Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome_gvcf.cwl Branch/Commit ID: 0b6e8fd8ead7644cf5398395b76af5cf4011686f |
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cram_to_bam workflow
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Path: definitions/subworkflows/cram_to_bam_and_index.cwl Branch/Commit ID: 449bc7e45bb02316d040f73838ef18359e770268 |
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STAR-RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq_star_fusion.cwl Branch/Commit ID: 0b6e8fd8ead7644cf5398395b76af5cf4011686f |
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Alignment without BQSR
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Path: definitions/subworkflows/sequence_to_bqsr_nonhuman.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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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: 0b6e8fd8ead7644cf5398395b76af5cf4011686f |
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env-wf1.cwl
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Path: cwltool/schemas/v1.0/v1.0/env-wf1.cwl Branch/Commit ID: 814bd0405a7701efc7d63e8f0179df394c7766f7 |
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Alignment without BQSR
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Path: definitions/subworkflows/sequence_to_bqsr_mouse.cwl Branch/Commit ID: 233f026ffce240071edda526391be0c03186fce8 |
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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: 457e101e3fb87e7fd792357afce00ed8ccbfbcdb |
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alignment for nonhuman with qc
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Path: definitions/pipelines/alignment_wgs_nonhuman.cwl Branch/Commit ID: 04d21c33a5f2950e86db285fa0a32a6659198d8a |
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Chipseq alignment with qc and creating homer tag directory
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Path: definitions/pipelines/chipseq.cwl Branch/Commit ID: 844c10a4466ab39c02e5bfa7a210c195b8efa77a |
