Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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gdc_dnaseq_ar_workflow.cwl
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![]() Path: subworkflows/main/gdc_dnaseq_ar_workflow.cwl Branch/Commit ID: master |
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gdc_dnaseq_main_workflow.cwl
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![]() Path: subworkflows/main/gdc_dnaseq_main_workflow.cwl Branch/Commit ID: master |
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count-lines15-wf.cwl
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![]() Path: tests/count-lines15-wf.cwl Branch/Commit ID: main |
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md5-validate.cwl
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![]() Path: cwl_awsem_v1/md5-validate.cwl Branch/Commit ID: dev2 |
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scRNA-seq pipeline using Salmon and Alevin
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![]() Path: pipeline.cwl Branch/Commit ID: 72cf42a |
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Exome QC workflow
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![]() Path: workflows/hello/exome_alignment_packed.cwl Branch/Commit ID: master Packed ID: workflow_exome.cwl |
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presto_nosort.cwl
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![]() Path: presto_nosort.cwl Branch/Commit ID: visualise |
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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 |
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rRNA_selection.cwl
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![]() Path: tools/rRNA_selection.cwl Branch/Commit ID: 3168316 |
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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 |