Explore Workflows
View already parsed workflows here or click here to add your own
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Align reference proteins plane complete workflow
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Path: protein_alignment/wf_protein_alignment.cwl Branch/Commit ID: be9d12a3f8e1924183a1dc6a0bda6ada4195ca71 |
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Subworkflow to allow calling different SV callers which require bam files as inputs
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Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: 049f4aeff4c4a1b8421cac9b1c1c1f0da5848315 |
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bacterial_orthology_cond
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Path: bacterial_orthology/wf_bacterial_orthology_conditional.cwl Branch/Commit ID: be9d12a3f8e1924183a1dc6a0bda6ada4195ca71 |
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Detect Variants workflow for WGS pipeline
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Path: definitions/pipelines/detect_variants_wgs.cwl Branch/Commit ID: 3bebaf9b70331de9f4845e2223c55082f5a812fb |
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kmer_top_n_extract
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Path: task_types/tt_kmer_top_n_extract.cwl Branch/Commit ID: 7b21dc40840852f3942c31b9c472346ea3f9a3ca |
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js-expr-req-wf.cwl#wf
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Path: cwltool/schemas/v1.0/v1.0/js-expr-req-wf.cwl Branch/Commit ID: 48bd6c751aceef30614d9e43d91865980035781f Packed ID: wf |
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Bacterial Annotation, pass 3, structural annotation, functional annotation: ab initio GeneMark, by WP, by HMM (second pass)
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Path: bacterial_annot/wf_bacterial_annot_pass3.cwl Branch/Commit ID: be9d12a3f8e1924183a1dc6a0bda6ada4195ca71 |
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retrieve metadata from Zenodo community
For a given Zenodo community, retrieve its repository records as Zenodo JSON and (eventually) schema.org JSON-LD and DataCite v4 XML. |
Path: code/data-gathering/workflows/zenodo-records.cwl Branch/Commit ID: 7166c89aad278bdf438d593040948f3b95e6c410 |
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RNA-Seq pipeline paired-end strand specific
The original [BioWardrobe's](https://biowardrobe.com) [PubMed ID:26248465](https://www.ncbi.nlm.nih.gov/pubmed/26248465) **RNA-Seq** basic analysis for a **paired-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 paired-end RNA-Seq data. It performs the following steps: 1. Use STAR to align reads from input FASTQ files according to the predefined reference indices; generate unsorted BAM file and alignment statistics file 2. Use fastx_quality_stats to analyze input FASTQ files and generate quality statistics files 3. Use samtools sort to generate coordinate sorted BAM(+BAI) file pair from the unsorted BAM file obtained on the step 1 (after running STAR) 4. Generate BigWig file on the base of sorted BAM file 5. Map input FASTQ files to predefined rRNA reference indices using Bowtie to define the level of rRNA contamination; export resulted statistics to file 6. 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-pe-dutp.cwl Branch/Commit ID: 29bf638904709cfbf10908adcd51ba4886ace94a |
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Filter ChIP/ATAC peaks for Tag Density Profile or Motif Enrichment analyses
Filters ChIP/ATAC peaks with the neatest genes assigned for Tag Density Profile or Motif Enrichment analyses ============================================================================================================ Tool filters output from any ChIP/ATAC pipeline to create a file with regions of interest for Tag Density Profile or Motif Enrichment analyses. Peaks with duplicated coordinates are discarded. |
Path: workflows/filter-peaks-for-heatmap.cwl Branch/Commit ID: 00ea05e22788029370898fd4c17798b11edf0e57 |
