Explore Workflows
View already parsed workflows here or click here to add your own
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Run genomic CMsearch (5S rRNA)
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Path: bacterial_noncoding/wf_gcmsearch.cwl Branch/Commit ID: ba3e313e646f1dd3da3f5f93a1e6cb7f252be97b |
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mergeAndMarkBams_4_1_3.cwl
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Path: janis_pipelines/wgs_somatic/cwl/tools/mergeAndMarkBams_4_1_3.cwl Branch/Commit ID: 1d45492ae0085824a7ac532d0dfa6621c1cbe415 |
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kmer_cache_store
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Path: task_types/tt_kmer_cache_store.cwl Branch/Commit ID: 7c8eb4d23c3c9859f57421643710c0b6d57b606c |
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Run pindel on provided region
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Path: definitions/subworkflows/pindel_region.cwl Branch/Commit ID: 2ae0a374fab650757cdae4391c8cbd32f02edf97 |
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Replace legacy AML Trio Assay
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Path: definitions/pipelines/aml_trio_cle.cwl Branch/Commit ID: 2ae0a374fab650757cdae4391c8cbd32f02edf97 |
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umi per-lane alignment subworkflow
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Path: definitions/subworkflows/umi_alignment.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 |
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samtoolsW.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: samtoolsW.cwl Branch/Commit ID: 530e671c113e91fe6b9114eda32103bb980450c7 |
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scatter-valuefrom-wf3.cwl#main
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Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf3.cwl Branch/Commit ID: 819c81af5449ec912bbbbead042ad66b8d3fd8d4 Packed ID: main |
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count-lines10-wf.cwl
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Path: cwltool/schemas/v1.0/v1.0/count-lines10-wf.cwl Branch/Commit ID: 819c81af5449ec912bbbbead042ad66b8d3fd8d4 |
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varscan somatic workflow
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Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: 18d8efdc4c97c1c9222f603f529b909b36fa42e7 |
