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pipelines_germline_wgs.cwl
APipe Tester edited this page Jul 28, 2021
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wgs alignment and germline variant detection
| Name | Label | Description | Type | Secondary Files |
|---|---|---|---|---|
| reference | ['string', 'File'] | ['.fai', '^.dict', '.amb', '.ann', '.bwt', '.pac', '.sa'] | ||
| sequence | sequence: sequencing data and readgroup information | sequence represents the sequencing data as either FASTQs or BAMs with accompanying readgroup information. Note that in the @RG field ID and SM are required. | ../types/sequence_data.yml#sequence_data[] | |
| trimming | ['../types/trimming_options.yml#trimming_options', 'null'] | |||
| omni_vcf | File | ['.tbi'] | ||
| picard_metric_accumulation_level | string | |||
| gvcf_gq_bands | string[] | |||
| intervals | {'type': 'array', 'items': {'type': 'array', 'items': 'string'}} | |||
| ploidy | int? | |||
| qc_intervals | File | |||
| variant_reporting_intervals | File | |||
| vep_cache_dir | ['string', 'Directory'] | |||
| vep_ensembl_assembly | genome assembly to use in vep. Examples: GRCh38 or GRCm38 | string | ||
| vep_ensembl_version | ensembl version - Must be present in the cache directory. Example: 95 | string | ||
| vep_ensembl_species | ensembl species - Must be present in the cache directory. Examples: homo_sapiens or mus_musculus | string | ||
| vep_plugins | array of plugins to use when running vep | string[]? | ||
| synonyms_file | File? | |||
| annotate_coding_only | boolean? | |||
| bqsr_known_sites | One or more databases of known polymorphic sites used to exclude regions around known polymorphisms from analysis. | File[] | ['.tbi'] | |
| bqsr_intervals | string[]? | |||
| minimum_mapping_quality | int? | |||
| minimum_base_quality | int? | |||
| per_base_intervals | ../types/labelled_file.yml#labelled_file[] | |||
| per_target_intervals | ../types/labelled_file.yml#labelled_file[] | |||
| summary_intervals | ../types/labelled_file.yml#labelled_file[] | |||
| vep_custom_annotations | custom type, check types directory for input format | ../types/vep_custom_annotation.yml#vep_custom_annotation[] | ||
| cnvkit_diagram | boolean? | |||
| cnvkit_drop_low_coverage | boolean? | |||
| cnvkit_method | ['null', {'type': 'enum', 'symbols': ['hybrid', 'amplicon', 'wgs']}] | |||
| cnvkit_reference_cnn | File? | |||
| cnvkit_scatter_plot | boolean? | |||
| cnvkit_male_reference | boolean? | |||
| cnvkit_vcf_name | string? | |||
| manta_call_regions | File? | ['.tbi'] | ||
| manta_non_wgs | boolean? | |||
| manta_output_contigs | boolean? | |||
| smoove_exclude_regions | File? | |||
| merge_max_distance | int | |||
| merge_min_svs | int | |||
| merge_same_type | boolean | |||
| merge_same_strand | boolean | |||
| merge_estimate_sv_distance | boolean | |||
| merge_min_sv_size | int | |||
| sv_filter_alt_abundance_percentage | double? | |||
| sv_filter_paired_count | int? | |||
| sv_filter_split_count | int? | |||
| cnv_filter_deletion_depth | double? | |||
| cnv_filter_duplication_depth | double? | |||
| variants_to_table_fields | string[]? | |||
| variants_to_table_genotype_fields | string[]? | |||
| vep_to_table_fields | string[]? | |||
| cnv_filter_min_size | int? | |||
| blocklist_bedpe | File? | |||
| disclaimer_text | string? |
| Name | Label | Description | Type | Secondary Files |
|---|---|---|---|---|
| cram | File | |||
| mark_duplicates_metrics | File | |||
| insert_size_metrics | File | |||
| insert_size_histogram | File | |||
| alignment_summary_metrics | File | |||
| gc_bias_metrics | File | |||
| gc_bias_metrics_chart | File | |||
| gc_bias_metrics_summary | File | |||
| wgs_metrics | File | |||
| flagstats | File | |||
| verify_bam_id_metrics | File | |||
| verify_bam_id_depth | File | |||
| raw_vcf | File | ['.tbi'] | ||
| final_vcf | File | ['.tbi'] | ||
| filtered_vcf | File | ['.tbi'] | ||
| vep_summary | File | |||
| per_base_coverage_metrics | File[] | |||
| per_base_hs_metrics | File[] | |||
| per_target_coverage_metrics | File[] | |||
| per_target_hs_metrics | File[] | |||
| summary_hs_metrics | File[] | |||
| cn_diagram | File? | |||
| cn_scatter_plot | File? | |||
| tumor_antitarget_coverage | File | |||
| tumor_target_coverage | File | |||
| tumor_bin_level_ratios | File | |||
| tumor_segmented_ratios | File | |||
| cnvkit_vcf | File | |||
| cnvnator_cn_file | File | |||
| cnvnator_root | File | |||
| cnvnator_vcf | File | |||
| manta_diploid_variants | File? | |||
| manta_somatic_variants | File? | |||
| manta_all_candidates | File | |||
| manta_small_candidates | File | |||
| manta_tumor_only_variants | File? | |||
| smoove_output_variants | File | |||
| final_tsv | File | |||
| filtered_tsv | File | |||
| cnvkit_filtered_vcf | File | |||
| cnvnator_filtered_vcf | File | |||
| manta_filtered_vcf | File | |||
| smoove_filtered_vcf | File | |||
| survivor_merged_vcf | File | |||
| survivor_merged_annotated_tsv | File | |||
| bcftools_merged_vcf | File | |||
| bcftools_merged_annotated_tsv | File | |||
| bcftools_merged_filtered_annotated_tsv | File |
| Name | CWL Run |
|---|---|
| alignment_and_qc | pipelines/alignment_wgs.cwl |
| extract_freemix | |
| detect_variants | subworkflows/germline_detect_variants.cwl |
| add_disclaimer_filtered_vcf | tools/add_string_at_line_bgzipped.cwl |
| index_disclaimer_filtered_vcf | tools/index_vcf.cwl |
| add_disclaimer_final_vcf | tools/add_string_at_line_bgzipped.cwl |
| index_disclaimer_final_vcf | tools/index_vcf.cwl |
| add_disclaimer_filtered_tsv | tools/add_string_at_line.cwl |
| add_disclaimer_final_tsv | tools/add_string_at_line.cwl |
| sv_detect_variants | subworkflows/single_sample_sv_callers.cwl |
| add_disclaimer_survivor_sv_vcf | tools/add_string_at_line_bgzipped.cwl |
| add_disclaimer_bcftools_sv_vcf | tools/add_string_at_line_bgzipped.cwl |
| add_disclaimer_survivor_sv_tsv | tools/add_string_at_line.cwl |
| add_disclaimer_bcftools_sv_tsv | tools/add_string_at_line.cwl |
| add_disclaimer_bcftools_filtered_sv_tsv | tools/add_string_at_line.cwl |
| bam_to_cram | tools/bam_to_cram.cwl |
| index_cram | tools/index_cram.cwl |