Explore Workflows
View already parsed workflows here or click here to add your own
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io-int-default-wf.cwl
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Path: tests/io-int-default-wf.cwl Branch/Commit ID: master |
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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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hi-c-processing-pairs-nonorm.cwl
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Path: cwl_awsem_v1/hi-c-processing-pairs-nonorm.cwl Branch/Commit ID: master |
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star-stringtie_wf_se.cwl
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Path: workflows/star-stringtie/single_end/star-stringtie_wf_se.cwl Branch/Commit ID: master |
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: 9c57dba |
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bulk_analysis.cwl
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Path: steps/bulk_analysis.cwl Branch/Commit ID: bb023f9 |
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Salmon quantification, FASTQ -> H5AD count matrix
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Path: steps/salmon-quantification.cwl Branch/Commit ID: 6591870 |
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PerformanceSummaryGenome_v0_1_0.cwl
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Path: janis_pipelines/wgs_somatic/cwl/tools/PerformanceSummaryGenome_v0_1_0.cwl Branch/Commit ID: master |
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tt_univec_wnode.cwl
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Path: task_types/tt_univec_wnode.cwl Branch/Commit ID: master |
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qiime2 demux sequences
Demultiplexing sequences from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
Path: subworkflows/qiime2-02-demux-emp-single.cwl Branch/Commit ID: develop |
