Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
exome alignment with qc
|
Path: definitions/pipelines/exome_alignment.cwl Branch/Commit ID: No_filters_detect_variants |
|
|
|
main-somatic.cwl
|
Path: somatic/somatic-workflow/main-somatic.cwl Branch/Commit ID: master |
|
|
|
wf_get_peaks_scatter_se_nostats.cwl
The \"main\" workflow. Takes fastq files generated using the seCLIP protocol (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991800/) and outputs candidate RBP binding regions (peaks). runs: wf_get_peaks_se.cwl through scatter across multiple samples. |
Path: cwl/wf_get_peaks_scatter_se_nostats.cwl Branch/Commit ID: master |
|
|
|
filtering.cwl
|
Path: workflows/subworkflows/filtering.cwl Branch/Commit ID: master |
|
|
|
wgs alignment and somatic variant detection
|
Path: definitions/pipelines/somatic_wgs_nonhuman.cwl Branch/Commit ID: master |
|
|
|
epigenome-chip-seq.packed.cwl#macs2.cwl
|
Path: workflow/epigenome-chip-seq/epigenome-chip-seq.packed.cwl Branch/Commit ID: main Packed ID: macs2.cwl |
|
|
|
scatter-valuefrom-wf2.cwl
|
Path: tests/scatter-valuefrom-wf2.cwl Branch/Commit ID: main |
|
|
|
wf-variantcall.cwl
|
Path: wes-agha-test/wes_chr21_test-workflow-gcp/wf-variantcall.cwl Branch/Commit ID: master |
|
|
|
wf_demultiplex_se.cwl
This workflow takes in single-end reads, and performs the following steps in order: demux_se.cwl (does not actually demux for single end, but mirrors the paired-end processing protocol) |
Path: cwl/wf_demultiplex_se.cwl Branch/Commit ID: master |
|
|
|
msi.cwl
|
Path: workflows/subworkflows/msi.cwl Branch/Commit ID: master |
