Explore Workflows
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AltAnalyze Build Reference Indices
AltAnalyze Build Reference Indices ================================== |
Path: workflows/altanalyze-prepare-genome.cwl Branch/Commit ID: 7ae3b75bbe614e59cdeaba06047234a6c40c0fe9 |
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count-lines7-single-source-wf_v1_0.cwl
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Path: testdata/count-lines7-single-source-wf_v1_0.cwl Branch/Commit ID: 77669d4dd1d1ebd2bdd9810f911608146d9b8e51 |
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Chipseq alignment for mouse with qc and creating homer tag directory
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Path: definitions/pipelines/chipseq_alignment_mouse.cwl Branch/Commit ID: 27dcb1ae121be6a23057b74332b8c752ea425735 |
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Bacterial Annotation, pass 2, blastp-based functional annotation (first pass)
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Path: bacterial_annot/wf_bacterial_annot_pass2.cwl Branch/Commit ID: ae781871782805632f8947c1b11f65507c80cd43 |
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gathered exome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_exome_gathered.cwl Branch/Commit ID: 27dcb1ae121be6a23057b74332b8c752ea425735 |
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allele-alignreads-se-pe.cwl
Workflow maps FASTQ files from `fastq_files` input into reference genome `reference_star_indices_folder` and insilico generated `insilico_star_indices_folder` genome (concatenated genome for both `strain1` and `strain2` strains). For both genomes STAR is run with `outFilterMultimapNmax` parameter set to 1 to discard all of the multimapped reads. For insilico genome SAM file is generated. Then it's splitted into two SAM files based on strain names and then sorted by coordinates into the BAM format. For reference genome output BAM file from STAR slignment is also coordinate sorted. |
Path: subworkflows/allele-alignreads-se-pe.cwl Branch/Commit ID: c602e3cdd72ff904dd54d46ba2b5146eb1c57022 |
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contig LCA
create LCA consistant across input contigs contigs order of precedence - rRNA, single copy gene, LCA of genes |
Path: CWL/Workflows/contig-lca.workflow.cwl Branch/Commit ID: d9cf22cd615542c94f7974e8bce4cf29b24d985f |
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conditional_step_no_inputs.cwl
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Path: tests/wf/conditional_step_no_inputs.cwl Branch/Commit ID: e1a9100dff381ebd59b2a74806f705b7c68a8584 |
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umi duplex alignment fastq workflow
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Path: definitions/pipelines/umi_duplex_alignment.cwl Branch/Commit ID: f9600f9959acdc30259ba7e64de61104c9b01f0b |
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trim-rnaseq-se-dutp.cwl
Runs RNA-Seq dUTP BioWardrobe basic analysis with strand specific single-end data file. |
Path: workflows/trim-rnaseq-se-dutp.cwl Branch/Commit ID: b8e28a017f7b1a2900ec0fd3b3549f123f0c91b4 |
