Evidence map›Paper›PMID 28361694›Full record

ArticleBMC genomics2017

An empirical fuzzy multifactor dimensionality reduction method for detecting gene-gene interactions.

Sangseob Leem, Taesung Park

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Life (Basel, Switzerland) · 2025
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  8. Relationship BetweenPharmacogenomics and personalized medicine · 2021
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  15. Review
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Sangseob LeemDepartment of Statistics, Seoul National University, Seoul, 08826, South Korea.
Taesung ParkDepartment of Statistics, Seoul National University, Seoul, 08826, South Korea. tspark@stats.snu.ac.kr.

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundDetection of gene-gene interaction (GGI) is a key challenge towards solving the problem of missing heritability in genetics. The multifactor dimensionality reduction (MDR) method has been widely studied for detecting GGIs. MDR reduces the dimensionality of multi-factor by means of binary classification into high-risk (H) or low-risk (L) groups. Unfortunately, this simple binary classification does not reflect the uncertainty of H/L classification. Thus, we proposed Fuzzy MDR to overcome limitations of binary classification by introducing the degree of membership of two fuzzy sets H/L. While Fuzzy MDR demonstrated higher power than that of MDR, its performance is highly dependent on the several tuning parameters. In real applications, it is not easy to choose appropriate tuning parameter values.

resultIn this work, we propose an empirical fuzzy MDR (EF-MDR) which does not require specifying tuning parameters values. Here, we propose an empirical approach to estimating the membership degree that can be directly estimated from the data. In EF-MDR, the membership degree is estimated by the maximum likelihood estimator of the proportion of cases(controls) in each genotype combination. We also show that the balanced accuracy measure derived from this new membership function is a linear function of the standard chi-square statistics. This relationship allows us to perform the standard significance test using p-values in the MDR framework without permutation. Through two simulation studies, the power of the proposed EF-MDR is shown to be higher than those of MDR and Fuzzy MDR. We illustrate the proposed EF-MDR by analyzing Crohn's disease (CD) and bipolar disorder (BD) in the Wellcome Trust Case Control Consortium (WTCCC) dataset.

conclusionWe propose an empirical Fuzzy MDR for detecting GGI using the maximum likelihood of the proportion of cases(controls) as the membership degree of the genotype combination. The program written in R for EF-MDR is available at http://statgen.snu.ac.kr/software/EF-MDR .

Indexed as

Epistasis, GeneticModels, GeneticPolymorphism, Single NucleotideBipolar DisorderCrohn DiseaseDatasets as TopicFuzzy LogicGenotypeHumansInternetMultifactor Dimensionality ReductionSoftwareFuzzy MDRFuzzy set theoryGene-gene interactionMultifactor dimensionality reduction

Identifiers

PMID28361694
PMCPMC5374597

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LicenceCC BY
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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.