Explore Workflows
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trim-rnaseq-se.cwl
Runs RNA-Seq BioWardrobe basic analysis with single-end data file. |
Path: workflows/trim-rnaseq-se.cwl Branch/Commit ID: 896422c9ff1995024cb77675edcd4d973ae11f7a |
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
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Genomic regions intersection and visualization
Genomic regions intersection and visualization ============================================== 1. Merges intervals within each of the filtered peaks files from ChIP/ATAC experiments 2. Overlaps merged intervals and assigns the nearest genes to them |
Path: workflows/intervene.cwl Branch/Commit ID: d76110e0bfc40c874f82e37cef6451d74df4f908 |
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count-lines7-wf.cwl
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Path: tests/count-lines7-wf.cwl Branch/Commit ID: 3e90671b25f7840ef2926ad2bacbf447772dda94 |
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trim-chipseq-pe.cwl
Runs ChIP-Seq BioWardrobe basic analysis with paired-end input data files. |
Path: workflows/trim-chipseq-pe.cwl Branch/Commit ID: 896422c9ff1995024cb77675edcd4d973ae11f7a |
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Single-Cell WNN Cluster Analysis
Single-Cell WNN Cluster Analysis Clusters cells by similarity on the basis of both gene expression and chromatin accessibility data from the outputs of the “Single-Cell RNA-Seq Dimensionality Reduction Analysis” and “Single-Cell ATAC-Seq Dimensionality Reduction Analysis” pipelines run sequentially. The results of this workflow are used in the “Single-Cell Manual Cell Type Assignment”, “Single-Cell RNA-Seq Differential Expression Analysis”, “Single-Cell RNA-Seq Trajectory Analysis”, “Single-Cell Differential Abundance Analysis”, “Single-Cell ATAC-Seq Differential Accessibility Analysis”, and “Single-Cell ATAC-Seq Genome Coverage” pipelines. |
Path: workflows/sc-wnn-cluster.cwl Branch/Commit ID: d76110e0bfc40c874f82e37cef6451d74df4f908 |
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trim-rnaseq-pe-dutp.cwl
Runs RNA-Seq BioWardrobe basic analysis with strand specific pair-end data file. |
Path: workflows/trim-rnaseq-pe-dutp.cwl Branch/Commit ID: 896422c9ff1995024cb77675edcd4d973ae11f7a |
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cond-wf-006.cwl
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Path: tests/conditionals/cond-wf-006.cwl Branch/Commit ID: a5073143db4155e05df8d2e7eb59d9e62acd65a5 |
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Build Bismark indices
Copy fasta_file file to the folder and run run bismark_genome_preparation script to prepare indices for Bismark Methylation Analysis. Bowtie2 aligner is used by default. The name of the output indices folder is equal to the genome input. |
Path: workflows/bismark-index.cwl Branch/Commit ID: d76110e0bfc40c874f82e37cef6451d74df4f908 |
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advanced-header.cwl
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Path: metadata/advanced-header.cwl Branch/Commit ID: d76110e0bfc40c874f82e37cef6451d74df4f908 |
