Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
---|---|---|---|
|
Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
|
![]() Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 480c438a6a7e78c624712aec01bc4214d2bc179c |
|
|
exome alignment and tumor-only variant detection
|
![]() Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 844c10a4466ab39c02e5bfa7a210c195b8efa77a |
|
|
kmer_build_tree
|
![]() Path: task_types/tt_kmer_build_tree.cwl Branch/Commit ID: f6950321e5c9ee733ad68a273d2ad8e802a6b982 |
|
|
exome_metrics.cwl
|
![]() Path: workflows/bamfastq_align/exome_metrics.cwl Branch/Commit ID: b110a23e2efaaadfd4feca4f9e130946d1c5418d |
|
|
BD Rhapsody™ Targeted Analysis Pipeline
The BD Rhapsody™ assays are used to create sequencing libraries from single cell transcriptomes. After sequencing, the analysis pipeline takes the FASTQ files and a reference file for gene alignment. The pipeline generates molecular counts per cell, read counts per cell, metrics, and an alignment file. |
![]() Path: v1.8/rhapsody_targeted_1.8.cwl Branch/Commit ID: b9ec66d82bc04934fbe9f9088ae7e802d72c4a4e Packed ID: main |
|
|
Merge, annotate, and generate a TSV for SVs
|
![]() Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: e56f1024306aeb427d8aae2fff715ed2e8b8f86f |
|
|
bact_get_kmer_reference
|
![]() Path: task_types/tt_bact_get_kmer_reference.cwl Branch/Commit ID: 3897218b16b30a933beecd60a98a300d677207d8 |
|
|
tt_kmer_compare_wnode
|
![]() Path: task_types/tt_kmer_compare_wnode.cwl Branch/Commit ID: b12ec8c8e832151033b9e6c0a76a3c3df18d45da |
|
|
bact_get_kmer_reference
|
![]() Path: task_types/tt_bact_get_kmer_reference.cwl Branch/Commit ID: bb2f26dfe630179737ec2ff08a8614f1f47abcaf |
|
|
align_sort_sa
|
![]() Path: task_types/tt_align_sort_sa.cwl Branch/Commit ID: f18c1dce463509170ee3bf2844d5a3637ff706f5 |