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planemo upload for repository https://github.com/youyuh48/galaxy-tools/tree/master/tools/sniffles
author | youyuh48 |
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date | Sun, 25 Aug 2019 01:58:51 -0400 |
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children | ba3aaae7a229 |
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<tool id="sniffles" name="sniffles" version="0.1.0"> <description>Structural variation caller using third generation sequencing</description> <requirements> <requirement type="package" version="1.0.11">sniffles</requirement> </requirements> <command detect_errors="exit_code"> <![CDATA[ sniffles -t \${GALAXY_SLOTS:-2} -m '$input' --${output_format} '$output' ## general_options #if $general_options.s: -s $general_options.s #end if #if $general_options.max_num_splits: --max_num_splits $max_num_splits #end if #if $general_options.l: -l $general_options.l #end if #if $general_options.q: -q $general_options.q #end if #if $general_options.n: -n $general_options.n #end if #if $general_options.r: -r $general_options.r #end if ]]> </command> <inputs> <param type="data" name="input" format="bam" label="Input BAM file"/> <param name="output_format" type="select" label="Select an output format"> <option value="vcf">VCF</option> <option value="bedpe">bedpe</option> </param> <section name="general_options" title="Set general options" expanded="False"> <param argument="-s" type="integer" value="" optional="true" label="Minimum number of reads that support a SV. [10]"/> <param argument="--max_num_splits" name="max_num_splits" type="integer" value="" optional="true" label="Maximum number of splits per read to be still taken into account. [7]"/> <param argument="-l" type="integer" value="" optional="true" label="Minimum length of SV to be reported. [30]"/> <param argument="-q" type="integer" value="" optional="true" label="Minimum Mapping Quality. [20]"/> <param argument="-n" type="integer" value="" optional="true" label="Report up to N reads that support the SV in the vcf file. -1: report all. [0]"/> <param argument="-r" type="integer" value="" optional="true" label="Discard read if non of its segment is larger then this. [2000]"/> </section> </inputs> <outputs> <data name="output" format="vcf" label="${tool.name} on ${on_string} (${output_format} format)"> <change_format> <when input="output_format" value="bedpe" format="tabular"/> </change_format> </data> </outputs> <tests> <test> <param name="input" value="reads_region.bam"/> <param name="option" value="--vcf"/> <output name="output" file="expected_output.vcf"/> </test> </tests> <help> <![CDATA[ Usage: sniffles [options] -m <sorted.bam> -v <output.vcf> Input/Output: -m <string>, --mapped_reads <string> (required) Sorted bam File -v <string>, --vcf <string> VCF output file name [] -b <string>, --bedpe <string> bedpe output file name [] \--Ivcf <string> Input VCF file name. Enable force calling [] \--tmp_file <string> path to temporary file otherwise Sniffles will use the current directory. [] General: -s <int>, --min_support <int> Minimum number of reads that support a SV. [10] \--max_num_splits <int> Maximum number of splits per read to be still taken into account. [7] -d <int>, --max_distance <int> Maximum distance to group SV together. [1000] -t <int>, --threads <int> Number of threads to use. [3] -l <int>, --min_length <int> Minimum length of SV to be reported. [30] -q <int>, --minmapping_qual <int> Minimum Mapping Quality. [20] -n <int>, --num_reads_report <int> Report up to N reads that support the SV in the vcf file. -1: report all. [0] -r <int>, --min_seq_size <int> Discard read if non of its segment is larger then this. [2000] -z <int>, --min_zmw <int> Discard SV that are not supported by at least x zmws. This applies only for PacBio recognizable reads. [0] \--cs_string Enables the scan of CS string instead of Cigar and MD. [false] Clustering/phasing and genotyping: \--genotype Enables Sniffles to compute the genotypes. [false] \--cluster Enables Sniffles to phase SVs that occur on the same reads [false] \--cluster_support <int> Minimum number of reads supporting clustering of SV. [1] -f <float>, --allelefreq <float> Threshold on allele frequency (0-1). [0] \--min_homo_af <float> Threshold on allele frequency (0-1). [0.8] \--min_het_af <float> Threshold on allele frequency (0-1). [0.3] Advanced: \--report_BND Dont report BND instead use Tra in vcf output. [true] \--report_seq Report sequences for indels in vcf output. (Beta version!) [false] \--ignore_sd Ignores the sd based filtering. [false] \--report_read_strands Enables the report of the strand categories per read. (Beta) [false] \--ccs_reads Preset CCS Pacbio setting. (Beta) [false] Parameter estimation: \--skip_parameter_estimation Enables the scan if only very few reads are present. [false] \--del_ratio <float> Estimated ration of deletions per read (0-1). [0.0458369] \--ins_ratio <float> Estimated ratio of insertions per read (0-1). [0.049379] \--max_diff_per_window <int> Maximum differences per 100bp. [50] \--max_dist_aln_events <int> Maximum distance between alignment (indel) events. [4] ]]> </help> <citations> <citation type="doi">10.1038/s41592-018-0001-7</citation> </citations> </tool>