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/cle_somatic_exome.cwl Branch/Commit ID: 4ae14dd3a447c90022e3dfeb53fc05b8436e2775 |
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conflict.cwl#main
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![]() Path: tests/wf/conflict.cwl Branch/Commit ID: main Packed ID: main |
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count-lines9-wf-noET.cwl
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![]() Path: tests/count-lines9-wf-noET.cwl Branch/Commit ID: master |
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SVision-Pro workflow for structural variant detection in cancer samples
A workflow that uses SVision-Pro to identify structural variants in tumor/normal paired samples from Oxford Nanopore Technology (ONT) long-read sequencing data. |
![]() Path: workflow/main.cwl Branch/Commit ID: main |
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BD Rhapsody™ Sequence Analysis Pipeline
The BD Rhapsody™ assays are used to create sequencing libraries from single cell transcriptomes. After sequencing, the analysis pipeline takes the FASTQ files and a reference file for gene alignment. The pipeline generates molecular counts per cell, read counts per cell, metrics, and an alignment file. |
![]() Path: rhapsody_pipeline_2.0.cwl Branch/Commit ID: main Packed ID: main |
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cond-wf-012.cwl
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![]() Path: tests/conditionals/cond-wf-012.cwl Branch/Commit ID: main |
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nmrpipe_workflow.cwl
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![]() Path: nmrpipe_workflow.cwl Branch/Commit ID: master |
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workflow-transeq-blast-clustalo.cwl
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![]() Path: workflows/workflow-transeq-blast-clustalo.cwl Branch/Commit ID: master |
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scatter-valuefrom-wf3.cwl#main
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![]() Path: tests/scatter-valuefrom-wf3.cwl Branch/Commit ID: main Packed ID: main |
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assm_assm_blastn_wnode
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![]() Path: task_types/tt_assm_assm_blastn_wnode.cwl Branch/Commit ID: master |