Explore Workflows
View already parsed workflows here or click here to add your own
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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: 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: workflow1_11.cwl Branch/Commit ID: main Packed ID: main |
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ST520111.cwl
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![]() Path: wf5201/ST520111.cwl Branch/Commit ID: main |
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exomeseq-01-preprocessing.cwl
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![]() Path: subworkflows/exomeseq-01-preprocessing.cwl Branch/Commit ID: gatk4-fixes |
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cmsearch-multimodel.cwl
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![]() Path: workflows/cmsearch-multimodel.cwl Branch/Commit ID: c211071 |
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repliseq-parta.cwl
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![]() Path: cwl_awsem_v1/repliseq/repliseq-parta.cwl Branch/Commit ID: master |
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snapanalysis_setup_and_analyze.cwl
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![]() Path: steps/snapanalysis_setup_and_analyze.cwl Branch/Commit ID: bb023f9 |
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WGS processing workflow for single sample
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![]() Path: WGS-processing/cwl/helper/bwamem-gatk-report-wf.cwl Branch/Commit ID: main |
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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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Apply filters to VCF file
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![]() Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: master |