Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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oxog_varbam_annotate_wf.cwl
This workflow will run OxoG, variantbam, and annotate. Run this as `dockstore --script --debug workflow launch --descriptor cwl --local-entry --entry ./oxog_varbam_annotate_wf.cwl --json oxog_varbam_annotat_wf.input.json ` |
https://github.com/svonworl/OxoG-Dockstore-Tools.git
Path: oxog_varbam_annotate_wf.cwl Branch/Commit ID: b38a8a4785746b8267913ea5389e21ae6dc921a3 |
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Trim Galore RNA-Seq pipeline paired-end
The original [BioWardrobe's](https://biowardrobe.com) [PubMed ID:26248465](https://www.ncbi.nlm.nih.gov/pubmed/26248465) **RNA-Seq** basic analysis for a **pair-end** experiment. A corresponded input [FASTQ](http://maq.sourceforge.net/fastq.shtml) file has to be provided. Current workflow should be used only with the single-end RNA-Seq data. It performs the following steps: 1. Trim adapters from input FASTQ files 2. Use STAR to align reads from input FASTQ files according to the predefined reference indices; generate unsorted BAM file and alignment statistics file 3. Use fastx_quality_stats to analyze input FASTQ files and generate quality statistics files 4. Use samtools sort to generate coordinate sorted BAM(+BAI) file pair from the unsorted BAM file obtained on the step 1 (after running STAR) 5. Generate BigWig file on the base of sorted BAM file 6. Map input FASTQ files to predefined rRNA reference indices using Bowtie to define the level of rRNA contamination; export resulted statistics to file 7. Calculate isoform expression level for the sorted BAM file and GTF/TAB annotation file using GEEP reads-counting utility; export results to file |
https://github.com/datirium/workflows.git
Path: workflows/trim-rnaseq-pe.cwl Branch/Commit ID: 7518b100d8cbc80c8be32e9e939dfbb27d6b4361 |
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oxog_sub_wf.cwl
This is a subworkflow of the main oxog_varbam_annotat_wf workflow - this is not meant to be run as a stand-alone workflow! |
https://github.com/svonworl/OxoG-Dockstore-Tools.git
Path: oxog_sub_wf.cwl Branch/Commit ID: b38a8a4785746b8267913ea5389e21ae6dc921a3 |
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preprocess_vcf.cwl
This workflow will perform preprocessing steps on VCFs for the OxoG/Variantbam/Annotation workflow. |
https://github.com/svonworl/OxoG-Dockstore-Tools.git
Path: preprocess_vcf.cwl Branch/Commit ID: b38a8a4785746b8267913ea5389e21ae6dc921a3 |
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Genome conversion and annotation
Workflow for genome annotation from EMBL format |
https://git.wur.nl/unlock/cwl.git
Path: cwl/workflows/workflow_sapp_microbes.cwl Branch/Commit ID: d944d61ddc34a5b24ebac6e1701efd6f8fdf54ae |
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fireprot.cwl
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https://github.com/CERIT-SC/fireprot.git
Path: fireprot.cwl Branch/Commit ID: a2b0c18f117dcf2b0d7e33c59c0f180b6a9bf709 |
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js-expr-req-wf.cwl#wf
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https://github.com/common-workflow-language/cwltool.git
Path: cwltool/schemas/v1.0/v1.0/js-expr-req-wf.cwl Branch/Commit ID: fc6ca8b1498926f705dcfde7ab0a365bd09a9675 Packed ID: wf |
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io-int-optional-wf.cwl
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https://github.com/common-workflow-language/common-workflow-language.git
Path: v1.0/v1.0/io-int-optional-wf.cwl Branch/Commit ID: 1f501e38ff692a408e16b246ac7d64d32f0822c2 |
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cnv_manta
CNV Manta calling |
https://gitlab.bsc.es/lrodrig1/structuralvariants_poc.git
Path: structuralvariants/cwl/abstract_operations/subworkflows/cnv_manta.cwl Branch/Commit ID: de9cb009f8fe0c8d5a94db5c882cf21ddf372452 |
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RNA-seq alelle specific pipeline for single-read data
Allele specific RNA-Seq single-read workflow |
https://github.com/datirium/workflows.git
Path: workflows/allele-rnaseq-se.cwl Branch/Commit ID: 6bf56698c6fe6e781723dea32bc922b91ef49cf3 |