Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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Apply filters to VCF file
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![]() Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: 480c438a6a7e78c624712aec01bc4214d2bc179c |
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exome alignment and somatic variant detection for cle purpose
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![]() Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: 7638b3075863ae8172f4adaec82fb2eb8e80d3d5 |
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SoupX (workflow) - an R package for the estimation and removal of cell free mRNA contamination
Wrapped in a workflow SoupX tool for easy access to Cell Ranger pipeline compressed outputs. |
![]() Path: tools/soupx-subworkflow.cwl Branch/Commit ID: 8049a781ac4aae579fbd3036fa0bf654532f15be |
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02-peakcall.cwl
DNase-seq 02 quantification |
![]() Path: v1.0/DNase-seq_pipeline/02-peakcall.cwl Branch/Commit ID: 1a0dd34d59ec983d1f7ad77bff35da2f016e3134 |
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umi duplex alignment fastq workflow
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![]() Path: definitions/pipelines/alignment_umi_duplex.cwl Branch/Commit ID: 43c790e2ee6a0f3f42e40fb4d9a9005eb8de747a |
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joint genotyping for trios or small cohorts
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![]() Path: definitions/subworkflows/joint_genotype.cwl Branch/Commit ID: 7638b3075863ae8172f4adaec82fb2eb8e80d3d5 |
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gdc_dnaseq.bamfastq_align.workflow.cwl
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![]() Path: workflows/gdc_dnaseq.bamfastq_align.workflow.cwl Branch/Commit ID: 27a6d99cd517538eb345e2319d0903a864ea5965 |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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![]() Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: 7638b3075863ae8172f4adaec82fb2eb8e80d3d5 |
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realignment.cwl
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![]() Path: modules/pair/realignment.cwl Branch/Commit ID: 54c9e02751dc65607f0e334c0eb1a5e646cc71d6 |
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downsample unaligned BAM and align
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![]() Path: definitions/subworkflows/downsampled_alignment.cwl Branch/Commit ID: 449bc7e45bb02316d040f73838ef18359e770268 |