Explore Workflows
View already parsed workflows here or click here to add your own
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umi duplex alignment workflow
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Path: definitions/subworkflows/duplex_alignment.cwl Branch/Commit ID: low-vaf |
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cmsearch-multimodel.cwl
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Path: workflows/cmsearch-multimodel.cwl Branch/Commit ID: f6b5196 |
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validate_interleaved_fq.cwl
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Path: cwls/validate_interleaved_fq.cwl Branch/Commit ID: develop |
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genomics-workspace-genome.cwl
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Path: flow_genomicsWorkspace/genomics-workspace-genome.cwl Branch/Commit ID: master |
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final_filtering
Final filtering |
Path: structuralvariants/cwl/subworkflows/final_filtering.cwl Branch/Commit ID: master |
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Gathered Downsample and HaplotypeCaller
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Path: definitions/pipelines/gathered_downsample_and_recall.cwl Branch/Commit ID: master |
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cnv_exomedepth
CNV ExomeDepth calling |
Path: structuralvariants/cwl/subworkflows/cnv_exome_depth.cwl Branch/Commit ID: 1.0.7 |
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Merge, annotate, and generate a TSV for SVs
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: master |
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WF5201.cwl
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Path: WF5201.cwl Branch/Commit ID: main |
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Ambarish_Kumar_SOP-GATK-SAR-CoV-2.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: Ambarish_Kumar_SOP/Ambarish_Kumar_SOP-GATK-SAR-CoV-2.cwl Branch/Commit ID: main |
