Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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Per-region pindel
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![]() Path: definitions/subworkflows/pindel_cat.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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chipseq-header.cwl
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![]() Path: metadata/chipseq-header.cwl Branch/Commit ID: 10ce6e113f749c7bd725e426445220c3bdc5ddf1 |
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Running cellranger count and lineage inference
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![]() Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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Replace legacy AML Trio Assay
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![]() Path: definitions/pipelines/aml_trio_cle.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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Apply filters to VCF file
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![]() Path: definitions/subworkflows/filter_vcf_nonhuman.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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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: b38b0070edf910984f29a4a495b5dfa525b8b305 |
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Varscan Workflow
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![]() Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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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: 061d3a2fbcd8a1c39c0b38c549e528deb24a9d54 |
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gdc_dnaseq.aligned_reads.workflow.cwl
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![]() Path: workflows/gdc_dnaseq.aligned_reads.workflow.cwl Branch/Commit ID: 27a6d99cd517538eb345e2319d0903a864ea5965 |
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umi duplex alignment fastq workflow
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![]() Path: definitions/pipelines/alignment_umi_duplex.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |