Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
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 |
|
|
|
wf-variantcall.cwl
|
Path: NA12878-chr20/NA12878-platinum-chr20-workflow/wf-variantcall.cwl Branch/Commit ID: master |
|
|
|
cnv_codex
CNV CODEX calling |
Path: structuralvariants/cwl/subworkflows/cnv_codex.cwl Branch/Commit ID: 1.0.7 |
|
|
|
validate_interleaved_fq.cwl
|
Path: cwls/validate_interleaved_fq.cwl Branch/Commit ID: 0.2.3 |
|
|
|
somatic_exome: exome alignment and somatic variant detection
somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml |
Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: master |
|
|
|
cpo-pipeline.cwl
|
Path: workflows/cpo-pipeline/cpo-pipeline.cwl Branch/Commit ID: master |
|
|
|
metaphlan_wfl.cwl
|
Path: metaphlan_wfl.cwl Branch/Commit ID: master |
|
|
|
filtering.cwl
|
Path: workflows/subworkflows/filtering.cwl Branch/Commit ID: master |
|
|
|
workflow_select_shape.cwl
|
Path: cwl/workflow_select_shape.cwl Branch/Commit ID: master |
|
|
|
wf-variantcall.cwl
|
Path: somatic/somatic-workflow/wf-variantcall.cwl Branch/Commit ID: master |
