Explore Workflows
View already parsed workflows here or click here to add your own
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md5sum.cwl
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Path: md5sum/md5sum.cwl Branch/Commit ID: develop |
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Gz_Fasta_GC_TRF_CpG.cwl
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Path: workflow/Gz_Fasta_GC_TRF_CpG.cwl Branch/Commit ID: master |
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rhapsody_targeted_1.9-beta.cwl#VDJ_tcr.cwl
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Path: v1.9-beta/rhapsody_targeted_1.9-beta.cwl Branch/Commit ID: master Packed ID: VDJ_tcr.cwl |
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1st-wf-generated.cwl
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Path: 1st-wf-generated.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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WES GATK4 Preprocessing
Whole Exome Sequence analysis GATK4 Preprocessing |
Path: workflows/exomeseq-gatk4-preprocessing.cwl Branch/Commit ID: master |
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EMG pipeline v4.0 (single end version)
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Path: workflows/emg-pipeline-v4-single.cwl Branch/Commit ID: master |
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Dockstore.cwl
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Path: Dockstore.cwl Branch/Commit ID: master |
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EMG pipeline v3.0 (paired end version)
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Path: workflows/emg-pipeline-v3-paired.cwl Branch/Commit ID: 0cf06f1 |
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EMG pipeline v3.0 (paired end version)
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Path: workflows/emg-pipeline-v3-paired.cwl Branch/Commit ID: 5dc7c5c |
