FractalSIM

FractalSIM simulates genome-wide genetic variation under multiple demographic and selective scenarios to model admixture and homogeneous population dynamics for medical population genetics research.


Key Features:

  • Multi-Scenario Simulation: Simulates genome-wide data under a variety of genetic models including admixed and homogeneous population scenarios.
  • Natural Selection Integration: Incorporates natural selection during both admixture and homogeneous processes to reflect evolutionary dynamics.
  • Genome-Wide Data Capability: Handles large-scale, genome-wide simulations rather than being limited to single chromosomes or specific regions.
  • Validation and Evaluation: Outputs have been assessed using popular analytical tools and used to evaluate performance of methods such as ancestry inference and GWAS.

Scientific Applications:

  • Ancestry Inference: Evaluating tools that determine ancestral origins using simulated admixed and homogeneous genomic data.
  • Genome-Wide Association Studies (GWAS): Assessing methodologies used to identify genetic variants associated with diseases under realistic demographic and selective scenarios.
  • Disease Genetics Research: Simulating genomic variation linked to specific diseases to investigate genetic architecture and effects of demography and selection.

Methodology:

Simulates genome-wide data across multiple genetic models, integrates natural selection during admixture and homogeneous processes, and evaluates outputs with analytical tools for ancestry inference and GWAS.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Mac
Programming Languages:
Python
Added:
6/14/2018
Last Updated:
11/25/2024

Operations

Publications

Mugo JW, Geza E, Defo J, Elsheikh SSM, Mazandu GK, Mulder NJ, Chimusa ER. A multi-scenario genome-wide medical population genetics simulation framework. Bioinformatics. 2017;33(19):2995-3002. doi:10.1093/bioinformatics/btx369. PMID:28957497. PMCID:PMC5870573.

PMID: 28957497
PMCID: PMC5870573
Funding: - National Institutes of Health: U41HG006941