Dahak
Dahak is a software suite that integrates state-of-the-art open source tools for metagenomic analyses. Tools in the dahak software suite will perform various steps in metagenomic analysis workflows including data pre-processing, metagenome assembly, taxonomic and functional classification, genome binning, and gene assignment. We aim to deliver the analytical framework as a robust and reliable containerized workflow system, which will be free from dependency, installation, and execution problems typically associated with other open-source bioinformatics solutions. This will maximize the transparency, data provenance (i.e., the process of tracing the origins of data and its movement through the workflow), and reproducibility.
Getting Started
Analysis protocols can be found in the workflows directory. It is assumed that analysis will begin with read filtering and instructions for Docker installation are included there.
You can run these protocols interactively using Docker or automate them using Snakemake and Singularity. See the workflows README for Docker, Snakemake and, Singularity istall instructions.
The assembly, comparison, functional inference, and taxonomic classification workflows are depednent upon the output of the read filtering workflow data. You can download our data to use in the read filtering protocol from the openscience framework. See the section below titled Data and the read filtering protocol for more information.
Prerequisites
Currently, for the sake of simplicity, it is assumed that all workflow steps will be run from Ubuntu 16.04 LTS.
dahak is not a standalone program, but rather a collection of workflows that are defined in snakemake files and that utilize bioconda and Docker to install and run software for different tasks.
See the workflows/
directory to get started.
Data
For purposes of benchmarking this project will use the following datasets:
Dataset | Description |
---|---|
Shakya complete | Complete metagenomic dataset from Shakya et al., 2013* containing bacterial and archaeal genomes |
Shakya subset 50 | 50 percent of the reads from Shakya complete |
Shakya subset 25 | 25 percent of the reads from Shakya complete |
Shakya subset 10 | 10 percent of the reads from Shakya complete |
Contributing
Please read CONTRIBUTING.md for details on our code of conduct and the process for submitting pull requests to us.
Contributors
Phillip Brooks1, Charles Reid1, Bruce Budowle2, Chris Grahlmann3, Stephanie L. Guertin3, F. Curtis Hewitt3, Alexander F. Koeppel4, Oana I. Lungu3, Krista L. Ternus3, Stephen D. Turner4,5, C. Titus Brown1
1School of Veterinary Medicine, University of California Davis, Davis, CA, United States of America
2Institute of Applied Genetics, Department of Molecular and Medical Genetics, University of North Texas Health Science Center, Fort Worth, Texas, United States of America
3Signature Science, LLC, Austin, Texas, United States of America
4Department of Public Health Sciences, University of Virginia, Charlottesville, VA, United States of America
5Bioinformatics Core, University of Virginia School of Medicine, Charlottesville, VA, United States of America
See also the list of contributors who participated in this project.
License
This project is licensed under the BSD 3-Clause License - see the LICENSE file for details.
Acknowledgments
- Bioconda
- Hat tip to anyone whose code was used