Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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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: 54846feabbf008c1946db2a86d87252e0edd95b0 |
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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: 742dbafb5fb103d8578f48a0576c14dd8dae3b2a |
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RNASelector as a CWL workflow
https://doi.org/10.1007/s12275-011-1213-z |
![]() Path: workflows/rna-selector.cwl Branch/Commit ID: cac44f2cf14110fde9951161c663c4525772f616 |
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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: 742dbafb5fb103d8578f48a0576c14dd8dae3b2a |
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Build Bismark indices
Copy fasta_file file to the folder and run run bismark_genome_preparation script to prepare indices for Bismark Methylation Analysis. Bowtie2 aligner is used by default. The name of the output indices folder is equal to the genome input. |
![]() Path: workflows/bismark-index.cwl Branch/Commit ID: 2f0db4b3c515f91c5cfda19c78cf90d339390986 |
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workflow_5_main.cwl
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![]() Path: ros/wf5/workflow_5_main.cwl Branch/Commit ID: 1037933fde07b9b5a55a8e610069263c7772fa0d |
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count-lines6-wf.cwl
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![]() Path: v1.0/v1.0/count-lines6-wf.cwl Branch/Commit ID: e67f19d8a713759d761ecad050966d1eb043b85c |
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gathered exome alignment and somatic variant detection
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![]() Path: definitions/pipelines/gathered_somatic_exome.cwl Branch/Commit ID: e56f1024306aeb427d8aae2fff715ed2e8b8f86f |
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count-lines10-wf.cwl
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![]() Path: v1.0/v1.0/count-lines10-wf.cwl Branch/Commit ID: e67f19d8a713759d761ecad050966d1eb043b85c |
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phase VCF
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![]() Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 844c10a4466ab39c02e5bfa7a210c195b8efa77a |