Evidence map›Paper›PMID 22172045›Full record

ArticleBMC bioinformatics2011

Performance analysis of novel methods for detecting epistasis.

Junliang Shang, Junying Zhang, Yan Sun, Dan Liu, Daojun Ye, Yaling Yin

Abstract read
In one paragraph

Article in BMC bioinformatics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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  18. Detecting epistasis in human complex traits.Nature reviews. Genetics · 2014
    Review
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Junliang ShangSchool of Computer Science & Technology, Xidian University, Xi'an 710071, China. jlshang@mail.xidian.edu.cn
Junying Zhang
Yan Sun
Dan Liu
Daojun Ye
Yaling Yin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpistasis is recognized fundamentally important for understanding the mechanism of disease-causing genetic variation. Though many novel methods for detecting epistasis have been proposed, few studies focus on their comparison. Undertaking a comprehensive comparison study is an urgent task and a pathway of the methods to real applications.

resultsThis paper aims at a comparison study of epistasis detection methods through applying related software packages on datasets. For this purpose, we categorize methods according to their search strategies, and select five representative methods (TEAM, BOOST, SNPRuler, AntEpiSeeker and epiMODE) originating from different underlying techniques for comparison. The methods are tested on simulated datasets with different size, various epistasis models, and with/without noise. The types of noise include missing data, genotyping error and phenocopy. Performance is evaluated by detection power (three forms are introduced), robustness, sensitivity and computational complexity.

conclusionsNone of selected methods is perfect in all scenarios and each has its own merits and limitations. In terms of detection power, AntEpiSeeker performs best on detecting epistasis displaying marginal effects (eME) and BOOST performs best on identifying epistasis displaying no marginal effects (eNME). In terms of robustness, AntEpiSeeker is robust to all types of noise on eME models, BOOST is robust to genotyping error and phenocopy on eNME models, and SNPRuler is robust to phenocopy on eME models and missing data on eNME models. In terms of sensitivity, AntEpiSeeker is the winner on eME models and both SNPRuler and BOOST perform well on eNME models. In terms of computational complexity, BOOST is the fastest among the methods. In terms of overall performance, AntEpiSeeker and BOOST are recommended as the efficient and effective methods. This comparison study may provide guidelines for applying the methods and further clues for epistasis detection.

Indexed as

Epistasis, GeneticSoftwareDiseaseGenotypeHumansPolymorphism, Single Nucleotide

Identifiers

PMID22172045
PMCPMC3259123

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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.