Genome-Wide Association Studies (GWASs), analyses that try to find a link between a given phenotype (such as a disease) and genetic markers, have been growing in popularity in the recent years. Relations between phenotypes and genotypes are not easy to identify, as most of the phenotypes are a product of the interaction between multiple genes, a phenomenon known as epistasis. Many authors have resorted to different approaches and hardware architectures in order to mitigate the exponential time complexity of the problem. However, these studies make some compromises in order to keep a reasonable execution time, such as limiting the number of genetic markers involved in the interaction, or discarding some of these markers in an initial filtering stage. This work presents MPI3SNP, a tool that implements a three-way exhaustive search for cluster architectures with the aim of mitigating the exponential growth of the run-time. Modern cluster solutions usually incorporate GPUs. Thus, MPI3SNP includes implementations for both multi-CPU and multi-GPU clusters. To contextualize the performance achieved, MPI3SNP is able to analyze an input of 6300 genetic markers and 3200 samples in less than 6 min using 768 CPU cores or 4 min using 8 NVIDIA K80 GPUs. The source code is available at https://github.com/chponte/mpi3snp .
Background: Epistasis is defined as the interaction between different genes when expressing a specific phenotype. The most common way to characterize an epistatic relationship is using a penetrance table, which contains the probability of expressing the phenotype under study given a particular allele combination. Available simulators can only create penetrance tables for well-known epistasis models involving a small number of genes and under a large number of limitations. Results: Toxo is a MATLAB library designed to calculate penetrance tables of epistasis models of any interaction order which resemble real data more closely. The user specifies the desired heritability (or prevalence) and the program maximizes the table's prevalence (or heritability) according to the input epistatic model boundaries. Conclusions: Toxo extends the capabilities of existing simulators that define epistasis using penetrance tables. These tables can be directly used as input for software simulators such as GAMETES so that they are able to generate data samples with larger interactions and more realistic prevalences/heritabilities.
Finding epistatic interactions among loci when expressing a phenotype is a widely employed strategy to understand the genetic architecture of complex traits in GWAS. The abundance of methods dedicated to the same purpose, however, makes it increasingly difficult for scientists to decide which method is more suitable for their studies. This work compares the different epistasis detection methods published during the last decade in terms of runtime, detection power and type I error rate, with a special emphasis on high-order interactions. Results show that in terms of detection power, the only methods that perform well across all experiments are the exhaustive methods, although their computational cost may be prohibitive in large-scale studies. Regarding non-exhaustive methods, not one could consistently find epistasis interactions when marginal effects are absent. If marginal effects are present, there are methods that perform well for high-order interactions, such as BADTrees, FDHE-IW, SingleMI or SNPHarvester. As for false-positive control, only SNPHarvester, FDHE-IW and DCHE show good results. The study concludes that there is no single epistasis detection method to recommend in all scenarios. Authors should prioritize exhaustive methods when sufficient computational resources are available considering the data set size, and resort to nonexhaustive methods when the analysis time is prohibitive.
Background Epistasis is the interaction between different genes when expressing a certain phenotype. If epistasis involves more than two loci it is called high-order epistasis. High-order epistasis is an area under active research because it could be the cause of many complex traits. The most common way to specify an epistasis interaction is through a penetrance table. Results This paper presents PyToxo, a Python tool for generating penetrance tables from any-order epistasis models. Unlike other tools available in the bibliography, PyToxo is able to work with high-order models and realistic penetrance and heritability values, achieving high-precision results in a short time. In addition, PyToxo is distributed as open-source software and includes several interfaces to ease its use. Conclusions PyToxo provides the scientific community with a useful tool to evaluate algorithms and methods that can detect high-order epistasis to continue advancing in the discovery of the causes behind complex diseases.
The interaction among different genes when expressing a particular phenotype is known as epistasis. High-order epistasis, when more than two loci are involved, is an active research area because it could be the cause of many complex traits. The most common abstraction for specifying an epistasis interaction is through a penetrance table, which captures the probability of expressing the studied phenotype given a particular genotype.Although it is very common for simulators to use penetrance tables, most of them do not allow the user to generate them directly, or present limitations for high-order interac- tions and/or realistic prevalence and heritability values. In this work, we present PyToxo, a Python tool for generating penetrance tables from any-order epistasis models. PyToxo allows to work with more appropriate scenarios than other state-of-the-art tools. Addi- tionally, it also improves in terms of accuracy, speed and ease of use, being available as a library, through a CLI or through a cross-platform GUI.
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