Explore Workflows
View already parsed workflows here or click here to add your own
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Detect Variants workflow
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Path: definitions/pipelines/detect_variants_nonhuman.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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count-lines1-wf.cwl
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Path: tests/wf/count-lines1-wf.cwl Branch/Commit ID: 1eb6bfe3c77aebaf69453a669d21ae7a5a78056f |
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wgs alignment with qc
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Path: definitions/pipelines/alignment_wgs.cwl Branch/Commit ID: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e |
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blastp_wnode_naming
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Path: task_types/tt_blastp_wnode_naming.cwl Branch/Commit ID: 861d9baa067af98d794ba0ed4e43aa42e37d8a24 |
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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: 861d9baa067af98d794ba0ed4e43aa42e37d8a24 |
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exome alignment and tumor-only variant detection
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Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 97572e3a088d79f6a4166385f79e79ea77b11470 |
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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: 97572e3a088d79f6a4166385f79e79ea77b11470 |
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hmmsearch_wnode and gpx_qdump combined workflow to apply scatter/gather
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Path: task_types/tt_hmmsearch_wnode_plus_qdump.cwl Branch/Commit ID: 5282690e0f634a5f83107ba878fe62cbbb347408 |
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: 5dc7c5ca618a248a99bd4bf5f3042cdb21947193 |
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kmer_seq_entry_extract_wnode
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Path: task_types/tt_kmer_seq_entry_extract_wnode.cwl Branch/Commit ID: 8fb4ac7f5a66897206c7469101a471108b06eada |
