subworkflows_varscan_germline.cwl - genome/analysis-workflows GitHub Wiki
Documentation for varscan_germline.cwl
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Overview
Varscan Workflow
Inputs
Name |
Label |
Description |
Type |
Secondary Files |
reference |
|
|
['string', 'File'] |
['.fai', '^.dict'] |
bam |
|
|
File |
['.bai', '^.bai'] |
interval_list |
|
|
File |
|
strand_filter |
|
|
int? |
|
min_coverage |
|
|
int? |
|
min_var_freq |
|
|
float? |
|
min_reads |
|
|
int? |
|
p_value |
|
|
float? |
|
max_normal_freq |
|
|
float? |
|
sample_name |
|
|
string |
|
Outputs
Name |
Label |
Description |
Type |
Secondary Files |
unfiltered_vcf |
|
|
File |
['.tbi'] |
filtered_vcf |
|
|
File |
['.tbi'] |
Steps