Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: 28d1065759cbd389594ee33b41fd1103ced5436d |
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phase VCF
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Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 67f56d3b9c70ad56019ed8aa8d50a128e02be43b |
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scatter-wf1.cwl
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Path: v1.0/v1.0/scatter-wf1.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b |
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bam to trimmed fastqs and HISAT alignments
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Path: definitions/subworkflows/bam_to_trimmed_fastq_and_hisat_alignments.cwl Branch/Commit ID: c625e05eefb1754353c1bdfa46c01dc61e6233dd |
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scatter GATK HaplotypeCaller over intervals
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Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: cfdcd0735e8fb1ac0b97f1a5cbe0cc7e00033dd0 |
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Whole genome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 |
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: f45b52a24c7b54a75368dcbab24b4eb2c5a9c75a |
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format_rrnas_from_seq_entry
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Path: task_types/tt_format_rrnas_from_seq_entry.cwl Branch/Commit ID: 47ccbd0bc7b45bf8b3c92d0a66c1a9a232367a5d |
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Gathered Downsample and HaplotypeCaller
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Path: definitions/pipelines/gathered_downsample_and_recall.cwl Branch/Commit ID: e8b7759826df40b8bb821b40b15aea960a4951c4 |
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FASTQ to BQSR
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Path: definitions/subworkflows/fastq_to_bqsr.cwl Branch/Commit ID: ac87e0584685fe04e4010ecd77ae4f055f21d788 |
