Explore Workflows
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trim-rnaseq-pe-dutp.cwl
Runs RNA-Seq BioWardrobe basic analysis with strand specific pair-end data file. |
![]() Path: workflows/trim-rnaseq-pe-dutp.cwl Branch/Commit ID: cf107bc24a37883ef01b959fd89c19456aaecc02 |
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qc_workflow.cwl
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![]() Path: workflows/QC/qc_workflow.cwl Branch/Commit ID: bccb338be356db83ad178be2aa9634ae86cb5211 |
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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. |
![]() Path: tools/bam-bedgraph-bigwig.cwl Branch/Commit ID: 5c0d21fe4f180730d4f6dd301e785bd6b00d5907 |
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compile1.cwl#main
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![]() Path: workflows//compile/compile1.cwl Branch/Commit ID: master Packed ID: main |
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xenbase-sra-to-fastq-pe.cwl
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![]() Path: subworkflows/xenbase-sra-to-fastq-pe.cwl Branch/Commit ID: bfa3843bcf36125ff258d6314f64b41336f06e6b |
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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. |
![]() Path: subworkflows/heatmap-prepare.cwl Branch/Commit ID: 3e2ad9c049ea96584c365559c687205e3b642146 |
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limit_detection.cwl
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![]() Path: limit_detection/limit_detection.cwl Branch/Commit ID: master |
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seqtk_sample_PE.cwl
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![]() Path: limit_detection/seqtk_sample_PE.cwl Branch/Commit ID: master |
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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. |
![]() Path: zip_and_index_vcf.cwl Branch/Commit ID: 40bf56daf9edab82e0f964dbd6961ca1111cd35f |
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workflow_localfiles.cwl
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![]() Path: workflow_localfiles.cwl Branch/Commit ID: c87304bce01c87346bf1b83558e18120ee834d28 |