Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
---|---|---|---|
|
exome alignment with qc, no bqsr, no verify_bam_id
|
![]() Path: definitions/pipelines/alignment_exome_mouse.cwl Branch/Commit ID: 9161ef43f7bf0e22b365fde9ec92edcb8601798e |
|
|
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: cbcea2fb2f01383d6b7f3102ee6a76ff100315ef |
|
|
adapter for sequence_align_and_tag
Some workflow engines won't stage files in our nested structure, so parse it out here |
![]() Path: definitions/subworkflows/sequence_align_and_tag_adapter.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 |
|
|
Motif Finding with HOMER with custom background regions
Motif Finding with HOMER with custom background regions --------------------------------------------------- HOMER contains a novel motif discovery algorithm that was designed for regulatory element analysis in genomics applications (DNA only, no protein). It is a differential motif discovery algorithm, which means that it takes two sets of sequences and tries to identify the regulatory elements that are specifically enriched in on set relative to the other. It uses ZOOPS scoring (zero or one occurrence per sequence) coupled with the hypergeometric enrichment calculations (or binomial) to determine motif enrichment. HOMER also tries its best to account for sequenced bias in the dataset. It was designed with ChIP-Seq and promoter analysis in mind, but can be applied to pretty much any nucleic acids motif finding problem. For more information please refer to: ------------------------------------- [Official documentation](http://homer.ucsd.edu/homer/motif/) |
![]() Path: workflows/homer-motif-analysis-bg.cwl Branch/Commit ID: d1bef74924efcb8bfaa00987b3f148d5a192b7a9 |
|
|
Exome QC workflow
|
![]() Path: definitions/subworkflows/qc_exome.cwl Branch/Commit ID: 700e73aaed6db1ad538dd27b2e1709f436ad3edb |
|
|
Downsample and HaplotypeCaller
|
![]() Path: definitions/pipelines/downsample_and_recall.cwl Branch/Commit ID: ac87e0584685fe04e4010ecd77ae4f055f21d788 |
|
|
varscan somatic workflow
|
![]() Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: 9161ef43f7bf0e22b365fde9ec92edcb8601798e |
|
|
strelka workflow
|
![]() Path: definitions/subworkflows/strelka_and_post_processing.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 |
|
|
Exome QC workflow
|
![]() Path: definitions/subworkflows/qc_exome.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 |
|
|
process VCF workflow
|
![]() Path: definitions/subworkflows/strelka_process_vcf.cwl Branch/Commit ID: ac87e0584685fe04e4010ecd77ae4f055f21d788 |