Explore Workflows
View already parsed workflows here or click here to add your own
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03-map-pe.cwl
STARR-seq 03 mapping - reads: PE |
Path: v1.0/STARR-seq_pipeline/03-map-pe.cwl Branch/Commit ID: master |
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kfdrc_RNAseq_workflow.cwl
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Path: workflow/kfdrc_RNAseq_workflow.cwl Branch/Commit ID: master |
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LodSeq
LodSeq performs the genetic linkage analysis across families, by computing lod-scores given a gvcf file and a related tfam pedigree file. |
Path: workflows/cwltoil/lodseq.cwl Branch/Commit ID: master |
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assm_assm_blastn_wnode
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Path: task_types/tt_assm_assm_blastn_wnode.cwl Branch/Commit ID: dev |
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count-lines6-wf.cwl
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Path: v1.0/v1.0/count-lines6-wf.cwl Branch/Commit ID: master |
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example_workflow.cwl
Example CWL workflow that uses some advanced features |
Path: cwl/example_workflow.cwl Branch/Commit ID: master |
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gatk4W.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.cwl Branch/Commit ID: release |
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stage_data_workflow.vcf_to_aliquot_maf.cwl
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Path: vcf-to-aliquot-maf/subworkflows/stage_data_workflow.vcf_to_aliquot_maf.cwl Branch/Commit ID: main |
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HS Metrics workflow
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Path: definitions/subworkflows/hs_metrics.cwl Branch/Commit ID: No_filters_detect_variants |
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workflow.cwl
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Path: cwl/console-CAD/workflow.cwl Branch/Commit ID: master |
