Explore Workflows
View already parsed workflows here or click here to add your own
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Uses Bruker TopSpin to convert a zipped NMR data directory to JCAMP-DX
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![]() Path: cwl/zipped2bruker2jcamp.cwl Branch/Commit ID: da8a0496d4fbe1815dc978a5ceaa183b7cb73cf1 |
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rnaseq-alignment-quantification
This workflow retrieve SRA fastqc data and execute QC, alignment and quantification from TPMCalculator |
![]() Path: workflows/RNA-Seq/rnaseq-quantification-qc.cwl Branch/Commit ID: 1b1cb5bbbe53a2dd5d7de7cdbff19c1bdbe23a49 |
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call_variants.cwl
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![]() Path: workflows/subworkflows/call_variants.cwl Branch/Commit ID: b0f226a9ac5152f3afe0d38c8cd54aa25b8b01cf |
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vcf.gz2bed.cwl
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![]() Path: multi-samples/Workflows/vcf.gz2bed.cwl Branch/Commit ID: main |
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no-inputs-wf.cwl
Workflow without inputs. |
![]() Path: tests/no-inputs-wf.cwl Branch/Commit ID: b1d4a69df86350059bd49aa127c02be0c349f7de |
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vqsr.cwl
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![]() Path: multi-samples/Workflows/vqsr.cwl Branch/Commit ID: main |
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vcf_concat.cwl
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![]() Path: workflows/subworkflows/vcf_concat.cwl Branch/Commit ID: b0f226a9ac5152f3afe0d38c8cd54aa25b8b01cf |
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BD Rhapsody™ WTA Analysis Pipeline
The BD Rhapsody™ WTA Analysis Pipeline is used to create sequencing libraries from single cell transcriptomes without having to specify a targeted panel. After sequencing, the analysis pipeline takes the FASTQ files, a reference genome file and a transcriptome annotation file for gene alignment. The pipeline generates molecular counts per cell, read counts per cell, metrics, and an alignment file. |
![]() Path: workflow1_11.cwl Branch/Commit ID: 46d4472af75afacfb13ed92d149a4decd015cf43 Packed ID: main |
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two-step-workflow.cwl
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![]() Path: _includes/cwl/two-step-workflow.cwl Branch/Commit ID: 4b43712319e2009c3867446b5dd1e8e31e897458 |
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dfast-filelist.cwl
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![]() Path: cwl/workflow/dfast-filelist.cwl Branch/Commit ID: e316f37f502005165ebd7f22b5257900c7c712ac |