Explore Workflows
View already parsed workflows here or click here to add your own
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fillout_index_prefilter.cwl
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Path: cwl/fillout_index_prefilter.cwl Branch/Commit ID: master |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: No_filters_detect_variants |
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Per-chromosome pindel
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Path: pindel/pindel_cat.cwl Branch/Commit ID: master |
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ST520101.cwl
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Path: wf5201/ST520101.cwl Branch/Commit ID: main |
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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: master |
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gathered exome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_exome_gathered.cwl Branch/Commit ID: low-vaf |
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heatmap.cwl
Generates ATDP heatmap centered on TSS from an array of input BAM files and genelist TSV file. Returns array of heatmap JSON files with the names that have the same basenames as input BAM files, but with .json extension |
Path: workflows/heatmap.cwl Branch/Commit ID: b25b17651171f32005e9d879a9a049382f044baf |
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02-trim-pe.cwl
STARR-seq 02 trimming - reads: PE |
Path: v1.0/STARR-seq_pipeline/02-trim-pe.cwl Branch/Commit ID: master |
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pipeline-pe-blacklist-removal.cwl
ATAC-seq pipeline - reads: PE - with blacklist removal |
Path: v1.0/ATAC-seq_pipeline/pipeline-pe-blacklist-removal.cwl Branch/Commit ID: master |
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bam-genomecov-bigwig.cwl
creates genome coverage bigWig file from .bam file |
Path: workflows/bam-genomecov-bigwig.cwl Branch/Commit ID: v0.0.2 |
