Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
---|---|---|---|
|
FASTQ to BQSR
|
![]() Path: definitions/subworkflows/fastq_to_bqsr.cwl Branch/Commit ID: 038cb3617a1966a1057386adcde97ce55d9e1139 |
|
|
Unaligned bam to sorted, markduped bam
|
![]() Path: definitions/subworkflows/align_sort_markdup.cwl Branch/Commit ID: 038cb3617a1966a1057386adcde97ce55d9e1139 |
|
|
cache_test_workflow.cwl
|
![]() Path: tests/wf/cache_test_workflow.cwl Branch/Commit ID: e4a52682f3bdefafe5c27e32983fed31116ac489 |
|
|
Detect Variants workflow
|
![]() Path: definitions/pipelines/detect_variants_mouse.cwl Branch/Commit ID: 74647cc0f1abac4ee22950cfa89c44cf2ca3cffd |
|
|
count-lines10-wf.cwl
|
![]() Path: v1.0/v1.0/count-lines10-wf.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b |
|
|
1st-workflow.cwl
|
![]() Path: tests/wf/1st-workflow.cwl Branch/Commit ID: 2a922ab11b2f9c21ae4955c74563543b87717b93 |
|
|
Subworkflow to allow calling different SV callers which require bam files as inputs
|
![]() Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: 038cb3617a1966a1057386adcde97ce55d9e1139 |
|
|
gatk4W.cwl
Author: AMBARISH KUMAR er.ambarish@gmail.com & ambari73_sit@jnu.ac.in This is a proposed standard operating procedure for genomic variant detection using GATK4. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
![]() Path: gatk4W.cwl Branch/Commit ID: fcab170f3e8a4bc70601650401cce2a9df42f484 |
|
|
bam2fasta.cwl
|
![]() Path: cwl/fastq2fasta/bam2fasta.cwl Branch/Commit ID: 24465ba219711f2828e633d25d9f183e0f0eaccd |
|
|
exome alignment and germline variant detection, with optitype for HLA typing
|
![]() Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: 3b6d0475c80f5e452793a46a38ee188742b86595 |