AlphaDrop beta
AlphaDrop beta simulates sequence, single nucleotide polymorphism (SNP), phased allele, genotype, and phenotype data within specified pedigree structures for genomic selection and genome-wide association study (GWAS) research.
Key Features:
- Flexible Simulation Capabilities: Allows definition of historical population structures and recent pedigree configurations to model complex genetic scenarios.
- Phased Alleles and Genotypes: Simulates sequence data and SNP-phased alleles and genotypes.
- Quantitative Trait Loci (QTL) Effects: Enables specification of the distribution of QTL effects for studies of additive genetic influence.
- Breeding Values Simulation: Simulates breeding values for use in genomic selection analyses.
- Pre-specified Pedigrees: Supports input of pre-defined pedigree structures to replicate specific breeding programs or population histories.
- Public Data Availability: Provides ten replicate datasets from a representative livestock genomic selection scenario that are publicly available for reproducibility and comparison.
Scientific Applications:
- Genomic Selection Studies: Model breeding programs, assess selection strategies, and predict genetic gains across generations.
- GWAS Simulations: Generate datasets with controlled QTL effects and population structures to validate GWAS methodologies and statistical models.
- Educational Purposes: Provide example datasets and simulation scenarios for teaching genomic data simulation and analysis techniques.
Methodology:
Uses the MaCS (Markov Chain Simulator) algorithm to drop simulated haplotypes through pedigrees, with configurable historical population structures, pedigree configurations, and QTL effect distributions.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Hickey JM, Gorjanc G. Simulated Data for Genomic Selection and Genome-Wide Association Studies Using a Combination of Coalescent and Gene Drop Methods. G3 Genes|Genomes|Genetics. 2012;2(4):425-427. doi:10.1534/g3.111.001297. PMID:22540033. PMCID:PMC3337470.