Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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pipeline-bam2vcf-distr.cwl
DNAseq pipeline from bam to vcf in distributed mode |
![]() Path: pipeline/pipeline-bam2vcf-distr.cwl Branch/Commit ID: d20382adfe7285cb517a25d95d2bcb7586546e23 |
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: 0798b3933ae3e6486596294984c7ffee50b94ef5 |
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chipseq-header.cwl
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![]() Path: metadata/chipseq-header.cwl Branch/Commit ID: 657eb494c880480574ac111dab4e11a06453d168 |
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exome alignment and germline variant detection, with optitype for HLA typing
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![]() Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: f615832615c3b41728df8e47b72ef11e37e6a9e5 |
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ATACseq.cwl
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![]() Path: CWL/workflows/ATACseq.cwl Branch/Commit ID: da07ef9c506ba921438df0bc9f6e1ee57b7d5910 |
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Identifies non-coding RNAs using Rfams covariance models
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![]() Path: workflows/cmsearch-multimodel-wf.cwl Branch/Commit ID: 55fad182885822a2927bba6bf9cd517e60d9330e |
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align_sort_sa
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![]() Path: task_types/tt_align_sort_sa.cwl Branch/Commit ID: 71e3a42eadc007b66ef4689086530dfc3123d32f |
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exome alignment and somatic variant detection for cle purpose
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![]() Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 |
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Running cellranger count and lineage inference
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![]() Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: c625e05eefb1754353c1bdfa46c01dc61e6233dd |
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bam to trimmed fastqs and biscuit alignments
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![]() Path: definitions/subworkflows/bam_to_trimmed_fastq_and_biscuit_alignments.cwl Branch/Commit ID: cfdcd0735e8fb1ac0b97f1a5cbe0cc7e00033dd0 |