Explore Workflows
View already parsed workflows here or click here to add your own
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1st-workflow.cwl
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Path: tests/wf/1st-workflow.cwl Branch/Commit ID: 37c6c78693a4b1e644db951ea964259734a50c6f |
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schemadef-wf.cwl
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Path: cwltool/schemas/v1.0/v1.0/schemadef-wf.cwl Branch/Commit ID: 047e69bb169e79fad6a7285ee798c4ecec3b218b |
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bulk_process.cwl
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Path: steps/bulk_process.cwl Branch/Commit ID: 53415520f94ac0d9a1fae89af0f6e8250240723a |
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Indices builder from GBOL RDF (TTL)
Workflow to build different indices for different tools from a genome and transcriptome. This workflow expects an (annotated) genome in GBOL ttl format. Steps: - SAPP: rdf2gtf (genome fasta) - SAPP: rdf2fasta (transcripts fasta) - STAR index (Optional for Eukaryotic origin) - bowtie2 index - kallisto index |
Path: cwl/workflows/workflow_indexbuilder.cwl Branch/Commit ID: b9097b82e6ab6f2c9496013ce4dd6877092956a0 |
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workflow.cwl
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Path: flow_dispatch/2blat/workflow.cwl Branch/Commit ID: 5910b4d88aca172252d9102ddb610a7dc9e1347f |
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RNA-Seq pipeline single-read stranded mitochondrial
Slightly changed original [BioWardrobe's](https://biowardrobe.com) [PubMed ID:26248465](https://www.ncbi.nlm.nih.gov/pubmed/26248465) **RNA-Seq** basic analysis for **strand specific single-read** experiment. An additional steps were added to map data to mitochondrial chromosome only and then merge the output. Experiment files in [FASTQ](http://maq.sourceforge.net/fastq.shtml) format either compressed or not can be used. Current workflow should be used only with single-read strand specific RNA-Seq data. It performs the following steps: 1. `STAR` to align reads from input FASTQ file according to the predefined reference indices; generate unsorted BAM file and alignment statistics file 2. `fastx_quality_stats` to analyze input FASTQ file and generate quality statistics file 3. `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 file 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 |
Path: workflows/rnaseq-se-dutp-mitochondrial.cwl Branch/Commit ID: 954bb2f213d97dfef1cddaf9e830169a92ad0c6b |
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standard_bam_to_collapsed_qc.cwl
This is a workflow to go from standard bams to collapsed bams and QC results. |
Path: workflows/subworkflows/standard_bam_to_collapsed_qc.cwl Branch/Commit ID: b0f226a9ac5152f3afe0d38c8cd54aa25b8b01cf |
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workflow.cwl
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Path: flow_dispatch/2other_species/workflow.cwl Branch/Commit ID: 5910b4d88aca172252d9102ddb610a7dc9e1347f |
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facets-suite-workflow.cwl
Workflow for running the facets suite workflow on a single tumor normal pair Includes handling of errors in case execution fails for the sample pair |
Path: cwl/facets-suite-workflow.cwl Branch/Commit ID: 59b69eed7ffefcffd81313ec8ffb84c0d716b933 |
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fillout_workflow.cwl
Workflow to run GetBaseCountsMultiSample fillout on a number of bam files with a single maf file |
Path: cwl/fillout_workflow.cwl Branch/Commit ID: 59b69eed7ffefcffd81313ec8ffb84c0d716b933 |
