Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
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Alignment without BQSR
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Path: definitions/subworkflows/sequence_to_bqsr_mouse.cwl Branch/Commit ID: downsample_and_recall |
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pipeline.cwl
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Path: CWLworkflow/pipeline.cwl Branch/Commit ID: master |
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wgs alignment and germline variant detection
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Path: wgs_workflow.cwl Branch/Commit ID: toil_compatibility |
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Functional analyis of sequences that match the 16S SSU
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Path: workflows/16S_taxonomic_analysis.cwl Branch/Commit ID: a8abd0e |
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exomeseq.cwl#exomeseq-02-variantdiscovery.cwl
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Path: packed/exomeseq.cwl Branch/Commit ID: qiime2-workflow-paired Packed ID: exomeseq-02-variantdiscovery.cwl |
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sc_atac_seq_initial_analysis.cwl
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Path: sc-atac-seq-pipeline/steps/sc_atac_seq_initial_analysis.cwl Branch/Commit ID: 68e0cc1 |
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biowardrobe_chipseq_se.cwl
The workflow is used to run CHIP-Seq basic analysis with single-end input FASTQ file. In outputs it returns coordinate sorted BAM file alongside with index BAI file, quality statistics of the input FASTQ file, reads coverage in a form of bigWig file, peaks calling data in a form of narrowPeak or broadPeak files. |
Path: biowardrobe_chipseq_se.cwl Branch/Commit ID: master |
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scatter GATK HaplotypeCaller over intervals
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Path: detect_variants/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: toil_compatibility |
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Apply filters to VCF file
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Path: definitions/subworkflows/germline_filter_vcf.cwl Branch/Commit ID: downsample_and_recall |
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collate_unique_SSU_headers.cwl
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Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: master |
