Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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cwlsite.cwl
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https://github.com/common-workflow-language/cwltool.git
Path: cwltool/schemas/site/cwlsite.cwl Branch/Commit ID: 03af16c9df2ee77485d4ab092cd64ae096d2e71c |
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Add snv and indel bam-readcount files to a vcf
|
https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/vcf_readcount_annotator.cwl Branch/Commit ID: ddd748516b25256a461ea9277303406fa2759b00 |
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merge_duprem_filter.cwl
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https://github.com/CompEpigen/ATACseq_workflows.git
Path: CWL/workflow_modules/merge_duprem_filter.cwl Branch/Commit ID: 52515b5c053d3cf157be070efac954043892429f |
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sum-wf.cwl
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https://github.com/common-workflow-language/cwltool.git
Path: cwltool/schemas/v1.0/v1.0/sum-wf.cwl Branch/Commit ID: 9e7c68c0834645ba53a7e2b5f70d53df9d051c92 |
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extract_capture_kit_http.cwl
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https://github.com/NCI-GDC/gdc-dnaseq-cwl.git
Path: workflows/bamfastq_align/extract_capture_kit_http.cwl Branch/Commit ID: 17823fcd036d134df803fbf76e23b0bc5eabedfd |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: ec5355f335852e51c6938809c16ea1d230a3f983 |
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Execute CRISPR
|
https://github.com/ncbi/pgap.git
Path: bacterial_mobile_elem/wf_bacterial_mobile_elem.cwl Branch/Commit ID: 8cc9b995bca666c54c673a5eb8d9b8c6f8e84490 |
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scatter-wf1.cwl
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https://github.com/common-workflow-language/cwltool.git
Path: cwltool/schemas/v1.0/v1.0/scatter-wf1.cwl Branch/Commit ID: 0db44e3c9805a070564f954222efff71cd791b70 |
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phase VCF
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: ec5355f335852e51c6938809c16ea1d230a3f983 |
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schemadef-wf.cwl
|
https://github.com/common-workflow-language/cwltool.git
Path: cwltool/schemas/v1.0/v1.0/schemadef-wf.cwl Branch/Commit ID: 9e7c68c0834645ba53a7e2b5f70d53df9d051c92 |