SELANSI

SELANSI simulates the stochastic dynamics of multidimensional gene regulatory networks (GRNs) to provide efficient approximations of stochastic effects in gene regulation.


Key Features:

  • Stochastic Simulation: Simulates the inherent stochasticity of gene regulation for multidimensional GRNs.
  • Efficient Approximation Methodology: Transforms the Chemical Master Equation into a partial integral differential equation and solves it using a semi-Lagrangian method to improve computational efficiency while preserving accuracy.
  • Flexible Network Modeling: Models complex networks with multiple genes exhibiting self- and cross-regulation, multiple transcription factors, and configurable topology, kinetics, and parameters.
  • Unrestricted Kinetic Validity: Is not confined to specific types of kinetics, enabling application across diverse kinetic rate laws.
  • MATLAB Environment Compatibility: Implements algorithms within the MATLAB environment for integration with MATLAB-based computational workflows.

Scientific Applications:

  • Reverse Engineering of Genetic Circuits: Supports inference of regulatory mechanisms by modeling stochastic effects in observed biological data.
  • De Novo Design of Genetic Networks: Enables design and evaluation of synthetic genetic circuits by predicting stochastic behavior under different designs.
  • Exploration of Gene Regulation Dynamics: Allows analysis of noise-driven dynamics in gene expression to study the impact of stochastic fluctuations on cellular processes.

Methodology:

Transforms the Chemical Master Equation into a partial integral differential equation using intrinsic structural properties of GRNs and solves it numerically with a semi-Lagrangian method.

Topics

Details

Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
MATLAB
Added:
6/21/2018
Last Updated:
11/25/2024

Operations

Publications

Pájaro M, Otero-Muras I, Vázquez C, Alonso AA. SELANSI: a toolbox for simulation of stochastic gene regulatory networks. Bioinformatics. 2017;34(5):893-895. doi:10.1093/bioinformatics/btx645. PMID:29040384. PMCID:PMC6030881.

Documentation