Explore Workflows
View already parsed workflows here or click here to add your own
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scatter-wf1_v1_1.cwl
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Path: testdata/scatter-wf1_v1_1.cwl Branch/Commit ID: 139c64b55f7693d22e6646b8afe585f90da11dcb |
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phase VCF
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Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 31a179d7a2f2ac86bfd7fcc4dc79832c3739ae76 |
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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: 93656ed6582073e434eab168c610625a835dce37 |
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 28d1065759cbd389594ee33b41fd1103ced5436d |
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any-type-compat.cwl
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Path: cwltool/schemas/v1.0/v1.0/any-type-compat.cwl Branch/Commit ID: ecdfe1ee769d05790f70ac87a711131f441f3753 |
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trim-chipseq-pe.cwl
Runs ChIP-Seq BioWardrobe basic analysis with paired-end input data files. |
Path: workflows/trim-chipseq-pe.cwl Branch/Commit ID: a8e4c1245950715d2e07682d3ac4865ce1d73777 |
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realignment.cwl
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Path: modules/pair/realignment.cwl Branch/Commit ID: eb1c641d3134e7e13bc1a15fe7d8de7937527aca |
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Whole genome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: efbbe5ed51f6ac583e87a348785c72818a33f56e |
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Unaligned to aligned BAM
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Path: definitions/subworkflows/align.cwl Branch/Commit ID: 86fbeb95ef85111f3b4c6bc2bba8f06cef64e157 |
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genome-kallisto-index.cwl
Generates a FASTA file with the DNA sequences for all transcripts in a GFF file and builds kallisto index |
Path: tools/genome-kallisto-index.cwl Branch/Commit ID: c82a2e766abba032f0bbe2aa76e0176e69064569 |
