Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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call_variants.cwl
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![]() Path: workflows/subworkflows/call_variants.cwl Branch/Commit ID: master |
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post-proccessing-go-pfam-stats-subwf.cwl
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![]() Path: workflows/subworkflows/functional-annotation/post-proccessing-go-pfam-stats-subwf.cwl Branch/Commit ID: eosc-life-gos |
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count-lines4-wf.cwl
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![]() Path: tests/count-lines4-wf.cwl Branch/Commit ID: main |
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qiime2 demux paired sequences
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![]() Path: packed/qiime2-step1-import-demux-paired.cwl Branch/Commit ID: qiime2-workflow-paired Packed ID: qiime2-02-demux-emp-paired.cwl |
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5fb4c1087a8d46e7885c74e0e3d79d90.cwl
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![]() Path: .renku/workflow/5fb4c1087a8d46e7885c74e0e3d79d90.cwl Branch/Commit ID: master |
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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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count-lines8-wf.cwl
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![]() Path: v1.0/v1.0/count-lines8-wf.cwl Branch/Commit ID: master |
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bams2gvcf.woBQSR_female_chrX_wXTR.multisapmles.cwl
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![]() Path: Workflows/bams2gvcf.woBQSR_female_chrX_wXTR.multisapmles.cwl Branch/Commit ID: master |
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WES GATK4
Whole Exome Sequence analysis GATK4 Preprocessing |
![]() Path: workflows/exomeseq-gatk4.cwl Branch/Commit ID: master |
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02-trim-se.cwl
RNA-seq 02 trimming - reads: SE |
![]() Path: v1.0/RNA-seq_pipeline/02-trim-se.cwl Branch/Commit ID: master |