Explore Workflows
View already parsed workflows here or click here to add your own
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: 9c57dba |
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preprocess-ont.cwl
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Path: PreProcessing/preprocess-ont.cwl Branch/Commit ID: master |
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kfdrc-jointgenotyping-refinement-workflow.cwl
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Path: workflow/kfdrc-jointgenotyping-refinement-workflow.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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indexing_bed
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Path: structuralvariants/cwl/subworkflows/indexing_bed.cwl Branch/Commit ID: 1.0.7 |
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workflow1.cwl
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Path: actions/workflow1.cwl Branch/Commit ID: master |
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bulk_analysis.cwl
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Path: steps/bulk_analysis.cwl Branch/Commit ID: 302f1f3 |
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EMG assembly for paired end Illumina
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Path: workflows/emg-assembly.cwl Branch/Commit ID: 0fed1c9 |
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word-mapping-test-files-wf.cwl#align-texts-wf.cwl
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Path: ochre/cwl/word-mapping-test-files-wf.cwl Branch/Commit ID: master Packed ID: align-texts-wf.cwl |
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Indices builder from GBOL RDF (TTL)
Workflow to build different indices for different tools from a genome and transcriptome. This workflow expects an (annotated) genome in GBOL ttl format. Steps: - SAPP: rdf2gtf (genome fasta) - SAPP: rdf2fasta (transcripts fasta) - STAR index (Optional for Eukaryotic origin) - bowtie2 index - kallisto index |
Path: cwl/workflows/workflow_indexbuilder.cwl Branch/Commit ID: master |
