Explore Workflows
View already parsed workflows here or click here to add your own
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 |
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tt_hmmsearch_wnode.cwl
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Path: task_types/tt_hmmsearch_wnode.cwl Branch/Commit ID: f225cd99b0e0a5043dd102f8b33a6139fefe9ea4 |
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protein_extract
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Path: progs/protein_extract.cwl Branch/Commit ID: f225cd99b0e0a5043dd102f8b33a6139fefe9ea4 |
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Per-region pindel
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Path: definitions/subworkflows/pindel_cat.cwl Branch/Commit ID: 2ae0a374fab650757cdae4391c8cbd32f02edf97 |
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cluster_blastp_wnode and gpx_qdump combined
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Path: task_types/tt_cluster_and_qdump.cwl Branch/Commit ID: 146df33e2e44afa2a608ac72c036e6b6b871af93 |
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pindel parallel workflow
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Path: definitions/subworkflows/pindel.cwl Branch/Commit ID: 74647cc0f1abac4ee22950cfa89c44cf2ca3cffd |
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fail-unconnected.cwl
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Path: v1.0/v1.0/fail-unconnected.cwl Branch/Commit ID: 40fcfc01812046f012acf5153cc955ee848e69e3 |
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BioExcel-CWL-MDSetup.cwl
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Path: biobb_wf_cwl_tutorial/examples/BioExcel-CWL-MDSetup.cwl Branch/Commit ID: 0d77918a9347b12af11fe71273b0c1f9dccbd2d3 |
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varscanW.cwl
Author: AMBARISH KUMAR er.ambarish@gmail.com; ambari73_sit@jnu.ac.in This is a proposed standard operating procedure for genomic variant detection using VARSCAN. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
Path: varscanW.cwl Branch/Commit ID: 690ff2fa1ef356c42003e4b9986d39f4e44806a8 |
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assm_assm_blastn_wnode
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Path: task_types/tt_assm_assm_blastn_wnode.cwl Branch/Commit ID: 0514ffe248dd11068a3f2268bc67b6ce5ab051d2 |
