Explore Workflows
View already parsed workflows here or click here to add your own
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minibam_sub_wf.cwl
This is a subworkflow of the main oxog_varbam_annotat_wf workflow - this is not meant to be run as a stand-alone workflow! |
Path: minibam_sub_wf.cwl Branch/Commit ID: develop |
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Calculate FDA-requested metrics on all aligned and unaligned sequence files
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Path: definitions/subworkflows/generate_fda_metrics.cwl Branch/Commit ID: master |
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stats.cwl
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Path: cwl/stats/stats.cwl Branch/Commit ID: demo |
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bulk_process.cwl
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Path: steps/bulk_process.cwl Branch/Commit ID: 302f1f3 |
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map medium and long reads (> 100 bp) against reference genome
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Path: bwa/BWA-Mem2-single.cwl Branch/Commit ID: release |
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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: v0.0.3 |
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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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umi per-lane alignment subworkflow
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Path: definitions/subworkflows/umi_alignment.cwl Branch/Commit ID: master |
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simple_two_step.cwl
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Path: blast-pipelines/simple_two_step.cwl Branch/Commit ID: master |
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SAMSA2 pipeline
SAMSA2 complete workflow for meta-omics read annotation Steps: - Diamond read blastx - Refseq - SEED - SAMSA2 processing |
Path: cwl/workflows/workflow_samsa2.cwl Branch/Commit ID: master |
