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

Modelling and simulation

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.

Documentation

Links