Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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xenbase-fastq-bowtie-bigwig-se-pe.cwl
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https://github.com/datirium/workflows.git
Path: subworkflows/xenbase-fastq-bowtie-bigwig-se-pe.cwl Branch/Commit ID: d6ec0dee61ef65a110e10141bde1a79332a64ab0 |
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pangenome-generate.cwl
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https://github.com/arvados/bh20-seq-resource.git
Path: workflows/pangenome-generate/pangenome-generate.cwl Branch/Commit ID: fdb1b012fc04ee07f401541e181e28fe442c9454 |
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workflow.cwl
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https://github.com/nal-i5k/organism_onboarding.git
Path: flow_dispatch/2other_species/workflow.cwl Branch/Commit ID: 0ecf492419ddaa015f14a163381948c53b3deea6 |
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zip_and_index_vcf.cwl
This is a very simple workflow of two steps. It will zip an input VCF file and then index it. The zipped file and the index file will be in the workflow output. |
https://github.com/icgc-tcga-pancancer/pcawg-oxog-filter.git
Path: zip_and_index_vcf.cwl Branch/Commit ID: 123a3151d35f98e442e703d903dc3e1d72f3c4b0 |
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oxog_sub_wf.cwl
This is a subworkflow - this is not meant to be run as a stand-alone workflow! |
https://github.com/icgc-tcga-pancancer/pcawg-oxog-filter.git
Path: oxog_sub_wf.cwl Branch/Commit ID: 123a3151d35f98e442e703d903dc3e1d72f3c4b0 |
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heatmap-prepare.cwl
Workflow runs homer-make-tag-directory.cwl tool using scatter for the following inputs - bam_file - fragment_size - total_reads `dotproduct` is used as a `scatterMethod`, so one element will be taken from each array to construct each job: 1) bam_file[0] fragment_size[0] total_reads[0] 2) bam_file[1] fragment_size[1] total_reads[1] ... N) bam_file[N] fragment_size[N] total_reads[N] `bam_file`, `fragment_size` and `total_reads` arrays should have the identical order. |
https://github.com/datirium/workflows.git
Path: tools/heatmap-prepare.cwl Branch/Commit ID: 799575ce58746813f066a665adeacdda252d8cab |
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allele-process-reference.cwl
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https://github.com/datirium/workflows.git
Path: subworkflows/allele-process-reference.cwl Branch/Commit ID: e627079d8431e4f1f1c7531af1ca2e7dcc684b90 |
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Transcriptome assembly workflow (paired-end version)
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https://github.com/mscheremetjew/workflow-is-cwl.git
Path: workflows/TranscriptomeAssembly-wf.paired-end.cwl Branch/Commit ID: e9bbe2917384efc75ba067db23612bc8e22f3f06 |
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bam-bedgraph-bigwig.cwl
Workflow converts input BAM file into bigWig and bedGraph files. Input BAM file should be sorted by coordinates (required by `bam_to_bedgraph` step). If `split` input is not provided use true by default. Default logic is implemented in `valueFrom` field of `split` input inside `bam_to_bedgraph` step to avoid possible bug in cwltool with setting default values for workflow inputs. `scale` has higher priority over the `mapped_reads_number`. The last one is used to calculate `-scale` parameter for `bedtools genomecov` (step `bam_to_bedgraph`) only in a case when input `scale` is not provided. All logic is implemented inside `bedtools-genomecov.cwl`. `bigwig_filename` defines the output name only for generated bigWig file. `bedgraph_filename` defines the output name for generated bedGraph file and can influence on generated bigWig filename in case when `bigwig_filename` is not provided. All workflow inputs and outputs don't have `format` field to avoid format incompatibility errors when workflow is used as subworkflow. |
https://github.com/Barski-lab/workflows.git
Path: tools/bam-bedgraph-bigwig.cwl Branch/Commit ID: 64e85970dbecba89c3380ab285c108d221e76fe6 |
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indexing_bed
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https://gitlab.bsc.es/lrodrig1/structuralvariants_poc.git
Path: structuralvariants/cwl/abstract_operations/subworkflows/indexing_bed.cwl Branch/Commit ID: 82e533a98a763a258bd841ed0032c79445478d56 |