Explore Workflows
View already parsed workflows here or click here to add your own
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: fbeea265295ae596d5a3ba563e766be0c4fc26e8 |
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blastp_wnode_struct
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Path: task_types/tt_blastp_wnode_struct.cwl Branch/Commit ID: 61eaea2f746c8a1fc2a2b731056b068e28ca4e20 |
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assemble.cwl
Assemble a set of reads using SKESA |
Path: assemble.cwl Branch/Commit ID: 17bae57a1f00f5c6db8f3a82d86262f12b8153cf |
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wgs alignment and germline variant detection
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Path: definitions/pipelines/germline_wgs.cwl Branch/Commit ID: fbeea265295ae596d5a3ba563e766be0c4fc26e8 |
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gk-parse-current.cwl
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Path: cwl/gk-parse-current.cwl Branch/Commit ID: 48f4b8266a5a199cfc100d45148996f10a092f3b |
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Unaligned bam to sorted, markduped bam
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Path: definitions/subworkflows/align_sort_markdup.cwl Branch/Commit ID: ef7f3345b352319ec22dffba26c79df033b141f9 |
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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: fbeea265295ae596d5a3ba563e766be0c4fc26e8 |
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bam to trimmed fastqs and HISAT alignments
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Path: definitions/subworkflows/bam_to_trimmed_fastq_and_hisat_alignments.cwl Branch/Commit ID: 6949082038c1ad36d6e9848b97a2537aef2d3805 |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf_nonhuman.cwl Branch/Commit ID: 2f65fc96207a71b1cda4e246f808bed056608cd0 |
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align_sort_sa
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Path: task_types/tt_align_sort_sa.cwl Branch/Commit ID: add6b7724698694e0e72d972e2e85e1ae4e67902 |
