Explore Workflows
View already parsed workflows here or click here to add your own
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filter-pcr-artifacts.cwl
DNase-seq - map - Filter PCR Artifacts |
Path: v1.0/map/filter-pcr-artifacts.cwl Branch/Commit ID: v1.0.0 |
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wf_vecscreen.cwl
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Path: contam_filter/wf_vecscreen.cwl Branch/Commit ID: master |
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hisat2_samtools_htseq-dexseq.stringtie-prepDE-DESeq2.cwl
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Path: workflows/hisat2_samtools_htseq-dexseq.stringtie-prepDE-DESeq2.cwl Branch/Commit ID: master |
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kf_alignment_fq_input_wf.cwl
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Path: workflows/kf_alignment_fq_input_wf.cwl Branch/Commit ID: dev |
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pipeline-fastq2vcf-parallel-bwa.cwl
DNAseq pipeline from fastq to vcf |
Path: pipeline/pipeline-fastq2vcf-parallel-bwa.cwl Branch/Commit ID: master |
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picard_markduplicates
Mark duplicates |
Path: structuralvariants/cwl/subworkflows/picard_markduplicates.cwl Branch/Commit ID: 1.1.3 |
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qc_workflow_wo_waltz.cwl
This workflow is intended to be used to test the QC module, without having to run the long waltz step |
Path: workflows/QC/qc_workflow_wo_waltz.cwl Branch/Commit ID: 0.0.33_dmp |
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gathered exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle_gathered.cwl Branch/Commit ID: low-vaf |
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exome alignment and germline variant detection, with optitype for HLA typing
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Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: low-vaf |
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no-outputs-wf.cwl
Workflow without outputs. |
Path: tests/no-outputs-wf.cwl Branch/Commit ID: main |
