Explore Workflows
View already parsed workflows here or click here to add your own
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ani_top_n
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Path: task_types/tt_ani_top_n.cwl Branch/Commit ID: 33414c888997d558bdcb558ca33c3a728a3e6143 |
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Subworkflow to allow calling different SV callers which require bam files as inputs
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Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: 43c790e2ee6a0f3f42e40fb4d9a9005eb8de747a |
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wf_get_peaks_scatter_se.cwl
The \"main\" workflow. Takes fastq files generated using the seCLIP protocol (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991800/) and outputs candidate RBP binding regions (peaks). runs: wf_get_peaks_se.cwl through scatter across multiple samples. |
Path: cwl/wf_get_peaks_scatter_se.cwl Branch/Commit ID: b389f7fe3e76cb6e3f31c3a8e2e3b59bb400e74c |
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workflow.cwl
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Path: flow_dispatch/2working_files/workflow.cwl Branch/Commit ID: 39b1d1a39a2ccdadd52db15b41422ecccc66e605 |
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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: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71 |
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blastp_wnode_naming
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Path: task_types/tt_blastp_wnode_naming.cwl Branch/Commit ID: e2a6cbcc36212433d8fbc804919442787a5e2a49 |
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gathered exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle_gathered.cwl Branch/Commit ID: 43c790e2ee6a0f3f42e40fb4d9a9005eb8de747a |
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bam_readcount workflow
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Path: definitions/subworkflows/bam_readcount.cwl Branch/Commit ID: 43c790e2ee6a0f3f42e40fb4d9a9005eb8de747a |
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gathered exome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_exome_gathered.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a |
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EMG QC workflow, (paired end version). Benchmarking with MG-RAST expt.
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Path: workflows/emg-qc-single.cwl Branch/Commit ID: 7bb76f33bf40b5cd2604001cac46f967a209c47f |
