Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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Dockstore.cwl
INTEGRATE workflow: untar, tophat align, samtools index, Integrate fusion |
![]() Path: Dockstore.cwl Branch/Commit ID: master |
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pcr-bottleneck-coef.cwl
ChIP-seq - map - PCR Bottleneck Coefficients |
![]() Path: v1.0/map/pcr-bottleneck-coef.cwl Branch/Commit ID: v1.0.0 |
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04-quantification-pe-stranded.cwl
RNA-seq 04 quantification |
![]() Path: v1.0/RNA-seq_pipeline/04-quantification-pe-stranded.cwl Branch/Commit ID: master |
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ValidateOpticalPSF
Validate telescope (whole dish) optical point-spread function |
![]() Path: workflows/ValidateOpticalPSF.cwl Branch/Commit ID: main |
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output-arrays-file-wf.cwl
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![]() Path: v1.0/v1.0/output-arrays-file-wf.cwl Branch/Commit ID: master |
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createindex.cwl
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![]() Path: workflow/createindex.cwl Branch/Commit ID: master |
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bwa_mem
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![]() Path: structuralvariants/cwl/subworkflows/bwa_mem.cwl Branch/Commit ID: 1.0.9 |
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wf_step3.cwl
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![]() Path: yw_cwl_modeling/additional_test_cases/wf_step3.cwl Branch/Commit ID: master |
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01-qc-pe.cwl
RNA-seq 01 QC - reads: PE |
![]() Path: v1.0/RNA-seq_pipeline/01-qc-pe.cwl Branch/Commit ID: master |
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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 |