Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and germline variant detection, with optitype for HLA typing
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Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: low-vaf |
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cnv_codex
CNV CODEX calling |
Path: structuralvariants/subworkflows/cnv_codex.cwl Branch/Commit ID: 3bb03c9b |
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preprocess fasta
Remove reads from fasta files based on sequence stats. Return fasta files with reads passed and reads removed. |
Path: CWL/Workflows/preprocess-fasta.workflow.cwl Branch/Commit ID: master |
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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 |
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apply_cal.cwl
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Path: utils/IM/LINC/lincSun/workflow/apply_cal.cwl Branch/Commit ID: master |
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pass-unconnected.cwl
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Path: tests/pass-unconnected.cwl Branch/Commit ID: main |
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pipeline-pe.cwl
ATAC-seq pipeline - reads: PE |
Path: v1.0/ATAC-seq_pipeline/pipeline-pe.cwl Branch/Commit ID: master |
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step-valuefrom-wf.cwl
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Path: tests/step-valuefrom-wf.cwl Branch/Commit ID: main |
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Seed Search Compartments
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Path: protein_alignment/wf_seed.cwl Branch/Commit ID: master |
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rmats_wf.cwl
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Path: workflow/rmats_wf.cwl Branch/Commit ID: master |
