Explore Workflows
View already parsed workflows here or click here to add your own
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checkm
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Path: checkm/wf_checkm.cwl Branch/Commit ID: test |
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spurious_annot
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Path: spurious_annot/wf_spurious_annot_pass1.cwl Branch/Commit ID: dev |
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rnaseq_pipeline_fastq.cwl
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Path: topmed-workflows/TOPMed_RNAseq_pipeline/rnaseq_pipeline_fastq.cwl Branch/Commit ID: master |
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methylCtools_multilib_start_with_trimmed.cwl
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Path: workflows/methylCtools/methylCtools_multilib_start_with_trimmed.cwl Branch/Commit ID: main |
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02-peakcall.cwl
DNase-seq 02 quantification |
Path: v1.0/DNase-seq_pipeline/02-peakcall.cwl Branch/Commit ID: master |
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sorter.cwl
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Path: steps/sorter.cwl Branch/Commit ID: master |
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gpas_gatk4.2.4.1_mutect2_tumor_only_workflow.cwl
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Path: gatk4-mutect2-tumor-only-cwl/gpas_gatk4.2.4.1_mutect2_tumor_only_workflow.cwl Branch/Commit ID: master |
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exomeseq.cwl#exomeseq-03-organizedirectories.cwl
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Path: packed/exomeseq.cwl Branch/Commit ID: qiime2-workflow Packed ID: exomeseq-03-organizedirectories.cwl |
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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: downsample_and_recall |
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scRNA-seq pipeline using Salmon and Alevin
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Path: pipeline.cwl Branch/Commit ID: baee233 |
