ArticleBMC bioinformatics2008
GENOMEPOP: a program to simulate genomes in populations.
Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.
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Who cites it
35 citing papers in PubMed.
- Probabilities of two alleles being identity by state at unobserved loci predicted by observed loci in cattle populations.Scientific reports · 2026Article
- Generating realistic artificial human genomes using adversarial autoencoders.NAR genomics and bioinformatics · 2025Article
- iHDSel software: The price equation and the population stability index to detect genomic patterns compatible with selective sweeps. An example with SARS-CoV-2.Biology methods & protocols · 2024Article
- The statistical power of genome-wide association studies for threshold traits with different frequencies of causal variants.Genetica · 2022Article
- Simulating within host human immunodeficiency virus 1 genome evolution in the persistent reservoir.Virus evolution · 2020Article
- A multihost bacterial pathogen overcomes continuous population bottlenecks to adapt to new host species.Science advances · 2019Article
- SANTA-SIM: simulating viral sequence evolution dynamics under selection and recombination.Virus evolution · 2019Article
- PhenotypeSimulator: A comprehensive framework for simulating multi-trait, multi-locus genotype to phenotype relationships.Bioinformatics (Oxford, England) · 2018Article
- Simulating variance heterogeneity in quantitative genome wide association studies.BMC bioinformatics · 2018Article
- An Eigenvalue test for spatial principal component analysis.BMC bioinformatics · 2017Article
- The Bacterial Sequential Markov Coalescent.Genetics · 2017Article
- HacDivSel: Two new methods (haplotype-based and outlier-based) for the detection of divergent selection in pairs of populations.PloS one · 2017Article
- Detecting the Genomic Signature of Divergent Selection in Presence of Gene Flow.Current genomics · 2015Article
- A C++ template library for efficient forward-time population genetic simulation of large populations.Genetics · 2014Article
- SMARTPOP: inferring the impact of social dynamics on genetic diversity through high speed simulations.BMC bioinformatics · 2014Article
- πBUSS: a parallel BEAST/BEAGLE utility for sequence simulation under complex evolutionary scenarios.BMC bioinformatics · 2014Article
- Simulation of genome-wide evolution under heterogeneous substitution models and complex multispecies coalescent histories.Molecular biology and evolution · 2014Article
- Genome evolution by matrix algorithms: cellular automata approach to population genetics.Genome biology and evolution · 2014Article
- forqs: forward-in-time simulation of recombination, quantitative traits and selection.Bioinformatics (Oxford, England) · 2014Article
- SLiM: simulating evolution with selection and linkage.Genetics · 2013Article
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1 author.
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Abstract
backgroundThere are several situations in population biology research where simulating DNA sequences is useful. Simulation of biological populations under different evolutionary genetic models can be undertaken using backward or forward strategies. Backward simulations, also called coalescent-based simulations, are computationally efficient. The reason is that they are based on the history of lineages with surviving offspring in the current population. On the contrary, forward simulations are less efficient because the entire population is simulated from past to present. However, the coalescent framework imposes some limitations that forward simulation does not. Hence, there is an increasing interest in forward population genetic simulation and efficient new tools have been developed recently. Software tools that allow efficient simulation of large DNA fragments under complex evolutionary models will be very helpful when trying to better understand the trace left on the DNA by the different interacting evolutionary forces. Here I will introduce GenomePop, a forward simulation program that fulfills the above requirements. The use of the program is demonstrated by studying the impact of intracodon recombination on global and site-specific dN/dS estimation.
resultsI have developed algorithms and written software to efficiently simulate, forward in time, different Markovian nucleotide or codon models of DNA mutation. Such models can be combined with recombination, at inter and intra codon levels, fitness-based selection and complex demographic scenarios.
conclusionGenomePop has many interesting characteristics for simulating SNPs or DNA sequences under complex evolutionary and demographic models. These features make it unique with respect to other simulation tools. Namely, the possibility of forward simulation under General Time Reversible (GTR) mutation or GTRxMG94 codon models with intra-codon recombination, arbitrary, user-defined, migration patterns, diploid or haploid models, constant or variable population sizes, etc. It also allows simulation of fitness-based selection under different distributions of mutational effects. Under the 2-allele model it allows the simulation of recombination hot-spots, the definition of different frequencies in different populations, etc. GenomePop can also manage large DNA fragments. In addition, it has a scaling option to save computation time when simulating large sequences and population sizes under complex demographic and evolutionary situations. These and many other features are detailed in its web page [1].
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