Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
tRNA_selection.cwl
|
Path: tools/tRNA_selection.cwl Branch/Commit ID: ca6ca613 |
|
|
|
tRNA_selection.cwl
|
Path: tools/tRNA_selection.cwl Branch/Commit ID: c1f8b22 |
|
|
|
tRNA_selection.cwl
|
Path: tools/tRNA_selection.cwl Branch/Commit ID: 3b602cb |
|
|
|
rRNA_selection.cwl
|
Path: tools/rRNA_selection.cwl Branch/Commit ID: c1f8b22 |
|
|
|
tRNA_selection.cwl
|
Path: tools/tRNA_selection.cwl Branch/Commit ID: 6c856cd |
|
|
|
samtoolsW.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: samtoolsW.cwl Branch/Commit ID: release |
|
|
|
gk-full-step-qeheat.cwl
|
Path: cwl/gk-full-step-qeheat.cwl Branch/Commit ID: master |
|
|
|
scRNA-seq pipeline using Salmon and Alevin
|
Path: pipeline.cwl Branch/Commit ID: 8af5a1c |
|
|
|
tRNA_selection.cwl
|
Path: tools/tRNA_selection.cwl Branch/Commit ID: 3039744 |
|
|
|
rRNA_selection.cwl
|
Path: tools/rRNA_selection.cwl Branch/Commit ID: 5833078 |
