Explore Workflows
View already parsed workflows here or click here to add your own
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Spliced RNAseq workflow
Workflow for Spliced RNAseq data Steps: - workflow_illumina_quality: - FastQC (Read Quality Control) - fastp (Read Trimming) - STAR (Read mapping) - featurecounts (transcript read counts) - kallisto (transcript [pseudo]counts) |
Path: cwl/workflows/workflow_RNAseq_Spliced.cwl Branch/Commit ID: master |
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exome alignment with qc
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Path: definitions/pipelines/alignment_exome.cwl Branch/Commit ID: low-vaf |
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scatter-wf3.cwl#main
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Path: v1.0/v1.0/scatter-wf3.cwl Branch/Commit ID: master Packed ID: main |
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preprocess_vcf.cwl
This workflow will perform preprocessing steps on VCFs for the OxoG/Variantbam/Annotation workflow. |
Path: preprocess_vcf.cwl Branch/Commit ID: develop |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: low-vaf |
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scatter-valuefrom-wf5.cwl
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Path: v1.0/v1.0/scatter-valuefrom-wf5.cwl Branch/Commit ID: master |
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GRO_run_nested.cwl
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Path: test_workflow_notables_clean/nested_workflow/GRO_run_nested.cwl Branch/Commit ID: master |
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main.cwl
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Path: main.cwl Branch/Commit ID: master |
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Unaligned bam to sorted, markduped bam
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Path: definitions/subworkflows/align_sort_markdup.cwl Branch/Commit ID: low-vaf |
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CODEX analysis pipeline using Cytokit
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Path: pipeline.cwl Branch/Commit ID: 221f7c4 |
