Evidence map›Paper›PMID 31380425›Full record

ArticleBioMed research international2019

Multivariate Cluster-Based Multifactor Dimensionality Reduction to Identify Genetic Interactions for Multiple Quantitative Phenotypes.

Hyein Kim, Hoe-Bin Jeong, Hye-Young Jung, Taesung Park, Mira Park

Abstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Overview of frequent pattern mining.Genomics & informatics · 2022
    Article
  3. Article
  4. Article
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Hyein KimDepartment of Statistics, Korea University, Seoul,02841, Republic of Korea.ORCID https://orcid.org/0000-0001-8611-5703
Hoe-Bin JeongDepartment of Statistics, Korea University, Seoul,02841, Republic of Korea.
Hye-Young JungDepartment of Statistics, Seoul National University, Seoul, 08826, Republic of Korea.
Taesung ParkDepartment of Statistics, Seoul National University, Seoul, 08826, Republic of Korea.ORCID https://orcid.org/0000-0002-8294-590X
Mira ParkDepartment of Preventive Medicine, Eulji University, Daejeon, 34824, Republic of Korea.ORCID https://orcid.org/0000-0003-3827-9089

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To understand the pathophysiology of complex diseases, including hypertension, diabetes, and autism, deleterious phenotypes are unlikely due to the effects of single genes, but rather, gene-gene interactions (GGIs), which are widely analyzed by multifactor dimensionality reduction (MDR). Early MDR methods mainly focused on binary traits. More recently, several extensions of MDR have been developed for analyzing various traits such as quantitative traits and survival times. Newer technologies, such as genome-wide association studies (GWAS), have now been developed for assessing multiple traits, to simultaneously identify genetic variants associated with various pathological phenotypes. It has also been well demonstrated that analyzing multiple traits has several advantages over single trait analysis. While there remains a need to find GGIs for multiple traits, such studies have become more difficult, due to a lack of novel methods and software. Herein, we propose a novel multi-CMDR method, by combining fuzzy clustering and MDR, to find GGIs for multiple traits. Multi-CMDR showed similar power to existing methods, when phenotypes followed bivariate normal distributions, and showed better power than others for skewed distributions. The validity of multi-CMDR was confirmed by analyzing real-life Korean GWAS data.

Indexed as

AlgorithmsCluster AnalysisEpistasis, GeneticGenome-Wide Association StudyHumansMultifactor Dimensionality ReductionPolymorphism, Single NucleotideQuantitative Trait LociSoftware

Identifiers

PMID31380425
PMCPMC6657635

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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.