Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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allele-rnaseq-pe.cwl
Allele specific RNA-Seq paired-end workflow |
![]() Path: workflows/allele-rnaseq-pe.cwl Branch/Commit ID: 94471ee6c01b7bc17102e45e56e7366c2a52acdf |
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Apply filters to VCF file
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![]() Path: definitions/subworkflows/germline_filter_vcf.cwl Branch/Commit ID: 295e7b7f51727c0f2d6cc86ce817449b2e8dba3c |
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gathered exome alignment and somatic variant detection for cle purpose
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![]() Path: definitions/pipelines/somatic_exome_cle_gathered.cwl Branch/Commit ID: 061d3a2fbcd8a1c39c0b38c549e528deb24a9d54 |
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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: 146df33e2e44afa2a608ac72c036e6b6b871af93 |
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umi molecular alignment fastq workflow
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![]() Path: definitions/pipelines/alignment_umi_molecular.cwl Branch/Commit ID: 061d3a2fbcd8a1c39c0b38c549e528deb24a9d54 |
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Unaligned to aligned BAM
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![]() Path: definitions/subworkflows/align.cwl Branch/Commit ID: 789267ce0e3fed674ea5212a562315218fcf1bfc |
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Detect Variants workflow
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![]() Path: definitions/pipelines/detect_variants.cwl Branch/Commit ID: 2decd55996b912feb48be5db1b052aa3274ee405 |
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Add snv and indel bam-readcount files to a vcf
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![]() Path: definitions/subworkflows/vcf_readcount_annotator.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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gatk4_cohort_genotyping.cwl
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![]() Path: genomel/cwl/workflows/variant_calling/gatk4_cohort_genotyping.cwl Branch/Commit ID: 13c106834d6c9031de08496faeff521740a0c95f |
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Varscan Workflow
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![]() Path: definitions/subworkflows/varscan_pre_and_post_processing.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |