Explore Workflows
View already parsed workflows here or click here to add your own
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biowardrobe_chipseq_se.cwl
The workflow is used to run CHIP-Seq basic analysis with single-end input FASTQ file. In outputs it returns coordinate sorted BAM file alongside with index BAI file, quality statistics of the input FASTQ file, reads coverage in a form of bigWig file, peaks calling data in a form of narrowPeak or broadPeak files. |
Path: biowardrobe_chipseq_se.cwl Branch/Commit ID: v0.0.5 |
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kfdrc_bwamem_subwf.cwl
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Path: workflows/dev/ultra-opt/kfdrc_bwamem_subwf.cwl Branch/Commit ID: master |
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EMG pipeline v3.0 (paired end version)
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Path: workflows/emg-pipeline-v3-paired.cwl Branch/Commit ID: 9c57dba |
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scRNA-seq pipeline using Salmon and Alevin
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Path: pipeline.cwl Branch/Commit ID: 16dd8ca |
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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: v1.0 |
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bam_readcount workflow
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Path: definitions/subworkflows/bam_readcount.cwl Branch/Commit ID: master |
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wf.cwl
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Path: NF_Hello/wf.cwl Branch/Commit ID: master |
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pipeline.cwl
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Path: pipeline.cwl Branch/Commit ID: 20ea8da |
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bulk_analysis.cwl
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Path: steps/bulk_analysis.cwl Branch/Commit ID: v1.0 |
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Merge, annotate, and generate a TSV for SVs
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: low-vaf |
