ArticleBioData mining2012
GAMETES: a fast, direct algorithm for generating pure, strict, epistatic models with random architectures.
Article in BioData mining, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.
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71 citing papers in PubMed, 226 citations in OpenAlex.
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- Designing interpretable deep learning applications for functional genomics: a quantitative analysis.Briefings in bioinformatics · 2024Review
- GWASTool: A web pipeline for detecting SNP-phenotype associations.Fundamental research · 2024Article
- Distributed transformer for high order epistasis detection in large-scale datasets.Scientific reports · 2024Article
- SimHOEPI: A resampling simulator for generating single nucleotide polymorphism data with a high-order epistasis model.Quantitative biology (Beijing, China) · 2024Article
- SEEI: spherical evolution with feedback mechanism for identifying epistatic interactions.BMC genomics · 2024Article
- Deep learning captures the effect of epistasis in multifactorial diseases.Frontiers in medicine · 2024Article
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- Missing Causality and Heritability of Autoimmune Hepatitis.Digestive diseases and sciences · 2023Article
- NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution.Bioinformatics advances · 2023Article
- Article
11 more citing papers are in PubMed but not listed here.
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
Abstract
backgroundGeneticists who look beyond single locus disease associations require additional strategies for the detection of complex multi-locus effects. Epistasis, a multi-locus masking effect, presents a particular challenge, and has been the target of bioinformatic development. Thorough evaluation of new algorithms calls for simulation studies in which known disease models are sought. To date, the best methods for generating simulated multi-locus epistatic models rely on genetic algorithms. However, such methods are computationally expensive, difficult to adapt to multiple objectives, and unlikely to yield models with a precise form of epistasis which we refer to as pure and strict. Purely and strictly epistatic models constitute the worst-case in terms of detecting disease associations, since such associations may only be observed if all n-loci are included in the disease model. This makes them an attractive gold standard for simulation studies considering complex multi-locus effects.
resultsWe introduce GAMETES, a user-friendly software package and algorithm which generates complex biallelic single nucleotide polymorphism (SNP) disease models for simulation studies. GAMETES rapidly and precisely generates random, pure, strict n-locus models with specified genetic constraints. These constraints include heritability, minor allele frequencies of the SNPs, and population prevalence. GAMETES also includes a simple dataset simulation strategy which may be utilized to rapidly generate an archive of simulated datasets for given genetic models. We highlight the utility and limitations of GAMETES with an example simulation study using MDR, an algorithm designed to detect epistasis.
conclusionsGAMETES is a fast, flexible, and precise tool for generating complex n-locus models with random architectures. While GAMETES has a limited ability to generate models with higher heritabilities, it is proficient at generating the lower heritability models typically used in simulation studies evaluating new algorithms. In addition, the GAMETES modeling strategy may be flexibly combined with any dataset simulation strategy. Beyond dataset simulation, GAMETES could be employed to pursue theoretical characterization of genetic models and epistasis.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.