Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment with qc
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Path: definitions/pipelines/exome_alignment.cwl Branch/Commit ID: 051074fce4afd9732ef34db9dd43d3a1d8e979d6 |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: b7d9ace34664d3cedb16f2512c8a6dc6debfc8ca |
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tt_fscr_calls_pass1
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Path: task_types/tt_fscr_calls_pass1.cwl Branch/Commit ID: 953d7866bc70e14c02a6bb8c5a72305caa823bfc |
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conflict.cwl#main
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Path: tests/wf/conflict.cwl Branch/Commit ID: efb40a812cdba2df6699f130ee5aeea9b63045cd Packed ID: main |
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Feature expression merge - combines feature expression from several experiments
Feature expression merge - combines feature expression from several experiments ========================================================================= Workflows merges RPKM (by default) gene expression from several experiments based on the values from GeneId, Chrom, TxStart, TxEnd and Strand columns (by default). Reported unique columns are renamed based on the experiments names. |
Path: workflows/feature-merge.cwl Branch/Commit ID: bf80c9339d81a78aefb8de661bff998ed86e836e |
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scatter-valuefrom-wf6.cwl
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Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf6.cwl Branch/Commit ID: 65aedc5e7e1f3ccace7f9022f8a54b3f0d5c9a8c |
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conflict-wf.cwl#collision
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Path: cwltool/schemas/v1.0/v1.0/conflict-wf.cwl Branch/Commit ID: c6cced7a2e6389d2eb43342e702677ccb7c7497c Packed ID: collision |
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genome-kallisto-index.cwl
Generates a FASTA file with the DNA sequences for all transcripts in a GFF file and builds kallisto index |
Path: tools/genome-kallisto-index.cwl Branch/Commit ID: 80d64741638b14de5cf58236b6d6d99713c62086 |
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stdout-wf_v1_0.cwl
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Path: testdata/stdout-wf_v1_0.cwl Branch/Commit ID: 7af75226f084349e401b1114f25bdcdee060e127 |
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grepsort workflow
a workflow that performs grep followed by sort |
Path: tests/data/grepsort-run-1/snapshot/grepsort.cwl Branch/Commit ID: 376f6b2c6332a4742d4512d6e1fb785a2f8b7285 |
