.name) + #elif str( $fastq_input.fastq_input_selector ) == "single" + #set $dir_name = re.sub('[^\w_]', '_', $fastq_input.fastq_input_single.element_identifier) + #elif str( $fastq_input.fastq_input_selector ) == "paired_iv" + #set $dir_name = re.sub('[^\w_]', '_', $fastq_input.fastq_input_interleaved.element_identifier) #end if - mkdir -p ${dir_name} && cp -r out/reference out/snps.tab out/snps.aligned.fa ${dir_name}/ && + mkdir -p ${dir_name} && cp -r out/reference out/snps.tab out/snps.aligned.fa out/snps.vcf ${dir_name}/ && tar -czf out.tgz ${dir_name} + #if "outcon" in str($outputs) and $adv.rename_cons + && sed -i 's/>.*/>${dir_name}/' out/snps.consensus.fa + #end if - ]]></command> + ]]> </command> <inputs> - <param label="Select a reference" name="snippy_ref" type="select"> - <options from_data_table="snippy"> - <validator message="No database is available" type="no_options" /> - </options> - </param> + + <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. If you would like to perform self-mapping select `history` here, then choose your input file as reference."> + <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="all_fasta"> + <validator type="no_options" message="No reference genomes are available" /> + </options> + </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 or FASTQ sequence to the history and use it as reference" /> + </when> + </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> @@ -80,13 +96,13 @@ <param name="fastq_input2" type="data" format="fastqsanger,fasta" label="Select second set of reads" help="Specify dataset with reverse reads"/> </when> <when value="single"> - <param name="fastq_input" type="data" format="fastqsanger,fasta" label="Select fastq dataset" help="Specify dataset with single reads"/> + <param name="fastq_input_single" type="data" format="fastqsanger,fasta" label="Select fastq dataset" help="Specify dataset with single reads"/> </when> <when value="paired_collection"> <param name="fastq_input" format="fastqsanger,fasta" type="data_collection" collection_type="paired" label="Select a paired collection" help="See help section for an explanation of dataset collections"/> </when> <when value="paired_iv"> - <param name="fastq_input" type="data" format="fastqsanger" label="Select fastq dataset" help="Specify dataset with interleaved reads"/> + <param name="fastq_input_interleaved" type="data" format="fastqsanger" label="Select fastq dataset" help="Specify dataset with interleaved reads"/> </when> </conditional> @@ -94,8 +110,10 @@ <param name="mapqual" type="integer" value="60" label="Minimum mapping quality" help="Minimum mapping quality to allow" /> <param name="mincov" type="integer" value="10" label="Minimum coverage" help="Minimum coverage to call a snp" /> <param name="minfrac" type="float" value="0.9" label="Minumum proportion for variant evidence" help="Minumum proportion for variant evidence" /> + <param name="minqual" type="float" value="100.0" label="Minumum QUALITY in VCF column 6" help="Minumum QUALITY in VCF column 6" /> <param name="rgid" type="text" value="" label="Bam header @RG ID" help="Use this @RG ID: in the BAM header" /> <param name="bwaopt" type="text" value="" label="Extra BWA MEM options" help="Extra BWA MEM options, eg. -x pacbio" /> + <param name="rename_cons" type="boolean" truevalue="rename_cons" falsevalue="" help="When producing an output of the reference genome with variants instantiated, edit the header so that it is named after the input VCF" /> </section> <param name="outputs" type="select" multiple="true" display="checkboxes" label="Output selection"> @@ -150,73 +168,76 @@ <tests> - <test> <!-- test 1 - fasta ref default --> - <param name="ref" value="wildtype.fna" ftype="fasta" /> + <test> <!-- test 0 - fasta ref no snps --> + <!-- <param name="ref" value="reference.fasta" ftype="fasta" /> --> + <param name="reference_source|reference_source_selector" value="history"/> + <param name="reference_source|ref_file" value="reference.fasta" ftype="fasta"/> <param name="fastq_input_selector" value="paired" /> - <param name="fastq_input1" ftype="fastqsanger" value="mutant_R1.fastq" /> - <param name="fastq_input2" ftype="fastqsanger" value="mutant_R2.fastq" /> + <param name="fastq_input1" ftype="fastqsanger" value="a_1.fastq" /> + <param name="fastq_input2" ftype="fastqsanger" value="a_2.fastq" /> + <param name="mincov" value="2" /> + <param name="minqual" value="60" /> <param name="outputs" value="outgff,outsum" /> - <output name="snpsum" ftype="tabular" file="fna_ref/snps.txt" lines_diff="6" /> - <output name="snpgff" ftype="gff3" file="fna_ref/snps.gff" /> - </test> - - <test> <!-- test 2 - gbk ref default --> - <param name="ref" value="wildtype.gbk" ftype="genbank" /> - <param name="fastq_input_selector" value="paired" /> - <param name="fastq_input1" ftype="fastqsanger" value="mutant_R1.fastq" /> - <param name="fastq_input2" ftype="fastqsanger" value="mutant_R2.fastq" /> - <param name="outputs" value="outgff,outsum" /> - <output name="snpsum" ftype="tabular" file="gbk_ref/snps.txt" lines_diff="6" /> - <output name="snpgff" ftype="gff3" file="gbk_ref/snps.gff" /> + <output name="snpsum" ftype="tabular" file="a_fna_ref_mincov_2_minqual_60.snps.txt" lines_diff="6" /> + <output name="snpgff" ftype="gff3" file="a_fna_ref_mincov_2_minqual_60.snps.gff" /> </test> - <test> <!-- test 3 - gbk mapqual=40 --> - <param name="ref" value="wildtype.gbk" ftype="genbank" /> + <test> <!-- test 1 - fasta ref one snp --> + <!-- <param name="ref" value="reference.fasta" ftype="fasta" /> --> + <param name="reference_source|reference_source_selector" value="history"/> + <param name="reference_source|ref_file" value="reference.fasta" ftype="fasta"/> <param name="fastq_input_selector" value="paired" /> - <param name="fastq_input1" ftype="fastqsanger" value="mutant_R1.fastq" /> - <param name="fastq_input2" ftype="fastqsanger" value="mutant_R2.fastq" /> + <param name="fastq_input1" ftype="fastqsanger" value="b_1.fastq" /> + <param name="fastq_input2" ftype="fastqsanger" value="b_2.fastq" /> + <param name="mincov" value="2" /> + <param name="minqual" value="60" /> <param name="outputs" value="outgff,outsum" /> - <param name="mapqual" value="40" /> - <output name="snpsum" ftype="tabular" file="map_qual/snps.txt" lines_diff="6" /> - <output name="snpgff" ftype="gff3" file="map_qual/snps.gff" /> + <output name="snpsum" ftype="tabular" file="b_fna_ref_mincov_2_minqual_60.snps.txt" lines_diff="6" /> + <output name="snpgff" ftype="gff3" file="b_fna_ref_mincov_2_minqual_60.snps.gff" /> </test> - <test> <!-- test 4 - gbk mincov=15 --> - <param name="ref" value="wildtype.gbk" ftype="genbank" /> - <param name="fastq_input_selector" value="paired" /> - <param name="fastq_input1" ftype="fastqsanger" value="mutant_R1.fastq" /> - <param name="fastq_input2" ftype="fastqsanger" value="mutant_R2.fastq" /> - <param name="mincov" value="15" /> - <param name="outputs" value="outgff,outsum" /> - <output name="snpsum" ftype="tabular" file="min_cov/snps.txt" lines_diff="6" /> - <output name="snpgff" ftype="gff3" file="min_cov/snps.gff" /> - </test> - - <test> <!-- test 5 - gbk minfrac=0.7 --> - <param name="ref" value="wildtype.gbk" ftype="genbank" /> - <param name="fastq_input_selector" value="paired" /> - <param name="fastq_input1" ftype="fastqsanger" value="mutant_R1.fastq" /> - <param name="fastq_input2" ftype="fastqsanger" value="mutant_R2.fastq" /> - <param name="minfrac" value="0.7" /> - <param name="outputs" value="outgff,outsum" /> - <output name="snpsum" ftype="tabular" file="min_frac/snps.txt" lines_diff="6" /> - <output name="snpgff" ftype="gff3" file="min_frac/snps.gff" /> - </test> - - <test> <!-- test 6 - fasta ref default paired_collection --> - <param name="ref" value="wildtype.fna" ftype="fasta" /> + <test> <!-- test 2 - fasta ref one snp paired_collection --> + <!-- <param name="ref" value="reference.fasta" ftype="fasta" /> --> + <param name="reference_source|reference_source_selector" value="history"/> + <param name="reference_source|ref_file" value="reference.fasta" ftype="fasta"/> <param name="fastq_input_selector" value="paired_collection" /> <param name="fastq_input"> <collection type="paired"> - <element name="forward" ftype="fastqsanger" value="mutant_R1.fastq" /> - <element name="reverse" ftype="fastqsanger" value="mutant_R2.fastq" /> + <element name="forward" ftype="fastqsanger" value="b_1.fastq" /> + <element name="reverse" ftype="fastqsanger" value="b_2.fastq" /> </collection> </param> + <param name="mincov" value="2" /> + <param name="minqual" value="60" /> <param name="outputs" value="outgff,outsum" /> - <output name="snpsum" ftype="tabular" file="fna_ref/snps.txt" lines_diff="6" /> - <output name="snpgff" ftype="gff3" file="fna_ref/snps.gff" /> + <output name="snpsum" ftype="tabular" file="b_fna_ref_mincov_2_minqual_60.snps.txt" lines_diff="6" /> + <output name="snpgff" ftype="gff3" file="b_fna_ref_mincov_2_minqual_60.snps.gff" /> </test> + <test> <!-- test 3 - fasta ref one snp single --> + <!-- <param name="ref" value="reference.fasta" ftype="fasta" /> --> + <param name="reference_source|reference_source_selector" value="history"/> + <param name="reference_source|ref_file" value="reference.fasta" ftype="fasta"/> + <param name="fastq_input_selector" value="single" /> + <param name="fastq_input_single" value="b_2.fastq" ftype="fastqsanger" /> + <param name="mincov" value="2" /> + <param name="minqual" value="60" /> + <param name="outputs" value="outgff,outsum" /> + <output name="snpsum" ftype="tabular" file="b_fna_ref_mincov_2_minqual_60.snps.txt" lines_diff="6" /> + <output name="snpgff" ftype="gff3" file="b_2_fna_ref_mincov_2_minqual_60.snps.gff" /> + </test> + + <test> <!-- test 4 - reference source as cached --> + <param name="reference_source|reference_source_selector" value="cached"/> + <param name="reference_source|ref_file" value="test_id"/> + <param name="fastq_input_selector" value="single" /> + <param name="fastq_input_single" value="b_2.fastq" ftype="fastqsanger" /> + <param name="mincov" value="2" /> + <param name="minqual" value="60" /> + <param name="outputs" value="outgff,outsum" /> + <output name="snpsum" ftype="tabular" file="b_fna_ref_mincov_2_minqual_60.snps.txt" lines_diff="6" /> + <output name="snpgff" ftype="gff3" file="b_2_fna_ref_mincov_2_minqual_60.snps.gff" /> + </test> </tests> @@ -245,6 +266,8 @@ - minimum fraction - Float - Minumum proportion for variant evidence (default '0.9') + - minimum quality - Float - Minumum QUALITY in VCF column 6 (default '100.0') + - rgid - String - Use this @RG ID: in the BAM header (default '') - bwaopt - Extra BWA MEM options, eg. -x pacbio (default '') @@ -253,7 +276,7 @@ For a much more in depth description of snippy and how it works, see https://github.com/tseemann/snippy - ]]></help> - <expand macro="citations"/> + ]]> </help> + <expand macro="citations"/> </tool>
