Explore Workflows
View already parsed workflows here or click here to add your own
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TransDecoder 2 step workflow, running TransDecoder.LongOrfs (step 1) followed by TransDecoder.Predict (step2)
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Path: workflows/TransDecoder-v5-wf-2steps.cwl Branch/Commit ID: fix_sbg_namespace |
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LodSeq
LodSeq performs the genetic linkage analysis across families, by computing lod-scores given a gvcf file and a related tfam pedigree file. |
Path: workflows/cwltoil/lodseq.cwl Branch/Commit ID: master |
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extract_gencoll_ids
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Path: task_types/tt_extract_gencoll_ids.cwl Branch/Commit ID: master |
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hi-c-processing-pairs-nore.cwl
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Path: cwl_awsem_v1/hi-c-processing-pairs-nore.cwl Branch/Commit ID: master |
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cnv_exomedepth
CNV ExomeDepth calling |
Path: structuralvariants/cwl/subworkflows/cnv_exome_depth.cwl Branch/Commit ID: master |
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transform.cwl
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Path: workflows/dnaseq/transform.cwl Branch/Commit ID: 1.1 |
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preprocess_vcf.cwl
This workflow will perform preprocessing steps on VCFs for the OxoG/Variantbam/Annotation workflow. |
Path: preprocess_vcf.cwl Branch/Commit ID: 1.0.0 |
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PGAP Pipeline, simple user input, PGAPX-134
PGAP pipeline for external usage, powered via containers, simple user input: (FASTA + yaml only, no template) |
Path: pgap.cwl Branch/Commit ID: test |
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NonSpliced RNAseq workflow
Workflow for NonSpliced RNAseq data alignment with multiple aligners. Steps: - workflow_illumina_quality.cwl: - FastQC (control) - fastp (trimming) - bowtie2 (read mapping) - sam_to_sorted-bam - featurecounts (transcript read counts) - kallisto (transcript [pseudo]counts) |
Path: cwl/workflows/workflow_RNAseq_NonSpliced.cwl Branch/Commit ID: master |
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sum-wf-noET.cwl
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Path: tests/sum-wf-noET.cwl Branch/Commit ID: main |
