Explore Workflows
View already parsed workflows here or click here to add your own
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EMG pipeline v3.0 (single end version)
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Path: workflows/emg-pipeline-v3.cwl Branch/Commit ID: 5dc7c5c |
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bam_filtering
BAM filtering |
Path: structuralvariants/cwl/subworkflows/bam_filtering.cwl Branch/Commit ID: 1.0.6 |
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functional analysis prediction with InterProScan
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Path: workflows/functional_analysis.cwl Branch/Commit ID: 0cd2d70 |
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biowardrobe_chipseq_se.cwl
Current 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: v0.0.2 |
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02-trim-pe.cwl
STARR-seq 02 trimming - reads: PE |
Path: v1.0/STARR-seq_pipeline/02-trim-pe.cwl Branch/Commit ID: master |
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Trim and reformat reads (single and paired end version)
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Path: workflows/trim_and_reformat_reads.cwl Branch/Commit ID: master |
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mutect parallel workflow
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Path: mutect/workflow.cwl Branch/Commit ID: master |
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wf_fastqc.cwl
This workflow takes in single-end reads, and performs the following steps in order: demux_se.cwl (does not actually demux for single end, but mirrors the paired-end processing protocol) |
Path: cwl/wf_fastqc.cwl Branch/Commit ID: master |
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A workflow that aligns a fasta file and provides statistics on the SAM file
A workflow that aligns a fasta file and provides statistics on the SAM file |
Path: version_1_2/sub_workflow_metrics.cwl Branch/Commit ID: develop |
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qiime2 identify differentially abundant features
Differential abundance testing with ANCOM from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
Path: packed/qiime2-step2-dada2.cwl Branch/Commit ID: qiime2-workflow-paired Packed ID: qiime2-09-ancom.cwl |
