subworkflows_varscan.cwl - genome/analysis-workflows GitHub Wiki
Documentation for varscan.cwl
This page is auto-generated. Do not edit.
Overview
varscan somatic workflow
Inputs
Name |
Label |
Description |
Type |
Secondary Files |
reference |
|
|
['string', 'File'] |
['.fai', '^.dict'] |
tumor_bam |
|
|
File |
['^.bai'] |
normal_bam |
|
|
File |
['^.bai'] |
roi_bed |
|
|
File? |
|
strand_filter |
|
|
int? |
|
min_coverage |
|
|
int? |
|
min_var_freq |
|
|
float? |
|
p_value |
|
|
float? |
|
max_normal_freq |
|
|
float? |
|
Outputs
Name |
Label |
Description |
Type |
Secondary Files |
snvs |
|
|
File |
|
indels |
|
|
File |
|
somatic_hc_snvs |
|
|
File |
|
somatic_snvs |
|
|
File |
|
germline_hc_snvs |
|
|
File |
|
germline_snvs |
|
|
File |
|
loh_hc_snvs |
|
|
File |
|
loh_snvs |
|
|
File |
|
somatic_hc_indels |
|
|
File |
|
somatic_indels |
|
|
File |
|
germline_hc_indels |
|
|
File |
|
germline_indels |
|
|
File |
|
loh_hc_indels |
|
|
File |
|
loh_indels |
|
|
File |
|
Steps