Explore Workflows
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multiple.cwl
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![]() Path: multiple.cwl Branch/Commit ID: tutorial |
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collapsed_fastq_to_bam.cwl
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![]() Path: workflows/marianas/collapsed_fastq_to_bam.cwl Branch/Commit ID: master |
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SPRM pipeline
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![]() Path: pipeline.cwl Branch/Commit ID: 2ddb0ce |
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EMG pipeline v3.0 (single end version)
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![]() Path: workflows/emg-pipeline-v3.cwl Branch/Commit ID: master |
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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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dna.cwl#main
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![]() Path: workflows/make-to-cwl/dna.cwl Branch/Commit ID: master Packed ID: main |
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ST520108.cwl
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![]() Path: ST520108.cwl Branch/Commit ID: main |
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Dockstore.cwl
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![]() Path: Dockstore.cwl Branch/Commit ID: master |
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realignment.cwl
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![]() Path: modules/pair/realignment.cwl Branch/Commit ID: master |
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rRNA_selection.cwl
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![]() Path: tools/rRNA_selection.cwl Branch/Commit ID: caea457 |