Abstract
BackgroundMachine learning methods have gained popularity and practicality in identifying linear and non-linear effects of variants associated with complex disease/traits. Detection of epistatic interactions still remains a challenge due to the large number of features and relatively small sample size as input, thus leading to the so-called “short fat data” problem. The efficiency of machine learning methods can be increased by limiting the number of input features. Thus, it is very important to perform variable selection before searching for epistasis. Many methods have been evaluated and proposed to perform feature selection, but no single method works best in all scenarios. We demonstrate this by conducting two separate simulation analyses to evaluate the proposed collective feature selection approach.ResultsThrough our simulation study we propose a collective feature selection approach to select features that are in the “union” of the best performing methods. We explored various parametric, non-parametric, and data mining approaches to perform feature selection. We choose our top performing methods to select the union of the resulting variables based on a user-defined percentage of variants selected from each method to take to downstream analysis. Our simulation analysis shows that non-parametric data mining approaches, such as MDR, may work best under one simulation criteria for the high effect size (penetrance) datasets, while non-parametric methods designed for feature selection, such as Ranger and Gradient boosting, work best under other simulation criteria. Thus, using a collective approach proves to be more beneficial for selecting variables with epistatic effects also in low effect size datasets and different genetic architectures. Following this, we applied our proposed collective feature selection approach to select the top 1% of variables to identify potential interacting variables associated with Body Mass Index (BMI) in ~ 44,000 samples obtained from Geisinger’s MyCode Community Health Initiative (on behalf of DiscovEHR collaboration).ConclusionsIn this study, we were able to show that selecting variables using a collective feature selection approach could help in selecting true positive epistatic variables more frequently than applying any single method for feature selection via simulation studies. We were able to demonstrate the effectiveness of collective feature selection along with a comparison of many methods in our simulation analysis. We also applied our method to identify non-linear networks associated with obesity.
Highlights
Machine learning methods have gained popularity and practicality in identifying linear and non-linear effects of variants associated with complex disease/ traits
In order to do so, many feature selection methods have been proposed in the past and have been applied in the context of detecting statistical epistasis to identify non-linear associations of genetic variants with a disease trait
Simulation studies Simulated data experiment 1 We simulated multiple data sets consisting of Single Nucleotide Polymorphism (SNP), referred to as variables, using an additive genetic encoding (AA = 0, Aa = 1, aa = 2) with case-control status to test for binary outcome
Summary
Machine learning methods have gained popularity and practicality in identifying linear and non-linear effects of variants associated with complex disease/ traits. Regression approaches are frequently used to model pairwise interactions but many machine learning approaches such as multi-factor dimensionality reduction (MDR) [7, 8], neural networks [9], support vector machines [10], Bayesian methods [11], among others are contemporary methods more commonly applied. Most of these methods are limited in the number of features they can handle, and dealing with the computational burden poses a challenge in the application of these methods. All methods have some advantages and disadvantages, and they do not follow a “one method fits all” criterion
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