Explore Workflows
View already parsed workflows here or click here to add your own
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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: release |
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env-wf3.cwl
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Path: v1.0/v1.0/env-wf3.cwl Branch/Commit ID: master |
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ST610106.cwl
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Path: ST610106.cwl Branch/Commit ID: remove-cycles |
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scatter-wf3_v1_1.cwl#main
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Path: testdata/scatter-wf3_v1_1.cwl Branch/Commit ID: main Packed ID: main |
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abundance
abundace profiles from annotated files, for protein and/or rna |
Path: CWL/Workflows/abundance.workflow.cwl Branch/Commit ID: master |
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wgs alignment with qc
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Path: definitions/pipelines/alignment_wgs.cwl Branch/Commit ID: master |
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HS Metrics workflow
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Path: definitions/subworkflows/hs_metrics.cwl Branch/Commit ID: low-vaf |
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oxog_sub_wf.cwl
This is a subworkflow - this is not meant to be run as a stand-alone workflow! |
Path: oxog_sub_wf.cwl Branch/Commit ID: develop |
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EMG assembly for paired end Illumina
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Path: workflows/emg-assembly.cwl Branch/Commit ID: master |
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wf.cwl#main
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Path: wf.cwl Branch/Commit ID: master Packed ID: main |
