Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and tumor-only variant detection
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Path: definitions/pipelines/exome.cwl Branch/Commit ID: No_filters_detect_variants |
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qc_workflow.cwl
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Path: workflows/QC/qc_workflow.cwl Branch/Commit ID: master |
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BD Rhapsody™ WTA Analysis Pipeline
The BD Rhapsody™ WTA Analysis Pipeline is used to create sequencing libraries from single cell transcriptomes without having to specify a targeted panel. After sequencing, the analysis pipeline takes the FASTQ files, a reference genome file and a transcriptome annotation file for gene alignment. The pipeline generates molecular counts per cell, read counts per cell, metrics, and an alignment file. |
Path: wf.cwl Branch/Commit ID: main Packed ID: main |
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helloworld.cwl
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Path: workflow/cwl/helloworld.cwl Branch/Commit ID: master |
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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: downsample_and_recall |
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trnascan_wnode and gpx_qdump combined
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Path: bacterial_trna/wf_scan_and_dump.cwl Branch/Commit ID: dev |
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step_valuefrom5_wf_v1_0.cwl
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Path: testdata/step_valuefrom5_wf_v1_0.cwl Branch/Commit ID: aa13f7bad47e8df2349bdebd163e1830537d7f93 |
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no-outputs-wf.cwl
Workflow without outputs. |
Path: tests/no-outputs-wf.cwl Branch/Commit ID: master |
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cram_to_bam workflow
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Path: definitions/subworkflows/cram_to_bam_and_index.cwl Branch/Commit ID: No_filters_detect_variants |
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Produce a list of residue-mapped structural domain instances from CATH ids
Retrieve and process the PDB structures corresponding to the CATH superfamily ids resulting in a list of residue-mapped structural domain instances along with lost structural instances (requires Data/cath_domain_description_file.txt downloaded from CATH and uses SIFTS resource for PDB to UniProt residue Mapping) |
Path: Tools/resmapping_cath_instances_subwf.cwl Branch/Commit ID: main |
