Explore Workflows
View already parsed workflows here or click here to add your own
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Workflow that executes the SBG L1 Workflow
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Path: L1-to-L2-e2e.cwl Branch/Commit ID: 1.1.1 |
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epigenome-chip-seq.packed.cwl#macs2.cwl
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Path: workflow/epigenome-chip-seq/epigenome-chip-seq.packed.cwl Branch/Commit ID: main Packed ID: macs2.cwl |
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scatter_head.cwl
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Path: tests/cwl/scatter_head.cwl Branch/Commit ID: master |
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maf2vcf_gz_workflow.cwl
Workflow to convert a maf file into a vcf.gz with .tbi index |
Path: cwl/maf2vcf_gz_workflow.cwl Branch/Commit ID: master |
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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: master Packed ID: main |
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qiime2 DADA2 detect/correct sequence data
Option 1: DADA2 from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
Path: packed/qiime2-step2-dada2.cwl Branch/Commit ID: qiime2-workflow Packed ID: qiime2-03-dada2.cwl |
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revcomp.cwl
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Path: workflows/sanbi_cwltutorial/revcomp/revcomp.cwl Branch/Commit ID: master |
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wf_rescue_ratio_2inputs.cwl
Calculates the rescue ratio (see Gabe's protocols paper), given two eCLIP IP samples and 2 size-matched input samples. Also returns the reproducible peaks given these two samples. This is different from the 1input workflow in that each INPUT is first merged together and is used downstream instead of the 1input version, which remains unmodified. Merged inputs are NOT used in calculating true reproducible peaks. |
Path: cwl/wf_rescue_ratio_2inputs.cwl Branch/Commit ID: master |
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realign-distr.cwl
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Path: stage/realign-distr.cwl Branch/Commit ID: master |
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wgs alignment and tumor-only variant detection
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Path: definitions/pipelines/tumor_only_wgs.cwl Branch/Commit ID: master |
