Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
---|---|---|---|
|
step-valuefrom2-wf.cwl
|
![]() Path: v1.0/v1.0/step-valuefrom2-wf.cwl Branch/Commit ID: f24c797ea017a467185b516ea4862c9c494c9d33 |
|
|
Downsample and HaplotypeCaller
|
![]() Path: definitions/pipelines/downsample_and_recall.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |
|
|
bact_get_kmer_reference
|
![]() Path: task_types/tt_bact_get_kmer_reference.cwl Branch/Commit ID: 41dfc42a730087189122a2f74b2f547a4665a225 |
|
|
umi duplex alignment fastq workflow
|
![]() Path: definitions/pipelines/alignment_umi_duplex.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |
|
|
wgs alignment with qc
|
![]() Path: definitions/pipelines/alignment_wgs.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |
|
|
Running cellranger count and lineage inference
|
![]() Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: 27dcb1ae121be6a23057b74332b8c752ea425735 |
|
|
exome alignment and somatic variant detection for cle purpose
|
![]() Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |
|
|
Raw sequence data to BQSR
|
![]() Path: definitions/subworkflows/sequence_to_bqsr.cwl Branch/Commit ID: 27dcb1ae121be6a23057b74332b8c752ea425735 |
|
|
Immunotherapy Workflow
|
![]() Path: definitions/pipelines/immuno.cwl Branch/Commit ID: 8eb189a4a34dc8cd86380685f814c79a444a7601 |
|
|
Apply filters to VCF file
|
![]() Path: definitions/subworkflows/filter_vcf_mouse.cwl Branch/Commit ID: 27dcb1ae121be6a23057b74332b8c752ea425735 |