- Selected
 - |
 - Default Values
 - Nested Workflows
 - Tools
 - Inputs/Outputs
 
                This workflow is Open Source and may be reused according to the terms of:
                
                    MIT License
                
                
            
            Note that the tools invoked by the workflow may have separate licenses.
            Inputs
| ID | Type | Title | Doc | 
|---|---|---|---|
| mills | File | ||
| docm_vcf | File | ||
| omni_vcf | File | ||
| vep_pick | |||
| dbsnp_vcf | File | ||
| reference | String | ||
| cosmic_vcf | File (Optional) | ||
| tumor_bams | File[] | ||
| normal_bams | File[] | ||
| known_indels | File | ||
| interval_list | File | ||
| manta_non_wgs | Boolean (Optional) | ||
| synonyms_file | File (Optional) | ||
| vep_cache_dir | String | ||
| bait_intervals | File | ||
| bqsr_intervals | String[] | ||
| cle_vcf_filter | Boolean | ||
| tumor_cram_name | String (Optional) | ||
| varscan_p_value | Float (Optional) | ||
| normal_cram_name | String (Optional) | ||
| target_intervals | File | ||
| tumor_readgroups | String[] | ||
| custom_gnomad_vcf | File (Optional) | ||
| normal_readgroups | String[] | ||
| summary_intervals | https://w3id.org/cwl/view/git/68eda647259849ca81ac0bb07a24bc8a4465a630/definitions/types/labelled_file.yml#labelled_file[] | ||
| custom_clinvar_vcf | File (Optional) | ||
| manta_call_regions | File (Optional) | ||
| per_base_intervals | https://w3id.org/cwl/view/git/68eda647259849ca81ac0bb07a24bc8a4465a630/definitions/types/labelled_file.yml#labelled_file[] | ||
| pindel_insert_size | Integer | ||
| vep_to_table_fields | String[] | ||
| annotate_coding_only | Boolean (Optional) | ||
| manta_output_contigs | Boolean (Optional) | ||
| mutect_scatter_count | Integer | ||
| panel_of_normals_vcf | File (Optional) | ||
| per_target_intervals | https://w3id.org/cwl/view/git/68eda647259849ca81ac0bb07a24bc8a4465a630/definitions/types/labelled_file.yml#labelled_file[] | ||
| strelka_cpu_reserved | Integer (Optional) | ||
| varscan_min_coverage | Integer (Optional) | ||
| varscan_min_var_freq | Float (Optional) | ||
| varscan_strand_filter | Integer (Optional) | ||
| qc_minimum_base_quality | Integer (Optional) | ||
| varscan_max_normal_freq | Float (Optional) | ||
| variants_to_table_fields | String[] | ||
| qc_minimum_mapping_quality | Integer (Optional) | ||
| mutect_artifact_detection_mode | Boolean | ||
| picard_metric_accumulation_level | String | ||
| variants_to_table_genotype_fields | String[] | ||
| mutect_max_alt_alleles_in_normal_count | Integer (Optional) | ||
| mutect_max_alt_allele_in_normal_fraction | Float (Optional) | 
Steps
| ID | Runs | Label | Doc | 
|---|---|---|---|
| manta | 
                                 
                                    
                                    ../tools/manta_somatic.cwl
                                    (CommandLineTool)
                                 
                                
                             | 
                            Set up and execute manta | |
| cnvkit | 
                                 
                                    ../subworkflows/cram_to_cnvkit.cwl
                                    
                                    (Workflow)
                                 
                                
                             | 
                            Subworkflow to allow calling cnvkit with cram instead of bam files | |
| detect_variants | 
                                 
                                    detect_variants.cwl
                                    
                                    (Workflow)
                                 
                                
                             | 
                            Detect Variants workflow | |
| tumor_alignment_and_qc | 
                                 
                                    exome_alignment.cwl
                                    
                                    (Workflow)
                                 
                                
                             | 
                            exome alignment with qc | |
| normal_alignment_and_qc | 
                                 
                                    exome_alignment.cwl
                                    
                                    (Workflow)
                                 
                                
                             | 
                            exome alignment with qc | 
Outputs
| ID | Type | Label | Doc | 
|---|---|---|---|
| final_tsv | File | ||
| final_vcf | File | ||
| cn_diagram | File (Optional) | ||
| tumor_cram | File | ||
| normal_cram | File | ||
| vep_summary | File | ||
| all_candidates | File | ||
| cn_scatter_plot | File (Optional) | ||
| tumor_flagstats | File | ||
| diploid_variants | File (Optional) | ||
| intervals_target | File (Optional) | ||
| normal_flagstats | File | ||
| small_candidates | File | ||
| somatic_variants | File (Optional) | ||
| tumor_hs_metrics | File | ||
| docm_filtered_vcf | File | ||
| normal_hs_metrics | File | ||
| final_filtered_vcf | File | ||
| reference_coverage | File (Optional) | ||
| docm_unfiltered_vcf | File | ||
| mutect_filtered_vcf | File | ||
| pindel_filtered_vcf | File | ||
| tumor_only_variants | File (Optional) | ||
| intervals_antitarget | File (Optional) | ||
| strelka_filtered_vcf | File | ||
| varscan_filtered_vcf | File | ||
| mutect_unfiltered_vcf | File | ||
| pindel_unfiltered_vcf | File | ||
| tumor_target_coverage | File | ||
| normal_target_coverage | File | ||
| strelka_unfiltered_vcf | File | ||
| tumor_bin_level_ratios | File | ||
| tumor_segmented_ratios | File | ||
| varscan_unfiltered_vcf | File | ||
| tumor_summary_hs_metrics | File[] | ||
| normal_summary_hs_metrics | File[] | ||
| tumor_antitarget_coverage | File | ||
| tumor_insert_size_metrics | File | ||
| tumor_per_base_hs_metrics | File[] | ||
| tumor_verify_bam_id_depth | File | ||
| normal_antitarget_coverage | File | ||
| normal_insert_size_metrics | File | ||
| normal_per_base_hs_metrics | File[] | ||
| normal_verify_bam_id_depth | File | ||
| tumor_per_target_hs_metrics | File[] | ||
| tumor_snv_bam_readcount_tsv | File | ||
| tumor_verify_bam_id_metrics | File | ||
| normal_per_target_hs_metrics | File[] | ||
| normal_snv_bam_readcount_tsv | File | ||
| normal_verify_bam_id_metrics | File | ||
| tumor_indel_bam_readcount_tsv | File | ||
| tumor_mark_duplicates_metrics | File | ||
| normal_indel_bam_readcount_tsv | File | ||
| normal_mark_duplicates_metrics | File | ||
| tumor_alignment_summary_metrics | File | ||
| tumor_per_base_coverage_metrics | File[] | ||
| normal_alignment_summary_metrics | File | ||
| normal_per_base_coverage_metrics | File[] | ||
| tumor_per_target_coverage_metrics | File[] | ||
| normal_per_target_coverage_metrics | File[] | 
      Permalink:
        
https://w3id.org/cwl/view/git/68eda647259849ca81ac0bb07a24bc8a4465a630/definitions/pipelines/somatic_exome.cwl
      
    