Workflows
What is a Workflow?Filters
Generate annotated gb for fragments and add them to DB
Automatically generate annotated GenBank files for your fragments based on your constraints and store them in your database.
steps:
input: GenBank files : If your fragments are not in the database, you can generate GenBank files for each fragment to be used as input for the annotation workflow and then passed to the evaluate_manufacturability tool.
evaluate_manufacturability
- Set the constraints for the annotations. ...
CWL + RO-Crate Workflow Descriptions
This repository stores computational workflows described using the Common Workflow Language (CWL) and enriched with metadata using Research Object Crate (RO-Crate) conforming to the Workflow Run RO-Crate profile.
Each workflow is contained in its own directory (e.g., WF5201
, WF6101
, ...). Inside each workflow directory you will typically find at least:
- The CWL workflow definition (with the same name as the directory, e.g.,
WF5201.cwl
). ...
Digitial Twin Component for Earthquakes (DTC-E5) WorkFlow 1 (WF7501) uses new data to create a multi-scale model of the Earth, which is used to update the REVEAL/CSEMv3 velocity model. The WF7501 workflow models an inversion-based update process for CSEMv3 (Computational Seismic Earth Model). Below is a simple explanation of the STEPs:
- ST750101 - Data Catalog Update: Collects external data sources and updates the database for further processing.
- ST750102 - Inversion Setup: Configures ...
Type: Common Workflow Language
Creators: Johannes Kemper, Marta Pienkowska, Andreas Fichtner, Christian Böhm, Scott Keating
Submitter: Johannes Kemper
This workflow extracts protein-coding sequences from whole genome sequencing (WGS) data obtained from the European Nucleotide Archive (ENA). It automates the preprocessing, annotation, and selection of relevant protein sequences using tools such as Prokka, FASTA-to-Tabular, and pattern-based selection. The resulting dataset supports downstream analyses including comparative genomics, phylogenetics, and functional annotation.
This workflow supports processing of bulk ACT-Seq data from raw reads to genome-wide accessiblity tracks (bigWig) and ACT-Seq peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.
This workflow supports processing of bulk CUT'N'RUN data from raw reads to genome-wide accessiblity tracks (bigWig) and CUT'N'RUN peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.
This workflow supports primary processing of ChIP-Seq data from raw reads to genome-wide ChIP signal tracks and ChIP peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.
This workflow supports processing of bulk ATAC-Seq data from raw reads to genome-wide accessiblity tracks (bigWig) and ATAC peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.