Explore Workflows
View already parsed workflows here or click here to add your own
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picard_markduplicates
Mark duplicates |
Path: structuralvariants/cwl/subworkflows/picard_markduplicates.cwl Branch/Commit ID: 1.0.5 |
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fail-unconnected.cwl
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Path: v1.0/v1.0/fail-unconnected.cwl Branch/Commit ID: master |
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consensus_maf.cwl
Workflow to merge a large number of maf files into a single consensus maf file for use with GetBaseCountsMultiSample |
Path: cwl/consensus_maf.cwl Branch/Commit ID: master |
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kallisto-demo.cwl
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Path: workflows/workflows/kallisto-demo.cwl Branch/Commit ID: master |
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fastqPE2bam.multisamples.cwl
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Path: Workflows/fastqPE2bam.multisamples.cwl Branch/Commit ID: master |
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step-valuefrom3-wf.cwl
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Path: tests/step-valuefrom3-wf.cwl Branch/Commit ID: master |
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trim-rnaseq-pe.cwl
Runs RNA-Seq BioWardrobe basic analysis with pair-end data file. |
Path: workflows/trim-rnaseq-pe.cwl Branch/Commit ID: master |
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samtools_sort
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Path: structuralvariants/cwl/subworkflows/samtools_sort.cwl Branch/Commit ID: master |
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gatk4W-spark.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 GATK4. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
Path: gatk4W-spark.cwl Branch/Commit ID: release |
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timelimit2-wf.cwl
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Path: tests/timelimit2-wf.cwl Branch/Commit ID: master |
