Workflow: Detect Variants workflow for nonhuman WGS pipeline
Fetched 2024-11-25 12:16:31 GMT
Verified with cwltool version 3.1.20230201224320
- Selected
- |
- Default Values
- Nested Workflows
- Tools
- Inputs/Outputs
Inputs
| ID | Type | Title | Doc |
|---|---|---|---|
| vep_pick | |||
| reference | File | ||
| tumor_bam | File | ||
| normal_bam | File | ||
| vep_plugins | String[] (Optional) | ||
| roi_intervals | File | ||
| scatter_count | Integer (Optional) |
scatters each supported variant detector (varscan, mutect) into this many parallel jobs |
|
| synonyms_file | File (Optional) | ||
| vep_cache_dir | Directory | ||
| cle_vcf_filter | Boolean (Optional) | ||
| varscan_p_value | Float (Optional) | ||
| tumor_sample_name | String | ||
| normal_sample_name | String | ||
| strelka_exome_mode | Boolean | ||
| vep_ensembl_species | String |
ensembl species - Must be present in the cache directory. Examples: homo_sapiens or mus_musculus |
|
| vep_ensembl_version | String |
ensembl version - Must be present in the cache directory. Example: 95 |
|
| vep_to_table_fields | String[] (Optional) | ||
| annotate_coding_only | Boolean (Optional) | ||
| filter_minimum_depth | Integer (Optional) | ||
| strelka_cpu_reserved | Integer (Optional) | ||
| varscan_min_coverage | Integer (Optional) | ||
| varscan_min_var_freq | Float (Optional) | ||
| vep_ensembl_assembly | String |
genome assembly to use in vep. Examples: GRCh38 or GRCm38 |
|
| varscan_strand_filter | Integer (Optional) | ||
| filter_mapq0_threshold | Float (Optional) | ||
| varscan_max_normal_freq | Float (Optional) | ||
| variants_to_table_fields | String[] (Optional) | ||
| filter_somatic_llr_threshold | Float |
Sets the stringency (log-likelihood ratio) used to filter out non-somatic variants. Typical values are 10=high stringency, 5=normal, 3=low stringency. Low stringency may be desirable when read depths are low (as in WGS) or when tumor samples are impure. |
|
| readcount_minimum_base_quality | Integer (Optional) | ||
| filter_somatic_llr_tumor_purity | Float |
Sets the purity of the tumor used in the somatic llr filter, used to remove non-somatic variants. Probably only needs to be adjusted for low-purity (< 50%). Range is 0 to 1 |
|
| readcount_minimum_mapping_quality | Integer (Optional) | ||
| variants_to_table_genotype_fields | String[] (Optional) | ||
| filter_somatic_llr_normal_contamination_rate | Float |
Sets the fraction of tumor present in the normal sample (range 0 to 1), used in the somatic llr filter. Useful for heavily contaminated adjacent normals. Range is 0 to 1 |
Steps
| ID | Runs | Label | Doc |
|---|---|---|---|
| index |
../tools/index_vcf.cwl
(CommandLineTool)
|
vcf index | |
| mutect |
../subworkflows/mutect.cwl
(Workflow)
|
mutect parallel workflow | |
| combine |
../tools/combine_variants_wgs.cwl
(CommandLineTool)
|
CombineVariants (GATK 3.6) | |
| strelka | strelka workflow | ||
| varscan | Varscan Workflow | ||
| decompose |
../tools/vt_decompose.cwl
(CommandLineTool)
|
run vt decompose | |
| filter_vcf |
../subworkflows/filter_vcf_nonhuman.cwl
(Workflow)
|
Apply filters to VCF file | |
| decompose_index |
../tools/index_vcf.cwl
(CommandLineTool)
|
vcf index | |
| annotate_variants |
../tools/vep.cwl
(CommandLineTool)
|
Ensembl Variant Effect Predictor | |
| variants_to_table |
../tools/variants_to_table.cwl
(CommandLineTool)
|
SelectVariants (GATK 4.1.8.1) | |
| tumor_bam_readcount |
../tools/bam_readcount.cwl
(CommandLineTool)
|
run bam-readcount | |
| normal_bam_readcount |
../tools/bam_readcount.cwl
(CommandLineTool)
|
run bam-readcount | |
| annotated_filter_bgzip |
../tools/bgzip.cwl
(CommandLineTool)
|
bgzip VCF | |
| annotated_filter_index |
../tools/index_vcf.cwl
(CommandLineTool)
|
vcf index | |
| add_vep_fields_to_table |
../tools/add_vep_fields_to_table.cwl
(CommandLineTool)
|
add VEP annotation to report | |
| add_tumor_bam_readcount_to_vcf |
../subworkflows/vcf_readcount_annotator.cwl
(Workflow)
|
Add snv and indel bam-readcount files to a vcf | |
| add_normal_bam_readcount_to_vcf |
../subworkflows/vcf_readcount_annotator.cwl
(Workflow)
|
Add snv and indel bam-readcount files to a vcf |
Outputs
| ID | Type | Label | Doc |
|---|---|---|---|
| final_tsv | File | ||
| final_vcf | File | ||
| vep_summary | File | ||
| final_filtered_vcf | File | ||
| mutect_filtered_vcf | File | ||
| strelka_filtered_vcf | File | ||
| varscan_filtered_vcf | File | ||
| mutect_unfiltered_vcf | File | ||
| strelka_unfiltered_vcf | File | ||
| varscan_unfiltered_vcf | File | ||
| tumor_snv_bam_readcount_tsv | File | ||
| normal_snv_bam_readcount_tsv | File | ||
| tumor_indel_bam_readcount_tsv | File | ||
| normal_indel_bam_readcount_tsv | File |
https://w3id.org/cwl/view/git/bfcb5ffbea3d00a38cc03595d41e53ea976d599d/definitions/pipelines/detect_variants_wgs_nonhuman.cwl
