Explore Workflows
View already parsed workflows here or click here to add your own
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: adcae308fdccaa1190083616118dfadb4df65dca |
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1st-workflow.cwl
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Path: tests/wf/1st-workflow.cwl Branch/Commit ID: ca7f7687b39611c295dc9d21c542214f2b462093 |
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome_gvcf.cwl Branch/Commit ID: 39ac49f5d080bbb6bfa97246f46a5b621254f622 |
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: 27aa22e6f5d2fca75abca42d52867259fd0725b9 |
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step_valuefrom5_wf_v1_1.cwl
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Path: testdata/step_valuefrom5_wf_v1_1.cwl Branch/Commit ID: 0ad6983898f0d9001fe0f416f97c4d8b940e384a |
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timelimit-wf.cwl
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Path: tests/timelimit-wf.cwl Branch/Commit ID: ad91c844b5adfef514c059af364e20afc935e598 |
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Filter single sample sv vcf from paired read callers(Manta/Smoove)
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Path: definitions/subworkflows/sv_paired_read_caller_filter.cwl Branch/Commit ID: 1585504ccffafac53b1594349ed934f45206ee2b |
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xenbase-sra-to-fastq-pe.cwl
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Path: subworkflows/xenbase-sra-to-fastq-pe.cwl Branch/Commit ID: 68ccda2aeaac01375bc25d3994fb1ec44572a63b |
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align_merge_sas
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Path: task_types/tt_align_merge_sas.cwl Branch/Commit ID: 6d04f5d65d1d4893706d9ae7e27341633333054f |
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step-valuefrom2-wf_v1_1.cwl
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Path: testdata/step-valuefrom2-wf_v1_1.cwl Branch/Commit ID: 139c64b55f7693d22e6646b8afe585f90da11dcb |
