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: master |
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Downsample and HaplotypeCaller
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Path: definitions/pipelines/downsample_and_recall.cwl Branch/Commit ID: downsample_and_recall |
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WF6101.cwl
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Path: WF6101.cwl Branch/Commit ID: main |
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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: ca6ca613 |
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RNASelector as a CWL workflow
https://doi.org/10.1007/s12275-011-1213-z |
Path: workflows/rna-selector.cwl Branch/Commit ID: caea457 |
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chksum_seqval_wf_interleaved_fq.cwl
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Path: cwls/chksum_seqval_wf_interleaved_fq.cwl Branch/Commit ID: master |
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wgetkegg_ids.cwl
get KGML by multiple ids |
Path: wgetkegg_ids.cwl Branch/Commit ID: master |
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genomel_cohort_genotyping.cwl
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Path: genomel/genomel_cohort_genotyping.cwl Branch/Commit ID: master |
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bgzip and index VCF
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Path: definitions/subworkflows/bgzip_and_index.cwl Branch/Commit ID: No_filters_detect_variants |
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SAMSA2 pipeline
SAMSA2 complete workflow for meta-omics read annotation Steps: - Diamond read blastx - Refseq - SEED - SAMSA2 processing |
Path: cwl/workflows/workflow_samsa2.cwl Branch/Commit ID: master |
