Explore Workflows
View already parsed workflows here or click here to add your own
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collate_unique_SSU_headers.cwl
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Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: 6c856cd2d7dd1c21016341feb942ada0fb5630cb |
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fastq2fasta-create-bwaindex.cwl
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Path: cwl/fastq2fasta/fastq2fasta-create-bwaindex.cwl Branch/Commit ID: 1b1139d72e1bcc870424c87c7325e27ed79bc42c |
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process VCF workflow
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Path: definitions/subworkflows/strelka_process_vcf.cwl Branch/Commit ID: 0b6e8fd8ead7644cf5398395b76af5cf4011686f |
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integrity.cwl
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Path: workflows/bamfastq_align/integrity.cwl Branch/Commit ID: 1046947f8d2923e6563b3aceac9e435554c5bea1 |
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: adcae308fdccaa1190083616118dfadb4df65dca |
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: c23dc7f113ca0b0a3127a5d6c696e98d4799460c |
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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: c23dc7f113ca0b0a3127a5d6c696e98d4799460c |
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CODEX analysis pipeline using Cytokit
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Path: pipeline.cwl Branch/Commit ID: f3d6e97408b1c542641b313c1ea8d3115d72e3f8 |
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cluster_blastp_wnode and gpx_qdump combined
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Path: task_types/tt_cluster_and_qdump.cwl Branch/Commit ID: 7c8eb4d23c3c9859f57421643710c0b6d57b606c |
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Detect Variants workflow
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Path: definitions/pipelines/detect_variants_mouse.cwl Branch/Commit ID: c23dc7f113ca0b0a3127a5d6c696e98d4799460c |
