Explore Workflows
View already parsed workflows here or click here to add your own
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Sort and merge input bed file and generate a .sorted.merged.bed file
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Path: sort_merge.cwl Branch/Commit ID: main |
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pcawg_minibam_wf.cwl
This workflow will run OxoG, variantbam, and annotate. Run this as `dockstore --script --debug workflow launch --descriptor cwl --local-entry --entry ./oxog_varbam_annotate_wf.cwl --json oxog_varbam_annotat_wf.input.json ` |
Path: pcawg_minibam_wf.cwl Branch/Commit ID: 1.0.0 |
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ani_top_n
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Path: task_types/tt_ani_top_n.cwl Branch/Commit ID: dev |
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: 5dc7c5c |
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wgs_variant_calling_bam.cwl
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Path: workflows/wgs_variant_calling_bam.cwl Branch/Commit ID: dev |
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EMG QC workflow, (paired end version). Benchmarking with MG-RAST expt.
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Path: workflows/emg-qc-paired.cwl Branch/Commit ID: 5833078 |
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binning.cwl
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Path: workflows/binning.cwl Branch/Commit ID: master |
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: downsample_and_recall |
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scatter GATK HaplotypeCaller over intervals
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Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: No_filters_detect_variants |
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contaminant_cleanup
This workflow detect and remove contamination from a DNA fasta file |
Path: workflows/Contamination/contaminant-cleanup.cwl Branch/Commit ID: master |
