Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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bam_filtering
BAM filtering |
![]() Path: structuralvariants/cwl/subworkflows/bam_filtering.cwl Branch/Commit ID: 1.0.5 |
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record-in-secondaryFiles-missing-wf.cwl
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![]() Path: tests/record-in-secondaryFiles-missing-wf.cwl Branch/Commit ID: master |
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emep_workflow.cwl
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![]() Path: workflows/emep_workflow.cwl Branch/Commit ID: develop |
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chksum_seqval_wf_interleaved_fq.cwl
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![]() Path: cwls/chksum_seqval_wf_interleaved_fq.cwl Branch/Commit ID: 0.4.1 |
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adapter for sequence_align_and_tag
Some workflow engines won't stage files in our nested structure, so parse it out here |
![]() Path: definitions/subworkflows/sequence_align_and_tag_adapter.cwl Branch/Commit ID: master |
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pipeline-se.cwl
ATAC-seq pipeline - reads: SE |
![]() Path: v1.0/ATAC-seq_pipeline/pipeline-se.cwl Branch/Commit ID: master |
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03-map-pe-blacklist-removal.cwl
ATAC-seq 03 mapping - reads: PE |
![]() Path: v1.0/ATAC-seq_pipeline/03-map-pe-blacklist-removal.cwl Branch/Commit ID: v1.0.0 |
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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: workflow1_11.cwl Branch/Commit ID: main Packed ID: main |
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SSU-from-tablehits.cwl
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![]() Path: tools/SSU-from-tablehits.cwl Branch/Commit ID: master |
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wf-variantcall.cwl
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![]() Path: NA12878-chr20/NA12878-platinum-chr20-workflow/wf-variantcall.cwl Branch/Commit ID: master |