Mercurial > repos > trinity_ctat > ctat_mutations
diff ctat_mutations.xml @ 0:de4e183593ac draft
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author | trinity_ctat |
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date | Wed, 14 Nov 2018 12:15:15 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/ctat_mutations.xml Wed Nov 14 12:15:15 2018 -0500 @@ -0,0 +1,68 @@ +<tool id="ctat_mutations" name="ctat_mutations" version="1.0.0" profile="17.05"> + <description>Mutation Pipeline for calling SNPs and variants</description> + <requirements> + <requirement type="package" version="2.0.1">ctat-mutations</requirement> + </requirements> + <command detect_errors="default"> + <![CDATA[ + ctat_mutations \ + --plot \ + --out_dir varcalling.outdir \ + --threads 8 \ + --variant_filtering_mode GATK \ + --left "$left" \ + --right "$right" \ + --genome_lib_dir "${genome_resource_lib.fields.path}" \ + --variant_call_mode GATK \ + --tissue_type "$tissue_type" \ + --email "$cravat_email" + ]]> + </command> + <inputs> + <param format="fastq" name="left" type="data" label="Left/Forward strand reads" help="Left read"/> + <param format="fastq" name="right" type="data" label="Right/Reverse strand reads" help="Right read"/> + <param name="tissue_type" type="select" label="Select a pathology" help="If you don't know, just choose 'General Purpose'"> + <options from_data_table="ctat_cravat_tissues"> + <filter type="sort_by" column="1"/> + <validator type="no_options" message="No indexes are available for the selected input dataset"/> + </options> + </param> + <param name="genome_resource_lib" type="select" label="Select a reference genome"> + <options from_data_table="ctat_genome_resource_libs"> + <filter type="sort_by" column="2" /> + <validator type="no_options" message="No indexes are available" /> + </options> + </param> + <param name="cravat_email" type="text" label="CRAVAT email" help="CRAVAT registered email id"/> + <section name="adv" title="This service uses the GATK4. GATK4 is licensed by the Broad Institute and is made available to academic users of this service for non-commercial use only. The full text of the license is available here: https://www.broadinstitute.org/gatk/about/license.html. For more information about GATK and full documentation, please visit the GATK website: https://www.broadinstitute.org." expanded="False"> + </section> + </inputs> + <outputs> + <data format="tabular" name="cancertab" label="${tool.name} on ${on_string}: Cancer Tab" from_work_dir="varcalling.outdir/cancer.tab"/> + <data format="vcf" name="cancerVariants" label="${tool.name} on ${on_string}: Cancer VCF" from_work_dir="varcalling.outdir/cancer.vcf"/> + <data format="vcf" name="allVariants" label="${tool.name} on ${on_string}: All Variants VCF" from_work_dir="varcalling.outdir/variants.vcf"/> + <data format="bam" name="bamfile" label="Bam used in haplotype calling" from_work_dir="varcalling.outdir/misc/recalibrated.bam"/> + <data format="txt" name="cravat" label="Annotated (lightly filtered) VCF file" from_work_dir="varcalling.outdir/variants_initial_filtering_clean_snp_RNAedit.vcf_snpeff_updated.vcf.gz"/> + </outputs> + <tests> + <test> + <param name="left" value="reads_1.fastq.gz"/> + <param name="right" value="reads_2.fastq.gz"/> + <param name="tissue_type" value="Other"/> + <output name="cancertab" file="varcalling.outdir/cancer.tab" /> + <output name="cancerVariants" file="varcalling.outdir/cancer.vcf" /> + <output name="allVariants" file="varcalling.outdir/variants.vcf" /> + <output name="bamfile" file="varcalling.outdir/misc/recalibrated.bam" /> + <output name="cravat" file="varcalling.outdir/variants_initial_filtering_clean_snp_RNAedit.vcf_snpeff_updated.vcf.gz"/> + </test> + </tests> + <help> + +.. class:: warningmark + +Mutation detection in RNA-Seq highlights the GATK Best Practices in RNA-Seq variant calling, several sources of variant annotation, and filtering based on CRAVAT. + + </help> + <citations> + </citations> +</tool>