Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
genome-kallisto-index.cwl
Generates a FASTA file with the DNA sequences for all transcripts in a GFF file and builds kallisto index |
Path: tools/genome-kallisto-index.cwl Branch/Commit ID: 896422c9ff1995024cb77675edcd4d973ae11f7a |
|
|
|
umi duplex alignment fastq workflow
|
Path: definitions/pipelines/alignment_umi_duplex.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
|
|
|
Single-Cell RNA-Seq Trajectory Analysis
Single-Cell RNA-Seq Trajectory Analysis Infers developmental trajectories and pseudotime from cells clustered by similarity of gene expression data. |
Path: workflows/sc-rna-trajectory.cwl Branch/Commit ID: d76110e0bfc40c874f82e37cef6451d74df4f908 |
|
|
|
Unaligned to aligned BAM
|
Path: definitions/subworkflows/align.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
|
|
|
DESeq2 Multi-factor Analysis
DESeq2 Multi-factor Analysis Runs DeSeq2 multi-factor analysis with manual control over major parameters |
Path: workflows/deseq-multi-factor.cwl Branch/Commit ID: d76110e0bfc40c874f82e37cef6451d74df4f908 |
|
|
|
FastQC - a quality control tool for high throughput sequence data
FastQC - a quality control tool for high throughput sequence data ===================================== FastQC aims to provide a simple way to do some quality control checks on raw sequence data coming from high throughput sequencing pipelines. It provides a modular set of analyses which you can use to give a quick impression of whether your data has any problems of which you should be aware before doing any further analysis. The main functions of FastQC are: - Import of data from FastQ files (any variant) - Providing a quick overview to tell you in which areas there may be problems - Summary graphs and tables to quickly assess your data - Export of results to an HTML based permanent report - Offline operation to allow automated generation of reports without running the interactive application |
Path: workflows/fastqc.cwl Branch/Commit ID: d76110e0bfc40c874f82e37cef6451d74df4f908 |
|
|
|
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 |
|
|
|
RNA-Seq alignment and transcript/gene abundance workflow
|
Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
|
|
|
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 |
|
|
|
count-lines7-wf.cwl
|
Path: tests/count-lines7-wf.cwl Branch/Commit ID: 3e90671b25f7840ef2926ad2bacbf447772dda94 |
