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pipelines_tumor_only_detect_variants.cwl
Travis CI User edited this page Feb 3, 2020
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Tumor-Only Detect Variants workflow
Name | Label | Description | Type | Secondary Files |
---|---|---|---|---|
reference | ['string', 'File'] | ['.fai', '^.dict'] | ||
bam | File | ['^.bai', '.bai'] | ||
interval_list | File | |||
varscan_strand_filter | int? | |||
varscan_min_coverage | int? | |||
varscan_min_var_freq | float? | |||
varscan_p_value | float? | |||
varscan_min_reads | int? | |||
maximum_population_allele_frequency | float? | |||
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 | ||
synonyms_file | File? | |||
annotate_coding_only | boolean | |||
vep_pick | ['null', {'type': 'enum', 'symbols': ['pick', 'flag_pick', 'pick_allele', 'per_gene', 'pick_allele_gene', 'flag_pick_allele', 'flag_pick_allele_gene']}] | |||
variants_to_table_fields | string[] | |||
variants_to_table_genotype_fields | string[] | |||
vep_to_table_fields | string[] | |||
vep_plugins | string[] | |||
sample_name | string | |||
docm_vcf | File | ['.tbi'] | ||
vep_custom_annotations | custom type, check types directory for input format | ../types/vep_custom_annotation.yml#vep_custom_annotation[] | ||
readcount_minimum_mapping_quality | int? | |||
readcount_minimum_base_quality | int? |
Name | Label | Description | Type | Secondary Files |
---|---|---|---|---|
varscan_vcf | File | ['.tbi'] | ||
docm_gatk_vcf | File | |||
annotated_vcf | File | ['.tbi'] | ||
final_vcf | File | ['.tbi'] | ||
final_tsv | File | |||
vep_summary | File | |||
tumor_snv_bam_readcount_tsv | File | |||
tumor_indel_bam_readcount_tsv | File |
Name | CWL Run |
---|---|
varscan | subworkflows/varscan_germline.cwl |
docm | subworkflows/docm_germline.cwl |
combine_variants | tools/germline_combine_variants.cwl |
decompose | tools/vt_decompose.cwl |
annotate_variants | tools/vep.cwl |
bam_readcount | tools/bam_readcount.cwl |
add_bam_readcount_to_vcf | subworkflows/vcf_readcount_annotator.cwl |
index | tools/index_vcf.cwl |
hard_filter | tools/select_variants.cwl |
af_filter | tools/filter_vcf_custom_allele_freq.cwl |
coding_variant_filter | tools/filter_vcf_coding_variant.cwl |
bgzip_filtered | tools/bgzip.cwl |
index_filtered | tools/index_vcf.cwl |
variants_to_table | tools/variants_to_table.cwl |
add_vep_fields_to_table | tools/add_vep_fields_to_table.cwl |