Explore Workflows
View already parsed workflows here or click here to add your own
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wgs alignment and germline variant detection
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Path: definitions/pipelines/germline_wgs.cwl Branch/Commit ID: ffd73951157c61c1581d346628d75b61cdd04141 |
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revsort_datetime.cwl
Reverse the lines in a document, then sort those lines. |
Path: tests/wf/revsort_datetime.cwl Branch/Commit ID: 7a058fed2987bc0046ffbc9a2b8a39b5b4fec6e1 |
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Hello World
Outputs a message using echo |
Path: tests/wf/hello-workflow.cwl Branch/Commit ID: 135a0c67afd67383c44e89fba136ccd9ce6afb1f |
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cond-wf-007.cwl
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Path: tests/conditionals/cond-wf-007.cwl Branch/Commit ID: 979083396fee912fca8ef778174216d317338a00 |
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output_reference_workflow_input.cwl
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Path: tests/output_reference_workflow_input.cwl Branch/Commit ID: 31bda22357987171f02ae6513fcc26e011e6afed |
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allele-alignreads-se-pe.cwl
Workflow maps FASTQ files from `fastq_files` input into reference genome `reference_star_indices_folder` and insilico generated `insilico_star_indices_folder` genome (concatenated genome for both `strain1` and `strain2` strains). For both genomes STAR is run with `outFilterMultimapNmax` parameter set to 1 to discard all of the multimapped reads. For insilico genome SAM file is generated. Then it's splitted into two SAM files based on strain names and then sorted by coordinates into the BAM format. For reference genome output BAM file from STAR slignment is also coordinate sorted. |
Path: subworkflows/allele-alignreads-se-pe.cwl Branch/Commit ID: 68ccda2aeaac01375bc25d3994fb1ec44572a63b |
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schemadef-wf.cwl
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Path: tests/schemadef-wf.cwl Branch/Commit ID: 979083396fee912fca8ef778174216d317338a00 |
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mut.cwl
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Path: tests/wf/mut.cwl Branch/Commit ID: 190415a46a7249ab85fde87d797ec1ea688a8cc5 |
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scatter-wf4.cwl#main
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Path: cwltool/schemas/v1.0/v1.0/scatter-wf4.cwl Branch/Commit ID: 639229b1159cf484e70e52da10194561b3fad719 Packed ID: main |
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03-map-pe.cwl
ATAC-seq 03 mapping - reads: PE |
Path: v1.0/ATAC-seq_pipeline/03-map-pe.cwl Branch/Commit ID: 6d9457382f0b7cc2510e148d21383261280d17ed |
