Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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alignment_novoalign.cwl
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![]() Path: genomel/cwl/workflows/harmonization/alignment_novoalign.cwl Branch/Commit ID: master |
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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: 14985c972d540929cacbdf33925af2d4c6c9edb1 |
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pindel parallel workflow
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![]() Path: pindel/workflow.cwl Branch/Commit ID: master |
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check_md5_wf.cwl
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![]() Path: workflow/checker-workflows/check_md5_wf.cwl Branch/Commit ID: master |
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pipeline-bam2vcf-distr.cwl
DNAseq pipeline from bam to vcf in distributed mode |
![]() Path: pipeline/pipeline-bam2vcf-distr.cwl Branch/Commit ID: master |
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paramref_arguments_self.cwl
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![]() Path: tests/wf/paramref_arguments_self.cwl Branch/Commit ID: main |
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bulk-atac-seq-pipeline.cwl
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![]() Path: bulk-atac-seq-pipeline.cwl Branch/Commit ID: 5465f66 |
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revsort_step_bad_schema.cwl
Reverse the lines in a document, then sort those lines. |
![]() Path: tests/wf/revsort_step_bad_schema.cwl Branch/Commit ID: main |
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NonSpliced RNAseq workflow
Workflow for NonSpliced RNAseq data alignment with multiple aligners. Steps: - workflow_illumina_quality.cwl: - FastQC (control) - fastp (trimming) - bowtie2 (read mapping) - sam_to_sorted-bam - featurecounts (transcript read counts) - kallisto (transcript [pseudo]counts) |
![]() Path: cwl/workflows/workflow_RNAseq_NonSpliced.cwl Branch/Commit ID: master |
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kmer_top_n_extract
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![]() Path: task_types/tt_kmer_top_n_extract.cwl Branch/Commit ID: master |