Workflow: wgs alignment and germline variant detection

Fetched 2023-01-11 11:01:11 GMT
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Inputs

ID Type Title Doc
ploidy Integer (Optional)
omni_vcf File
sequence https://w3id.org/cwl/view/git/87faba2fff8007ecc95160729b1c7cd0376e46f2/definitions/types/sequence_data.yml#sequence_data[] 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.

trimming https://w3id.org/cwl/view/git/87faba2fff8007ecc95160729b1c7cd0376e46f2/definitions/types/trimming_options.yml#trimming_options (Optional)
intervals c4e7364b5433a0c4b16888dfda08e30d[]
reference File
vep_plugins String[] (Optional)

array of plugins to use when running vep

qc_intervals File
cnvkit_method
gvcf_gq_bands String[]
manta_non_wgs Boolean (Optional)
merge_min_svs Integer
synonyms_file File (Optional)
vep_cache_dir Directory
bqsr_intervals String[] (Optional)
cnvkit_diagram Boolean (Optional)
blocklist_bedpe File (Optional)
cnvkit_vcf_name String (Optional)
disclaimer_text String (Optional)
merge_same_type Boolean
bqsr_known_sites File[]

One or more databases of known polymorphic sites used to exclude regions around known polymorphisms from analysis.

merge_min_sv_size Integer
merge_same_strand Boolean
summary_intervals https://w3id.org/cwl/view/git/87faba2fff8007ecc95160729b1c7cd0376e46f2/definitions/types/labelled_file.yml#labelled_file[]
manta_call_regions File (Optional)
merge_max_distance Integer
per_base_intervals https://w3id.org/cwl/view/git/87faba2fff8007ecc95160729b1c7cd0376e46f2/definitions/types/labelled_file.yml#labelled_file[]
cnv_filter_min_size Integer (Optional)
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 (Optional)
manta_output_contigs Boolean (Optional)
minimum_base_quality Integer (Optional)
per_target_intervals https://w3id.org/cwl/view/git/87faba2fff8007ecc95160729b1c7cd0376e46f2/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)
vep_custom_annotations https://w3id.org/cwl/view/git/87faba2fff8007ecc95160729b1c7cd0376e46f2/definitions/types/vep_custom_annotation.yml#vep_custom_annotation[]

custom type, check types directory for input format

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
merge_estimate_sv_distance Boolean
variant_reporting_intervals File
cnv_filter_duplication_depth Double (Optional)
picard_metric_accumulation_level String
variants_to_table_genotype_fields String[] (Optional)
sv_filter_alt_abundance_percentage Double (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 exome alignment and germline variant detection
extract_freemix
germline_wgs.cwl#extract_freemix/b1907029-9414-446b-8d1c-31396490983e (ExpressionTool)
alignment_and_qc
alignment_wgs.cwl (Workflow)
wgs alignment with qc
sv_detect_variants Subworkflow to allow calling different SV callers which require bam files as inputs
add_disclaimer_final_tsv
../tools/add_string_at_line.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a file
add_disclaimer_final_vcf
../tools/add_string_at_line_bgzipped.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a gzipped file
index_disclaimer_final_vcf
../tools/index_vcf.cwl (CommandLineTool)
vcf index
add_disclaimer_filtered_tsv
../tools/add_string_at_line.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a file
add_disclaimer_filtered_vcf
../tools/add_string_at_line_bgzipped.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a gzipped file
index_disclaimer_filtered_vcf
../tools/index_vcf.cwl (CommandLineTool)
vcf index
add_disclaimer_bcftools_sv_tsv
../tools/add_string_at_line.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a file
add_disclaimer_bcftools_sv_vcf
../tools/add_string_at_line_bgzipped.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a gzipped file
add_disclaimer_survivor_sv_tsv
../tools/add_string_at_line.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a file
add_disclaimer_survivor_sv_vcf
../tools/add_string_at_line_bgzipped.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a gzipped file
add_disclaimer_bcftools_filtered_sv_tsv
../tools/add_string_at_line.cwl (CommandLineTool)
Insert an arbitrary string at a specific line of a file

Outputs

ID Type Label Doc
cram File
raw_vcf File
final_tsv File
final_vcf File
flagstats File
cn_diagram File (Optional)
cnvkit_vcf File
vep_summary File
wgs_metrics File
cnvnator_vcf File
filtered_tsv File
filtered_vcf File
cnvnator_root File
cn_scatter_plot File (Optional)
gc_bias_metrics File
cnvnator_cn_file File
manta_filtered_vcf File
summary_hs_metrics File[]
bcftools_merged_vcf File
cnvkit_filtered_vcf File
insert_size_metrics File
per_base_hs_metrics File[]
smoove_filtered_vcf File
survivor_merged_vcf File
verify_bam_id_depth File
manta_all_candidates File
cnvnator_filtered_vcf 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
alignment_summary_metrics File
manta_tumor_only_variants File (Optional)
per_base_coverage_metrics File[]
tumor_antitarget_coverage File
per_target_coverage_metrics File[]
bcftools_merged_annotated_tsv File
survivor_merged_annotated_tsv File
bcftools_merged_filtered_annotated_tsv File
Permalink: https://w3id.org/cwl/view/git/87faba2fff8007ecc95160729b1c7cd0376e46f2/definitions/pipelines/germline_wgs.cwl