Workflow: wgs alignment and germline variant detection
Fetched 2023-01-10 20:01:55 GMT
Verified with cwltool version 3.1.20221201130942
- 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 | ||
| omni_vcf | File | ||
| sequence | https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/sequence_data.yml#sequence_data[] | ||
| dbsnp_vcf | File | ||
| intervals | fd165d0c15801d066fd2e811dc4bbdbb[] | ||
| reference | String | ||
| vep_plugins | String[] (Optional) |
array of plugins to use when running vep |
|
| known_indels | File | ||
| qc_intervals | File | ||
| cnvkit_method | String (Optional) | ||
| gvcf_gq_bands | String[] | ||
| manta_non_wgs | Boolean (Optional) | ||
| merge_min_svs | Integer | ||
| synonyms_file | File (Optional) | ||
| vep_cache_dir | String | ||
| bqsr_intervals | String[] (Optional) | ||
| cnvkit_diagram | Boolean (Optional) | ||
| cnvkit_vcf_name | String (Optional) | ||
| merge_same_type | Boolean | ||
| custom_gnomad_vcf | File (Optional) | ||
| merge_min_sv_size | Integer | ||
| merge_same_strand | Boolean | ||
| summary_intervals | https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/labelled_file.yml#labelled_file[] | ||
| custom_clinvar_vcf | File (Optional) | ||
| manta_call_regions | File (Optional) | ||
| merge_max_distance | Integer | ||
| per_base_intervals | https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/labelled_file.yml#labelled_file[] | ||
| cnvkit_scatter_plot | Boolean (Optional) | ||
| 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) | ||
| cnvkit_reference_cnn | File | ||
| manta_output_contigs | Boolean (Optional) | ||
| minimum_base_quality | Integer (Optional) | ||
| per_target_intervals | https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/labelled_file.yml#labelled_file[] | ||
| vep_ensembl_assembly | String |
genome assembly to use in vep. Examples: GRCh38 or GRCm38 |
|
| cnvkit_male_reference | Boolean (Optional) | ||
| sv_filter_split_count | Integer (Optional) | ||
| smoove_exclude_regions | File (Optional) | ||
| sv_filter_paired_count | Integer (Optional) | ||
| minimum_mapping_quality | Integer (Optional) | ||
| cnvkit_drop_low_coverage | Boolean (Optional) | ||
| variants_to_table_fields | String[] (Optional) | ||
| cnv_filter_deletion_depth | Double (Optional) | ||
| emit_reference_confidence | String | ||
| merge_estimate_sv_distance | Boolean | ||
| sv_filter_split_percentage | Double (Optional) | ||
| sv_filter_paired_percentage | Double (Optional) | ||
| variant_reporting_intervals | File | ||
| cnv_filter_duplication_depth | Double (Optional) | ||
| picard_metric_accumulation_level | String | ||
| variants_to_table_genotype_fields | String[] (Optional) |
Steps
| ID | Runs | Label | Doc |
|---|---|---|---|
| index_cram |
../tools/index_cram.cwl
(CommandLineTool)
|
samtools index cram | |
| bam_to_cram |
../tools/bam_to_cram.cwl
(CommandLineTool)
|
BAM to CRAM conversion | |
| detect_variants |
../subworkflows/germline_detect_variants.cwl
(Workflow)
|
exome alignment and germline variant detection | |
| extract_freemix |
germline_wgs.cwl#extract_freemix/63d15a30-62d2-4c20-9ef1-e65051c424fc
(ExpressionTool)
|
||
| alignment_and_qc |
wgs_alignment.cwl
(Workflow)
|
wgs alignment with qc | |
| sv_detect_variants |
../subworkflows/single_sample_sv_callers.cwl
(Workflow)
|
Subworkflow to allow calling different SV callers which require bam files as inputs |
Outputs
| ID | Type | Label | Doc |
|---|---|---|---|
| cram | File | ||
| gvcf | File[] | ||
| final_tsv | File | ||
| final_vcf | File | ||
| flagstats | File | ||
| cn_diagram | File (Optional) | ||
| cnvkit_vcf | File | ||
| coding_vcf | File | ||
| limited_vcf | File | ||
| vep_summary | File | ||
| wgs_metrics | File | ||
| cnvnator_vcf | File | ||
| cnvnator_root | File | ||
| merged_sv_vcf | File | ||
| cn_scatter_plot | File (Optional) | ||
| gc_bias_metrics | File | ||
| cnvnator_cn_file | File | ||
| filtered_sv_vcfs | File[] | ||
| bamcoverage_bigwig | File | ||
| summary_hs_metrics | File[] | ||
| insert_size_metrics | File | ||
| per_base_hs_metrics | File[] | ||
| verify_bam_id_depth | File | ||
| manta_all_candidates | File | ||
| gc_bias_metrics_chart | File | ||
| insert_size_histogram | File | ||
| per_target_hs_metrics | File[] | ||
| tumor_target_coverage | File | ||
| verify_bam_id_metrics | File | ||
| manta_diploid_variants | File (Optional) | ||
| manta_small_candidates | File | ||
| manta_somatic_variants | File (Optional) | ||
| smoove_output_variants | File | ||
| tumor_bin_level_ratios | File | ||
| tumor_segmented_ratios | File | ||
| gc_bias_metrics_summary | File | ||
| mark_duplicates_metrics | File | ||
| merged_annotated_sv_tsvs | File | ||
| alignment_summary_metrics | File | ||
| manta_tumor_only_variants | File (Optional) | ||
| per_base_coverage_metrics | File[] | ||
| tumor_antitarget_coverage | File | ||
| per_target_coverage_metrics | File[] |
Permalink:
https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/pipelines/germline_wgs.cwl
