ngs_simulation
ngs_simulation simulates Illumina sequencing runs to model sequencing errors and assess false positives and false negatives in genomic datasets.
Key Features:
- Simulation of Illumina Runs: Replicates Illumina next-generation DNA sequencing runs to generate simulated sequencing data.
- Visualization of Errors: Generates plots that delineate false positives and false negatives to visualize sequencing error profiles.
- Customizable Parameters: Allows adjustment of simulation parameters to mimic different experimental conditions.
Scientific Applications:
- Validate Analytical Methods: Test and refine computational methods for analyzing large-scale genomic data using simulated Illumina data.
- Optimize Experimental Design: Compare simulated experimental setups to identify conditions that minimize errors or improve detection sensitivity.
- Education and Training: Provide controlled datasets for training researchers on sequencing data characteristics and error interpretation.
Methodology:
Simulates Illumina sequencing runs using adjustable parameters, leverages advanced statistical and computational methods to produce realistic sequencing scenarios, and generates plots of false positives and false negatives.
Topics
Collections
Details
- Maturity:
- Mature
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 12/19/2016
- Last Updated:
- 11/25/2024
Operations
Data Inputs & Outputs
Publications
Mareuil F, Doppelt-Azeroual O, Ménager H. A public Galaxy platform at Pasteur used as an execution engine for web services. Unknown Journal. 2017. doi:10.7490/f1000research.1114334.1.
Afgan E, Baker D, van den Beek M, Blankenberg D, Bouvier D, Čech M, Chilton J, Clements D, Coraor N, Eberhard C, Grüning B, Guerler A, Hillman-Jackson J, Von Kuster G, Rasche E, Soranzo N, Turaga N, Taylor J, Nekrutenko A, Goecks J. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update. Nucleic Acids Research. 2016;44(W1):W3-W10. doi:10.1093/nar/gkw343. PMID:27137889. PMCID:PMC4987906.