Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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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: 39ac49f5d080bbb6bfa97246f46a5b621254f622 |
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format_rrnas_from_seq_entry
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![]() Path: task_types/tt_format_rrnas_from_seq_entry.cwl Branch/Commit ID: 041a234a935c7af7d3db95353ef80c61c88fc010 |
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phase VCF
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![]() Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: f45b52a24c7b54a75368dcbab24b4eb2c5a9c75a |
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RNA-Seq alignment and transcript/gene abundance workflow
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![]() Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 233f026ffce240071edda526391be0c03186fce8 |
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RNA-Seq alignment and transcript/gene abundance workflow
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![]() Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 68eda647259849ca81ac0bb07a24bc8a4465a630 |
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taxcheck.cwl
Perform taxonomic identification tasks on an input genome |
![]() Path: taxcheck.cwl Branch/Commit ID: 2229f26ec424f9ebeb3db7fec3bd3f84a38c7485 |
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Unaligned BAM to BQSR and VCF
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![]() Path: definitions/subworkflows/bam_to_bqsr_no_dup_marking.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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fp_filter workflow
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![]() Path: definitions/subworkflows/fp_filter.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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strelka workflow
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![]() Path: definitions/subworkflows/strelka_and_post_processing.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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mutect parallel workflow
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![]() Path: definitions/subworkflows/mutect.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |