Explore Workflows
View already parsed workflows here or click here to add your own
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count-lines1-wf.cwl
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![]() Path: tests/wf/count-lines1-wf.cwl Branch/Commit ID: main |
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minibam_sub_wf.cwl
This is a subworkflow of the main oxog_varbam_annotat_wf workflow - this is not meant to be run as a stand-alone workflow! |
![]() Path: minibam_sub_wf.cwl Branch/Commit ID: master |
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Functional analyis of sequences that match the 16S SSU
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![]() Path: workflows/16S_taxonomic_analysis.cwl Branch/Commit ID: ca6ca61 |
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Create Genomic Collection for Bacterial Pipeline
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![]() Path: genomic_source/wf_genomic_source.cwl Branch/Commit ID: master |
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Molecular Dynamics Simulation.
CWL version of the md_list.cwl workflow for HPC. This performs a system setup and runs a molecular dynamics simulation on the structure passed to this workflow. This workflow uses the md_gather.cwl sub-workflow to gather the outputs together to return these. To work with more than one structure this workflow can be called from either the md_launch.cwl workflow, or the md_launch_mutate.cwl workflow. These use scatter for parallelising the workflow. md_launch.cwl operates on a list of individual input molecule files. md_launch_mutate.cwl operates on a single input molecule file, and a list of mutations to apply to that molecule. Within that list of mutations, a value of 'WT' will indicate that the molecule should be simulated without any mutation being applied. |
![]() Path: md_list.cwl Branch/Commit ID: main |
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SSU-from-tablehits.cwl
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![]() Path: tools/SSU-from-tablehits.cwl Branch/Commit ID: 43d2fb8 |
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msi.cwl
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![]() Path: workflows/subworkflows/msi.cwl Branch/Commit ID: master |
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pipeline_cavatica.cwl
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![]() Path: pipeline_cavatica.cwl Branch/Commit ID: main |
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exome alignment and somatic variant detection
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![]() Path: definitions/pipelines/somatic_exome_nonhuman.cwl Branch/Commit ID: low-vaf |
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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/CWL/Ambarish_Kumar_SOP-GATK-SAR-CoV-2.cwl Branch/Commit ID: main |