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: v0.0.3 |
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Seed Search Compartments
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Path: protein_alignment/wf_seed.cwl Branch/Commit ID: master |
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cnv_codex
CNV CODEX calling |
Path: structuralvariants/cwl/subworkflows/cnv_codex.cwl Branch/Commit ID: 1.0.5 |
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ProteinInferenceWorkflow.cwl
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Path: ProteinInferenceWorkflow.cwl Branch/Commit ID: master |
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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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qiime2 Deblur detect/correct sequence data
Option 2: Deblur from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
Path: packed/qiime2-step2-deblur.cwl Branch/Commit ID: qiime2-workflow-paired Packed ID: qiime2-03-deblur.cwl |
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Preprocess fastq
Remove and trim low quality reads from fastq files. Return fasta files with reads passed and reads removed. |
Path: CWL/Workflows/preprocess-fastq.workflow.cwl Branch/Commit ID: master |
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Filter single sample sv vcf from paired read callers(Manta/Smoove)
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Path: definitions/subworkflows/sv_paired_read_caller_filter.cwl Branch/Commit ID: low-vaf |
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alignment_workflow_md5checker.cwl
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Path: aligner/topmed-cwl/workflow/alignment_workflow_md5checker.cwl Branch/Commit ID: develop |
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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 |
