Explore Workflows
View already parsed workflows here or click here to add your own
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kmer_top_n_extract
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Path: task_types/tt_kmer_top_n_extract.cwl Branch/Commit ID: 61e3752f1f5e2ee498fa024c235226f8580be942 |
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scatter-wf4.cwl#main
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Path: tests/wf/scatter-wf4.cwl Branch/Commit ID: dbc4c4c2ad30ed31367b4fbcc3bb4084fdcabaa2 Packed ID: main |
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Run pindel on provided region
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Path: definitions/subworkflows/pindel_region.cwl Branch/Commit ID: da335d9963418f7bedd84cb2791a0df1b3165ffe |
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Tumor-Only Detect Variants workflow
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Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 5cb188131f786ed33156e2f0e3dd63ab9c04245d |
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Single-cell RNA-Seq Dimensionality Reduction Analysis
Single-cell RNA-Seq Dimensionality Reduction Analysis Integrates multiple single-cell RNA-Seq datasets, reduces dimensionality using PCA. |
Path: workflows/sc-rna-reduce.cwl Branch/Commit ID: 7030da528559c7106d156284e50ff0ecedab0c4e |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: b7d9ace34664d3cedb16f2512c8a6dc6debfc8ca |
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prep.cwl
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Path: workflows/linc_target/prep.cwl Branch/Commit ID: 035f66ec0f260628424c9621aed97f7cbf35e737 |
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Build Bowtie indices
Workflow runs [Bowtie](http://bowtie-bio.sourceforge.net/tutorial.shtml) v1.2.0 (12/30/2016) to build indices for reference genome provided in a single FASTA file as fasta_file input. Generated indices are saved in a folder with the name that corresponds to the input genome |
Path: workflows/bowtie-index.cwl Branch/Commit ID: a1f6ca50fcb0881781b3ba0306dd61ebf555eaba |
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AltAnalyze CellHarmony
AltAnalyze CellHarmony ====================== |
Path: workflows/altanalyze-cellharmony.cwl Branch/Commit ID: c6bfa0de917efb536dd385624fc7702e6748e61d |
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Running cellranger count and lineage inference
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Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: da335d9963418f7bedd84cb2791a0df1b3165ffe |
