Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: 97572e3a088d79f6a4166385f79e79ea77b11470 |
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allele-process-strain.cwl
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Path: subworkflows/allele-process-strain.cwl Branch/Commit ID: 942f453603bc1df04cee28d6ac6b3b8b649fda55 |
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wgs alignment with qc
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Path: definitions/pipelines/alignment_wgs.cwl Branch/Commit ID: 0d2f354af9192a56af258a7d2426c7c160f4ec1a |
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allele-process-reference.cwl
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Path: subworkflows/allele-process-reference.cwl Branch/Commit ID: 942f453603bc1df04cee28d6ac6b3b8b649fda55 |
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Build Bowtie indices
Workflow runs [Bowtie](http://bowtie-bio.sourceforge.net/tutorial.shtml) v1.2.0 (12/30/2016) to build indices for reference genome provided in a single FASTA file as fasta_file input. Generated indices are saved in a folder with the name that corresponds to the input genome |
Path: workflows/bowtie-index.cwl Branch/Commit ID: ebbf23764ede324cabc064bd50647c1f643726fa |
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mut2.cwl
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Path: tests/wf/mut2.cwl Branch/Commit ID: 49cd284a8fc7884de763573075d3e1d6a4c1ffdd |
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bacterial_kmer
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Path: bacterial_kmer/wf_bacterial_kmer.cwl Branch/Commit ID: 8af4e2aabf43d5e3c7162efae4ad4649df5601e2 |
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Alignment without BQSR
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Path: definitions/subworkflows/sequence_to_bqsr_mouse.cwl Branch/Commit ID: b7d9ace34664d3cedb16f2512c8a6dc6debfc8ca |
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basename-fields-test.cwl
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Path: v1.0/v1.0/basename-fields-test.cwl Branch/Commit ID: 4fd45edb9531a03223c18a586e32d0baf0d5acb2 |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: bfcb5ffbea3d00a38cc03595d41e53ea976d599d |
