Explore Workflows
View already parsed workflows here or click here to add your own
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final_filtering
Final filtering |
Path: structuralvariants/cwl/subworkflows/final_filtering.cwl Branch/Commit ID: master |
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chksum_seqval_wf_interleaved_fq.cwl
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Path: cwls/chksum_seqval_wf_interleaved_fq.cwl Branch/Commit ID: 0.2.1 |
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find_hotspots_in_normals.cwl
Workflow to find hotspot VAFs from duplex (for Tumor sample) and unfiltered (for Normal sample) pileups. These inputs are all required to be sorted in the same order: sample_ids patient_ids sample_classes unfiltered_pileups duplex_pileups |
Path: workflows/subworkflows/find_hotspots_in_normals.cwl Branch/Commit ID: master |
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Tumor-Only Detect Variants workflow
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Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: master |
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fp_filter workflow
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Path: subworkflows/fp_filter.cwl Branch/Commit ID: master |
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BD Rhapsody™ WTA Analysis Pipeline
The BD Rhapsody™ WTA Analysis Pipeline is used to create sequencing libraries from single cell transcriptomes without having to specify a targeted panel. After sequencing, the analysis pipeline takes the FASTQ files, a reference genome file and a transcriptome annotation file for gene alignment. The pipeline generates molecular counts per cell, read counts per cell, metrics, and an alignment file. |
Path: v1.8/rhapsody_wta_1.8.cwl Branch/Commit ID: master Packed ID: main |
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oxog_sub_wf.cwl
This is a subworkflow of the main oxog_varbam_annotat_wf workflow - this is not meant to be run as a stand-alone workflow! |
Path: oxog_sub_wf.cwl Branch/Commit ID: 1.0.0 |
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cmsearch-multimodel.cwl
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Path: workflows/cmsearch-multimodel.cwl Branch/Commit ID: 0cd2d70 |
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bqsr-distr.cwl
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Path: stage/bqsr-distr.cwl Branch/Commit ID: master |
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EMG assembly for paired end Illumina
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Path: workflows/emg-assembly.cwl Branch/Commit ID: 708fd97 |
