Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
Add snv and indel bam-readcount files to a vcf
|
Path: subworkflows/vcf_readcount_annotator.cwl Branch/Commit ID: master |
|
|
|
sum-wf-noET.cwl
|
Path: tests/sum-wf-noET.cwl Branch/Commit ID: main |
|
|
|
EMG QC workflow, (paired end version). Benchmarking with MG-RAST expt.
|
Path: workflows/emg-qc-paired.cwl Branch/Commit ID: c1f8b22 |
|
|
|
running cellranger mkfastq and count
|
Path: definitions/subworkflows/cellranger_mkfastq_and_count.cwl Branch/Commit ID: No_filters_detect_variants |
|
|
|
alignment_prep.cwl
|
Path: genomel/cwl/workflows/harmonization/alignment_prep.cwl Branch/Commit ID: a83f16e804bc36a2823e32fa2fb649ebe2e05f4c |
|
|
|
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 |
|
|
|
wf_amr_prot.cwl
|
Path: amr_finder/wf_amr_prot.cwl Branch/Commit ID: master |
|
|
|
collate_unique_SSU_headers.cwl
|
Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: d3b8e45 |
|
|
|
raw-reads-2.cwl
|
Path: workflows/conditionals/raw-reads/raw-reads-2.cwl Branch/Commit ID: master |
|
|
|
preprocess_vcf.cwl
This workflow will perform preprocessing steps on VCFs for the OxoG/Variantbam/Annotation workflow. |
Path: preprocess_vcf.cwl Branch/Commit ID: develop |
