Explore Workflows
View already parsed workflows here or click here to add your own
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wf_full_IDR_pipeline_2inputs_sample.cwl
This workflow essentially restructures the inputs before sending to wf_full_IDR_pipeline_2inputs.cwl |
Path: cwl/wf_full_IDR_pipeline_2inputs_sample.cwl Branch/Commit ID: master |
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preprocess.cwl
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Path: cwl_s/preprocess.cwl Branch/Commit ID: master |
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chksum_seqval_wf_interleaved_fq.cwl
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Path: cwls/chksum_seqval_wf_interleaved_fq.cwl Branch/Commit ID: 0.4.1 |
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exome alignment with qc, no bqsr, no verify_bam_id
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Path: definitions/pipelines/alignment_exome_nonhuman.cwl Branch/Commit ID: master |
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somatic_exome: exome alignment and somatic variant detection
somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml |
Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: master |
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Exome QC workflow
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Path: qc/workflow_exome.cwl Branch/Commit ID: toil_compatibility |
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Subworkflow to allow calling cnvkit with cram instead of bam files
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Path: definitions/subworkflows/cram_to_cnvkit.cwl Branch/Commit ID: master |
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Gathered Downsample and HaplotypeCaller
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Path: definitions/pipelines/gathered_downsample_and_recall.cwl Branch/Commit ID: master |
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abc_step01
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Path: abc_enhancer_gene_prediction/abc-enchancer-gene-prediction-wf.cwl.steps/abc_step01.cwl Branch/Commit ID: main |
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pindel parallel workflow
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Path: pindel/workflow.cwl Branch/Commit ID: master |
