Explore Workflows
View already parsed workflows here or click here to add your own
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cnv.cwl
Copynumber variation workflow, runs ADTEx and Varscan |
Path: cnv.cwl Branch/Commit ID: 1.0.1 |
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diadem_workflow_test1.cwl
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Path: diadem_workflow_test1.cwl Branch/Commit ID: main |
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PGAP Pipeline, simple user input, PGAPX-134
PGAP pipeline for external usage, powered via containers, simple user input: (FASTA + yaml only, no template) |
Path: pgap.cwl Branch/Commit ID: test |
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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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rnaseq_pipeline_fastq_checker.cwl
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Path: workflow/checker-workflows/rnaseq_pipeline_fastq_checker.cwl Branch/Commit ID: master |
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Chipseq alignment with qc and creating homer tag directory
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Path: definitions/pipelines/chipseq.cwl Branch/Commit ID: low-vaf |
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Single-cell Reference Indices
Single-cell Reference Indices Builds a Cell Ranger and Cell Ranger ARC compatible reference folders from the custom genome FASTA and gene GTF annotation files |
Path: workflows/sc-ref-indices-wf.cwl Branch/Commit ID: main |
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Bacterial Annotation, pass 1, genemark training, by HMMs (first pass)
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Path: bacterial_annot/wf_orf_hmms.cwl Branch/Commit ID: test |
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02-trim-se.cwl
ATAC-seq 02 trimming - reads: SE |
Path: v1.0/ATAC-seq_pipeline/02-trim-se.cwl Branch/Commit ID: master |
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kf-cram2gvcf-bam-input.cwl
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Path: workflows/kf-cram2gvcf-bam-input.cwl Branch/Commit ID: dev |
