Explore Workflows
View already parsed workflows here or click here to add your own
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black-diamond-workflow.cwl
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Path: black-diamond-workflow/cwl/black-diamond-workflow.cwl Branch/Commit ID: master |
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prefetch_fastq.cwl
Worfklow combining an SRA fetch from NCBI with a fastq-dump cmd |
Path: bio-cwl-tools/sratoolkit/prefetch_fastq.cwl Branch/Commit ID: master |
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exomeseq-00-prepare-reference-data.cwl
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Path: subworkflows/exomeseq-00-prepare-reference-data.cwl Branch/Commit ID: gatk4-fixes |
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GRO_run.cwl
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Path: test_workflow_notables_clean/workflow/GRO_run.cwl Branch/Commit ID: master |
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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: release |
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Run genomic CMsearch
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Path: bacterial_noncoding/wf_gcmsearch.cwl Branch/Commit ID: test |
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msi.cwl
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Path: workflows/subworkflows/msi.cwl Branch/Commit ID: master |
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delay-calibration.cwl
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Path: workflows/delay-calibration.cwl Branch/Commit ID: master |
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wf-loadContents4.cwl
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Path: tests/wf-loadContents4.cwl Branch/Commit ID: main |
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Run genomic CMsearch (Rfam rRNA)
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Path: bacterial_ncrna/wf_gcmsearch.cwl Branch/Commit ID: test |
