Explore Workflows
View already parsed workflows here or click here to add your own
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STAR-Alignment-PE
This workflow aligns the fastq files using STAR for no spliced genomes |
Path: workflows/Alignments/star-alignment-nosplice.cwl Branch/Commit ID: master |
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two-step-workflow.cwl
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Path: _includes/cwl/two-step-workflow.cwl Branch/Commit ID: gh-pages |
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cnv_exomedepth
CNV ExomeDepth calling |
Path: structuralvariants/cwl/subworkflows/cnv_exome_depth.cwl Branch/Commit ID: 1.0.7 |
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SSU-from-tablehits.cwl
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Path: tools/SSU-from-tablehits.cwl Branch/Commit ID: master |
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biowardrobe_chipseq_se.cwl
The workflow is used to run CHIP-Seq basic analysis with single-end input FASTQ file. In outputs it returns coordinate sorted BAM file alongside with index BAI file, quality statistics of the input FASTQ file, reads coverage in a form of bigWig file, peaks calling data in a form of narrowPeak or broadPeak files. |
Path: biowardrobe_chipseq_se.cwl Branch/Commit ID: v0.0.5 |
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TOPMed Alignment
A CWL wrapper of the TopMed alignment workflow described here: https://github.com/statgen/docker-alignment Tool Author: Hyun Min Kang (hmkang@umich.edu) and Adrian Tan (atks@umich.edu) Wrapper Author: Marko Zecevic (marko.zecevic@sbgenomics.com) |
Path: aligner/sbg-alignment-cwl/topmed-alignment.cwl Branch/Commit ID: no-id |
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03-map-se-blacklist-removal.cwl
ATAC-seq 03 mapping - reads: SE |
Path: v1.0/ATAC-seq_pipeline/03-map-se-blacklist-removal.cwl Branch/Commit ID: v1.0.0 |
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Protein_Inference_workflow_challenge.cwl
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Path: Protein_Inference_workflow_challenge.cwl Branch/Commit ID: master |
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EMG assembly for paired end Illumina
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Path: workflows/emg-assembly.cwl Branch/Commit ID: master |
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md5sum-workflow.cwl
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Path: md5sum/md5sum-workflow.cwl Branch/Commit ID: 1.0.1 |
