Workflow: Immunotherapy Workflow

Fetched 2023-01-04 21:16:59 GMT
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Inputs

ID Type Title Doc
mills File
strand
refFlat File
docm_vcf File
expn_val Float (Optional)
omni_vcf File
rna_bams File[]
tdna_cov Integer (Optional)
tdna_vaf Float (Optional)
trna_cov Integer (Optional)
trna_vaf Float (Optional)
vep_pick
dbsnp_vcf File
reference String
cosmic_vcf File (Optional)
fasta_size Integer (Optional)
normal_cov Integer (Optional)
normal_vaf Float (Optional)
tumor_name String (Optional)
exclude_nas Boolean (Optional)
netmhc_stab Boolean (Optional)
normal_name String (Optional)
sample_name String
known_indels File
somalier_vcf File
gvcf_gq_bands String[]
interval_list File
manta_non_wgs Boolean (Optional)
optitype_name String (Optional)
synonyms_file File (Optional)
vep_cache_dir String
bait_intervals File
bqsr_intervals String[]
cle_vcf_filter Boolean
kallisto_index File
reference_dict File
rna_readgroups String[]
tumor_sequence https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/sequence_data.yml#sequence_data[]
epitope_lengths Integer[] (Optional)
net_chop_method
normal_sequence https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/sequence_data.yml#sequence_data[]
pvacseq_threads Integer (Optional)
reference_index File
varscan_p_value Float (Optional)
target_intervals File
top_score_metric
binding_threshold Integer (Optional)
custom_gnomad_vcf File (Optional)
read_group_fields fae9a8bff1795302954eb94e27d9c959[]
summary_intervals https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/labelled_file.yml#labelled_file[]
trimming_adapters File
custom_clinvar_vcf File (Optional)
manta_call_regions File (Optional)
net_chop_threshold Float (Optional)
per_base_intervals https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/labelled_file.yml#labelled_file[]
pindel_insert_size Integer
minimum_fold_change Float (Optional)
ribosomal_intervals File
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[]
annotate_coding_only Boolean (Optional)
filter_docm_variants Boolean (Optional)
manta_output_contigs Boolean (Optional)
mutect_scatter_count Integer
panel_of_normals_vcf File (Optional)
per_target_intervals https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/types/labelled_file.yml#labelled_file[]
reference_annotation File
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

prediction_algorithms String[]
trimming_max_uncalled Integer
varscan_strand_filter Integer (Optional)
peptide_sequence_length Integer (Optional)
qc_minimum_base_quality Integer (Optional)
reference_transcriptome File
trimming_min_readlength Integer
varscan_max_normal_freq Float (Optional)
immuno_tumor_sample_name String
variants_to_table_fields String[]
additional_report_columns
emit_reference_confidence String
immuno_normal_sample_name String
trimming_adapter_trim_end String
downstream_sequence_length String (Optional)
qc_minimum_mapping_quality Integer (Optional)
gene_transcript_lookup_table File
phased_proximal_variants_vcf File (Optional)
trimming_adapter_min_overlap Integer
gatk_haplotypecaller_intervals 7b52c4e333f21d1b46580f69b5c4f6c9[]
mutect_artifact_detection_mode Boolean
readcount_minimum_base_quality Integer (Optional)
maximum_transcript_support_level
picard_metric_accumulation_level String
readcount_minimum_mapping_quality Integer (Optional)
variants_to_table_genotype_fields String[]
allele_specific_binding_thresholds Boolean (Optional)
mutect_max_alt_alleles_in_normal_count Integer (Optional)
mutect_max_alt_allele_in_normal_fraction Float (Optional)

Steps

ID Runs Label Doc
rnaseq
rnaseq.cwl (Workflow)
RNA-Seq alignment and transcript/gene abundance workflow
pvacseq Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
somatic
somatic_exome.cwl (Workflow)
exome alignment and somatic variant detection
germline exome alignment and germline variant detection, with optitype for HLA typing
phase_vcf phase VCF
extract_alleles
../tools/extract_hla_alleles.cwl (CommandLineTool)
index_renamed_somatic
../tools/index_vcf.cwl (CommandLineTool)
vcf index
rename_somatic_vcf_tumor_sample
../tools/replace_vcf_sample_name.cwl (CommandLineTool)
rename_somatic_vcf_normal_sample
../tools/replace_vcf_sample_name.cwl (CommandLineTool)

Outputs

ID Type Label Doc
cram File
gvcf File[]
chart File
metrics File
final_bam File
final_tsv File
flagstats File
cn_diagram File (Optional)
coding_vcf File
hs_metrics File
phased_vcf File
tumor_cram File
limited_vcf File
normal_cram File
optitype_tsv File
allele_string String[]
annotated_tsv File
annotated_vcf File
optitype_plot File
all_candidates File
gene_abundance File
cn_scatter_plot File (Optional)
fusion_evidence File
tumor_flagstats File
diploid_variants File (Optional)
intervals_target File (Optional)
normal_flagstats File
small_candidates File
somatic_variants File (Optional)
tumor_hs_metrics File
docm_filtered_vcf File
normal_hs_metrics File
somatic_final_vcf File
final_filtered_vcf File
final_fusion_calls File
germline_final_vcf File
mhc_i_all_epitopes File (Optional)
reference_coverage File (Optional)
summary_hs_metrics File[]
insert_size_metrics File
mhc_ii_all_epitopes File (Optional)
mutect_filtered_vcf File
per_base_hs_metrics File[]
pindel_filtered_vcf File
somatic_vep_summary File
tumor_only_variants File (Optional)
verify_bam_id_depth File
filtered_fusion_seqs File
germline_vep_summary File
intervals_antitarget File (Optional)
strelka_filtered_vcf File
varscan_filtered_vcf File
combined_all_epitopes File (Optional)
filtered_fusions_json File
insert_size_histogram File
mhc_i_ranked_epitopes File (Optional)
mutect_unfiltered_vcf File
per_target_hs_metrics File[]
pindel_unfiltered_vcf File
tumor_target_coverage File
verify_bam_id_metrics File
mhc_ii_ranked_epitopes File (Optional)
normal_target_coverage File
strelka_unfiltered_vcf File
tumor_bin_level_ratios File
tumor_segmented_ratios File
unfiltered_fusion_seqs File
varscan_unfiltered_vcf File
mark_duplicates_metrics File
mhc_i_filtered_epitopes File (Optional)
transcript_abundance_h5 File
unfiltered_fusions_json File
combined_ranked_epitopes File (Optional)
mhc_ii_filtered_epitopes File (Optional)
stringtie_transcript_gtf File
transcript_abundance_tsv File
tumor_summary_hs_metrics File[]
alignment_summary_metrics File
normal_summary_hs_metrics File[]
per_base_coverage_metrics File[]
tumor_antitarget_coverage File
tumor_insert_size_metrics File
tumor_per_base_hs_metrics File[]
tumor_verify_bam_id_depth File
combined_filtered_epitopes File (Optional)
normal_antitarget_coverage File
normal_insert_size_metrics File
normal_per_base_hs_metrics File[]
normal_verify_bam_id_depth File
per_target_coverage_metrics File[]
tumor_per_target_hs_metrics File[]
tumor_snv_bam_readcount_tsv File
tumor_verify_bam_id_metrics File
normal_per_target_hs_metrics File[]
normal_snv_bam_readcount_tsv File
normal_verify_bam_id_metrics File
somalier_concordance_metrics File
stringtie_gene_expression_tsv File
tumor_indel_bam_readcount_tsv File
tumor_mark_duplicates_metrics File
normal_indel_bam_readcount_tsv File
normal_mark_duplicates_metrics File
somalier_concordance_statistics File
tumor_alignment_summary_metrics File
tumor_per_base_coverage_metrics File[]
normal_alignment_summary_metrics File
normal_per_base_coverage_metrics File[]
tumor_per_target_coverage_metrics File[]
normal_per_target_coverage_metrics File[]
Permalink: https://w3id.org/cwl/view/git/e56f1024306aeb427d8aae2fff715ed2e8b8f86f/definitions/pipelines/immuno.cwl