simMSG

simMSG simulates hybrid genomes from two parental genomes and evaluates ancestry-assignment accuracy using Multiplexed Shotgun Genotyping (MSG) and next-generation sequencing data to inform genetic mapping and introgression analyses.


Key Features:

  • Simulation of Hybrid Genomes: Generates in silico hybrids by crossing two parental genomes to produce controlled hybrid genotypes.
  • Integration with MSG Pipeline: Produces inputs compatible with the Multiplexed Shotgun Genotyping (MSG) pipeline and supports evaluation of MSG-based genotype calls from next-generation sequencing data.
  • Parameter Customization: Allows adjustment of simulation and genotyping parameters prior to MSG analysis.
  • Ancestry Assignment Accuracy: Enables assessment of ancestry assignment accuracy by simulating variation in ancestry tract length and the number of ancestry-informative markers.

Scientific Applications:

  • Mapping Quantitative Trait Loci (QTL): Uses hybrids with known ancestry to test and validate QTL mapping approaches.
  • Genotyping Introgressed Lines: Simulates and evaluates genotyping scenarios for introgressed lines to study gene flow and introgression.
  • Admixture Mapping: Simulates admixed genomes to assess methods for admixture mapping in populations with mixed ancestry.

Methodology:

Simulates hybrids by crossing two parental genomes, adjusts simulation and genotyping parameters, runs simulated hybrids through the Multiplexed Shotgun Genotyping (MSG) pipeline, and assesses ancestry-assignment accuracy by varying ancestry tract length and the number of ancestry-informative markers.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux
Programming Languages:
Shell, Perl
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Schumer M, Cui R, Rosenthal GG, Andolfatto P. simMSG: an experimental design tool for high‐throughput genotyping of hybrids. Molecular Ecology Resources. 2015;16(1):183-192. doi:10.1111/1755-0998.12434. PMID:26032857.

PMID: 26032857
Funding: - National Science Foundation: IOS‐0923825

Documentation

Links