Explore Workflows
View already parsed workflows here or click here to add your own
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step-valuefrom2-wf.cwl
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Path: tests/step-valuefrom2-wf.cwl Branch/Commit ID: 664835e83eb5e57eee18a04ce7b05fb9d70d77b7 |
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Chipseq alignment for mouse with qc and creating homer tag directory
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Path: definitions/pipelines/chipseq_alignment_mouse.cwl Branch/Commit ID: 22fce2dbdada0c4135b6f0677f78535cf980cb07 |
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scatter GATK HaplotypeCaller over intervals
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Path: detect_variants/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: ee1afbcbe01fd17715b54d23e556a23086aeec57 |
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FASTQ to BQSR
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Path: definitions/subworkflows/fastq_to_bqsr.cwl Branch/Commit ID: 39ac49f5d080bbb6bfa97246f46a5b621254f622 |
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wffail.cwl
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Path: tests/wf/wffail.cwl Branch/Commit ID: dbc4c4c2ad30ed31367b4fbcc3bb4084fdcabaa2 |
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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: 22880e0f41d0420a17d643e8a6e8ee18165bbfbf |
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Whole genome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71 |
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sec-wf-out.cwl
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Path: tests/wf/sec-wf-out.cwl Branch/Commit ID: 63f539ba60e91f0cb3ce7cda2c5da5c65525c375 |
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umi duplex alignment fastq workflow
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Path: definitions/pipelines/alignment_umi_duplex.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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scatter GATK HaplotypeCaller over intervals
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Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: b7d9ace34664d3cedb16f2512c8a6dc6debfc8ca |
