ArticleBMC bioinformatics2010
A genetic ensemble approach for gene-gene interaction identification.
Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 26 citations in OpenAlex.
- GEP-EpiSeeker: a gene expression programming-based method for epistatic interaction detection in genome-wide association studies.BMC genomics · 2021Article
- Feature selection revisited in the single-cell era.Genome biology · 2021Review
- Article
- Deep mixed model for marginal epistasis detection and population stratification correction in genome-wide association studies.BMC bioinformatics · 2019Article
- A novel adaptive ensemble classification framework for ADME prediction.RSC advances · 2018Article
- FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm.PloS one · 2016Article
- Cuckoo search epistasis: a new method for exploring significant genetic interactions.Heredity · 2014Article
- Interaction between γ-aminobutyric acid A receptor genes: new evidence in migraine susceptibility.PloS one · 2013Article
- Mining functional gene modules linked with rheumatoid arthritis using a SNP-SNP network.Genomics, proteomics & bioinformatics · 2012Article
- Gene-gene interaction filtering with ensemble of filters.BMC bioinformatics · 2011Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundIt has now become clear that gene-gene interactions and gene-environment interactions are ubiquitous and fundamental mechanisms for the development of complex diseases. Though a considerable effort has been put into developing statistical models and algorithmic strategies for identifying such interactions, the accurate identification of those genetic interactions has been proven to be very challenging.
methodsIn this paper, we propose a new approach for identifying such gene-gene and gene-environment interactions underlying complex diseases. This is a hybrid algorithm and it combines genetic algorithm (GA) and an ensemble of classifiers (called genetic ensemble). Using this approach, the original problem of SNP interaction identification is converted into a data mining problem of combinatorial feature selection. By collecting various single nucleotide polymorphisms (SNP) subsets as well as environmental factors generated in multiple GA runs, patterns of gene-gene and gene-environment interactions can be extracted using a simple combinatorial ranking method. Also considered in this study is the idea of combining identification results obtained from multiple algorithms. A novel formula based on pairwise double fault is designed to quantify the degree of complementarity.
conclusionsOur simulation study demonstrates that the proposed genetic ensemble algorithm has comparable identification power to Multifactor Dimensionality Reduction (MDR) and is slightly better than Polymorphism Interaction Analysis (PIA), which are the two most popular methods for gene-gene interaction identification. More importantly, the identification results generated by using our genetic ensemble algorithm are highly complementary to those obtained by PIA and MDR. Experimental results from our simulation studies and real world data application also confirm the effectiveness of the proposed genetic ensemble algorithm, as well as the potential benefits of combining identification results from different algorithms.
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