Workflow: Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
- Selected
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- Default Values
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- 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 |
---|---|---|---|
alleles | String[] | ||
expn_val | Float (Optional) | ||
tdna_cov | Integer (Optional) | ||
tdna_vaf | Float (Optional) | ||
trna_cov | Integer (Optional) | ||
trna_vaf | Float (Optional) | ||
n_threads | Integer (Optional) | ||
fasta_size | Integer (Optional) | ||
normal_cov | Integer (Optional) | ||
normal_vaf | Float (Optional) | ||
rnaseq_bam | File | ||
exclude_nas | Boolean (Optional) | ||
netmhc_stab | Boolean (Optional) | ||
sample_name | String (Optional) | ||
epitope_lengths | Integer[] (Optional) | ||
expression_tool | String (Optional) | ||
net_chop_method | |||
reference_fasta | File | ||
top_score_metric | |||
binding_threshold | Integer (Optional) | ||
net_chop_threshold | Float (Optional) | ||
normal_sample_name | String (Optional) | ||
detect_variants_vcf | File | ||
minimum_fold_change | Float (Optional) | ||
vep_to_table_fields | String[] (Optional) | ||
gene_expression_file | File | ||
prediction_algorithms | String[] | ||
peptide_sequence_length | Integer (Optional) | ||
variants_to_table_fields | String[] (Optional) | ||
additional_report_columns | |||
downstream_sequence_length | String (Optional) | ||
transcript_expression_file | File | ||
phased_proximal_variants_vcf | File (Optional) | ||
readcount_minimum_base_quality | Integer (Optional) | ||
maximum_transcript_support_level | |||
readcount_minimum_mapping_quality | Integer (Optional) | ||
variants_to_table_genotype_fields | String[] (Optional) | ||
allele_specific_binding_thresholds | Boolean (Optional) |
Steps
ID | Runs | Label | Doc |
---|---|---|---|
index |
../tools/index_vcf.cwl
(CommandLineTool)
|
vcf index | |
pvacseq |
../tools/pvacseq.cwl
(CommandLineTool)
|
run pVACseq | |
variants_to_table |
../tools/variants_to_table.cwl
(CommandLineTool)
|
SelectVariants (GATK 3.6) | |
add_vep_fields_to_table |
../tools/add_vep_fields_to_table.cwl
(CommandLineTool)
|
add VEP annotation to report | |
tumor_rna_bam_readcount |
bam_readcount.cwl
(Workflow)
|
bam_readcount workflow | |
add_gene_expression_data_to_vcf |
../tools/vcf_expression_annotator.cwl
(CommandLineTool)
|
add expression info to vcf | |
add_tumor_rna_bam_readcount_to_vcf |
vcf_readcount_annotator.cwl
(Workflow)
|
Add snv and indel bam-readcount files to a vcf | |
add_transcript_expression_data_to_vcf |
../tools/vcf_expression_annotator.cwl
(CommandLineTool)
|
add expression info to vcf |
Outputs
ID | Type | Label | Doc |
---|---|---|---|
annotated_tsv | File | ||
annotated_vcf | File | ||
pvacseq_predictions | Directory |
Permalink:
https://w3id.org/cwl/view/git/9143dc4ebacb9e1df36a712b0be6fa5d982b0c4f/definitions/subworkflows/pvacseq.cwl